Radiochemical and chemical constituents in water from selected wells and springs from the southern boundary of the Idaho National Laboratory to the Hagerman Area, Idaho, 2003

Science.gov (United States)

Rattray, Gordon W.; Wehnke, Amy J.; Hall, L. Flint; Campbell, Linford J.

2005-01-01

The U.S. Geological Survey and the Idaho Department of Water Resources, in cooperation with the U.S. Department of Energy, sampled water from 14 sites as part of an ongoing study to monitor the water quality of the eastern Snake River Plain aquifer between the southern boundary of the Idaho National Laboratory (INL) and the Burley-Twin Falls-Hagerman area. The State of Idaho, Department of Environmental Quality, Division of INL Oversight and Radiation Control cosampled with the U.S. Geological Survey and the Idaho Department of Water Resources and their analytical results are included in this report. The samples were collected from four domestic wells, two dairy wells, two springs, four irrigation wells, one observation well, and one stock well and analyzed for selected radiochemical and chemical constituents. Two quality-assurance samples, sequential replicates, also were collected and analyzed. None of the concentrations of radiochemical or organic-chemical constituents exceeded the maximum contaminant levels for drinking water established by the U.S. Environmental Protection Agency. However, the concentration of one inorganic-chemical constituent, nitrate (as nitrogen), in water from site MV-43 was 20 milligrams per liter which exceeded the maximum contaminant level for that constituent. Of the radiochemical and chemical concentrations analyzed for in the replicate-sample pairs, 267 of the 270 pairs (with 95 percent confidence) were statistically equivalent.

Radionuclides, inorganic constituents, organic compounds, and bacteria in water from selected wells and springs from the southern boundary of the Idaho National Engineering Laboratory to the Hagerman Area, Idaho, 1990

International Nuclear Information System (INIS)

Bartholomay, R.C.; Edwards, D.D.; Campbell, L.J.

1992-03-01

The US Geological Survey and the Idaho Department of Water Resources, in response to a request from the US Department of Energy, sampled 19 sites as part of a long-term project to monitor water quality of the Snake River Plain aquifer from the southern boundary of the Idaho National Engineering Laboratory to the Hagerman area. Water samples were collected and analyzed for manmade pollutants and naturally occurring constituents. The samples were collected from seven irrigation wells, five domestic wells, two springs, one stock well, two dairy wells, one observation well, and one commercial well. Two quality assurance samples also were collected and analyzed. The water samples were analyzed for selected radionuclides, inorganic constituents, organic compounds, and bacteria. None of the radionuclides, inorganic constituents, or organic compounds exceeded the established maximum contaminant levels for drinking water. Most of the radionuclide and inorganic constituent concentrations exceeded their respective reporting levels. All samples analyzed for surfactants and dissolved organic carbon had concentrations that exceeded their reporting level. Toluene concentrations exceeded the reporting level in one water sample. Two samples contained fecal coliform bacteria counts that exceeded established maximum contaminant levels for drinking water

Concentration and fractionation of hydrophobic organic acid constituents from natural waters by liquid chromatography

Science.gov (United States)

Thurman, E.M.; Malcolm, R.L.

1979-01-01

A scheme is presented which used adsorption chromatography with pH gradient elution and size-exclusion chromatography to concentrate and separate hydrophobic organic acids from water. A review of chromatographic processes involved in the flow scheme is also presented. Organic analytes which appear in each aqueous fraction are quantified by dissolved organic carbon analysis. Hydrophobic organic acids in a water sample are concentrated on a porous acrylic resin. These acids usually constitute approximately 30-50 percent of the dissolved organic carbon in an unpolluted water sample and are eluted with an aqueous eluent (dilute base). The concentrate is then passed through a column of polyacryloylmorpholine gel, which separates the acids into high- and low-molecular-weight fractions. The high- and low-molecular-weight eluates are reconcentrated by adsorption chromatography, then are eluted with a pH gradient into strong acids (predominately carboxylic acids) and weak acids (predominately phenolic compounds). For standard compounds and samples of unpolluted waters, the scheme fractionates humic substances into strong and weak acid fractions that are separated from the low molecular weight acids. A new method utilizing conductivity is also presented to estimate the acidic components in the methanol fraction.

Regression model development and computational procedures to support estimation of real-time concentrations and loads of selected constituents in two tributaries to Lake Houston near Houston, Texas, 2005-9

Science.gov (United States)

Lee, Michael T.; Asquith, William H.; Oden, Timothy D.

2012-01-01

In December 2005, the U.S. Geological Survey (USGS), in cooperation with the City of Houston, Texas, began collecting discrete water-quality samples for nutrients, total organic carbon, bacteria (Escherichia coli and total coliform), atrazine, and suspended sediment at two USGS streamflow-gaging stations that represent watersheds contributing to Lake Houston (08068500 Spring Creek near Spring, Tex., and 08070200 East Fork San Jacinto River near New Caney, Tex.). Data from the discrete water-quality samples collected during 2005–9, in conjunction with continuously monitored real-time data that included streamflow and other physical water-quality properties (specific conductance, pH, water temperature, turbidity, and dissolved oxygen), were used to develop regression models for the estimation of concentrations of water-quality constituents of substantial source watersheds to Lake Houston. The potential explanatory variables included discharge (streamflow), specific conductance, pH, water temperature, turbidity, dissolved oxygen, and time (to account for seasonal variations inherent in some water-quality data). The response variables (the selected constituents) at each site were nitrite plus nitrate nitrogen, total phosphorus, total organic carbon, E. coli, atrazine, and suspended sediment. The explanatory variables provide easily measured quantities to serve as potential surrogate variables to estimate concentrations of the selected constituents through statistical regression. Statistical regression also facilitates accompanying estimates of uncertainty in the form of prediction intervals. Each regression model potentially can be used to estimate concentrations of a given constituent in real time. Among other regression diagnostics, the diagnostics used as indicators of general model reliability and reported herein include the adjusted R-squared, the residual standard error, residual plots, and p-values. Adjusted R-squared values for the Spring Creek models ranged

Continuous real-time water-quality monitoring and regression analysis to compute constituent concentrations and loads in the North Fork Ninnescah River upstream from Cheney Reservoir, south-central Kansas, 1999–2012

Science.gov (United States)

Stone, Mandy L.; Graham, Jennifer L.; Gatotho, Jackline W.

2013-01-01

Cheney Reservoir, located in south-central Kansas, is the primary water supply for the city of Wichita. The U.S. Geological Survey has operated a continuous real-time water-quality monitoring station since 1998 on the North Fork Ninnescah River, the main source of inflow to Cheney Reservoir. Continuously measured water-quality physical properties include streamflow, specific conductance, pH, water temperature, dissolved oxygen, and turbidity. Discrete water-quality samples were collected during 1999 through 2009 and analyzed for sediment, nutrients, bacteria, and other water-quality constituents. Regression models were developed to establish relations between discretely sampled constituent concentrations and continuously measured physical properties to compute concentrations of those constituents of interest that are not easily measured in real time because of limitations in sensor technology and fiscal constraints. Regression models were published in 2006 that were based on data collected during 1997 through 2003. This report updates those models using discrete and continuous data collected during January 1999 through December 2009. Models also were developed for four new constituents, including additional nutrient species and indicator bacteria. In addition, a conversion factor of 0.68 was established to convert the Yellow Springs Instruments (YSI) model 6026 turbidity sensor measurements to the newer YSI model 6136 sensor at the North Ninnescah River upstream from Cheney Reservoir site. Newly developed models and 14 years of hourly continuously measured data were used to calculate selected constituent concentrations and loads during January 1999 through December 2012. The water-quality information in this report is important to the city of Wichita because it allows the concentrations of many potential pollutants of interest to Cheney Reservoir, including nutrients and sediment, to be estimated in real time and characterized over conditions and time scales that

Characterization of Formation Water Constituents and the Effect of ...

African Journals Online (AJOL)

Michael Horsfall

ABSTRACT: The research work examined the constituents of formation water and fresh water dilution effects from a land location in the Niger Delta Area of Nigeria. Some selected physicochemical and microbiological analyses were determined at ambient temperature (82oF) and formation temperature (185oF). Analysis of ...

Distribution of radioactive constituents in river waters

International Nuclear Information System (INIS)

Herranz, M.; Elejalde, C.; Legarda, F.; Romero, F.

1994-01-01

For a research project on the distribution and evaluation of natural and artificial radioactive constituents in ecological segments of Biscay (northeast spain), the amounts of nuclides present in the main river waters were measured. Radioactive procedures include i) total alpha and beta indexes with a gas flow detector, dry residues near to 2 and 10 mg/ cm sup 2, respectively and counting periods of 1000 mn, ii) gamma emitters with a low level gamma spectrometer (Ge-HP detector + 8000 channels analyser) using the dry residue from 8 litres and a counting period of 4 days and iii) statistical treatment of data at 95% confidence.In this paper, ten water samples from the nervion river basin are included. Physical and chemical parameters of samples were also determined by standard procedures, because there is a sharp change in the composition of this river in the first part of the course. Radioactive constituents were identified as follows: a sample has a detectable alpha index, all samples contains beta emitters with a high variability, natural nuclides from uranium and thorium families were detected in some cases. A parallel behaviour is found between samples where K-40 and Cs-137 were found. The paper tries at last to find relations among chemical and radioactive constituents by the application of multivariate statistical methods, specially for the case of Cs-137, the only artificial nuclide identified in this work. 1 tab., 2 figs., 5 refs. (author)

Model documentation for relations between continuous real-time and discrete water-quality constituents in Cheney Reservoir near Cheney, Kansas, 2001--2009

Science.gov (United States)

Stone, Mandy L.; Graham, Jennifer L.; Gatotho, Jackline W.

2013-01-01

Cheney Reservoir, located in south-central Kansas, is one of the primary water supplies for the city of Wichita, Kansas. The U.S. Geological Survey has operated a continuous real-time water-quality monitoring station in Cheney Reservoir since 2001; continuously measured physicochemical properties include specific conductance, pH, water temperature, dissolved oxygen, turbidity, fluorescence (wavelength range 650 to 700 nanometers; estimate of total chlorophyll), and reservoir elevation. Discrete water-quality samples were collected during 2001 through 2009 and analyzed for sediment, nutrients, taste-and-odor compounds, cyanotoxins, phytoplankton community composition, actinomycetes bacteria, and other water-quality measures. Regression models were developed to establish relations between discretely sampled constituent concentrations and continuously measured physicochemical properties to compute concentrations of constituents that are not easily measured in real time. The water-quality information in this report is important to the city of Wichita because it allows quantification and characterization of potential constituents of concern in Cheney Reservoir. This report updates linear regression models published in 2006 that were based on data collected during 2001 through 2003. The update uses discrete and continuous data collected during May 2001 through December 2009. Updated models to compute dissolved solids, sodium, chloride, and suspended solids were similar to previously published models. However, several other updated models changed substantially from previously published models. In addition to updating relations that were previously developed, models also were developed for four new constituents, including magnesium, dissolved phosphorus, actinomycetes bacteria, and the cyanotoxin microcystin. In addition, a conversion factor of 0.74 was established to convert the Yellow Springs Instruments (YSI) model 6026 turbidity sensor measurements to the newer YSI

Radionuclides, stable isotopes, inorganic constituents, and organic compounds in water from selected wells and springs from the southern boundary of the Idaho National Engineering Laboratory to the Hagerman Area, Idaho, 1995

International Nuclear Information System (INIS)

Bartholomay, R.C.; Williams, L.M.; Campbell, L.J.

1996-09-01

The US Geological Survey and the Idaho Department of Water Resources, in cooperation with the US Department of Energy, sampled 17 sites as part of a long-term project to monitor water quality of the Snake River Plain aquifer from the southern boundary of the Idaho National Engineering Laboratory to the Hagerman area. Water samples were collected and analyzed for selected radionuclides, stable isotopes, inorganic constituents, and organic compounds. The samples were collected from 11 irrigation wells, 2 domestic wells, 2 stock wells, 1 spring, and 1 public-supply well. Two quality assurance samples also were collected and analyzed. None of the radionuclide, inorganic constituents, or organic compound concentrations exceeded the established maximum contaminant levels for drinking water. Many of the radionuclide and inorganic constituent concentrations were greater than their respective reporting levels. All samples analyzed for dissolved organic carbon had concentrations that were greater than the minimum reporting level

Streamflow, water quality, and constituent loads and yields, Scituate Reservoir drainage area, Rhode Island, water year 2013

Science.gov (United States)

Smith, Kirk P.

2015-01-01

Streamflow and concentrations of sodium and chloride estimated from records of specific conductance were used to calculate loads of sodium and chloride during water year (WY) 2013 (October 1, 2012, through September 30, 2013) for tributaries to the Scituate Reservoir, Rhode Island. Streamflow and water-quality data used in the study were collected by the U.S. Geological Survey (USGS) or the Providence Water Supply Board (PWSB) in the cooperative study. Streamflow was measured or estimated by the USGS following standard methods at 23 streamgages; 14 of these streamgages are equipped with instrumentation capable of continuously monitoring water level, specific conductance, and water temperature. Water-quality samples were collected at 37 sampling stations by the PWSB and at 14 continuous-record streamgages by the USGS during WY 2013 as part of a long-term sampling program; all stations are in the Scituate Reservoir drainage area. Water-quality data collected by the PWSB are summarized by using values of central tendency and are used, in combination with measured (or estimated) streamflows, to calculate loads and yields (loads per unit area) of selected water-quality constituents for WY 2013.

Multi-Scale Analysis for Characterizing Near-Field Constituent Concentrations in the Context of a Macro-Scale Semi-Lagrangian Numerical Model

Science.gov (United States)

Yearsley, J. R.

2017-12-01

The semi-Lagrangian numerical scheme employed by RBM, a model for simulating time-dependent, one-dimensional water quality constituents in advection-dominated rivers, is highly scalable both in time and space. Although the model has been used at length scales of 150 meters and time scales of three hours, the majority of applications have been at length scales of 1/16th degree latitude/longitude (about 5 km) or greater and time scales of one day. Applications of the method at these scales has proven successful for characterizing the impacts of climate change on water temperatures in global rivers and on the vulnerability of thermoelectric power plants to changes in cooling water temperatures in large river systems. However, local effects can be very important in terms of ecosystem impacts, particularly in the case of developing mixing zones for wastewater discharges with pollutant loadings limited by regulations imposed by the Federal Water Pollution Control Act (FWPCA). Mixing zone analyses have usually been decoupled from large-scale watershed influences by developing scenarios that represent critical scenarios for external processes associated with streamflow and weather conditions . By taking advantage of the particle-tracking characteristics of the numerical scheme, RBM can provide results at any point in time within the model domain. We develop a proof of concept for locations in the river network where local impacts such as mixing zones may be important. Simulated results from the semi-Lagrangian numerical scheme are treated as input to a finite difference model of the two-dimensional diffusion equation for water quality constituents such as water temperature or toxic substances. Simulations will provide time-dependent, two-dimensional constituent concentration in the near-field in response to long-term basin-wide processes. These results could provide decision support to water quality managers for evaluating mixing zone characteristics.

Inversion of In Situ Light Absorption and Attenuation Measurements to Estimate Constituent Concentrations in Optically Complex Shelf Seas

Science.gov (United States)

Ramírez-Pérez, M.; Twardowski, M.; Trees, C.; Piera, J.; McKee, D.

2018-01-01

A deconvolution approach is presented to use spectral light absorption and attenuation data to estimate the concentration of the major nonwater compounds in complex shelf sea waters. The inversion procedure requires knowledge of local material-specific inherent optical properties (SIOPs) which are determined from natural samples using a bio-optical model that differentiates between Case I and Case II waters and uses least squares linear regression analysis to provide optimal SIOP values. A synthetic data set is used to demonstrate that the approach is fundamentally consistent and to test the sensitivity to injection of controlled levels of artificial noise into the input data. Self-consistency of the approach is further demonstrated by application to field data collected in the Ligurian Sea, with chlorophyll (Chl), the nonbiogenic component of total suspended solids (TSSnd), and colored dissolved organic material (CDOM) retrieved with RMSE of 0.61 mg m-3, 0.35 g m-3, and 0.02 m-1, respectively. The utility of the approach is finally demonstrated by application to depth profiles of in situ absorption and attenuation data resulting in profiles of optically significant constituents with associated error bar estimates. The advantages of this procedure lie in the simple input requirements, the avoidance of error amplification, full exploitation of the available spectral information from both absorption and attenuation channels, and the reasonably successful retrieval of constituent concentrations in an optically complex shelf sea.

An update of hydrologic conditions and distribution of selected constituents in water, Snake River Plain aquifer, Idaho National Laboratory, Idaho, Emphasis 1999-2001

Science.gov (United States)

Davis, Linda C.

2006-01-01

Radiochemical and chemical wastewater discharged since 1952 to infiltration ponds, evaporation ponds, and disposal wells at the Idaho National Laboratory (INL) has affected water quality in the Snake River Plain aquifer underlying the INL. The U.S. Geological Survey (USGS), in cooperation with the U.S. Department of Energy, maintains ground-water monitoring networks at the INL to determine hydrologic trends, and to delineate the movement of radiochemical and chemical wastes in the aquifer. This report presents an analysis of water-level and water-quality data collected from wells in the USGS ground-water monitoring networks during 1999-2001. Water in the Snake River Plain aquifer moves principally through fractures and interflow zones in basalt, generally flows southwestward, and eventually discharges at springs along the Snake River. The aquifer is recharged principally from infiltration of irrigation water, infiltration of streamflow, ground-water inflow from adjoining mountain drainage basins, and infiltration of precipitation. Water levels in wells rose in the northern and west-central parts of the INL by 1 to 3 feet, and declined in the southwestern parts of the INL by up to 4 feet during 1999-2001. Detectable concentrations of radiochemical constituents in water samples from wells in the Snake River Plain aquifer at the INL generally decreased or remained constant during 1999-2001. Decreases in concentrations were attributed to decreased rates of radioactive-waste disposal, radioactive decay, changes in waste-disposal methods, and dilution from recharge. Tritium concentrations in water samples decreased as much as 8.3 picocuries per milliliter (pCi/mL) during 1999-2001, ranging from 0.43?0.14 to 13.6?0.6 pCi/mL in October 2001. Tritium concentrations in five wells near the Idaho Nuclear Technology and Engineering Center (INTEC) increased a few picocuries per milliliter from October 2000 to October 2001. Strontium-90 concentrations decreased or remained

Water quality of storm runoff and comparison of procedures for estimating storm-runoff loads, volume, event-mean concentrations, and the mean load for a storm for selected properties and constituents for Colorado Springs, southeastern Colorado, 1992

Science.gov (United States)

Von Guerard, Paul; Weiss, W.B.

1995-01-01

The U.S. Environmental Protection Agency requires that municipalities that have a population of 100,000 or greater obtain National Pollutant Discharge Elimination System permits to characterize the quality of their storm runoff. In 1992, the U.S. Geological Survey, in cooperation with the Colorado Springs City Engineering Division, began a study to characterize the water quality of storm runoff and to evaluate procedures for the estimation of storm-runoff loads, volume and event-mean concentrations for selected properties and constituents. Precipitation, streamflow, and water-quality data were collected during 1992 at five sites in Colorado Springs. Thirty-five samples were collected, seven at each of the five sites. At each site, three samples were collected for permitting purposes; two of the samples were collected during rainfall runoff, and one sample was collected during snowmelt runoff. Four additional samples were collected at each site to obtain a large enough sample size to estimate storm-runoff loads, volume, and event-mean concentrations for selected properties and constituents using linear-regression procedures developed using data from the Nationwide Urban Runoff Program (NURP). Storm-water samples were analyzed for as many as 186 properties and constituents. The constituents measured include total-recoverable metals, vola-tile-organic compounds, acid-base/neutral organic compounds, and pesticides. Storm runoff sampled had large concentrations of chemical oxygen demand and 5-day biochemical oxygen demand. Chemical oxygen demand ranged from 100 to 830 milligrams per liter, and 5.-day biochemical oxygen demand ranged from 14 to 260 milligrams per liter. Total-organic carbon concentrations ranged from 18 to 240 milligrams per liter. The total-recoverable metals lead and zinc had the largest concentrations of the total-recoverable metals analyzed. Concentrations of lead ranged from 23 to 350 micrograms per liter, and concentrations of zinc ranged from 110

Interlaboratory quality assurance studies: Their use in certifying natural waters for major constituents and trace elements

International Nuclear Information System (INIS)

Alkema, H.; Simser, J.; Hjelm, L.

1998-01-01

Environmental programs throughout North America have demonstrated a strong awareness of the usefulness of interlaboratory studies for disclosing the quality of analytical results. The Ecosystem Interlaboratory Quality Assurance Program offered by the National Water Research Institute has a wide participation base of laboratories. Many of these laboratories are accredited and employ a number of recognized analytical methods. The interlaboratory study data archives contain a wealth of data for natural surface and rain waters from across the continent. These archives have proven to be a reliable means of characterizing a variety of constituents. Data assessments from these studies accurately identify the variability of data and the presence of any outliers. Repeated use of selected samples in a regular QA program confirms their stability. Time charts and statistical techniques are used to illustrate this stability and yield the precision of pooled analyses. The availability of archived data from interlaboratory studies has enabled the Institute to develop and certify natural water and trace element standards. The natural water CRM, ION-911, has been available for several years. Its historical aspects are discussed as well as the processes leading to the certification of TMRain-95, a soft water standard certifying 22 trace elements. This paper focuses on the use of select laboratories in round-robin evaluations to provide accurate values for constituent concentrations. Natural water and fortified trace element CRMs meet a recognized need in the generation of accurate data for environmental programs. (orig.)

Chemical and Radiochemical Constituents in Water from Wells in the Vicinity of the Naval Reactors Facility, Idaho National Engineering and Environmental Laboratory, Idaho, 1997-98

Energy Technology Data Exchange (ETDEWEB)

R. C. Bartholomay; L. L. Knobel; B. J. Tucker; B. V. Twining (USGS)

2000-06-01

The US Geological Survey, in response to a request from the U.S Department of Energy's Pittsburgh Naval Reactors Office, Idaho Branch Office, sampled water from 13 wells during 1997-98 as part of a long-term project to monitor water quality of the Snake River Plain aquifer in the vicinity of the Naval Reactors Facility, Idaho National Engineering and Environmental Laboratory, Idaho. Water samples were analyzed for naturally occurring constituents and man-made contaminants. A total of 91 samples were collected from the 13 monitoring wells. The routine samples contained detectable concentrations of total cations and dissolved anions, and nitrite plus nitrate as nitrogen. Most of the samples also had detectable concentrations of gross alpha- and gross beta-particle radioactivity and tritium. Fourteen quality-assurance samples were also collected and analyzed; seven were field-blank samples, and seven were replicate samples. Most of the field blank samples contained less than detectable concentrations of target constituents; however some blank samples did contain detectable concentrations of calcium, magnesium, barium, copper, manganese, nickel, zinc, nitrite plus nitrate, total organic halogens, tritium, and selected volatile organic compounds.

Radionuclides, stable isotopes, inorganic constituents, and organic compounds in water from selected wells and springs from the southern boundary of the Idaho National Engineering Laboratory to the Hagerman area, Idaho, 1993

Science.gov (United States)

Bartholomay, Roy C.; Edwards, Daniel D.; Campbell, Linford J.

1994-01-01

The U.S. Geological Survey and the Idaho Department of Water Resources, in response to a request from the U.S. Department of Energy, sampled 19 sites as part of a long-term project to monitor water quality of the Snake River Plain aquifer from the southern boundary of the Idaho National Engineering Laboratory to the Hagerman area. Water samples were collected and analyzed for selected radionuclides, stable isotopes, inorganic constituents, and organic compounds. The samples were collected from seven irrigation wells, four domestic wells, two springs, one stock well, three dairy wells, one observation well, and one commercial well. Two quality assurance samples also were collected and analyzed. None of the radionuclides, inorganic constituents, or organic compounds exceeded the established maximum contaminant levels for drinking water. Most of the radionuclide and inorganic constituent concen- trations exceeded their respective laboratory reporting levels. All samples analyzed for surfactants and dissolved organic carbon had concentrations that exceeded their reporting level. Ethylbenzene concentrations exceeded the reporting level in one water sample.

Concentrations of polycyclic aromatic hydrocarbons and inorganic constituents in ambient surface soils, Chicago, Illinois: 2001-2002

Science.gov (United States)

Kay, R.T.; Arnold, T.L.; Cannon, W.F.; Graham, D.

2008-01-01

Samples of ambient surface soils were collected from 56 locations in Chicago, Illinois, using stratified random sampling techniques and analyzed for polycyclic aromatic hydrocarbon (PAH) compounds and inorganic constituents. PAHs appear to be derived primarily from combustion of fossil fuels and may be affected by proximity to industrial operations, but do not appear to be substantially affected by the organic carbon content of the soil, proximity to nonindustrial land uses, or proximity to a roadway. Atmospheric settling of particulate matter appears to be an important mechanism for the placement of PAH compounds into soils. Concentrations of most inorganic constituents are affected primarily by soil-forming processes. Concentrations of lead, arsenic, mercury, calcium, magnesium, phosphorus, copper, molybdenum, zinc, and selenium are elevated in ambient surface soils in Chicago in comparison to the surrounding area, indicating anthropogenic sources for these elements in Chicago soils. Concentrations of calcium and magnesium in Chicago soils appear to reflect the influence of the carbonate bedrock parent material on the chemical composition of the soil, although the effects of concrete and road fill cannot be discounted. Concentrations of inorganic constituents appear to be largely unaffected by the type of nearby land use. Copyright ?? Taylor & Francis Group, LLC.

Variations in statewide water quality of New Jersey streams, water years 1998-2009

Science.gov (United States)

Heckathorn, Heather A.; Deetz, Anna C.

2012-01-01

Statistical analyses were conducted for six water-quality constituents measured at 371 surface-water-quality stations during water years 1998-2009 to determine changes in concentrations over time. This study examined year-round concentrations of total dissolved solids, dissolved nitrite plus nitrate, dissolved phosphorus, total phosphorus, and total nitrogen; concentrations of dissolved chloride were measured only from January to March. All the water-quality data analyzed were collected by the New Jersey Department of Environmental Protection and the U.S. Geological Survey as part of the cooperative Ambient Surface-Water-Quality Monitoring Network. Stations were divided into groups according to the 1-year or 2-year period that the stations were part of the Ambient Surface-Water-Quality Monitoring Network. Data were obtained from the eight groups of Statewide Status stations for water years 1998, 1999, 2000, 2001-02, 2003-04, 2005-06, 2007-08, and 2009. The data from each group were compared to the data from each of the other groups and to baseline data obtained from Background stations unaffected by human activity that were sampled during the same time periods. The Kruskal-Wallis test was used to determine whether median concentrations of a selected water-quality constituent measured in a particular 1-year or 2-year group were different from those measured in other 1-year or 2-year groups. If the median concentrations were found to differ among years or groups of years, then Tukey's multiple comparison test on ranks was used to identify those years with different or equal concentrations of water-quality constituents. A significance level of 0.05 was selected to indicate significant changes in median concentrations of water-quality constituents. More variations in the median concentrations of water-quality constituents were observed at Statewide Status stations (randomly chosen stations scattered throughout the State of New Jersey) than at Background stations

Radiochemical and Chemical Constituents in Water from Selected Wells and Springs from the Southern Boundary of the Idaho National Engineering and Environmental Laboratory to the Hagerman Area, Idaho, 1997

Energy Technology Data Exchange (ETDEWEB)

R. C. Bartholomay (USGS); L. M. Williams (USGS); L. J. Campbell (Idaho Department of Water Resources)

1998-12-01

The U.S. Geological Survey and the Idaho Department of Water Resources, in cooperation with the U.S. Department of Energy, sampled 18 sites as part of the fourth round of a long-term project to monitor water quality of the Snake River Plain aquifer from the southern boundary of the Idaho National Engineering and Environmental Laboratory to the Hagerman area. Water samples were collected and analyzed for selected radiochemical and chemical constituents. The samples were collected from seven domestic wells, six irrigation wells, two springs, one dairy well, one observation well, and one stock well. Two quality-assurance samples also were collected and analyzed. None of the radiochemical or chemical constituents exceeded the established maximum contaminant levels for drinking water. Many of the radionuclide- and inorganic-constituent concentrations were greater than their respective reporting levels.

Hydrologic conditions and distribution of selected radiochemical and chemical constituents in water, Snake River Plain aquifer, Idaho National Engineering Laboratory, Idaho, 1989 through 1991

International Nuclear Information System (INIS)

Bartholomay, R.C.; Orr, B.R.; Liszewski, M.J.; Jensen, R.G.

1995-08-01

Radiochemical and chemical wastewater discharged since 1952 to infiltration ponds and disposal wells at the Idaho National Engineering Laboratory (INEL) has affected water quality in the Snake River Plain aquifer. The U.S. Geological Survey, in cooperation with the U.S. Department of Energy, maintains a continuous monitoring network at the INEL to determine hydrologic trends and to delineate the movement of radiochemical and chemical wastes in the aquifer. This report presents an analysis of water-level and water-quality data collected from the Snake River Plain aquifer during 1989-91. Water in the eastern Snake River Plain aquifer moves principally through fractures and interflow zones in basalt, generally flows southwestward, and eventually discharges at springs along the Snake River. The aquifer is recharged principally from irrigation water, infiltration of streamflow, and ground-water inflow from adjoining mountain drainage basins. Water levels in wells throughout the INEL generally declined during 1989-91 due to drought. Detectable concentrations of radiochemical constituents in water samples from wells in the Snake River Plain aquifer at the INEL decreased or remained constant during 1989-91. Decreased concentrations are attributed to reduced rates of radioactive-waste disposal, sorption processes, radioactive decay, and changes in waste-disposal practices. Detectable concentrations of chemical constituents in water from the Snake River Plain aquifer at the INEL were variable during 1989-91. Sodium and chloride concentrations in the southern part of the INEL increased slightly during 1989-91 because of increased waste-disposal rates and a lack of recharge from the Big Lost River. Plumes of 1,1,1-trichloroethane have developed near the Idaho Chemical Processing Plant and the Radioactive Waste Management Complex as a result of waste disposal practices

Streamflow, Water Quality, and Constituent Loads and Yields, Scituate Reservoir Drainage Area, Rhode Island, Water Year 2006

Science.gov (United States)

Breault, Robert F.; Campbell, Jean P.

2010-01-01

Streamflow and water-quality data were collected by the U.S. Geological Survey (USGS) or the Providence Water Supply Board, Rhode Island's largest drinking-water supplier. Streamflow was measured or estimated by the USGS following standard methods at 23 streamgage stations; 10 of these stations were also equipped with instrumentation capable of continuously monitoring specific conductance. Streamflow and concentrations of sodium and chloride estimated from records of specific conductance were used to calculate instantaneous (15-minute) loads of sodium and chloride during water year (WY) 2006 (October 1, 2005, to September 30, 2006). Water-quality samples were also collected at 37 sampling stations in the Scituate Reservoir drainage area by the Providence Water Supply Board during WY 2006 as part of a long-term sampling program. Water-quality data are summarized by using values of central tendency and are used, in combination with measured (or estimated) streamflows, to calculate loads and yields (loads per unit area) of selected water-quality constituents for WY 2006. The largest tributary to the reservoir (the Ponaganset River, which was monitored by the USGS) contributed about 42 cubic feet per second (ft3/s) to the reservoir during WY 2006. For the same time period, annual mean streamflows1 measured (or estimated) for the other monitoring stations in this study ranged from about 0.60 to 26 ft3/s. Together, tributary streams (equipped with instrumentation capable of continuously monitoring specific conductance) transported about 1,600,000 kilograms (kg) of sodium and 2,500,000 kg of chloride to the Scituate Reservoir during WY 2006; sodium and chloride yields for the tributaries ranged from 15,000 to 100,000 kilograms per square mile (kg/mi2) and from 22,000 to 180,000 kg/mi2, respectively. At the stations where water-quality samples were collected by the Providence Water Supply Board, the median of the median chloride concentrations was 24.6 milligrams per liter

Streamflow, water quality, and constituent loads and yields, Scituate Reservoir drainage area, Rhode Island, water year 2003

Science.gov (United States)

Breault, Robert F.; Campbell, Jean P.

2010-01-01

Streamflow and water-quality data were collected by the U.S. Geological Survey (USGS) or the Providence Water Supply Board, Rhode Island's largest drinking-water supplier. Streamflow was measured or estimated by the USGS following standard methods at 23 streamgage stations; 10 of these stations were also equipped with instrumentation capable of continuously monitoring specific conductance. Streamflow and concentrations of sodium and chloride estimated from records of specific conductance were used to calculate instantaneous (15-minute) loads of sodium and chloride during water year (WY) 2003 (October 1, 2002, to September 30, 2003). Water-quality samples were also collected at 37 sampling stations in the Scituate Reservoir drainage area by the Providence Water Supply Board during WY 2003 as part of a long-term sampling program. Water-quality data are summarized by using values of central tendency and are used, in combination with measured (or estimated) streamflows, to calculate loads and yields (loads per unit area) of selected water-quality constituents for WY 2003. The largest tributary to the reservoir (the Ponaganset River, which was monitored by the USGS) contributed about 31 cubic feet per second (ft3/s) to the reservoir during WY 2003. For the same time period, annual mean streamflows1 measured (or estimated) for the other monitoring stations in this study ranged from about 0.44 to 20 ft3/s. Together, tributary streams (equipped with instrumentation capable of continuously monitoring specific conductance) transported about 1,200,000 kilograms (kg) of sodium and 1,900,000 kg of chloride to the Scituate Reservoir during WY 2003; sodium and chloride yields for the tributaries ranged from 10,000 to 61,000 kilograms per square mile (kg/mi2) and from 15,000 to 100,000 kg/mi2, respectively. At the stations where water-quality samples were collected by the Providence Water Supply Board, the median of the median chloride concentrations was 21.3 milligrams per liter

Streamflow, Water Quality, and Constituent Loads and Yields, Scituate Reservoir Drainage Area, Rhode Island, Water Year 2005

Science.gov (United States)

Breault, Robert F.; Campbell, Jean P.

2010-01-01

Streamflow and water-quality data were collected by the U.S. Geological Survey (USGS) or the Providence Water Supply Board, Rhode Island’s largest drinking-water supplier. Streamflow was measured or estimated by the USGS following standard methods at 23 streamgage stations; 10 of these stations were also equipped with instrumentation capable of continuously monitoring specific conductance. Streamflow and concentrations of sodium and chloride estimated from records of specific conductance were used to calculate instantaneous (15-minute) loads of sodium and chloride during water year (WY) 2005 (October 1, 2004, to September 30, 2005). Water-quality samples were also collected at 37 sampling stations in the Scituate Reservoir drainage area by the Providence Water Supply Board during WY 2005 as part of a long-term sampling program. Water-quality data are summarized by using values of central tendency and are used, in combination with measured (or estimated) streamflows, to calculate loads and yields (loads per unit area) of selected water-quality constituents for WY 2005. The largest tributary to the reservoir (the Ponaganset River, which was monitored by the USGS) contributed about 30 cubic feet per second (ft3/s) to the reservoir during WY 2005. For the same time period, annual mean streamflows1 measured (or estimated) for the other monitoring stations in this study ranged from about 0.42 to 19 ft3/s. Together, tributary streams (equipped with instrumentation capable of continuously monitoring specific conductance) transported about 1,300,000 kilograms (kg) of sodium and 2,000,000 kg of chloride to the Scituate Reservoir during WY 2005; sodium and chloride yields for the tributaries ranged from 13,000 to 77,000 kilograms per square mile (kg/mi2) and from 19,000 to 130,000 kg/mi2, respectively. At the stations where water-quality samples were collected by the Providence Water Supply Board, the median of the median chloride concentrations was 25.3 milligrams per

Streamflow, water quality, and constituent loads and yields, Scituate Reservoir drainage area, Rhode Island, water year 2004

Science.gov (United States)

Breault, Robert F.; Campbell, Jean P.

2010-01-01

Streamflow and water-quality data were collected by the U.S. Geological Survey (USGS) or the Providence Water Supply Board, Rhode Island's largest drinking-water supplier. Streamflow was measured or estimated by the USGS following standard methods at 23 streamgage stations; 10 of these stations were also equipped with instrumentation capable of continuously monitoring specific conductance. Streamflow and concentrations of sodium and chloride estimated from records of specific conductance were used to calculate instantaneous (15-minute) loads of sodium and chloride during water year (WY) 2004 (October 1, 2003, to September 30, 2004). Water-quality samples were also collected at 37 sampling stations in the Scituate Reservoir drainage area by the Providence Water Supply Board during WY 2004 as part of a long-term sampling program. Water-quality data are summarized by using values of central tendency and are used, in combination with measured (or estimated) streamflows, to calculate loads and yields (loads per unit area) of selected water-quality constituents for WY 2004. The largest tributary to the reservoir (the Ponaganset River, which was monitored by the USGS) contributed about 27 cubic feet per second (ft3/s) to the reservoir during WY 2004. For the same time period, annual mean1 streamflows measured (or estimated) for the other monitoring stations in this study ranged from about 0.42 to 19 ft3/s. Together, tributary streams (equipped with instrumentation capable of continuously monitoring specific conductance) transported about 1,100,000 kilograms (kg) of sodium and 1,700,000 kg of chloride to the Scituate Reservoir during WY 2004; sodium and chloride yields for the tributaries ranged from 12,000 to 61,000 kilograms per square mile (kg/mi2) and from 17,000 to 100,000 kg/mi2, respectively. At the stations where water-quality samples were collected by the Providence Water Supply Board, the median of the median chloride concentrations was 24.8 milligrams per liter

Streamflow, water quality and constituent loads and yields, Scituate Reservoir drainage area, Rhode Island, water year 2014

Science.gov (United States)

Smith, Kirk P.

2016-05-03

Streamflow and concentrations of sodium and chloride estimated from records of specific conductance were used to calculate loads of sodium and chloride during water year (WY) 2014 (October 1, 2013, through September 30, 2014) for tributaries to the Scituate Reservoir, Rhode Island. Streamflow and water-quality data used in the study were collected by the U.S. Geological Survey and the Providence Water Supply Board in the cooperative study. Streamflow was measured or estimated by the U.S. Geological Survey following standard methods at 23 streamgages; 14 of these streamgages are equipped with instrumentation capable of continuously monitoring water level, specific conductance, and water temperature. Water-quality samples were collected at 37 sampling stations by the Providence Water Supply Board and at 14 continuous-record streamgages by the U.S. Geological Survey during WY 2014 as part of a long-term sampling program; all stations are in the Scituate Reservoir drainage area. Water-quality data collected by the Providence Water Supply Board are summarized by using values of central tendency and are used, in combination with measured (or estimated) streamflows, to calculate loads and yields (loads per unit area) of selected water-quality constituents for WY 2014.The largest tributary to the reservoir (the Ponaganset River, which was monitored by the U.S. Geological Survey) contributed a mean streamflow of 23 cubic feet per second to the reservoir during WY 2014. For the same time period, annual mean streamflows measured (or estimated) for the other monitoring stations in this study ranged from about 0.35 to about 14 cubic feet per second. Together, tributaries (equipped with instrumentation capable of continuously monitoring specific conductance) transported about 1,200,000 kilograms of sodium and 2,100,000 kilograms of chloride to the Scituate Reservoir during WY 2014; sodium and chloride yields for the tributaries ranged from 7,700 to 45,000 kilograms per year per

An update of the distribution of selected radiochemical and chemical constituents in perched ground water, Idaho National Laboratory, Idaho, Emphasis 1999-2001

Science.gov (United States)

Davis, Linda C.

2006-01-01

Radiochemical and chemical wastes generated at facilities at the Idaho National Laboratory (INL) were discharged since 1952 to infiltration ponds at the Reactor Technology Complex (RTC) (known as the Test Reactor Area [TRA] until 2005), and the Idaho Nuclear Technology and Engineering Center (INTEC) and buried at the Radioactive Waste Management Complex (RWMC). Disposal of wastewater to infiltration ponds and infiltration of surface water at waste burial sites resulted in formation of perched ground water in basalts and in sedimentary interbeds above the Snake River Plain aquifer. Perched ground water is an integral part of the pathway for waste-constituent migration to the aquifer. The U.S. Geological Survey (USGS), in cooperation with the U.S. Department of Energy, maintains ground-water monitoring networks at the INL to determine hydrologic trends, and to monitor the movement of radiochemical and chemical constituents in wastewater discharged from facilities to both perched ground water and the aquifer. This report presents an analysis of water-quality and water-level data collected from wells completed in perched ground water at the INL during 1999-2001, and summarizes historical disposal data and water-level-and water-quality trends. At the RTC, tritium, strontium-90, cesium-137, dissolved chromium, chloride, sodium, and sulfate were monitored in shallow and deep perched ground water. In shallow perched ground water, no tritium was detected above the reporting level. In deep perched ground water, tritium concentrations generally decreased or varied randomly during 1999-2001. During October 2001, tritium concentrations ranged from less than the reporting level to 39.4?1.4 picocuries per milliliter (pCi/mL). Reportable concentrations of tritium during July-October 2001 were smaller than the reported concentrations measured during July-December 1998. Tritium concentrations in water from wells at the RTC were likely affected by: well's distance from the

Water-quality assessment of south-central Texas : comparison of water quality in surface-water samples collected manually and by automated samplers

Science.gov (United States)

Ging, Patricia B.

1999-01-01

Surface-water sampling protocols of the U.S. Geological Survey National Water-Quality Assessment (NAWQA) Program specify samples for most properties and constituents to be collected manually in equal-width increments across a stream channel and composited for analysis. Single-point sampling with an automated sampler (autosampler) during storms was proposed in the upper part of the South-Central Texas NAWQA study unit, raising the question of whether property and constituent concentrations from automatically collected samples differ significantly from those in samples collected manually. Statistical (Wilcoxon signed-rank test) analyses of 3 to 16 paired concentrations for each of 26 properties and constituents from water samples collected using both methods at eight sites in the upper part of the study unit indicated that there were no significant differences in concentrations for dissolved constituents, other than calcium and organic carbon.

Semi-analytical Model for Estimating Absorption Coefficients of Optically Active Constituents in Coastal Waters

Science.gov (United States)

Wang, D.; Cui, Y.

2015-12-01

The objectives of this paper are to validate the applicability of a multi-band quasi-analytical algorithm (QAA) in retrieval absorption coefficients of optically active constituents in turbid coastal waters, and to further improve the model using a proposed semi-analytical model (SAA). The ap(531) and ag(531) semi-analytically derived using SAA model are quite different from the retrievals procedures of QAA model that ap(531) and ag(531) are semi-analytically derived from the empirical retrievals results of a(531) and a(551). The two models are calibrated and evaluated against datasets taken from 19 independent cruises in West Florida Shelf in 1999-2003, provided by SeaBASS. The results indicate that the SAA model produces a superior performance to QAA model in absorption retrieval. Using of the SAA model in retrieving absorption coefficients of optically active constituents from West Florida Shelf decreases the random uncertainty of estimation by >23.05% from the QAA model. This study demonstrates the potential of the SAA model in absorption coefficients of optically active constituents estimating even in turbid coastal waters. Keywords: Remote sensing; Coastal Water; Absorption Coefficient; Semi-analytical Model

Streamflow, water quality, and constituent loads and yields, Scituate Reservoir drainage area, Rhode Island, water year 2012

Science.gov (United States)

Smith, Kirk P.

2014-01-01

Streamflow and concentrations of sodium and chloride estimated from records of specific conductance were used to calculate loads of sodium and chloride during water year (WY) 2012 (October 1, 2011, through September 30, 2012), for tributaries to the Scituate Reservoir, Rhode Island. Streamflow and water-quality data used in the study were collected by the U.S. Geological Survey (USGS) or the Providence Water Supply Board (PWSB). Streamflow was measured or estimated by the USGS following standard methods at 23 streamgages; 14 of these streamgages were equipped with instrumentation capable of continuously monitoring water level, specific conductance, and water temperature. Water-quality samples were collected at 37 sampling stations by the PWSB and at 14 continuous-record streamgages by the USGS during WY 2012 as part of a long-term sampling program; all stations were in the Scituate Reservoir drainage area. Water-quality data collected by the PWSB were summarized by using values of central tendency and used, in combination with measured (or estimated) streamflows, to calculate loads and yields (loads per unit area) of selected water-quality constituents for WY 2012. The largest tributary to the reservoir (the Ponaganset River, which was monitored by the USGS) contributed a mean streamflow of about 26 cubic feet per second (ft3/s) to the reservoir during WY 2012. For the same time period, annual mean1 streamflows measured (or estimated) for the other monitoring stations in this study ranged from about 0.40 to about 17 ft3/s. Together, tributaries (equipped with instrumentation capable of continuously monitoring specific conductance) transported about 1,100,000 kilograms (kg) of sodium and 1,900,000 kg of chloride to the Scituate Reservoir during WY 2012; sodium and chloride yields for the tributaries ranged from 8,700 to 51,000 kilograms per square mile (kg/mi2) and from 14,000 to 87,000 kg/mi2, respectively. At the stations where water-quality samples were collected

Streamflow, water quality, and constituent loads and yields, Scituate Reservoir drainage area, Rhode Island, water year 2011

Science.gov (United States)

Smith, Kirk P.

2013-01-01

Streamflow and concentrations of sodium and chloride estimated from records of specific conductance were used to calculate loads of sodium and chloride during water year (WY) 2011 (October 1, 2010, to September 30, 2011), for tributaries to the Scituate Reservoir, Rhode Island. Streamflow and water-quality data used in the study were collected by the U.S. Geological Survey (USGS) or the Providence Water Supply Board (PWSB). Streamflow was measured or estimated by the USGS following standard methods at 23 streamgages; 14 of these streamgages were also equipped with instrumentation capable of continuously monitoring water level, specific conductance, and water temperature. Water-quality samples also were collected at 37 sampling stations by the PWSB and at 14 continuous-record streamgages by the USGS during WY 2011 as part of a long-term sampling program; all stations were in the Scituate Reservoir drainage area. Water-quality data collected by PWSB are summarized by using values of central tendency and are used, in combination with measured (or estimated) streamflows, to calculate loads and yields (loads per unit area) of selected water-quality constituents for WY 2011. The largest tributary to the reservoir (the Ponaganset River, which was monitored by the USGS) contributed a mean streamflow of about 37 cubic feet per second (ft3/s) to the reservoir during WY 2011. For the same time period, annual mean1 streamflows measured (or estimated) for the other monitoring stations in this study ranged from about 0.5 to about 21 ft3/s. Together, tributaries (equipped with instrumentation capable of continuously monitoring specific conductance) transported about 1,600,000 kg (kilograms) of sodium and 2,600,000 kg of chloride to the Scituate Reservoir during WY 2011; sodium and chloride yields for the tributaries ranged from 9,800 to 53,000 kilograms per square mile (kg/mi2) and from 15,000 to 90,000 kg/mi2, respectively. At the stations where water-quality samples were

[Spectral absorption properties of the water constituents in the estuary of Zhujiang River].

Science.gov (United States)

Wang, Shan-shan; Wang, Yong-bo; Fu, Qing-hua; Yin, Bin; Li, Yun-mei

2014-12-01

Spectral absorption properties of the water constituents is the main factor affecting the light field under the surface of the water and the spectrum above the surface of the water. Thus, the study is useful for understanding of the water spectral property and the remote reversing of water quality parameters. Absorption properties of total suspended particles, non-algal particles, phytoplankton and CDOM were analyzed using the 30 samples collected in July 2013 in the estuary of Zhujiang River. The results indicated that: (1) the non-algal particles absorption dominated the absorption of the total suspended particles; (2) the absorption coefficient of the non-algal particles, which mainly came from the terrigenous deposits, decreased exponentially from short to long wavelength. In addition, the average value and spatial variation of the slope S(d) were higher than those in inland case- II waters; (3) the absorption coefficient of phytoplankton in 440 nm showed a better polynomial relationship with chlorophyll a concentration, while the absorption coefficient of phytoplankton in 675 nm linearly related with the chlorophyll a concentration. Moreover, the influence of accessory pigments on phytoplankton absorption coefficient mainly existed in the range of short wavelength, and Chlorophyll a was the main influencing factor for phytoplankton absorption in long wavelength. The specific absorption coefficient of phytoplankton decreased the power exponentially with the increase of the chlorophyll a concentration; (4) CDOM mainly came from the terrigenous sources and its spectral curve had an absorption shoulder between 250-290 nm. Thus, a piecewise S(g) fitting function could effectively express CDOM absorption properties, i.e., M value and S(g) value in period A (240-260 nm) showed a strong positive correlation. The M value was low, and the humic acid had a high proportion in CDOM; (5) the non-algal particles absorption dominated the total absorption in the estuary of

Prediction of meat spectral patterns based on optical properties and concentrations of the major constituents.

Science.gov (United States)

ElMasry, Gamal; Nakauchi, Shigeki

2016-03-01

A simulation method for approximating spectral signatures of minced meat samples was developed depending on concentrations and optical properties of the major chemical constituents. Minced beef samples of different compositions scanned on a near-infrared spectroscopy and on a hyperspectral imaging system were examined. Chemical composition determined heuristically and optical properties collected from authenticated references were simulated to approximate samples' spectral signatures. In short-wave infrared range, the resulting spectrum equals the sum of the absorption of three individual absorbers, that is, water, protein, and fat. By assuming homogeneous distributions of the main chromophores in the mince samples, the obtained absorption spectra are found to be a linear combination of the absorption spectra of the major chromophores present in the sample. Results revealed that developed models were good enough to derive spectral signatures of minced meat samples with a reasonable level of robustness of a high agreement index value more than 0.90 and ratio of performance to deviation more than 1.4.

Assessment of selected inorganic constituents in streams in the Central Arizona Basins Study Area, Arizona and northern Mexico, through 1998

Science.gov (United States)

Anning, David W.

2003-01-01

Stream properties and water-chemistry constituent concentrations from data collected by the National Water-Quality Assessment and other U.S. Geological Survey water-quality programs were analyzed to (1) assess water quality, (2) determine natural and human factors affecting water quality, and (3) compute stream loads for the surface-water resources in the Central Arizona Basins study area. Stream temperature, pH, dissolved-oxygen concentration and percent saturation, and dissolved-solids, suspended-sediment, and nutrient concentration data collected at 41 stream-water quality monitoring stations through water year 1998 were used in this assessment. Water-quality standards applicable to the stream properties and water-chemistry constituent concentration data for the stations investigated in this study generally were met, although there were some exceedences. In a few samples from the White River, the Black River, and the Salt River below Stewart Mountain Dam, the pH in reaches designated as a domestic drinking water source was higher than the State of Arizona standard. More than half of the samples from the Salt River below Stewart Mountain Dam and almost all of the samples from the stations on the Central Arizona Project Canal?two of the three most important surface-water sources used for drinking water in the Central Arizona Basins study area?exceeded the U.S. Environmental Protection Agency drinking water Secondary Maximum Contaminant Level for dissolved solids. Two reach-specific standards for nutrients established by the State of Arizona were exceeded many times: (1) the annual mean concentration of total phosphorus was exceeded during several years at stations on the main stems of the Salt and Verde Rivers, and (2) the annual mean concentration of total nitrogen was exceeded during several years at the Salt River near Roosevelt and at the Salt River below Stewart Mountain Dam. Stream properties and water-chemistry constituent concentrations were related to

Surface-water-quality assessment of the Upper Illinois River basin in Illinois, Indiana, and Wisconsin; cross-sectional and depth variation of water-quality constituents and properties in the Upper Illinois River basin, 1987-88

Science.gov (United States)

Marron, Donna C.; Blanchard, Stephen F.

1995-01-01

Data on water velocity, temperature, specific con- ductance, pH, dissolved oxygen concentration, chlorophyll concentration, suspended sediment con- centration, fecal-coliform counts, and the percen- tage of suspended sediment finer than 62 micrometers ranged up to 21 percent; and cross-section coefficients of variation of the concentrations of suspended sediment, fecal coliform, and chlorophyll ranged from 7 to 115 percent. Midchannel measure- ments of temperature, specific conductance, and pH were within 5 percent of mean cross-sectional values of these properties at the eight sampling sites, most of which appear well mixed because of the effect of dams and reservoirs. Measurements of the concentration of dissolved oxygen at various cross- section locations and at variable sampling depths are required to obtain a representative value of this constituent at these sites. The large varia- bility of concentrations of chlorophyll and suspended sediment, and fecal-coliform counts at the eight sampling sites indicates that composite rather than midchannel or mean values of these constituents are likely to be most representative of the channel cross section.

Logistic and linear regression model documentation for statistical relations between continuous real-time and discrete water-quality constituents in the Kansas River, Kansas, July 2012 through June 2015

Science.gov (United States)

Foster, Guy M.; Graham, Jennifer L.

2016-04-06

The Kansas River is a primary source of drinking water for about 800,000 people in northeastern Kansas. Source-water supplies are treated by a combination of chemical and physical processes to remove contaminants before distribution. Advanced notification of changing water-quality conditions and cyanobacteria and associated toxin and taste-and-odor compounds provides drinking-water treatment facilities time to develop and implement adequate treatment strategies. The U.S. Geological Survey (USGS), in cooperation with the Kansas Water Office (funded in part through the Kansas State Water Plan Fund), and the City of Lawrence, the City of Topeka, the City of Olathe, and Johnson County Water One, began a study in July 2012 to develop statistical models at two Kansas River sites located upstream from drinking-water intakes. Continuous water-quality monitors have been operated and discrete-water quality samples have been collected on the Kansas River at Wamego (USGS site number 06887500) and De Soto (USGS site number 06892350) since July 2012. Continuous and discrete water-quality data collected during July 2012 through June 2015 were used to develop statistical models for constituents of interest at the Wamego and De Soto sites. Logistic models to continuously estimate the probability of occurrence above selected thresholds were developed for cyanobacteria, microcystin, and geosmin. Linear regression models to continuously estimate constituent concentrations were developed for major ions, dissolved solids, alkalinity, nutrients (nitrogen and phosphorus species), suspended sediment, indicator bacteria (Escherichia coli, fecal coliform, and enterococci), and actinomycetes bacteria. These models will be used to provide real-time estimates of the probability that cyanobacteria and associated compounds exceed thresholds and of the concentrations of other water-quality constituents in the Kansas River. The models documented in this report are useful for characterizing changes

Chemical constituents in water from wells in the vicinity of the Naval Reactors Facility, Idaho National Engineering Laboratory, Idaho, 1990--91

International Nuclear Information System (INIS)

Bartholomay, R.C.; Knobel, L.L.; Tucker, B.J.

1993-01-01

The US Geological Survey, in response to a request from the US Department of Energy's Pittsburgh Naval Reactors Office, Idaho Branch Office, sampled 12 wells as part of a long-term project to monitor water quality of the Snake River Plain aquifer in the vicinity of the Naval Reactors Facility, Idaho National Engineering Laboratory, Idaho. Water samples were analyzed for manmade contaminants and naturally occurring constituents. Sixty samples were collected from eight groundwater monitoring wells and four production wells. Ten quality-assurance samples also were collected and analyzed. Most of the samples contained concentrations of total sodium and dissolved anions that exceeded reporting levels. The predominant category of nitrogen-bearing compounds was nitrite plus nitrate as nitrogen. Concentrations of total organic carbon ranged from less than 0.1 to 2.2 milligrams per liter. Total phenols in 52 of 69 samples ranged from 1 to 8 micrograms per liter. Extractable acid and base/neutral organic compounds were detected in water from 16 of 69 samples. Concentrations of dissolved gross alpha- and gross beta-particle radioactivity in all samples exceeded the reporting level. Radium-226 concentrations were greater than the reporting level in 63 of 68 samples

Arsenic, Boron, and Fluoride Concentrations in Ground Water in and Near Diabase Intrusions, Newark Basin, Southeastern Pennsylvania

Science.gov (United States)

Senior, Lisa A.; Sloto, Ronald A.

2006-01-01

During an investigation in 2000 by the U.S. Environmental Protection Agency (USEPA) of possible contaminant releases from an industrial facility on Congo Road near Gilbertsville in Berks and Montgomery Counties, southeastern Pennsylvania, concentrations of arsenic and fluoride above USEPA drinking-water standards of 10 ?g/L and 4 mg/L, respectively, and of boron above the USEPA health advisory level of 600 ?g/L were measured in ground water in an area along the northwestern edge of the Newark Basin. In 2003, the USEPA requested technical assistance from the U.S. Geological Survey (USGS) to help identify sources of arsenic, boron, and fluoride in the ground water in the Congo Road area, which included possible anthropogenic releases and naturally occurring mineralization in the local bedrock aquifer, and to identify other areas in the Newark Basin of southeastern Pennsylvania with similarly elevated concentrations of these constituents. The USGS reviewed available data and collected additional ground-water samples in the Congo Road area and four similar hydrogeologic settings. The Newark Basin is the largest of the 13 major exposed Mesozoic rift basins that stretch from Nova Scotia to South Carolina. Rocks in the Newark Basin include Triassic through Jurassic-age sedimentary sequences of sandstones and shales that were intruded by diabase. Mineral deposits of hydrothermal origin are associated with alteration zones bordering intrusions of diabase and also occur as strata-bound replacement deposits of copper and zinc in sedimentary rocks. The USGS review of data available in 2003 showed that water from about 10 percent of wells throughout the Newark Basin of southeastern Pennsylvania had concentrations of arsenic greater than the USEPA maximum contaminant level (MCL) of 10 ?g/L; the highest reported arsenic concentration was at about 70 ?g/L. Few data on boron were available, and the highest reported boron concentration in well-water samples was 60 ?g/L in contrast

Application of a Weighted Regression Model for Reporting Nutrient and Sediment Concentrations, Fluxes, and Trends in Concentration and Flux for the Chesapeake Bay Nontidal Water-Quality Monitoring Network, Results Through Water Year 2012

Science.gov (United States)

Chanat, Jeffrey G.; Moyer, Douglas L.; Blomquist, Joel D.; Hyer, Kenneth E.; Langland, Michael J.

2016-01-13

In the Chesapeake Bay watershed, estimated fluxes of nutrients and sediment from the bay’s nontidal tributaries into the estuary are the foundation of decision making to meet reductions prescribed by the Chesapeake Bay Total Maximum Daily Load (TMDL) and are often the basis for refining scientific understanding of the watershed-scale processes that influence the delivery of these constituents to the bay. Two regression-based flux and trend estimation models, ESTIMATOR and Weighted Regressions on Time, Discharge, and Season (WRTDS), were compared using data from 80 watersheds in the Chesapeake Bay Nontidal Water-Quality Monitoring Network (CBNTN). The watersheds range in size from 62 to 70,189 square kilometers and record lengths range from 6 to 28 years. ESTIMATOR is a constant-parameter model that estimates trends only in concentration; WRTDS uses variable parameters estimated with weighted regression, and estimates trends in both concentration and flux. WRTDS had greater explanatory power than ESTIMATOR, with the greatest degree of improvement evident for records longer than 25 years (30 stations; improvement in median model R2= 0.06 for total nitrogen, 0.08 for total phosphorus, and 0.05 for sediment) and the least degree of improvement for records of less than 10 years, for which the two models performed nearly equally. Flux bias statistics were comparable or lower (more favorable) for WRTDS for any record length; for 30 stations with records longer than 25 years, the greatest degree of improvement was evident for sediment (decrease of 0.17 in median statistic) and total phosphorus (decrease of 0.05). The overall between-station pattern in concentration trend direction and magnitude for all constituents was roughly similar for both models. A detailed case study revealed that trends in concentration estimated by WRTDS can operationally be viewed as a less-constrained equivalent to trends in concentration estimated by ESTIMATOR. Estimates of annual mean flow

Concentration of ions in selected bottled water samples sold in Malaysia

Science.gov (United States)

Aris, Ahmad Zaharin; Kam, Ryan Chuan Yang; Lim, Ai Phing; Praveena, Sarva Mangala

2013-03-01

Many consumers around the world, including Malaysians, have turned to bottled water as their main source of drinking water. The aim of this study is to determine the physical and chemical properties of bottled water samples sold in Selangor, Malaysia. A total of 20 bottled water brands consisting of `natural mineral (NM)' and `packaged drinking (PD)' types were randomly collected and analyzed for their physical-chemical characteristics: hydrogen ion concentration (pH), electrical conductivity (EC) and total dissolved solids (TDS), selected major ions: calcium (Ca), potassium (K), magnesium (Mg) and sodium (Na), and minor trace constituents: copper (Cu) and zinc (Zn) to ascertain their suitability for human consumption. The results obtained were compared with guideline values recommended by World Health Organization (WHO) and Malaysian Ministry of Health (MMOH), respectively. It was found that all bottled water samples were in accordance with the guidelines set by WHO and MMOH except for one sample (D3) which was below the pH limit of 6.5. Both NM and PD bottled water were dominated by Na + K > Ca > Mg. Low values for EC and TDS in the bottled water samples showed that water was deficient in essential elements, likely an indication that these were removed by water treatment. Minerals like major ions were present in very low concentrations which could pose a risk to individuals who consume this water on a regular basis. Generally, the overall quality of the supplied bottled water was in accordance to standards and guidelines set by WHO and MMOH and safe for consumption.

Mesoporous Carbon Produced from Tri-constituent Mesoporous Carbon-silica Composite for Water Purification

KAUST Repository

Yu, Yanjie

2012-01-01

Highly ordered mesoporous carbon-silica nanocomposites with interpenetrating carbon and silica networks were synthesized by the evaporation-induced tri-constituent co- assembly approach. The removal of silica by concentrated NaOH solution produced mesoporous carbons, which contained not only the primary large pores, but also the secondary mesopores in the carbon walls. The thus synthesized mesoporous carbon was further activated by using ZnCl2. The activated mesoporous carbon showed an improved surface area and pore volume. The synthesized mesoporous carbon was tested for diuron removal from water and the results showed that the carbon gave a fast diuron adsorption kinetics and a high diuron removal capacity, which was attributable to the primary mesopore channels being the highway for mass transfer, which led to short diffusion path length and easy accessibility of the interpenetrated secondary mesopores. The optimal adsorption capacity of the porous carbon was determined to be 390 mg/g, the highest values ever reported for diuron adsorption on carbon-based materials.

Mesoporous Carbon Produced from Tri-constituent Mesoporous Carbon-silica Composite for Water Purification

KAUST Repository

Yu, Yanjie

2012-05-01

Highly ordered mesoporous carbon-silica nanocomposites with interpenetrating carbon and silica networks were synthesized by the evaporation-induced tri-constituent co- assembly approach. The removal of silica by concentrated NaOH solution produced mesoporous carbons, which contained not only the primary large pores, but also the secondary mesopores in the carbon walls. The thus synthesized mesoporous carbon was further activated by using ZnCl2. The activated mesoporous carbon showed an improved surface area and pore volume. The synthesized mesoporous carbon was tested for diuron removal from water and the results showed that the carbon gave a fast diuron adsorption kinetics and a high diuron removal capacity, which was attributable to the primary mesopore channels being the highway for mass transfer, which led to short diffusion path length and easy accessibility of the interpenetrated secondary mesopores. The optimal adsorption capacity of the porous carbon was determined to be 390 mg/g, the highest values ever reported for diuron adsorption on carbon-based materials.

Ground-water-quality assessment of the Central Oklahoma aquifer, Oklahoma; hydrologic, water-quality, and quality-assurance data 1987-90

Science.gov (United States)

Ferree, D.M.; Christenson, S.C.; Rea, A.H.; Mesander, B.A.

1992-01-01

This report presents data collected from 202 wells between June 1987 and September 1990 as part of the Central Oklahoma aquifer pilot study of the National Water-Quality Assessment Program. The report describes the sampling networks, the sampling procedures, and the results of the ground-water quality and quality-assurance sample analyses. The data tables consist of information about the wells sampled and the results of the chemical analyses of ground water and quality-assurance sampling. Chemical analyses of ground-water samples in four sampling networks are presented: A geochemical network, a low-density survey bedrock network, a low-density survey alluvium and terrace deposits network, and a targeted urban network. The analyses generally included physical properties, major ions, nutrients, trace substances, radionuclides, and organic constituents. The chemical analyses of the ground-water samples are presented in five tables: (1) Physical properties and concentrations of major ions, nutrients, and trace substances; (2) concentrations of radionuclides and radioactivities; (3) carbon isotope ratios and delta values (d-values) of selected isotopes; (4) concentrations of organic constituents; and (5) organic constituents not reported in ground-water samples. The quality of the ground water sampled varied substantially. The sum of constituents (dissolved solids) concentrations ranged from 71 to 5,610 milligrams per liter, with 38 percent of the wells sampled exceeding the Secondary Maximum Contaminant Level of 500 milligrams per liter established under the Safe Drinking Water Act. Values of pH ranged from 5.7 to 9.2 units with 20 percent of the wells outside the Secondary Maximum Contaminant Level of 6.5 to 8.5 units. Nitrite plus nitrate concentrations ranged from less than 0.1 to 85 milligrams per liter with 8 percent of the wells exceeding the proposed Maximum Contaminant Level of 10 milligrams per liter. Concentrations of trace substances were highly variable

Retrieval of Water Constituents from Hyperspectral In-Situ Measurements under Variable Cloud Cover—A Case Study at Lake Stechlin (Germany

Directory of Open Access Journals (Sweden)

Anna Göritz

2018-01-01

Full Text Available Remote sensing and field spectroscopy of natural waters is typically performed under clear skies, low wind speeds and low solar zenith angles. Such measurements can also be made, in principle, under clouds and mixed skies using airborne or in-situ measurements; however, variable illumination conditions pose a challenge to data analysis. In the present case study, we evaluated the inversion of hyperspectral in-situ measurements for water constituent retrieval acquired under variable cloud cover. First, we studied the retrieval of Chlorophyll-a (Chl-a concentration and colored dissolved organic matter (CDOM absorption from in-water irradiance measurements. Then, we evaluated the errors in the retrievals of the concentration of total suspended matter (TSM, Chl-a and the absorption coefficient of CDOM from above-water reflectance measurements due to highly variable reflections at the water surface. In order to approximate cloud reflections, we extended a recent three-component surface reflectance model for cloudless atmospheres by a constant offset and compared different surface reflectance correction procedures. Our findings suggest that in-water irradiance measurements may be used for the analysis of absorbing compounds even under highly variable weather conditions. The extended surface reflectance model proved to contribute to the analysis of above-water reflectance measurements with respect to Chl-a and TSM. Results indicate the potential of this approach for all-weather monitoring.

Analysis of gamma irradiated pepper constituents, 1

International Nuclear Information System (INIS)

Takagi, Kazuko; Okuyama, Tsuneo

1988-01-01

A reversed phase high performance liquid chromatographic (HPLC) method was developed for the analysis of many constituents of pepper at the same time. And a extraction method of ultraviolet absorbing constituents from pepper was developed for the HPLC analysis. The Ultraviolet absorbing constituents were extracted by precooled Automatic Air-Hammer from frozen pepper with 20% acetonitrile in water. The process of extraction was achieved under cooling by liquid nitrogen from start to end. The extracted constituents were separated on a reversed phase C 8 (LiChrospher 300 RP - 8 10 μm 0.4 I.D. x 0.4 cm and LiChrosorb RP - 8 SelectB 0.4 I. D. x 25 cm) column with a concave gradient from 0.1% trifluoro acetic acid (TFA) in water to 75% acetonitrile and 0.1% TFA in water for 60 minutes. The eluted constituents were detected 210 nm and 280 nm. The present method permits the detection of about 50 peaks by 280 nm. (author)

Water Quality in Big Cypress National Preserve and Everglades National Park - Trends and Spatial Characteristics of Selected Constituents

Science.gov (United States)

Miller, Ronald L.; McPherson, Benjamin F.; Sobczak, Robert; Clark, Christine

2004-01-01

Seasonal changes in water levels and flows in Big Cypress National Preserve (BICY) and Everglades National Park (EVER) affect water quality. As water levels and flows decline during the dry season, physical, geochemical and biological processes increase the breakdown of organic materials and the build-up of organic waste, nutrients, and other constituents in the remaining surface water. For example, concentrations of total phosphorus in the marsh are less than 0.01 milligram per liter (mg/L) during much of the year. Concentrations can rise briefly above this value during the dry season and occasionally exceed 0.1 mg/L under drought conditions. Long-term changes in water levels, flows, water management, and upstream land use also affect water quality in BICY and EVER, based on analysis of available data (1959-2000). During the 1980's and early 1990's, specific conductance and concentrations of chloride increased in the Taylor Slough and Shark River Slough. Chloride concentrations more than doubled from 1960 to 1990, primarily due to greater canal transport of high dissolved solids into the sloughs. Some apparent long-term trends in sulfate and total phosphorus were likely attributable, at least in part, to high percentages of less-than and zero values and to changes in reporting levels over the period of record. High values in nutrient concentrations were evident during dry periods of the 1980's and were attributable either to increased canal inflows of nutrient-rich water, increased nutrient releases from breakdown of organic bottom sediment, or increased build-up of nutrient waste from concentrations of aquatic biota and wildlife in remaining ponds. Long-term changes in water quality over the period of record are less pronounced in the western Everglades and the Big Cypress Swamp; however, short-term seasonal and drought-related changes are evident. Water quality varies spatially across the region because of natural variations in geology, hydrology, and vegetation

Concentration comparison of selected constituents between groundwater samples collected within the Missouri River alluvial aquifer using purge and pump and grab-sampling methods, near the city of Independence, Missouri, 2013

Science.gov (United States)

Krempa, Heather M.

2015-10-29

The U.S. Geological Survey, in cooperation with the City of Independence, Missouri, Water Department, has historically collected water-quality samples using the purge and pump method (hereafter referred to as pump method) to identify potential contamination in groundwater supply wells within the Independence well field. If grab sample results are comparable to the pump method, grab samplers may reduce time, labor, and overall cost. This study was designed to compare constituent concentrations between samples collected within the Independence well field using the pump method and the grab method.

Optical remote sensing of properties and concentrations of atmospheric trace constituents

Science.gov (United States)

Vladutescu, Daniela Viviana

application is the detection of water vapor in the atmosphere. Water vapor is an important greenhouse gas due to its high concentration in the atmosphere (parts per thousand), among the trace constituents, and its interaction with tropospheric aerosols particles. The upward convection of water vapor and aerosols due to intense heating of the ground lead to aggregation of water particles or ice on aerosols in the air forming different types of clouds at various altitudes. In this regard a reliable method of retrieving atmospheric water vapor profiles is presented in the third part of the paper. The proposed technique here is the Raman lidar procedure that is calibrated afterwards. The accuracy of the water vapor measurements is obtained by calibration techniques based on different techniques that where compared and validated. The calibration method is based on data fusion from different sources like: GPS (global positioning system) sunphotometer, radiosonde. The condensation of water vapor on aerosols is affecting their size, shape, refractive index and chemical composition. The warming or cooling effect of the clouds hence formed are both possible depending on the cloud location, cover, composition and structure. The effect of these clouds on radiative global forcing and therefore on the short and long term global climate is of high interest in the scientific world. In an effort to understand the hygroscopic properties of aerosols, a major interest is manifested in obtaining accurate vertical water vapor profiles simultaneously with aerosol extinction and backscatter profiles. A reliable method of retrieving atmospheric water vapor profiles and aerosols backscatter and extinction in the same atmospheric volume is presented in the fourth chapter of the paper. As mentioned above the determination of greenhouse gases and other molecular pollutants is important in process control as well as environmental monitoring. Since many molecular vibrational modes are in the infrared

Effectiveness of a stormwater collection and detention system for reducing constituent loads from bridge runoff in Pinellas County, Florida

Science.gov (United States)

Stoker, Y.E.

1996-01-01

The quantity and quality of stormwater runoff from the Bayside Bridge were evaluated to determine the effectiveness of the stormwater collection and detention pond system of the bridge in reducing constituent loads to Old Tampa Bay. Water-quality samples of stormwater runoff from the bridge and outflow from the detention pond were collected during and after selected storms. These samples were used to compute loads for selected constituents. Stormwater on the Bayside Bridge drained rapidly during rain events. The volume of stormwater runoff from 24 storms measured during the study ranged from 4,086 to 103,705 cubic feet. Storms were most frequent during July through September and were least frequent from February through May. Concentrations of most constituents in stormwater runoff before the bridge opened to traffic were less than or equal to concentrations measured after the bridge was opened to traffic. However, concentrations of arsenic in the outflow from the detention pond generally were greater before the bridge opened than concentrations after, and concentrations of orthophosphorus in the stormwater runoff and outflow from the pond were greater before the bridge opened than during over half the sampled storms after the bridge opened. Concentrations of most constituents measured in stormwater runoff from the bridge were greatest at the beginning of the storm and decreased as the storm continued. Variations in suspended solids, nutrients, and trace element concentrations were not always concurrent with each other. The source of the measured constituent (rainfall or road debris) and the phase of the constituent (suspended or dissolved) probably affected the timing of concentration changes. The quality of stormwater runoff from the Bayside Bridge varied with total runoff volume, with the length of the dry period before the storm, and with season. Average concentrations of suspended solids, ammonia plus organic nitrogen, nitrite plus nitrate nitrogen

An Update of Hydrologic Conditions and Distribution of Selected Constituents in Water, Snake River Plain Aquifer and Perched-Water Zones, Idaho National Laboratory, Idaho, Emphasis 2002-05

Science.gov (United States)

Davis, Linda C.

2008-01-01

Radiochemical and chemical wastewater discharged since 1952 to infiltration ponds, evaporation ponds, and disposal wells at the Idaho National Laboratory (INL) has affected water quality in the Snake River Plain aquifer and perched-water zones underlying the INL. The U.S. Geological Survey, in cooperation with the U.S. Department of Energy, maintains ground-water monitoring networks at the INL to determine hydrologic trends, and to delineate the movement of radiochemical and chemical wastes in the aquifer and in perched-water zones. This report presents an analysis of water-level and water-quality data collected from aquifer and perched-water wells in the USGS ground-water monitoring networks during 2002-05. Water in the Snake River Plain aquifer primarily moves through fractures and interflow zones in basalt, generally flows southwestward, and eventually discharges at springs along the Snake River. The aquifer is recharged primarily from infiltration of irrigation water, infiltration of streamflow, ground-water inflow from adjoining mountain drainage basins, and infiltration of precipitation. From March-May 2001 to March-May 2005, water levels in wells declined throughout the INL area. The declines ranged from about 3 to 8 feet in the southwestern part of the INL, about 10 to 15 feet in the west central part of the INL, and about 6 to 11 feet in the northern part of the INL. Water levels in perched water wells declined also, with the water level dropping below the bottom of the pump in many wells during 2002-05. For radionuclides, concentrations that equal 3s, wheres s is the sample standard deviation, represent a measurement at the minimum detectable concentration, or 'reporting level'. Detectable concentrations of radiochemical constituents in water samples from wells in the Snake River Plain aquifer at the INL generally decreased or remained constant during 2002-05. Decreases in concentrations were attributed to decreased rates of radioactive-waste disposal

Use of Reflectance Ratios as a Proxy for Coastal Water Constituent Monitoring in the Pearl River Estuary

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Hong-Li Li

2009-01-01

Full Text Available Spectra, salinity, total suspended solids (TSS, in mg/L and colored dissolved organic matter (CDOM, ag(400 at 400 nm sampled in stations in 44 different locations on December 18, 19 and 21, in 2006 were measured and analyzed. The studied field covered a large variety of optically different waters, the absorption coefficient of CDOM ([ag(400] in m-1 varied between 0.488 and 1.41 m-1, and the TSS concentrations (mg/L varied between 7.0 and 241.1 mg/L. In order to detect salinity of the Pearl River Estuary, we analyzed the spectral properties of TSS and CDOM, and the relationships between field water reflectance spectra and water constituents’ concentrations based on the synchronous in-situ and satellite hyper-spectral image analysis. A good correlation was discovered (the positive correlation by linear fit, between in-situ reflectance ratio R680/R527 and TSS concentrations (R2 = 0.65 for the salinity range of 1.74-22.12. However, the result also showed that the absorption coefficient of CDOM was not tightly correlated with reflectance. In addition, we also observed two significant relationships (R2 > 0.77, one between TSS concentrations and surface salinity and the other between the absorption coefficient of CDOM and surface salinity. Finally, we develop a novel method to understand surface salinity distribution of estuarine waters from the calibrated EO-1 Hyperion reflectance data in the Pearl River Estuary, i.e. channels with high salinity and shoals with low salinity. The EO-1 Hyperion derived surface salinity and TSSconcentrations were validated using in-situ data that were collected on December 21, 2006, synchronous with EO-1 Hyperion satellite imagery acquisition. The results showed that the semi-empirical relationships are capable of predicting salinity from EO-1 Hyperion imagery in the Pearl River Estuary (RMSE < 2‰.

Filter-separable constituents of groundwater from the Columbia River plateau

International Nuclear Information System (INIS)

Seitz, M.G.; Boggs, S. Jr.

1984-01-01

The purpose of this procedure is to prepare groundwaters from the Columbia River basalt, northeastern Oregon, for batch partitioning experiments by concentration dissolved organic carbon (DOC) in water samples by ultrafiltration. Water samples were double-filtered through 0.4-μm Nuclepore polycarbonate filters to remove particulates before beginning the ultrafiltration process. The results of these experiments do not indicate a consistent relation between the distribution of americium with coexisting basalt and groundwater and the DOC content of the groundwater at 25 0 C, but there is some indication of increasing sorption of americium on basalt with increasing DOC at 90 0 C. However, any simple interpretation of the effects of DOC on the sorption behavior of americium must be made with caution, as there are other variables in the chemistry of the groundwaters that may also have important controls on this process. Another important observation from this set of experiments is that ultrafiltration does not seem to be an effective means of concentrating DOC without affecting the other trace constituents of groundwaters. The observed fractionation of groundwater chemistry as a result of the ultrafiltration procedure is not yet understood. However, for further progress in experiments of this type, it may be necessary to develop an alternative means of concentrating organic compounds that would allow the maintenance of constant values of other trace constituents as an experimental control

Streamflow, water quality, and constituent loads and yields, Scituate Reservoir Drainage Area, Rhode Island, water year 2015

Science.gov (United States)

Smith, Kirk P.

2018-05-11

Streamflow and concentrations of sodium and chloride estimated from records of specific conductance were used to calculate loads of sodium and chloride during water year (WY) 2015 (October 1, 2014, through September 30, 2015) for tributaries to the Scituate Reservoir, Rhode Island. Streamflow and water-quality data used in the study were collected by the U.S. Geological Survey and the Providence Water Supply Board. Streamflow was measured or estimated by the U.S. Geological Survey following standard methods at 23 streamgages; 14 of these streamgages are equipped with instrumentation capable of continuously monitoring water level, specific conductance, and water temperature. Water-quality samples were collected at 36 sampling stations by the Providence Water Supply Board and at 14 continuous-record streamgages by the U.S. Geological Survey during WY 2015 as part of a long-term sampling program; all stations are in the Scituate Reservoir drainage area. Water-quality data collected by the Providence Water Supply Board are summarized by using values of central tendency and are used, in combination with measured (or estimated) streamflows, to calculate loads and yields (loads per unit area) of selected water-quality constituents for WY 2015.The largest tributary to the reservoir (the Ponaganset River, which was monitored by the U.S. Geological Survey) contributed a mean streamflow of 25 cubic feet per second to the reservoir during WY 2015. For the same time period, annual mean streamflows measured (or estimated) for the other monitoring stations in this study ranged from about 0.38 to about 14 cubic feet per second. Together, tributaries (equipped with instrumentation capable of continuously monitoring specific conductance) transported about 1,500,000 kilograms of sodium and 2,400,000 kilograms of chloride to the Scituate Reservoir during WY 2015; sodium and chloride yields for the tributaries ranged from 8,000 to 54,000 kilograms per square mile and from 12,000 to 91

Investigation of selected water quality parameters in the Amargosa Drainage Basin

International Nuclear Information System (INIS)

Elliott, B.

1982-08-01

The purpose of this investigation was to determine whether Amargoso Desert water quality meets established federal drinking water standards. Samples were collected at selected drinking water supply sites and were analyzed for inorganic chemical constituents and radioactivity. The findings indicate that no concentrations of radioactivity in the drinking water exceeded the standards; however, some naturally occurring chemical constituent analysis indicate concentrations above federal drinking water standards. 18 references, 3 figures, 4 tables. (MF)

Refinement of the list of constituents for groundwater monitoring at M-area

International Nuclear Information System (INIS)

Wells, D.G.

1997-11-01

For several years Westinghouse Savannah River Company (WSRC) has been examining ways of reducing monitoring costs. Most of these efforts have been aimed at reducing the number of wells sampled or reducing sample frequency. With regards to monitoring around the M-Area Settling Basin, we are now examining a possible reduction in the number of constituents analyzed. Constituents that can be dropped entirely are nonhazardous inorganics generally referred to as water quality indicators. Monitoring for these parameters is sensible when a facility is in detection monitoring, but it is much less useful at a facility like the M-Area Basin. The water quality indicators are helpful in detecting whether or not a facility has impacted the environment. But their concentrations are not important in themselves. At M-Area, it is well documented that the facility has impacted groundwater quite seriously with a known group of hazardous constituents. So the concentrations of the nonhazardous constituents are of little interest. At M-Area there are 41 Point of Compliance (POC) wells monitoring an area of about .25 square miles and about 236 plume definition wells monitoring the surround 4 square miles. The POC wells form a picket line around the facility and are intended to detect any constituents leaching from it. They are also intended to determine whether such constituents exceed action levels. Plume definition wells are added to define the plume created a particular set or subset of contaminants. The M-Area plume definition wells were installed in several phases over a ten year time span as SRS struggled to define the extent of a large plume of TCE and PCE. These wells were not located for the purpose of monitoring the numerous inorganics and radionuclides on the unit's monitoring list. Many of the inorganics and radionuclides are relatively immobile in groundwater and cannot be expected to appear in the widely scattered TCE/PCE plume definition wells

Statistical summary of selected physical, chemical, and microbial characteristics, and estimates of constituent loads in urban stormwater, Maricopa County, Arizona

Science.gov (United States)

Lopes, T.J.; Fossum, K.D.; Phillips, J.V.; Monical, J.E.

1995-01-01

Stormwater and streamflow in the Phoenix, Arizona, area were monitored to determine the physical, chemical, and microbial characteristics of storm- water from areas having different land uses; to describe the characteristics of streamflow in a river that receives urban stormwater; and to estimate constituent loads in stormwater from unmonitored areas in Maricopa County, Arizona. Land use affects urban stormwater chemistry mostly because the percentage of impervious area controls the suspended-solids concentrations and varies with the type of land use. Urban activities also seem to concentrate cadmium, lead, and zinc in sediments. Urban stormwater had larger concentrations of chemical oxygen demand and biological oxygen demand, oil and grease, and higher counts of fecal bacteria than streamflow and could degrade the quality of the Salt River. Most regression equations for estimating constituent loads require three explanatory variables (total rainfall, drainage area, and per- centage of impervious area) and had standard errors that were from 65 to 266 percent. Localized areas that appear to contribute a large proportion of the constituent loads typically have 40 percent or more impervious area and are associated with industrial, commercial, and high-density residential land uses. The use of the mean value of the event-mean constituent concentrations measured in stormwater may be the best way of estimating constituent concentrations.

Social Position Influencing the Water Perception Gap Between Local Leaders and Constituents in a Socio-Hydrological System

Science.gov (United States)

Haeffner, Melissa; Jackson-Smith, Douglas; Flint, Courtney G.

2018-02-01

How well city leaders represent their constituents and meet their needs are key concerns in transitioning to local sustainable water governance. To date, however, there is little research documenting the influence of social position between elected leaders who make policy, career staff water managers who design and operate systems and implement policies, and the members of the public whose individual water use behaviors are important drivers of water sustainability outcomes. In this study, we ask: "How does social position explain variation in water perceptions and concerns between different actors in a socio-hydrological system?" Using a mixed method approach with survey and interview data, we explore the ways that positioning within the governance system, geographic context, and citizen engagement in local government mediate perceptions of the urban water system. Regardless of local biophysical water supply conditions, residents showed most concern about future water shortages and high water costs, while their leaders were consistently most concerned about deteriorating local water infrastructure. Further, constituents who received water-related information directly from public utility mailings or served on community committees and boards had perceptions that were more aligned with leaders' concerns. The importance of social structure over natural and built environments in shaping water issue perceptions underscores the value of social analysis in socio-hydrology studies. Further, practitioners looking to increase consensus for a transition to sustainable water governance might work to develop institutional mechanisms to increase opportunities for water user involvement in local water system governance.

Chloramination of Concentrated Drinking Water for Disinfection Byproduct Mixtures Creation- Indianapolis

Science.gov (United States)

Complex mixtures of disinfection by-products (DBPs) are formed when the disinfectant oxidizes constituents (e.g., natural organic matter (NOM) and organic pollutants) found in the source water. Since 1974, over 600 DBPs have been identified in drinking water. Despite intense iden...

Standards for heavy water concentration determinations in light water

International Nuclear Information System (INIS)

Varlam, M.; Steflea, D.; Pavelescu, M.

1995-01-01

The paper presents a method to prepare heavy water -light water standards within the range 144 ppm - 1%. A formula for computing standards concentration based on initial concentration of D 2 O and distilled water is given

An update of hydrologic conditions and distribution of selected constituents in water, eastern Snake River Plain aquifer and perched groundwater zones, Idaho National Laboratory, Idaho, emphasis 2009–11

Science.gov (United States)

Davis, Linda C.; Bartholomay, Roy C.; Rattray, Gordon W.

2013-01-01

Since 1952, wastewater discharged to infiltration ponds (also called percolation ponds) and disposal wells at the Idaho National Laboratory (INL) has affected water quality in the eastern Snake River Plain (ESRP) aquifer and perched groundwater zones underlying the INL. The U.S. Geological Survey (USGS), in cooperation with the U.S. Department of Energy, maintains groundwater monitoring networks at the INL to determine hydrologic trends, and to delineate the movement of radiochemical and chemical wastes in the aquifer and in perched groundwater zones. This report presents an analysis of water-level and water-quality data collected from aquifer, multilevel monitoring system (MLMS), and perched groundwater wells in the USGS groundwater monitoring networks during 2009–11. Water in the ESRP aquifer primarily moves through fractures and interflow zones in basalt, generally flows southwestward, and eventually discharges at springs along the Snake River. The aquifer primarily is recharged from infiltration of irrigation water, infiltration of streamflow, groundwater inflow from adjoining mountain drainage basins, and infiltration of precipitation. From March–May 2009 to March–May 2011, water levels in wells generally declined in the northern part of the INL. Water levels generally rose in the central and eastern parts of the INL. Detectable concentrations of radiochemical constituents in water samples from aquifer wells or MLMS equipped wells in the ESRP aquifer at the INL generally decreased or remained constant during 2009–11. Decreases in concentrations were attributed to radioactive decay, changes in waste-disposal methods, and dilution from recharge and underflow. In 2011, concentrations of tritium in groundwater from 50 of 127 aquifer wells were greater than or equal to the reporting level and ranged from 200±60 to 7,000±260 picocuries per liter. Tritium concentrations from one or more discrete zones from four wells equipped with MLMS were greater than or

A comparison of simultaneous plasma, atomic absorption, and iron colorimetric determinations of major and trace constituents in acid mine waters

Science.gov (United States)

Ball, J.W.; Nordstrom, D. Kirk

1994-01-01

Sixty-three water samples collected during June to October 1982 from the Leviathan/Bryant Creek drainage basin were originally analyzed by simultaneous multielement direct-current plasma (DCP) atomic-emission spectrometry, flame atomic-absorption spectrometry, graphite-furnace atomic-absorption spectrometry (GFAAS) (thallium only), ultraviolet-visible spectrometry, and hydride-generation atomic-absorption spectrometry.Determinations were made for the following metallic and semi-metallic constituents: AI, As, B, Ba, Be, Bi, Cd, Ca, Cr, Co, Cu, Fe(11), Fe(total), Li, Pb, Mg, Mn, Mo, Ni, K, Sb, Se, Si, Na, Sr, TI, V, and Zn. These samples were re-analyzed later by simultaneous multielement inductively coupled plasma (ICP) atomic-emission spectrometry and Zeeman-corrected GFAAS to determine the concentrations of many of the same constituents with improved accuracy, precision, and sensitivity. The result of this analysis has been the generation of comparative concentration values for a significant subset of the solute constituents. Many of the more recently determined values replace less-than-detection values for the trace metals; others constitute duplicate analyses for the major constituents. The multiple determinations have yielded a more complete, accurate, and precise set of analytical data. They also have resulted in an opportunity to compare the performance of the plasma-emission instruments operated in their respective simultaneous multielement modes. Flame atomic-absorption spectrometry was judged best for Na and K and hydride-generation atomic-absorption spectrometry was judged best for As because of their lower detection limit and relative freedom from interelement spectral effects. Colorimetric determination using ferrozine as the color agent was judged most accurate, precise, and sensitive for Fe. Cadmium, lead, and vanadium concentrations were too low in this set of samples to enable a determination of whether ICP or DCP is a more suitable technique. Of

PM2.5 constituents and hospital emergency-room visits in Shanghai, China.

Science.gov (United States)

Qiao, Liping; Cai, Jing; Wang, Hongli; Wang, Weibing; Zhou, Min; Lou, Shengrong; Chen, Renjie; Dai, Haixia; Chen, Changhong; Kan, Haidong

2014-09-02

Although ambient PM2.5 has been linked to adverse health effects, the chemical constituents that cause harm are largely unclear. Few prior studies in a developing country have reported the health impacts of PM2.5 constituents. In this study, we examined the short-term association between PM2.5 constituents and emergency room visits in Shanghai, China. We measured daily concentrations of PM2.5, organic carbon (OC), elemental carbon (EC), and eight water-soluble ions between January 1, 2011 and December 31, 2012. We analyzed the data using overdispersed generalized linear Poisson models. During our study period, the mean daily average concentration of PM2.5 in Shanghai was 55 μg/m(3). Major contributors to PM2.5 mass included OC, EC, sulfate, nitrate, and ammonium. For a 1-day lag, an interquartile range increment in PM2.5 mass (36.47 μg/m(3)) corresponded to 0.57% [95% confidence interval (CI): 0.13%, 1.01%] increase of emergency room visits. In all the three models used, we found significant positive associations of emergency room visits with OC and EC. Our findings suggest that PM2.5 constituents from the combustion of fossil fuel (e.g., OC and EC) may have an appreciable influence on the health impact attributable to PM2.5.

An assessment of stream water quality of the Rio San Juan, Nuevo Leon, Mexico, 1995-1996.

Science.gov (United States)

Flores Laureano, José Santos; Návar, José

2002-01-01

Good water quality of the Rio San Juan is critical for economic development of northeastern Mexico. However, water quality of the river has rapidly degraded during the last few decades. Societal concerns include indications of contamination problems and increased water diversions for agriculture, residential, and industrial water supplies. Eight sampling sites were selected along the river where water samples were collected monthly for 10 mo (October 1995-July 1996). The concentration of heavy metals and chemical constituents and measurements of bacteriological and physical parameters were determined on water samples. In addition, river discharge was recorded. Constituent concentrations in 18.7% of all samples exceeded at least one water quality standard. In particular, concentrations of fecal and total coliform bacteria, sulfate, detergent, dissolved solids, Al, Ba, Cr, Fe, and Cd, exceeded several water quality standards. Pollution showed spatial and temporal variations and trends. These variations were statistically explained by spatial and temporal changes of constituent inputs and discharge. Samples collected from the site upstream of El Cuchillo reservoir had large constituent concentrations when discharge was small; this reservoir supplies domestic and industrial water to the city of Monterrey.

Capturing optically important constituents and properties in a marine biogeochemical and ecosystem model

Science.gov (United States)

Dutkiewicz, S.; Hickman, A. E.; Jahn, O.; Gregg, W. W.; Mouw, C. B.; Follows, M. J.

2015-07-01

We present a numerical model of the ocean that couples a three-stream radiative transfer component with a marine biogeochemical-ecosystem component in a dynamic three-dimensional physical framework. The radiative transfer component resolves the penetration of spectral irradiance as it is absorbed and scattered within the water column. We explicitly include the effect of several optically important water constituents (different phytoplankton functional types; detrital particles; and coloured dissolved organic matter, CDOM). The model is evaluated against in situ-observed and satellite-derived products. In particular we compare to concurrently measured biogeochemical, ecosystem, and optical data along a meridional transect of the Atlantic Ocean. The simulation captures the patterns and magnitudes of these data, and estimates surface upwelling irradiance analogous to that observed by ocean colour satellite instruments. We find that incorporating the different optically important constituents explicitly and including spectral irradiance was crucial to capture the variability in the depth of the subsurface chlorophyll a (Chl a) maximum. We conduct a series of sensitivity experiments to demonstrate, globally, the relative importance of each of the water constituents, as well as the crucial feedbacks between the light field, the relative fitness of phytoplankton types, and the biogeochemistry of the ocean. CDOM has proportionally more importance at attenuating light at short wavelengths and in more productive waters, phytoplankton absorption is relatively more important at the subsurface Chl a maximum, and water molecules have the greatest contribution when concentrations of other constituents are low, such as in the oligotrophic gyres. Scattering had less effect on attenuation, but since it is important for the amount and type of upwelling irradiance, it is crucial for setting sea surface reflectance. Strikingly, sensitivity experiments in which absorption by any of the

Concentrations and annual fluxes of sediment-associated chemical constituents from conterminous US coastal rivers using bed sediment data

Science.gov (United States)

Horowitz, Arthur J.; Stephens, Verlin C.; Elrick, Kent A.; Smith, James J.

2012-01-01

Coastal rivers represent a significant pathway for the delivery of natural and anthropogenic sediment-associated chemical constituents to the Atlantic, Pacific and Gulf of Mexico coasts of the conterminous USA. This study entails an accounting segment using published average annual suspended sediment fluxes with published sediment-associated chemical constituent concentrations for (1) baseline, (2) land-use distributions, (3) population density, and (4) worldwide means to estimate concentrations/annual fluxes for trace/major elements and total phosphorus, total organic and inorganic carbon, total nitrogen, and sulphur, for 131 coastal river basins. In addition, it entails a sampling and subsequent chemical analysis segment that provides a level of ‘ground truth’ for the calculated values, as well as generating baselines for sediment-associated concentrations/fluxes against which future changes can be evaluated. Currently, between 260 and 270 Mt of suspended sediment are discharged annually from the conterminous USA; about 69% is discharged from Gulf rivers (n = 36), about 24% from Pacific rivers (n = 42), and about 7% from Atlantic rivers (n = 54). Elevated sediment-associated chemical concentrations relative to baseline levels occur in the reverse order of sediment discharges:Atlantic rivers (49%)>Pacific rivers (40%)>Gulf rivers (23%). Elevated trace element concentrations (e.g. Cu, Hg, Pb, Zn) frequently occur in association with present/former industrial areas and/or urban centres, particularly along the northeast Atlantic coast. Elevated carbon and nutrient concentrations occur along both the Atlantic and Gulf coasts but are dominated by rivers in the urban northeast and by southeastern and Gulf coast (Florida) ‘blackwater’ streams. Elevated Ca, Mg, K, and Na distributions tend to reflect local petrology, whereas elevated Ti, S, Fe, and Al concentrations are ubiquitous, possibly because they have substantial natural as well as anthropogenic sources

Biochar versus hydrochar as growth media constituents for ornamental plant cultivation

Directory of Open Access Journals (Sweden)

Fernando Fornes

Full Text Available ABSTRACT Biochar and hydrochar have been proposed as novel materials for providing soilless growth media. However, much more knowledge is required before reliable advice can be given on the use of these materials for this purpose. Depending on the material and the technology applied (pyrolysis or hydrothermal carbonization, phytotoxicity and greenhouse gas emissions have been found for certain chars. In this study, our aim was to assess the feasibility of three chars as substrate constituents. We compared two biochars, one from forest waste and the other from olive mill waste, and a hydrochar from forest waste. We studied how chars affected substrate characteristics, plant performance, water economy and respiratory CO2 emission. Substrates containing biochar from forest waste showed the best characteristics, with good air/water relationships and adequate electrical conductivity. Those with biochar from olive mill waste were highly saline and, consequently, low quality. The substrates with hydrochar retained too much water and were poorly aerated, presenting high CO2 concentrations due to high respiratory activity. Plants performed well only when grown in substrates containing a maximum of 25 % biochar from forest waste or hydrochar. After analyzing the char characteristics, we concluded that biochar from forest waste could be safely used as a substrate constituent and is environmentally friendly when applied due to its low salinity and low CO2 emission. However, biochar from olive mill waste and hydrochar need to be improved before they can be used as substrate constituents.

Mass imbalances in EPANET water-quality simulations

Energy Technology Data Exchange (ETDEWEB)

Davis, Michael J.; Janke, Robert; Taxon, Thomas N.

2018-04-06

EPANET is widely employed to simulate water quality in water distribution systems. However, the time-driven simulation approach used to determine concentrations of water-quality constituents provides accurate results, in general, only for small water-quality time steps; use of an adequately short time step may not be feasible. Overly long time steps can yield errors in concentrations and result in situations in which constituent mass is not conserved. Mass may not be conserved even when EPANET gives no errors or warnings. This paper explains how such imbalances can occur and provides examples of such cases; it also presents a preliminary event-driven approach that conserves mass with a water-quality time step that is as long as the hydraulic time step. Results obtained using the current approach converge, or tend to converge, to those obtained using the new approach as the water-quality time step decreases. Improving the water-quality routing algorithm used in EPANET could eliminate mass imbalances and related errors in estimated concentrations.

Influence from sea water constituents on the efficiency of water electrolysis by PEM-cells

DEFF Research Database (Denmark)

Agersted, Karsten; Bentzen, Janet Jonna; Yde-Andersen, S.

Among the sea-water specific impurities tested, magnesium has the most profound effect on PEM-cell degradation. Significant amounts of the cation was retrieved in the NAFION®-membrane structure after testing. Degradation was seen from a magnesium concentration as low as 3 10-7 mol/l, and increasing...... with concentration it led to a 86% increase of the area specific resistance at a concentration of 3 10-5 mol/l; equivalent to a conductivity of ~5 μS/cm. Other species (Cl-, Na+, SO4 2- ) seems to affect, though slowly, the performance negatively. If PEM will be used for electrolysis it seems therefore necessary...... to purify the feed water to ~1 μS/cm or even further while particularly focusing on the concentrations of polyvalent cations. e.g. magnesium....

Refinement of the list of constituents for groundwater monitoring at M-area

Energy Technology Data Exchange (ETDEWEB)

Wells, D.G.

1997-11-01

For several years Westinghouse Savannah River Company (WSRC) has been examining ways of reducing monitoring costs. Most of these efforts have been aimed at reducing the number of wells sampled or reducing sample frequency. With regards to monitoring around the M-Area Settling Basin, we are now examining a possible reduction in the number of constituents analyzed. It is our opinion that many constituents can be dropped entirely. Several others should be dropped from analyses in the plume definition wells, while retained for analyses at the point of compliance (POC) wells. Constituents that can be dropped entirely are nonhazardous inorganics generally referred to as water quality indicators. Monitoring for these parameters is sensible when a facility is in detection monitoring, but it is much less useful at a facility like the M-Area Basin. The water quality indicators are helpful in detecting whether or not a facility has impacted the environment. But their concentrations are not important in themselves. At M-Area, it is well documented that the facility has impacted groundwater quite seriously with a known group of hazardous constituents. So the concentrations of the nonhazardous constituents are of little interest. Obviously, monitoring for the hazardous constituents should continue, but it should only continue at wells that are likely to yield useful data. At M-Area there are 41 Point of Compliance (POC) wells monitoring an area of about .25 square miles and about 236 plume definition wells monitoring the surround 4 square miles. The locations of well clusters and the point of compliance are shown in figure 1. The POC wells and plume definition wells are intended to serve entirely different purposes and should not, necessarily, be monitored for the same things. The POC wells form a picket line around the facility and are intended to detect any constituents leaching from it. They are also intended to determine whether such constituents exceed action levels. Plume

Absorption mechanism of three curcumin constituents through in situ intestinal perfusion method

Directory of Open Access Journals (Sweden)

Y.-H. Wang

2017-09-01

Full Text Available This study aimed to investigate the absorption mechanism of three curcumin constituents in rat small intestines. Self-emulsification was used to solubilize the three curcumin constituents, and the rat in situ intestinal perfusion method was used to study factors on drug absorption, including drug mass concentration, absorption site, and the different types and concentrations of absorption inhibitors. Within the scope of experimental concentrations, three curcumin constituents were absorbed in rat small intestines through the active transport mechanism.

Performance of a pilot-scale constructed wetland system for treating simulated ash basin water.

Science.gov (United States)

Dorman, Lane; Castle, James W; Rodgers, John H

2009-05-01

A pilot-scale constructed wetland treatment system (CWTS) was designed and built to decrease the concentration and toxicity of constituents of concern in ash basin water from coal-burning power plants. The CWTS was designed to promote the following treatment processes for metals and metalloids: precipitation as non-bioavailable sulfides, co-precipitation with iron oxyhydroxides, and adsorption onto iron oxides. Concentrations of Zn, Cr, Hg, As, and Se in simulated ash basin water were reduced by the CWTS to less than USEPA-recommended water quality criteria. The removal efficiency (defined as the percent concentration decrease from influent to effluent) was dependent on the influent concentration of the constituent, while the extent of removal (defined as the concentration of a constituent of concern in the CWTS effluent) was independent of the influent concentration. Results from toxicity experiments illustrated that the CWTS eliminated influent toxicity with regard to survival and reduced influent toxicity with regard to reproduction. Reduction in potential for scale formation and biofouling was achieved through treatment of the simulated ash basin water by the pilot-scale CWTS.

Salinity impacts on water solubility and n-octanol/water partition coefficients of selected pesticides and oil constituents.

Science.gov (United States)

Saranjampour, Parichehr; Vebrosky, Emily N; Armbrust, Kevin L

2017-09-01

Salinity has been reported to influence the water solubility of organic chemicals entering marine ecosystems. However, limited data are available on salinity impacts for chemicals potentially entering seawater. Impacts on water solubility would correspondingly impact chemical sorption as well as overall bioavailability and exposure estimates used in the regulatory assessment. The pesticides atrazine, fipronil, bifenthrin, and cypermethrin, as well as the crude oil constituent dibenzothiophene together with 3 of its alkyl derivatives, all have different polarities and were selected as model compounds to demonstrate the impact of salinity on their solubility and partitioning behavior. The n-octanol/water partition coefficient (K OW ) was measured in both distilled-deionized water and artificial seawater (3.2%). All compounds had diminished solubility and increased K OW values in artificial seawater compared with distilled-deionized water. A linear correlation curve estimated salinity may increase the log K OW value by 2.6%/1 log unit increase in distilled water (R 2  = 0.97). Salinity appears to generally decrease the water solubility and increase the partitioning potential. Environmental fate estimates based on these parameters indicate elevated chemical sorption to sediment, overall bioavailability, and toxicity in artificial seawater. These dramatic differences suggest that salinity should be taken into account when exposure estimates are made for marine organisms. Environ Toxicol Chem 2017;36:2274-2280. © 2017 SETAC. © 2017 SETAC.

Recent Advances in Understanding Flow Dynamics and Transport of Water-Quality Constituents in the Sacramento–San Joaquin River Delta

Directory of Open Access Journals (Sweden)

David H. Schoellhamer

2016-12-01

Full Text Available doi: https://doi.org/10.15447/sfews.2016v14iss4art1This paper, part of the collection of research comprising the State of Bay–Delta Science 2016, describes advances during the past decade in understanding flow dynamics and how water-quality constituents move within California’s Sacramento–San Joaquin River Delta (Delta. Water-quality constituents include salinity, heat, oxygen, nutrients, contaminants, organic particles, and inorganic particles. These constituents are affected by water diversions and other human manipulations of flow, and they greatly affect the quantity and quality of benthic, pelagic, and intertidal habitat in the Delta. The Pacific Ocean, the Central Valley watershed, human intervention, the atmosphere, and internal biogeochemical processes are all drivers of flow and transport in the Delta. These drivers provide a conceptual framework for presenting recent findings. The tremendous expansion of acoustic and optical instruments deployed in the Delta over the past decade has greatly improved our understanding of how tidal variability affects flow and transport. Sediment is increasingly viewed as a diminishing resource needed to sustain pelagic habitat and tidal marsh, especially as sea level rises. Connections among the watershed, Delta, and San Francisco Bay that have been quantified recently highlight that a landscape view of this system is needed, rather than consideration of each region in isolation. We discuss interactions of multiple drivers and information gaps.

[Chemical constituents of Swertia macrosperma].

Science.gov (United States)

Wang, Hongling; Geng, Changan; Zhang, Xuemei; Ma, Yunbao; Jiang, Zhiyong; Chen, Jijun

2010-12-01

To study the chemical constituents of Swertia macrosperma. The air-dried whole plants of Swertia macrosperma were extracted with boiling water. The extract was concentrated to a small amount of volume and extracted with petroleum ether, EtOAc and n-BuOH, successively. The compounds were isolated and purified by column chromatography from the EtOAc fraction, and identified based on spectral analyses (MS, 1H-NMR, 13C-NMR). Thirteen compounds were isolated from S. macrosperma, and were characterized as norbellidifolin (1), 1-hydroxy-3,7, 8-trimethoxy-xanthone (2), norswertianolin (3), swertianolin (4), 1,3,7,8-tetrahydroxyxanthone-8-O-beta-D-glucopyranoside (5), swertiamatin (6), decentapicrin (7), coniferl aldehyde (8), sinapaldehyde (9), balanophonin (10), together with beta-sitosterol, daucosterol, and oleanolic acid . Compounds 2, 4-10 were obtained from Swertia macrosperma for the first time.

Water-assisted growth of graphene-carbon nanotube hybrids in plasma

Science.gov (United States)

Tewari, Aarti; Ghosh, Santanu; Srivastava, Pankaj

2018-04-01

The enhanced growth of graphene-carbon nanotube (CNT) hybrids in a hydrocarbon and hydrogen plasma assisted by water is numerically formulated. The catalyst activity and agglomeration of catalyst particles are the rate determining factors in the growth of hybrids and their constituents, i.e., the CNT and graphene. The water vapor concentration is varied to investigate its effect on the growth process. The enhanced catalyst activity on account of oxidation by hydroxyl ions of water to impede the agglomeration of catalyst particles and the removal of amorphous carbon through etching by hydrogen ions of water are seen to be the main driving forces behind the many fold increase in the dimensions of constituent nanostructures and the hybrids with water vapor concentration. Importantly, beyond a certain specific water vapor concentration, the growth rates dropped due to active oxidation of the catalyst particle.

Aqueous photochemical degradation of hydroxylated PAHs: Kinetics, pathways, and multivariate effects of main water constituents

Energy Technology Data Exchange (ETDEWEB)

Ge, Linke; Na, Guangshui [Key Laboratory for Ecological Environment in Coastal Areas (SOA), National Marine Environmental Monitoring Center, Dalian 116023 (China); Chen, Chang-Er [Lancaster Environment Centre, Lancaster University, Lancaster LA1 4YQ (United Kingdom); Li, Jun [Key Laboratory for Ecological Environment in Coastal Areas (SOA), National Marine Environmental Monitoring Center, Dalian 116023 (China); College of Marine Science, Shanghai Ocean University, Shanghai 201306 (China); Ju, Maowei; Wang, Ying; Li, Kai [Key Laboratory for Ecological Environment in Coastal Areas (SOA), National Marine Environmental Monitoring Center, Dalian 116023 (China); Zhang, Peng, E-mail: pzhang@nmemc.org.cn [Key Laboratory for Ecological Environment in Coastal Areas (SOA), National Marine Environmental Monitoring Center, Dalian 116023 (China); Yao, Ziwei [Key Laboratory for Ecological Environment in Coastal Areas (SOA), National Marine Environmental Monitoring Center, Dalian 116023 (China)

2016-03-15

Hydroxylated polycyclic aromatic hydrocarbons (OH-PAHs) are contaminants of emerging concern in the aquatic environment, so it is of great significance to understand their environmental transformation and toxicity. This study investigated the aqueous photochemical behavior of four OH-PAHs, 9-Hydroxyfluorene (9-OHFL), 2-Hydroxyfluorene, 9-Hydroxyphenanthrene and 1-Hydroxypyrene, under simulated sunlight irradiation (λ > 290 nm). It was observed that their photodegradation followed the pseudo-first-order kinetics. Based on the determined quantum yields, their calculated solar apparent photodegradation half-lives in surface waters at 45° N latitude ranged from 0.4 min for 9-Hydroxyphenanthrene to 7.5 × 10{sup 3} min for 9-OHFL, indicating that the OH-PAHs would intrinsically photodegrade fast in sunlit surface waters. Furthermore, 9-OHFL as an example was found to undergo direct photolysis, and self-sensitized photooxidation via ·OH rather than {sup 1}O{sub 2} in pure water. The potential photoreactions involved photoinduced hydroxylation, dehydrogenation and isomerization based on product identification by GC–MS/MS. 9-OHFL photodegraded slower in natural waters than in pure water, which was attributed to the integrative effects of the most photoreactive species, such as Fe(III), NO{sub 3}{sup −}, Cl{sup −} and humic acid. The photomodified toxicity was further examined using Vibrio fischeri, and it was found that the toxicity of photolyzed 9-OHFL did not decrease significantly (p > 0.05) either in pure water or in seawater, implying the comparable or higher toxicity of some intermediates. These results are important for assessing the fate and risks of OH-PAHs in surface waters. - Graphical abstract: Aqueous photochemical behavior of 4 hydroxylated PAHs is first reported on revealing the kinetics, mechanisms, toxicity, and multivariate effects of water constituents. - Highlights: • It is first reported on aqueous photochemical behavior of 4 hydroxylated

Measurement of concentration of heavy water

International Nuclear Information System (INIS)

Tsukamoto, Yuichi; Kondo, Mitsuo; Sakurai, Naoyuki

1979-01-01

The concentration of heavy water is measured as one of the technical management in the Fugen plant. The heavy water is used as the moderator in the reactor. The measuring method depends on the theory of light absorption. The light absorption range of heavy water spreads from near infrared to infrared zone. The near infrared absorption was adopted for the purpose, as the absorption is much larger in infrared zone, and the measurement has to be conducted, limiting the apparent absorption. This measuring method is available to determine the concentration of heavy water in the broad range exactly. The preparation of heavy water sample and the measurement of the absorption spectra of near infrared ray are explained, as the experimental procedure. The sample cell was made of quartz, and the spectroscope was the Hitachi 323 type. The resolving power is 100 nm and 27 nm for the wave length of 1000 nm and 2500 nm, respectively. Concerning the measured results, the absorption was recorded in the wave length range from 600 nm to 2600 nm, and for the heavy water concentration range from 0 to 99.77 wt. %. The peaks of absorption were located at the wave length of 1450, 1660, 1920, 1970, 2020 and 2600 nm. The three kinds of fundamental vibration mode of the molecules of both light and heavy water are shown, and the peaks belong to H 2 O, HDO and D 2 O, respectively. The relation between the absorption and the heavy water concentration, and that between the transmissivity and the wave length are shown, when the cell thickness was varied to 5 mm and 20 mm, and the heavy water concentration to 21%, 62% and 99.85%. (Nakai, Y.)

Hydrogeology and water quality of the shallow ground-water system in eastern York County, Virginia. Water resources investigation

International Nuclear Information System (INIS)

1993-01-01

The report describes the hydrogeology and water quality of the shallow ground-water system in the eastern part of York County, Va. The report includes a discussion of (1) the aquifers and confining units, (2) the flow of ground water, and (3) the quality of ground water. The report is an evaluation of the shallow ground-water system and focuses on the first 200 ft of sediments below land surface. Historical water-level and water-quality data were not available for the study area; therefore, a network of observation wells was constructed for the study. Water levels were measured to provide an understanding of the flow of ground water through the multiaquifer system. Water samples were collected and analyzed for major inorganic constituents, nutrients, and metals. The report presents maps that show the regional distribution of chloride and iron concentrations. Summary statistics and graphical summaries of selected chemical constituents provide a general assessment of the ground-water quality

Tritium concentrations of environmental waters in Aichi Prefecture

International Nuclear Information System (INIS)

Ohnuma, Shoko; Chaya, Kunio

1992-01-01

Tritium concentrations of environmental waters in Aichi Prefecture were determined from 1973 to 1989. They are rain water, river waters and sea waters. In 1970's, tritium concentrations of environmental waters were more than the natural levels under the influence of the atmospheric nuclear tests. However, atmospheric nuclear tests have not been carried out after Oct. 1980 and the tritium concentrations are going to return to the natural levels. Annual means of tritium concentration in 1989 were as follows: 0.67 Bq/l for rain water, 1.1 Bq/l for Kiso river and Shonai river, 0.85 Bq/l for Yahagi river, 0.70 Bq/l for Toyo river, and 0.41 Bq/l for surface sea water. Also tritium concentration of sea bottom water was 0.50±0.28 Bq/l and rather constant yearly. Among environmental waters, only rain water was previously having seasonal variation of tritium concentration and it was showing 'spring peak' when the troposphere and the stratosphere were mixed actively. At present, tritium concentration of rain water has a little seasonal variation, and is slightly lower in summer under the influence of the atmosphere coming over from the ocean. With regard to the direct influence of rain water to river waters, it was found by means of time series analysis that Kiso river was the least affected of river waters and Yahagi river was the most. The apparent residence time, in which rain water stayed in the underground before it flowed out as river water, was presumed to be 4.9 years for Kiso river, 3.6 years for Yahagi river, 2.0 years for Toyo river, respectively. (author)

Tritium concentrations of environmental waters in Aichi Prefecture

Energy Technology Data Exchange (ETDEWEB)

Ohnuma, Shoko; Chaya, Kunio (Aichi Prefectural Inst. of Public Health, Nagoya (Japan))

1992-09-01

Tritium concentrations of environmental waters in Aichi Prefecture were determined from 1973 to 1989. They are rain water, river waters and sea waters. In 1970's, tritium concentrations of environmental waters were more than the natural levels under the influence of the atmospheric nuclear tests. However, atmospheric nuclear tests have not been carried out after Oct. 1980 and the tritium concentrations are going to return to the natural levels. Annual means of tritium concentration in 1989 were as follows: 0.67 Bq/l for rain water, 1.1 Bq/l for Kiso river and Shonai river, 0.85 Bq/l for Yahagi river, 0.70 Bq/l for Toyo river, and 0.41 Bq/l for surface sea water. Also tritium concentration of sea bottom water was 0.50[+-]0.28 Bq/l and rather constant yearly. Among environmental waters, only rain water was previously having seasonal variation of tritium concentration and it was showing 'spring peak' when the troposphere and the stratosphere were mixed actively. At present, tritium concentration of rain water has a little seasonal variation, and is slightly lower in summer under the influence of the atmosphere coming over from the ocean. With regard to the direct influence of rain water to river waters, it was found by means of time series analysis that Kiso river was the least affected of river waters and Yahagi river was the most. The apparent residence time, in which rain water stayed in the underground before it flowed out as river water, was presumed to be 4.9 years for Kiso river, 3.6 years for Yahagi river, 2.0 years for Toyo river, respectively. (author).

Chloraminated Concentrated Drinking Water for Disinfection Byproduct Mixtures Research: Evaluating Free Chlorine Contact Times

Science.gov (United States)

Complex mixtures of disinfection by-products (DBPs) are formed when the disinfectant oxidizes constituents (e.g., natural organic matter (NOM) and organic pollutants) present in the source water. Since 1974, over 600 DBPs have been identified in drinking water, yet a large portio...

Chloramination of Concentrated Drinking Water: Evaluation of Disinfection Byproduct Formation and Dosing Scenarios - Portland

Science.gov (United States)

Complex mixtures of disinfection by-products (DBPs) are formed when the disinfectant oxidizes constituents (e.g., natural organic matter (NOM) and organic pollutants) found in the source water. Since 1974, over 600 DBPs have been identified in drinking water. Despite intense iden...

40 CFR 264.342 - Principal organic hazardous constituents (POHCs).

Science.gov (United States)

2010-07-01

...) Principal Organic Hazardous Constituents (POHCs) in the waste feed must be treated to the extent required by... organic constituents in the waste and on their concentration or mass in the waste feed, considering the... (CONTINUED) SOLID WASTES (CONTINUED) STANDARDS FOR OWNERS AND OPERATORS OF HAZARDOUS WASTE TREATMENT, STORAGE...

Trends in Surface-Water Quality at Selected Ambient-Monitoring Network Stations in Kentucky, 1979-2004

Science.gov (United States)

Crain, Angela S.; Martin, Gary R.

2009-01-01

stations. Flow-adjustment procedures were used with these techniques at all stations to remove the effects of streamflow on water-quality variability. Flow adjustments were used for all constituents, except temperature. A decreasing trend indicates a decrease in concentration of a particular constituent; whereas, an increasing trend indicates an increase in concentration and potential degradation in water quality. Trend results varied statewide by station and by physical property and water-quality constituent. The results for all stations and all physical properties and water-quality constituents examined had at least one statistically significant (p-value <0.05) increasing or decreasing trend during the specified period of record. Water temperature and concentrations of dissolved oxygen had no significant decreasing trends at any station. Water temperature had one significant increasing trend at the South Fork Cumberland River near Blue Heron station. Specific conductance and concentrations of hardness had one significant decreasing trend at the South Fork Cumberland River near Blue Heron station. pH also had a significant decreasing trend at the Mud River near Gus station. Concentrations of total suspended solids had 1 increasing trend at the Kentucky River at High Bridge station and 10 decreasing trends with 5 of those stations located in the Cumberland River Basin. Major ions analyzed for trends included chloride and sulfate. Concentrations of chloride at the 37 stations had increasing trends at 15 stations, decreasing trends at 3 stations, and no significant trend in concentration over time at 19 stations. Most of the increasing trends in concentrations of chloride are located in the northern part of Kentucky, possibly indicating an increase in the use of road salts for road deicing and (or) the result of resource extraction (oil, gas, and coal). Increasing trends of sulfate concentrations were detected at seven stations, all located in the Appalachian

Effects of physical and chemical heterogeneity on water-quality samples obtained from wells

Science.gov (United States)

Reilly, Thomas E.; Gibs, Jacob

1993-01-01

Factors that affect the mass of chemical constituents entering a well include the distributions of flow rate and chemical concentrations along and near the screened or open section of the well. Assuming a layered porous medium (with each layer being characterized by a uniform hydraulic conductivity and chemical concentration), a knowledge of the flow from each layer along the screened zone and of the chemical concentrations in each layer enables the total mass entering the well to be determined. Analyses of hypothetical systems and a site at Galloway, NJ, provide insight into the temporal variation of water-quality data observed when withdrawing water from screened wells in heterogeneous ground-water systems.The analyses of hypothetical systems quantitatively indicate the cause-and-effect relations that cause temporal variability in water samples obtained from wells. Chemical constituents that have relatively uniform concentrations with depth may not show variations in concentrations in the water discharged from a well after the well is purged (evacuation of standing water in the well casing). However, chemical constituents that do not have uniform concentrations near the screened interval of the well may show variations in concentrations in the well discharge water after purging because of the physics of ground-water flow in the vicinity of the screen.Water-quality samples were obtained through time over a 30 minute period from a site at Galloway, NJ. The water samples were analyzed for aromatic hydrocarbons, and the data for benzene, toluene, and meta+para xylene were evaluated for temporal variations. Samples were taken from seven discrete zones, and the flow-weighted concentrations of benzene, toluene, and meta+para xylene all indicate an increase in concentration over time during pumping. These observed trends in time were reproduced numerically based on the estimated concentration distribution in the aquifer and the flow rates from each zone.The results of

Effects of natural water constituents on the photo-decomposition of methylmercury and the role of hydroxyl radical

Energy Technology Data Exchange (ETDEWEB)

Kim, Moon-Kyung; Zoh, Kyung-Duk, E-mail: zohkd@snu.ac.kr

2013-04-01

Photo-decomposition of methylmercury (MeHg) in surface water is thought to be an important process that reduces the bioavailability of mercury (Hg) to aquatic organisms. In this study, photo-initiated decomposition of MeHg was investigated under UVA irradiation in the presence of natural water constituents including NO{sub 3}{sup −}, Fe{sup 3+}, and HCO{sub 3}{sup −} ions, and dissolved organic matter such as humic and fulvic acid. MeHg degradation followed the pseudo-first-order kinetics; the rate constant increased with increasing UVA intensity (0.3 to 3.0 mW cm{sup −2}). In the presence of NO{sub 3}{sup −}, Fe{sup 3+}, and fulvic acid, the decomposition rate of MeHg increased significantly due to photosensitization by reactive species such as hydroxyl radical. The presence of humic acid and HCO{sub 3}{sup −} ions lowered the degradation rate through a radical scavenging effect. Increasing the pH of the solution increased the degradation rate constant by enhancing the generation of hydroxyl radicals. Hydroxyl radicals play an important role in the photo-decomposition of MeHg in water, and natural constituents in water can affect the photo-decomposition of MeHg by changing radical production and inhibition. - Highlights: ► The abiotic photodecomposition of methylmercury (MeHg) in water was examined. ► UVA light is a primary factor inducing MeHg photodecomposition in water. ► Fulvic acid, NO{sub 3}{sup −}, and Fe{sup 3+} ion increased MeHg photo-decomposition rate significantly. ► Humic acid and HCO{sub 3}{sup −} ions inhibited photodecomposition through radical scavenging. ► OH radical is an important compound affecting photodecomposition of MeHg in water.

Evacuation of performance and significant chemical constituents and by products in drinking water treatment

International Nuclear Information System (INIS)

Jamrah, I. A.

1999-01-01

Drinking water treatment is a task that comprises of several processes that eventually lead to the addition of chemicals to achieve the objectives of treatment. This study was conducted to assess treatment performance, explain the presence of significant chemical species in water, and investigate the interactions and chemical by-products that are formed during the course of treatment. Grab water samples were collected on a regular basis from the influent and effluent of Zai water treatment plant. Chemical analysis were conducted to determine the concentrations of various chemical species of interest. Turbidity, temperature, and pH of the samples were also measured. The study concluded that Zai Water Treatment Plant produces potable drinking water in accordance with Jordanian Standards. The use of treatment chemical resulted in an increase in the concentrations of certain materials, such as manganese, aluminum, and sulfate. The turbidity of the raw water and the TOC of the samples were positively correlated, and the treatment results in approximately 20% TOC reduction, which demonstrates that the measures used for the control of TOC (carbon adsorption and permanganate pre-oxidation), are not very effective. The study also showed that the TOC content of our raw water samples and the concentration of tribalomethanes resulting after disinfection were positively correlated, and that bromoform was the dominant component. Also chloroform was the minor component of tribalomethanes formed during treatment. Positive correlation between the total concentration of tribalomethanes in water and the chlorine dose used for disinfection was also observed, and the total concentration of tribalomethanes increased with temperature. The formation of tribalomethanes was enhanced as the pH of water increased and as the concentration of bromide ion in raw water became significant. (author). 25 refs., 14 figs.1 table

Chester County ground-water atlas, Chester County, Pennsylvania

Science.gov (United States)

Ludlow, Russell A.; Loper, Connie A.

2004-01-01

Chester County encompasses 760 square miles in southeastern Pennsylvania. Groundwater-quality studies have been conducted in the county over several decades to address specific hydrologic issues. This report compiles and describes water-quality data collected during studies conducted mostly after 1990 and summarizes the data in a county-wide perspective.In this report, water-quality constituents are described in regard to what they are, why the constituents are important, and where constituent concentrations vary relative to geology or land use. Water-quality constituents are grouped into logical units to aid presentation: water-quality constituents measured in the field (pH, alkalinity, specific conductance, and dissolved oxygen), common ions, metals, radionuclides, bacteria, nutrients, pesticides, and volatile organic compounds. Water-quality constituents measured in the field, common ions (except chloride), metals, and radionuclides are discussed relative to geology. Bacteria, nutrients, pesticides, and volatile organic compounds are discussed relative to land use. If the U.S. Environmental Protection Agency (USEPA) or Chester County Health Department has drinking water standards for a constituent, the standards are included. Tables and maps are included to assist Chester County residents in understanding the water-quality constituents and their distribution in the county.Ground water in Chester County generally is of good quality and is mostly acidic except in the carbonate rocks and serpentinite, where it is neutral to strongly basic. Calcium carbonate and magnesium carbonate are major constituents of these rocks. Both compounds have high solubility, and, as such, both are major contributors to elevated pH, alkalinity, specific conductance, and the common ions. Elevated pH and alkalinity in carbonate rocks and serpentinite can indicate a potential for scaling in water heaters and household plumbing. Low pH and low alkalinity in the schist, quartzite, and

Concentration of tritium in precipitation and river water

International Nuclear Information System (INIS)

Chatani, Kunio

1983-01-01

The concentration of tritium in precipitation and river water has been measured sice 1973 in Aichi, Japan. The tritium in water samples was enriched by electrolysis, and measured by liquid scintillation counting. The concentration of tritium in precipitation decreased from 27 TU in 1973 to 17 TU in 1979, and showed seasonal variation. During this period, there was a rise of concentration because of Chinese nuclear detonation. The concentration of tritium in river water gradually decreased from 44 TU in 1973 to 24 TU in 1979, and the seasonal variation was not observed. Based on the observed values, the relation among precipitation, river water and ground water was analyzed. (J.P.N.)

Work plan for preliminary investigation of organic constituents in ground water at the New Rifle site, Rifle, Colorado. Revision 2

International Nuclear Information System (INIS)

1996-01-01

A special study screening for Appendix 9 (40 CFR Part 264) analytes identified the New Rifle site as a target for additional screening for organic constituents. Because of this recommendation and the findings in a recent independent technical review, the US Department of Energy (DOE) has requested that the Technical Assistance Contractor (TAC) perform a preliminary investigation of the potential presence of organic compounds in the ground water at the New Rifle Uranium Mill Tailings Remedial Action (UMTRA) Project site, Rifle, Colorado. From 1958 to 1972, organic chemicals were used in large quantities during ore processing at the New Rifle site, and it is possible that some fraction was released to the environment. Therefore, the primary objective of this investigation is to determine whether organic chemicals used at the milling facility are present in the ground water. The purpose of this document is to describe the work that will be performed and the procedures that will be followed during installation of ground water well points at the New Rifle site. The selection of analytes and the procedures for collecting ground water samples for analysis of organic constituents are also described

Exploratory Disposal and Reuse Feasibility Analysis of Winter Maintenance Wash Water.

Science.gov (United States)

Ullinger, Heather L; Kennedy, Marla J; Schneider, William H; Miller, Christopher M

2016-01-01

The Ohio Department of Transportation has more than 60 facilities without sewer access generating approximately 19 million gallons of winter maintenance wash water. Off-site disposal is costly, creating the need for sustainable management strategies. The objective of this study was to conduct an exploratory feasibility analysis to assess wash water disposal and potential reuse as brine. Based on a comprehensive literature review and relevant environmental chemistry, a sampling protocol consisting of 31 water quality constituents was utilized for monthly sampling at three geographically distinct Ohio Department of Transportation garages during the winter of 2012. Results were compared to local disposal and reuse guidance limits. Three constituents, including a maximum copper concentration of 858 ppb, exceeded disposal limits, and many constituents also failed to meet reuse limits. Some concentrations were orders of magnitude higher than reuse limits and suggest pre-treatment would be necessary if wash water were reused as brine. These water quality results, in conjunction with copper chemical equilibrium modeling, show pH and dissolved carbon both significantly impact the total dissolved copper concentration and should be measured to assess reuse potential. The sampling protocol and specific obstacles highlighted in this paper aid in the future development of sustainable wash water management strategies.

Exploratory Disposal and Reuse Feasibility Analysis of Winter Maintenance Wash Water.

Directory of Open Access Journals (Sweden)

Heather L Ullinger

Full Text Available The Ohio Department of Transportation has more than 60 facilities without sewer access generating approximately 19 million gallons of winter maintenance wash water. Off-site disposal is costly, creating the need for sustainable management strategies. The objective of this study was to conduct an exploratory feasibility analysis to assess wash water disposal and potential reuse as brine. Based on a comprehensive literature review and relevant environmental chemistry, a sampling protocol consisting of 31 water quality constituents was utilized for monthly sampling at three geographically distinct Ohio Department of Transportation garages during the winter of 2012. Results were compared to local disposal and reuse guidance limits. Three constituents, including a maximum copper concentration of 858 ppb, exceeded disposal limits, and many constituents also failed to meet reuse limits. Some concentrations were orders of magnitude higher than reuse limits and suggest pre-treatment would be necessary if wash water were reused as brine. These water quality results, in conjunction with copper chemical equilibrium modeling, show pH and dissolved carbon both significantly impact the total dissolved copper concentration and should be measured to assess reuse potential. The sampling protocol and specific obstacles highlighted in this paper aid in the future development of sustainable wash water management strategies.

Concentration and characterization of dissolved organic matter in the surface microlayer and subsurface water of the Bohai Sea, China

Science.gov (United States)

Chen, Yan; Yang, Gui-Peng; Wu, Guan-Wei; Gao, Xian-Chi; Xia, Qing-Yan

2013-01-01

A total of 19 sea-surface microlayer and corresponding subsurface samples collected from the Bohai Sea, China in April 2010 were analyzed for chlorophyll a, dissolved organic carbon (DOC) and its major compound classes including total dissolved carbohydrates (TDCHO, including monosaccharides, MCHO, and polysaccharides, PCHO) and total hydrolysable amino acids (THAA, including dissolved free, DFAA, and combined fraction, DCAA). The concentrations of DOC in the subsurface water ranged from 130.2 to 407.7 μM C, with an average of 225.9±75.4 μM C, while those in the surface microlayer varied between 140.1 and 330.9 μM C, with an average of 217.8±56.8 μM C. The concentrations of chlorophyll a, DOC, TDCHO and THAA in the microlayer were, respectively correlated with their subsurface water concentrations, implying that there was a strong exchange effect between the microlayer and subsurface water. The concentrations of DOC and TDCHO were negatively correlated with salinity, respectively, indicating that water mixing might play an important role in controlling the distribution of DOC and TDCHO in the water column. Major constituents of DCAA and DFAA present in the study area were glycine, alanine, glutamic acid, serine and histidine. Principal component analysis (PCA) was applied to examine the complex compositional differences that existed among the sampling sites. Our results showed that DFAA had higher mole percentages of glycine, valine and serine in the microlayer than in the subsurface water, while DCAA tended to have higher mole percentages of glutamic acid, aspartic acid, threonine, arginine, alanine, tyrosine, phenylalanine and leucine in the microlayer. The yields of TDCHO and THAA exhibited similar trends between the microlayer and subsurface water. Carbohydrate species displayed significant enrichment in the microlayer, whereas the DFAA and DCAA exhibited non-uniform enrichment in the microlayer.

[Nitrate concentrations in tap water in Spain].

Science.gov (United States)

Vitoria, Isidro; Maraver, Francisco; Sánchez-Valverde, Félix; Armijo, Francisco

2015-01-01

To determine nitrate concentrations in drinking water in a sample of Spanish cities. We used ion chromatography to analyze the nitrate concentrations of public drinking water in 108 Spanish municipalities with more than 50,000 inhabitants (supplying 21,290,707 potential individuals). The samples were collected between January and April 2012. The total number of samples tested was 324. The median nitrate concentration was 3.47 mg/L (range: 0.38-66.76; interquartile range: 4.51). The water from 94% of the municipalities contained less than 15 mg/L. The concentration was higher than 25mg/L in only 3 municipalities and was greater than 50mg/L in one. Nitrate levels in most public drinking water supplies in municipalities inhabited by almost half of the Spanish population are below 15 mg/L. Copyright © 2014 SESPAS. Published by Elsevier Espana. All rights reserved.

Tritium concentration and variation of environmental water in China

International Nuclear Information System (INIS)

Ren Tianshan; Zhao Qiufen; Liu Yan; Chen Bingru; Chen Jiashen; Deng Guolun; Gao Pingying; Kuan Yungu

2004-01-01

To estimate the baseline level of tritium concentrations of environmental waters before the operation of the first Chinese nuclear power plant, 1547 water samples of eight categories all over China were sampled in the early 1990s for tritium measurement. The measurements were performed with low background liquid scintillation technology. The average tritium radioactive concentrations were 8.96±4.30, 5.42±0.33, 4.77±1.15, 4.55±0.35, 4.04±0.10, 4.04±0.94, 2.38±0.30, 1.34±0.40 Bq/L for air vapor water, precipitation, river water, lake water, tap water, well water, spring water and sea water, respectively, as listed in Table 1. The results show that the tritium concentations in the early 1990s were significantly lower than that in the 1960s and almost reached to the nature tritium concentrations levels. The index of annual reduction rate of tritium concentrations for most water categories were in the range between -3.1%∼-6.3% in the period of 1978 to 1992, and -4.1%∼-5.7% in the 1990s, however, the averages for air vapor water, precipitation and spring water show slow increase with time in recent years. The regional distribution of tritium concentrations show a tendency being of higher in the north and northwest and lower in the south and southeast, indicating latitude and longitude distribution tendencies. The slopes of tritium concentration-latitude line were in the range of 0.33 - 0.18 (Bq/L)/ degree N for air vapor water, precipitation, river water and spring water, while in the range of 0.012-0.068 (Bq/L)/ degree N. The slopes of tritium concentration-longitude line were in the range of 0.15-0.071 (Bq/L)/ degree E for air vapor water, lake water, tap water and well water, however, the change of tritium concentrations with longitude are not significant. (authors)

Two-dimensional numerical modelling of sediment and chemical constituent transport within the lower reaches of the Athabasca River.

Science.gov (United States)

Kashyap, Shalini; Dibike, Yonas; Shakibaeinia, Ahmad; Prowse, Terry; Droppo, Ian

2017-01-01

Flows and transport of sediment and associated chemical constituents within the lower reaches of the Athabasca River between Fort McMurray and Embarrass Airport are investigated using a two-dimensional (2D) numerical model called Environmental Fluid Dynamics Code (EFDC). The river reach is characterized by complex geometry, including vegetated islands, alternating sand bars and an unpredictable thalweg. The models were setup and validated using available observed data in the region before using them to estimate the levels of cohesive sediment and a select set of chemical constituents, consisting of polycyclic aromatic hydrocarbons (PAHs) and metals, within the river system. Different flow scenarios were considered, and the results show that a large proportion of the cohesive sediment that gets deposited within the study domain originates from the main stem upstream inflow boundary, although Ells River may also contribute substantially during peak flow events. The floodplain, back channels and islands in the river system are found to be the major areas of concern for deposition of sediment and associated chemical constituents. Adsorbed chemical constituents also tend to be greater in the main channel water column, which has higher levels of total suspended sediments, compared to in the flood plain. Moreover, the levels of chemical constituents leaving the river system are found to depend very much on the corresponding river bed concentration levels, resulting in higher outflows with increases in their concentration in the bed sediment.

Tritium concentration in the heavy water upgrading plants

International Nuclear Information System (INIS)

Croitoru, C.; Pop, F.; Titescu, Gh.; Dumitrescu, M.; Ciortea, C.; Stefanescu, I.; Peculea, M.; Pitigoi, Gh.; Trancota, D. . E-mail of corresponding author: croitoru@icsi.ro; Croitoru, C.)

2005-01-01

In the course of time heavy water used in CANDU nuclear power plants, as moderator or coolant, degrades, as a result of its impurification with light water and tritium. Concentration diminution below 99.8% mol for moderator and 99.75% mol for coolant causes an inefficient functioning of CANDU reactor. By isotopic distillation, light water is removed. Simultaneously tritium concentration takes place. The heavy water upgrading plant from Cernavoda is an isotopic separation cascade with two stages. The paper presents, for this plant, a theoretical study of the tritium concentration. (author)

Separation of the constituents of coal

Energy Technology Data Exchange (ETDEWEB)

Betrand, M F

1938-12-06

A process is disclosed of separating, by means of dense aqueous solutions, the constituents of coal, isolated by preliminary crushing from each other and/or from barren and carbonaceous shales, comprising the addition to the washing water before treatment or during any stage of the preparation of the coal before separation, or to the dense separating solution of agents improving the wetting of the coal by water.

Radon concentrations in well water in Sichuan Province, China

International Nuclear Information System (INIS)

Chen Yibin; Wu Qun; Zhang Bo; Chen Daifu

1998-01-01

There are 110 million people in Sichuan Province, China. Although most of the people in cities of Sichuan use river water, which contains low levels of radon, as potable water, people in countryside and in some communities of big cities still use well water as domestic consumption. This paper reports the radon concentrations in well water investigated in four cities, i.e. Chengdu, Chongqing, Leshan and Leijiang in Sichuan Province. Of the 80 wells investigated, the radon concentrations range from 3.5 to 181.6 KBqm -3 . Of the four cities, Chongqing has the highest well water radon concentration with the average 49.6 ± 54.1 KBqm -3 and the greatest variation. The investigation in four cities showed that the radon concentrations in well water are much higher than that in tap-water. In Chongqing where there are complex geological structures, mainly granite stratum, for example, the average radon concentration in well water is 112 times higher than that in the tap-water, and even much higher than that in river water in Yangtse River, Jialing River, Jinsha River and Mingjiang River. The population in four cities is about one sixth of the total population in Sichuan Province. Because of the common use of well water and the high radon concentrations in well water in Sichuan Province, the health effect of radon in well water to the public should be stressed. (author)

Factors Affecting Source-Water Quality after Disturbance of Forests by Wildfire

Science.gov (United States)

Murphy, S. F.; Martin, D. A.; McCleskey, R. B.; Writer, J. H.

2015-12-01

Forests yield high-quality water supplies to communities throughout the world, in part because forest cover reduces flooding and the consequent transport of suspended and dissolved constituents to surface water. Disturbance by wildfire reduces or eliminates forest cover, leaving watersheds susceptible to increased surface runoff during storms and reduced ability to retain contaminants. We assessed water-quality response to hydrologic events for three years after a wildfire in the Fourmile Creek Watershed, near Boulder, Colorado, and found that hydrologic and geochemical responses downstream of a burned area were primarily driven by small, brief convective storms that had relatively high, but not unusual, rainfall intensity. Total suspended sediment, dissolved organic carbon, nitrate, and manganese concentrations were 10-156 times higher downstream of a burned area compared to upstream, and water quality was sufficiently impaired to pose water-treatment concerns. The response in both concentration and yield of water-quality constituents differed depending on source availability and dominant watershed processes controlling the constituent. For example, while all constituent concentrations were highest during storm events, annual sediment yields downstream of the burned area were controlled by storm events and subsequent mobilization, whereas dissolved organic carbon yields were more dependent on spring runoff from upstream areas. The watershed response was affected by a legacy of historical disturbance: the watershed had been recovering from extensive disturbance by mining, railroad and road development, logging, and fires in the late 19th and early 20th centuries, and we observed extensive erosion of mine waste in response to these summer storms. Therefore, both storm characteristics and historical disturbance in a burned watershed must be considered when evaluating the role of wildfire on water quality.

Radon concentration measurements in waters in Greece and Cyprus

International Nuclear Information System (INIS)

Louizi, A.; Nikolopoulos, D.; Tzortzi, A.; Thanassas, D.; Serefoglou, A.; Georgiou, E.; Vogiannis, E.; Koukouliou, V.

2004-01-01

The radon content of drinking water samples was determined with Alpha Guard Pro equipped with an appropriate unit (Aqua Kit). The samples were collected from water taps in dwellings located at various cities in Greece and Cyprus. In addition, surface water samples from rivers, lakes and seas as well as potable underground and hot spring water samples from Greece and Cyprus were also collected. For a precise determination of radon concentration in water samples, special procedures were followed both for sampling and transportation, as well as for measurement. Intercomparison experiments were designed and implemented before and during the study. Radon concentrations in drinking water samples in Greece ranged between 1.1 ± 0.5 Bq/L and 410±50 Bq/L. The corresponding concentrations in Cyprus ranged between 1.3 ± 0.8 Bq/L and 15±4 Bq/L. Three samples collected from the city of Arnea Chalkidikis (Northern Greece) exhibited high concentrations of 120±20 Bq/L, 320±40 Bq/L and 410±50 Bq/L. This city is identified as a high radon potential area. One water sample located in Lesvos Island (North-East part of Greece) exhibited radon concentration 140±20 Bq/L. Additional six samples displayed high concentrations in potable hot spring water samples. These samples which were collected from the city of Loutraki (Peloponnesus) ranged between 220-230 Bq/L. In addition, two samples characterized as 'medicinal drinking water' gave concentrations between 320 Bq/L and 340 Bq/L. For underground water samples the radon concentrations ranged between 1.2±0.7 Bq/L and 15±4 Bq/L, while for surface water samples the range was 2.7±0.8 Bq/L to 24±6 Bq/L. The observed concentrations of radon gas in potable water samples in Greece were found to be largely low. In Cyprus, they were all well below 15 Bq/L

Chemical constituents: water-soluble vitamins, free amino acids and sugar profile from Ganoderma adspersum.

Science.gov (United States)

Kıvrak, İbrahim

2015-01-01

Ganoderma adspersum presents a rigid fruiting body owing to chitin content and having a small quantity of water or moisture. The utility of bioactive constituent of the mushroom can only be available by extraction for human usage. In this study, carbohydrate, water-soluble vitamin compositions and amino acid contents were determined in G. adspersum mushroom. The composition in individual sugars was determined by HPLC-RID, mannitol (13.04 g/100 g) and trehalose (10.27 g/100 g) being the most abundant sugars. The examination of water-soluble vitamins and free amino acid composition was determined by UPLC-ESI-MS/MS. Essential amino acid constituted 67.79% of total amino acid, which is well worth the attention with regard to researchers and consumers. In addition, G. adspersum, which is also significantly rich in B group vitamins and vitamin C, can provide a wide range of notable applications in the pharmaceutics, cosmetics, food and dietary supplement industries. G. adspersum revealed its value for pharmacy and nutrition fields.

Urban Wastewater Impacts on the Spatial Distribution of Solutes and Microbial Constituents in the Musi River, India

Science.gov (United States)

Ensink, J.; Scott, C. A.; Cairncross, S.

2006-05-01

Wastewater discharge from expanding urban centers deteriorates the quality of receiving waters, a trend that has management and investment implications for cities around the world. This paper presents the results of a 14-month water quality evaluation over a 40-km longitudinal profile downstream of the city of Hyderabad, India (population 7 million) on the Musi River, a tributary to the Krishna River. Upstream to downstream improvements in Musi water quality for microbial constituents (nematode egg, faecal coliform), dissolved oxygen, and nitrate are attributed to natural attenuation processes (dilution, die-off, sedimentation and biological processes) coupled with the effects of in-stream hydraulic infrastructure (weirs and reservoirs). Conversely, upstream to downstream increases in total dissolved solids concentrations are caused by off- stream infrastructure and agricultural water use resulting in crop evapotranspiration and increased solute concentration in the return flow of irrigation diverted upstream in the wastewater system. Future water quality management challenges resulting from rampant urban growth, particularly in developing countries, are discussed.

Distribution of exposure concentrations and doses for constituents of environmental tobacco smoke

Energy Technology Data Exchange (ETDEWEB)

LaKind, J.S. [LaKind Associates (United States); Ginevan, M.E. [M.E. Ginevan and Associates (United States); Naiman, D.Q. [Johns Hopkins Univ., Baltimore, MD (United States). Dept. of Mathematical Sciences; James, A.C. [A.C. James and Associates (United States); Jenkins, R.A. [Oak Ridge National Lab., TN (United States); Dourson, M.L.; Felter, S.P. [TERA (United States); Graves, C.G.; Tardiff, R.G. [Sapphire Group, Inc., Bethesda, MD (United States)

1999-06-01

The ultimate goal of the research reported in this series of three articles is to derive distributions of doses of selected environmental tobacco smoke (ETS)-related chemicals for nonsmoking workers. This analysis uses data from the 16-City Study collected with personal monitors over the course of one workday in workplaces where smoking occurred. In this article, the authors describe distributions of ETS chemical concentrations and the characteristics of those distributions for the workplace exposure. Next, they present population parameters relevant for estimating dose distributions and the methods used for estimating those dose distributions. Finally, they derive distributions of doses of selected ETS-related constituents obtained in the workplace for people in smoking work environments. Estimating dose distributions provided information beyond the usual point estimate of dose and showed that the preponderance of individuals exposed to ETS in the workplace were exposed at the low end of the dose distribution curve. The results of this analysis include estimations of hourly maxima and time-weighted average (TWA) doses of nicotine from workplace exposures to ETS and doses derived from modeled lung burdens of ultraviolet-absorbing particulate matter (UVPM) and solanesol resulting from workplace exposures to ETS (extrapolated from 1 day to 1 year).

Radon concentration measurements in waters in Greece and Cyprus

International Nuclear Information System (INIS)

Louizi, A.; Nikolopoulos, D.; Tzortzi, A.; Thanassas, D.; Serefoglou, A.; Georgiou, E.; Vogiannis, E.; Koukouliou, V.

2004-01-01

A total of 35 measurements in Greece and 15 in Cyprus were performed. Radon concentrations in drinking water in Greece were from (1.1±0.5) to (410±50) Bq/L. The corresponding concentrations in underground potable waters in Cyprus ranged between (0.4±0.3) Bq/L and (15±4) Bq/L. High concentrations, viz. (120±20), (320±40) and (410±50) Bq/L, were observed in three samples collected from the city of Arnea Chalkidekis in northern Greece. One water sample from Lesvos Island (north-eastern part of Greece) exhibited a radon concentration of (140±20) Bq/L. Six samples of hot spring water from the city of Loutraki (Attica prefecture), characterized as 'medicinal drinking water', contained concentrations of radon between (220±10) and (340±20) Bq/L. Radon concentrations in potable and non-potable underground water in Greece and Cyprus ranged between (0.4±0.3) and (15±4) Bq/L, whereas in surface water the range was from (2.7±0.8) to (24±6) Bq/L. (P.A.)

Ground-Water Quality Data in the Central Sierra Study Unit, 2006 - Results from the California GAMA Program

Science.gov (United States)

Ferrari, Matthew J.; Fram, Miranda S.; Belitz, Kenneth

2008-01-01

the results for these samples were used to evaluate the quality of the data for the ground-water samples. Results from field blanks indicated contamination was not a noticeable source of bias in the data for ground-water samples. Differences between replicate samples were within acceptable ranges, indicating acceptably low variability. Matrix spike recoveries were within acceptable ranges for most constituents. This study did not attempt to evaluate the quality of water delivered to consumers; after withdrawal from the ground, water typically is treated, disinfected, or blended with other waters to maintain water quality. Regulatory thresholds apply to water that is served to the consumer, not to raw ground water. However, to provide some context for the results, concentrations of constituents measured in the raw ground water were compared with health-based thresholds established by the U.S. Environmental Protection Agency (USEPA) and California Department of Public Health (CDPH), and thresholds established for aesthetic concerns (Secondary Maximum Contaminant Levels, SMCL-CA) by CDPH. Therefore, any comparisons of the results of this study to drinking-water standards only is for illustrative purposes and is not indicative of compliance or non-compliance to those standards. Most constituents that were detected in ground-water samples were found at concentrations below drinking-water standards or thresholds. Six constituents? fluoride, arsenic, molybdenum, uranium, gross-alpha radioactivity, and radon-222?were detected at concentrations higher than thresholds set for health-based regulatory purposes. Three additional constituents?pH, iron and manganese?were detected at concentrations above thresholds set for aesthetic concerns. Volatile organic compounds (VOCs) and pesticides, were detected in less than one-third of the samples and generally at less than one one-hundredth of a health-based threshold.

Analysis of the Difference of Radon Concentration between Water Treatment Plant and Tap water in house

International Nuclear Information System (INIS)

Seo, Jeongil; Yoo, Donghan; Kim, Heereyoung

2013-01-01

As importance for the health, measurements and analysis about radon is active recently. Especially, radon concentration measurement about underground water which people drink was been carried out by the environment organizations in Korea and has been hot-issued because of the high radon concentration in water source. In present study, the difference of radon concentration among water source, water treatment plant and tap water in house is analyzed. It makes sense that the radon concentration in water treatment plant can represent the radon concentration in the tap water. Through the above experiments, the difference of the radon concentration between water treatment plant and tap water in house is figured out. It contributes to confirm more specific basis for estimating the annual radon exposure for the public. With further experiments and analysis, it is thought that it will be used as tool to assess more qualitatively for the radon concentration in tap water. Finally, this Fundamental approach will help in making new regulations about radon

Analysis of the Difference of Radon Concentration between Water Treatment Plant and Tap water in house

Energy Technology Data Exchange (ETDEWEB)

Seo, Jeongil; Yoo, Donghan; Kim, Heereyoung [Ulsan National Institute of Science and Technology, Ulsan (Korea, Republic of)

2013-05-15

As importance for the health, measurements and analysis about radon is active recently. Especially, radon concentration measurement about underground water which people drink was been carried out by the environment organizations in Korea and has been hot-issued because of the high radon concentration in water source. In present study, the difference of radon concentration among water source, water treatment plant and tap water in house is analyzed. It makes sense that the radon concentration in water treatment plant can represent the radon concentration in the tap water. Through the above experiments, the difference of the radon concentration between water treatment plant and tap water in house is figured out. It contributes to confirm more specific basis for estimating the annual radon exposure for the public. With further experiments and analysis, it is thought that it will be used as tool to assess more qualitatively for the radon concentration in tap water. Finally, this Fundamental approach will help in making new regulations about radon.

Radon concentrations in drinking water in Wakasa area, Fukui Prefecture

Energy Technology Data Exchange (ETDEWEB)

Tokuyama, Hideki; Igarashi, Shuichi [Fukui Prefectural Environmental Radiation Research and Monitoring Center, Tsuruga (Japan)

1997-02-01

Radon concentration in drinking water was surveyed to make basic data for the investigation of radiation dose due to natural radioisotopes in the general public. Here, the survey data in the Wakasa region were reported. Sampling was carried out at 126 points in this region (ca. 70x50 km{sup 2}). A total of 167 samples were taken from the tap of private wells, and small and large public water supplies. The radon concentration was determined by direct measuring method. The mean concentration of ground water from the wells was 28.5 Bq/l, significantly higher than those of the tap water from small and large water supplies, 5.0 and 11.2 Bq/l, respectively. Rn concentration of ground water was dependent on geological features and it was comparatively high in the granite region. Ground water containing a high concentration of Rn was mixed into the water of some large water supply in the cities, showing that its Rn concentration was higher compared to those for the small water supply. This survey was conducted only in the winter seasons from 1989 to 1993. Therefore, there are no data concerning seasonal changes in Rn concentration to drinking water. (M.N.)

Quality of ground water in Clark County, Washington, 1988

International Nuclear Information System (INIS)

Turney, G.L.

1990-01-01

Water samples were collected from 76 wells throughout Clark County, in southwest Washington, during April and May 1988, and were analyzed from concentrations of major ions, silica, nitrate, phosphorus, aluminum, manganese, radon, and bacteria. Samples from 20 wells were analyzed for concentrations of trace elements and organic compounds, including most of those on the US Environmental Protection Agency (USEPA) priority pollutant list. Dissolved solids concentrations range from 12 to 245 mg/L, with a median concentration of 132 mg/L. The major dissolved constituents are calcium, bicarbonate, and silica, and, in some samples, sodium. Nitrate concentrations exceeded 1.0 mg/L throughout the Vancouver urban area, and were as large as 6.7 mg/L. Comparison with limited historical data indicates that nitrate concentrations were somewhat correlated, possibly indicating similar sources. Volatile organic compound, including tetrachloroethane and 1,1,1-trichloroethane, were detected in samples from three wells in the Vancouver area. Trace amounts of volatile organic compounds were reported in samples from several other wells, but at concentrations too close to analytical detection limits to ascertain that they were in the groundwater. Trace elements and radiochemical constituents were present at small levels indicating natural sources for these constituents. Only pH, turbidity, iron, manganese, and total coliform bacteria had values that did not meet USEPA Drinking Water Standards

Remote Estimation of Chlorophyll-a in Inland Waters by a NIR-Red-Based Algorithm: Validation in Asian Lakes

Directory of Open Access Journals (Sweden)

Gongliang Yu

2014-04-01

Full Text Available Satellite remote sensing is a highly useful tool for monitoring chlorophyll-a concentration (Chl-a in water bodies. Remote sensing algorithms based on near-infrared-red (NIR-red wavelengths have demonstrated great potential for retrieving Chl-a in inland waters. This study tested the performance of a recently developed NIR-red based algorithm, SAMO-LUT (Semi-Analytical Model Optimizing and Look-Up Tables, using an extensive dataset collected from five Asian lakes. Results demonstrated that Chl-a retrieved by the SAMO-LUT algorithm was strongly correlated with measured Chl-a (R2 = 0.94, and the root-mean-square error (RMSE and normalized root-mean-square error (NRMS were 8.9 mg∙m−3 and 72.6%, respectively. However, the SAMO-LUT algorithm yielded large errors for sites where Chl-a was less than 10 mg∙m−3 (RMSE = 1.8 mg∙m−3 and NRMS = 217.9%. This was because differences in water-leaving radiances at the NIR-red wavelengths (i.e., 665 nm, 705 nm and 754 nm used in the SAMO-LUT were too small due to low concentrations of water constituents. Using a blue-green algorithm (OC4E instead of the SAMO-LUT for the waters with low constituent concentrations would have reduced the RMSE and NRMS to 1.0 mg∙m−3 and 16.0%, respectively. This indicates (1 the NIR-red algorithm does not work well when water constituent concentrations are relatively low; (2 different algorithms should be used in light of water constituent concentration; and thus (3 it is necessary to develop a classification method for selecting the appropriate algorithm.

Concentration data for anthropogenic organic compounds in ground water, surface water, and finished water of selected community water systems in the United States, 2002-05

Science.gov (United States)

Carter, Janet M.; Delzer, Gregory C.; Kingsbury, James A.; Hopple, Jessica A.

2007-01-01

combustion-derived compounds; (10) personal care and domestic use products; (11) plant- or animal-derived biochemicals; (12) refrigerants and propellants; and (13) solvents. Source and finished water samples were collected during phase 2 and analyzed for constituents that were detected frequently during phase 1. This report presents concentration data for AOCs in ground water, surface water, and finished water of CWSs sampled for SWQA studies during 2002-05. Specifically, this report presents the analytical results of samples collected during phase 1 including (1) samples from 221 wells that were analyzed for 258 AOCs; (2) monthly samples from 9 surface-water sites that were analyzed for 258 AOCs during phase 1; and (3) samples from a subset of the wells and surface-water sites located in areas with substantial agricultural production that were analyzed for 3 additional pesticides and 16 pesticide degradates. Samples collected during phase 2 were analyzed for selected AOCs that were detected most frequently in source water during phase 1 sampling; analytical results for phase 2 are presented for (1) samples of source water and finished water from 94 wells; and (2) samples of source water and finished water samples that were collected monthly and during selected flow conditions at 8 surface-water sites. Results of quality-assurance/quality-control samples collected for SWQA studies during 2002-05 also are presented.

Activity Concentrations of radionuclides in sea water in some Coastal Egyptian Regions and Their Public Health Impacts

International Nuclear Information System (INIS)

Sefien, S.M.; Abdel Malik, W.E.Y.; Ibrahim, A.S.; Yousef, S.K.

2008-01-01

Extensive investigations have been carried out monthly for one year period in order to find out the average activity concentrations of the natural radionuclide in some Egyptian coastal aquatic environment and to assess the annual radiation doses likely to be received by population near by. The determinations were mainly for the measurement of gross α, β and γ activities in sea water samples and some of its constituents. It has been found that; the average gross α, β and γ activities in sea water samples for the different studied locations ranged from (0-52) x 10 -3 ,(3-68) x10 -3 and (13-283) x10 -3 Bq.l -1 respectively but still below the recommended permissible limits in most locations. It was found that Rashid area posses the highest concentrations of uranium and thorium. The present results have shown that the radio activities of most of the locations are mainly due to naturally occurring radionuclide. No regular tendency increase was observed in activity concentrations of any particular radionuclide in the studied period. Calculations have shown that, the average external dose from the γ- emitting radionuclide is ranged over (0.5-177)x10 -3 nGy/hr with annual exposure dose ranged from (1.04-29)x10 -3 nGy in most locations except Rashid. This exposure dose does not present radiological injuries to the population

Composite measures of watershed health from a water quality perspective

Science.gov (United States)

Water quality data at gaging stations are typically compared with established federal, state, or local water quality standards to determine if violations (concentrations of specific constituents falling outside acceptable limits) have occurred. Based on the frequency and severity...

Storm water runoff concentration matrix for urban areas

Science.gov (United States)

Göbel, P.; Dierkes, C.; Coldewey, W. G.

2007-04-01

The infrastructure (roads, sidewalk, commercial and residential structures) added during the land development and urbanisation process is designed to collect precipitation and convey it out of the watershed, typically in existing surface water channels, such as streams and rivers. The quality of surface water, seepage water and ground water is influenced by pollutants that collect on impervious surfaces and that are carried by urban storm water runoff. Heavy metals, e.g. lead (Pb), zinc (Zn), copper (Cu), cadmium (Cd), polycyclic aromatic hydrocarbons (PAH), mineral oil hydrocarbons (MOH) and readily soluble salts in runoff, contribute to the degradation of water. An intensive literature search on the distribution and concentration of the surface-dependent runoff water has been compiled. Concentration variations of several pollutants derived from different surfaces have been averaged. More than 300 references providing about 1300 data for different pollutants culminate in a representative concentration matrix consisting of medians and extreme values. This matrix can be applied to long-term valuations and numerical modelling of storm water treatment facilities.

Identification of dissolved-constituent sources in mine-site ground water using batch mixing

International Nuclear Information System (INIS)

Clark, G.M.; Williams, R.S. Jr.

1991-01-01

Batch-mixing experiments were used to help identify lithologic mineralogic sources of increased concentrations of dissolved solids in water affected by surface coal mining in northwestern Colorado. Ten overburden core samples were analyzed for mineral composition and mixed with distilled water for 90 days until mineral-water equilibrium was reached. Dissolved-solids concentrations ranged from 200 to 8,700 mg/L in water samples extracted from the mixtures after 90 days. Mass-balance simulations were conducted using the geochemical models BALANCE and WATEQF to quantify mineral-water interactions occurring in five selected sample mixtures and in water collected from a spring at a reclaimed mine site. The spring water is affected by mineral-water interactions occurring in all of lithologic units comprising the overburden. Results of the simulations indicate that oxidation of pyrite, dissolution of dolomite, gypsum, and epsomite, and cation-exchange reactions are the primary mineral-water interactions occurring in the overburden. Three lithologic units in the overburden probably contribute most of the dissolved solids to the spring water. Water sample extracts from mixtures using core from these three units accounted for 85 percent of the total dissolved solids in the 10 sample extracts. Other lithologic units in the overburden probably contribute smaller quantities of dissolved solids to the spring water

Groundwater and surface-water interaction, water quality, and processes affecting loads of dissolved solids, selenium, and uranium in Fountain Creek near Pueblo, Colorado, 2012–2014

Science.gov (United States)

Arnold, L. Rick; Ortiz, Roderick F.; Brown, Christopher R.; Watts, Kenneth R.

2016-11-28

groundwater. However, during periods of high streamflow, the hydraulic gradient between groundwater and the stream temporarily reversed, causing the stream to lose flow to groundwater.Concentrations of dissolved solids, selenium, and uranium in groundwater generally had greater spatial variability than surface water or hyporheic-zone samples, and constituent concentrations in groundwater generally were greater than in surface water. Constituent concentrations in the hyporheic zone typically were similar to or intermediate between concentrations in groundwater and surface water. Concentrations of dissolved solids, selenium, uranium, and other constituents in groundwater samples collected from wells located on the east side of the north monitoring well transect were substantially greater than for other groundwater, surface-water, and hyporheic-zone samples. With one exception, groundwater samples collected from wells on the east side of the north transect exhibited oxic to mixed (oxic-anoxic) conditions, whereas most other groundwater samples exhibited anoxic to suboxic conditions. Concentrations of dissolved solids, selenium, and uranium in surface water generally increased in a downstream direction along Fountain Creek from the north transect to the south transect and exhibited an inverse relation to streamflow with highest concentration occurring during periods of low streamflow and lowest concentrations occurring during periods of high streamflow.Groundwater loads of dissolved solids, selenium, and uranium to Fountain Creek were small because of the small amount of groundwater flowing to the stream under typical low-streamflow conditions. In-stream loads of dissolved solids, selenium, and uranium in Fountain Creek varied by date, primarily in relation to streamflow at each transect and were much larger than computed constituent loads from groundwater. In-stream loads generally decreased with decreases in streamflow and increased as streamflow increased. In-stream loads of

Scientific substantination of maximum allowable concentration of fluopicolide in water

Directory of Open Access Journals (Sweden)

Pelo I.М.

2014-03-01

Full Text Available In order to substantiate fluopicolide maximum allowable concentration in the water of water reservoirs the research was carried out. Methods of study: laboratory hygienic experiment using organoleptic and sanitary-chemical, sanitary-toxicological, sanitary-microbiological and mathematical methods. The results of fluopicolide influence on organoleptic properties of water, sanitary regimen of reservoirs for household purposes were given and its subthreshold concentration in water by sanitary and toxicological hazard index was calculated. The threshold concentration of the substance by the main hazard criteria was established, the maximum allowable concentration in water was substantiated. The studies led to the following conclusions: fluopicolide threshold concentration in water by organoleptic hazard index (limiting criterion – the smell – 0.15 mg/dm3, general sanitary hazard index (limiting criteria – impact on the number of saprophytic microflora, biochemical oxygen demand and nitrification – 0.015 mg/dm3, the maximum noneffective concentration – 0.14 mg/dm3, the maximum allowable concentration - 0.015 mg/dm3.

Radon concentration of waters in Greece and Cyprus

Science.gov (United States)

Nikolopoulos, D.; Vogiannis, E.; Louizi, A.

2009-04-01

Radon (222Rn) is a radioactive gas generated by the decay of the naturally occurring 238U series. It is considered very important from radiological point of view, since it is the most significant natural source of human radiation exposure (approximately 50% from all natural sources). Radon is present in soil, rocks, building materials and waters. Through diffusion and convection, radon migrates and emanates to the atmosphere. Outdoors, radon concentrates at low levels (in the order of 10 Bq/m3). However indoors, radon accumulates significantly. It is trivial to observe indoor environments with high radon levels (in the order of 400 Bq/m3 or higher). Radon accumulation indoors, depends on the composition of the underlying soil and rock formation, on building materials, meteorological parameters, ventilation, heating and water use. Although soil and building materials are the most significant radon sources, there have been reported elevated radon concentrations in building structures due to entering water. It is the radon concentrations in the entering water, the volume and the way of water usage, separated or in combination, that result in large amounts of radon in indoor air. Moreover, radon is a factor of stomach radiation burden due to water consumption. This burden is estimated by measurements of radon concentrations in waters. Due to the health impact of radon exposure, the reporting team continuously measures radon. This work focused on the radon concentrations exposure due to water consumption and use in Greece and Cyprus. Various locations in Greece and Cyprus were accessed taking into consideration existing natural radioactivity data (mainly radon in water), however under the restriction of the capability of movement. Radon in water was measured by Alpha Guard (Genitron Ltd) via a special unit (Aqua Kit). This unit consists of a vessel used for forced degassing of radon diluted in water samples, a security vessel used for water drop deposition. Vessels and

Concentration of viruses from water on bituminous coal

Energy Technology Data Exchange (ETDEWEB)

Lakhe, S.B.; Parhad, N.M.

1988-05-01

The potential of bituminous coal for adsorption of viruses, using poliovirus as a model, was investigated. Influence of pH of water on the adsorption of viruses on a coal bed with and without addition of cation (Al/sup 3 +/) indicated that poliovirus could be adsorbed efficiently at pH 5 in presence of AlCl/sub 3/ at a concentration of 0.0005 M. studies on the effect of different concentrations of monovalent, divalent and trivalent cations showed that the trivalent cation was more effective and was required at a lower concentration than other cations tested. A coal bed of 1.5 g could adsorb as high as 204,000 PFU from water based on the absence of virus in the filtrate. Total organic carbon content of the water did not interfere in virus adsorption to coal. The results obtained indicated that a bituminous coal bed could be used as one of the methods for efficient concentration of viruses from water. 31 refs., 8 tabs.

Mass imbalances in EPANET water-quality simulations

Science.gov (United States)

Davis, Michael J.; Janke, Robert; Taxon, Thomas N.

2018-04-01

EPANET is widely employed to simulate water quality in water distribution systems. However, in general, the time-driven simulation approach used to determine concentrations of water-quality constituents provides accurate results only for short water-quality time steps. Overly long time steps can yield errors in concentration estimates and can result in situations in which constituent mass is not conserved. The use of a time step that is sufficiently short to avoid these problems may not always be feasible. The absence of EPANET errors or warnings does not ensure conservation of mass. This paper provides examples illustrating mass imbalances and explains how such imbalances can occur because of fundamental limitations in the water-quality routing algorithm used in EPANET. In general, these limitations cannot be overcome by the use of improved water-quality modeling practices. This paper also presents a preliminary event-driven approach that conserves mass with a water-quality time step that is as long as the hydraulic time step. Results obtained using the current approach converge, or tend to converge, toward those obtained using the preliminary event-driven approach as the water-quality time step decreases. Improving the water-quality routing algorithm used in EPANET could eliminate mass imbalances and related errors in estimated concentrations. The results presented in this paper should be of value to those who perform water-quality simulations using EPANET or use the results of such simulations, including utility managers and engineers.

Water-quality characteristics for selected sites on the Cape Fear River, North Carolina, 1955-80; variability, loads, and trends of selected constituents

Science.gov (United States)

Crawford, J. Kent

1983-01-01

. Nuisance algal growths have not been identified as a problem in the river. Comparisons of water-quality data for baseline (natural) and present conditions indicate that more than 50 percent of most dissolved substances and over 80 percent of certain forms of nitrogen and phosph6rus result from development. Over the past 25 years, increases in concentrations of specific conductance, dissolved magnesium, dissolved sodium, dissolved potassium, dissolved sulfate, dissolved solids, and total nitrite plus nitrate nitrogen were detected in the Cape Fear River at Lock 1. Values for pH and dissolved silica are decreasing. Concentrations of most dissolved constituents at Lock 1 are increasing. These increases are statistically related to increases in population and manufacturing employment in the basin but are unrelated to agricultural activity.

Water-Quality Constituents, Dissolved-Organic-Carbon Fractions, and Disinfection By-Product Formation in Water from Community Water-Supply Wells in New Jersey, 1998-99

Science.gov (United States)

Hopple, Jessica A.; Barringer, Julia L.; Koleis, Janece

2007-01-01

Water samples were collected from 20 community water-supply wells in New Jersey to assess the chemical quality of the water before and after chlorination, to characterize the types of organic carbon present, and to determine the disinfection by-product formation potential. Water from the selected wells previously had been shown to contain concentrations of dissolved organic carbon (DOC) that were greater than 0.2 mg/L. Of the selected wells, five are completed in unconfined (or semi-confined) glacial-sediment aquifers of the Piedmont and Highlands (New England) Physiographic Provinces, five are completed in unconfined bedrock aquifers of the Piedmont Physiographic Province, and ten are completed in unconsolidated sediments of the Coastal Plain Physiographic Province. Four of the ten wells in the Coastal Plain are completed in confined parts of the aquifers; the other six are in unconfined aquifers. One or more volatile organic compounds (VOCs) were detected in untreated water from all of the 16 wells in unconfined aquifers, some at concentrations greater than maximum contaminant levels. Those compounds detected included aliphatic compounds such as trichloroethylene and 1,1,1-trichloroethane, aromatic compounds such as benzene, the trihalomethane compound, chloroform, and the gasoline additive methyl tert-butyl ether (MTBE). Concentrations of sodium and chloride in water from one well in a bedrock aquifer and sulfate in water from another exceeded New Jersey secondary standards for drinking water. The source of the sulfate was geologic materials, but the sodium and chloride probably were derived from human inputs. DOC fractions were separated by passing water samples through XAD resin columns to determine hydrophobic fractions from hydrophilic fractions. Concentrations of hydrophobic acids were slightly lower than those of combined hydrophilic acids, neutral compounds, and low molecular weight compounds in most samples. Water samples from the 20 wells were adjusted

Analysis of gamma irradiated pepper constituents, 2

International Nuclear Information System (INIS)

Takagi, Kazuko; Ochiai, Junko; Okuyama, Tsuneo

1988-01-01

Black pepper, white pepper, frozen green pepper and real pink pepper (kept in vinegar) were analyzed by reversed phase IIPLC. The extraction method and HPLC conditions were same as the first report, that is, the extraction from pepper was performed by Automatic Air Hammer and the extracted samples were separated on a reversed phase C 8 column with a concave gradient from 0.1% trifluoro aceticacid (TFA) in water to 75% acetonitrile - 0.1% TFA in water for 60 minutes and detected at 210 nm, 280 nm. The different constituents were observed clearly on chromatogram between black pepper and white pepper. The different constituents were observed between different producing white peppers, and as the result that the analyzed pepper was distinguished its producing district by HPLC chromatogram. In order to investigate of effect of lyophilization on white pepper extracts, lyophilized extraction was analyzed by this HPLC method. Some peaks were decreased by lyophilization. The effect of heat on white pepper constituents was examined. White pepper was heated by electronic oven and thermostat. When the former method was used, decreased peak number (peak height was lower than without heat treatment) was more than latter method. These subtle change was able to be recognized by these HPLC chromatograms. (author)

Inorganic Constituents in Coal

Directory of Open Access Journals (Sweden)

Rađenović A.

2006-02-01

Full Text Available Coal contains not only organic matter but also small amounts of inorganic constituents. More thanone hundred different minerals and virtually every element in the periodic table have been foundin coal. Commonly found group minerals in coal are: major (quartz, pyrite, clays and carbonates,minor, and trace minerals. Coal includes a lot of elements of low mass fraction of the orderof w=0.01 or 0.001 %. They are trace elements connected with organic matter or minerals comprisedin coal. The fractions of trace elements usually decrease when the rank of coal increases.Fractions of the inorganic elements are different, depending on the coal bed and basin. A varietyof analytical methods and techniques can be used to determine the mass fractions, mode ofoccurrence, and distribution of organic constituents in coal. There are many different instrumentalmethods for analysis of coal and coal products but atomic absorption spectroscopy – AAS is theone most commonly used. Fraction and mode of occurrence are one of the main factors that haveinfluence on transformation and separation of inorganic constituents during coal conversion.Coal, as an important world energy source and component for non-fuels usage, will be continuouslyand widely used in the future due to its relatively abundant reserves. However, there is aconflict between the requirements for increased use of coal on the one hand and less pollution onthe other. It’s known that the environmental impacts, due to either coal mining or coal usage, canbe: air, water and land pollution. Although, minor components, inorganic constituents can exert asignificant influence on the economic value, utilization, and environmental impact of the coal.

Assessment of heavy metals concentration in drinking water ...

African Journals Online (AJOL)

The concentration of all the metals were considerably found to be below the limit permitted by WHO's drinking water guidelines (WHO 2005). Findings suggest that continues water quality monitoring should be carried out to check the concentration levels of heavy metals in that area, to prevent them from been above the limit ...

Water Quality of Combined Sewer Overflows, Stormwater, and Streams, Omaha, Nebraska, 2006-07

Science.gov (United States)

Vogel, Jason R.; Frankforter, Jill D.; Rus, David L.; Hobza, Christopher M.; Moser, Matthew T.

2009-01-01

The U.S. Geological Survey, in cooperation with the City of Omaha, investigated the water quality of combined sewer overflows, stormwater, and streams in the Omaha, Nebraska, area by collecting and analyzing 1,175 water samples from August 2006 through October 2007. The study area included the drainage area of Papillion Creek at Capeheart Road near Bellevue, Nebraska, which encompasses the tributary drainages of the Big and Little Papillion Creeks and Cole Creek, along with the Missouri River reach that is adjacent to Omaha. Of the 101 constituents analyzed during the study, 100 were detected in at least 1 sample during the study. Spatial and seasonal comparisons were completed for environmental samples. Measured concentrations in stream samples were compared to water-quality criteria for pollutants of concern. Finally, the mass loads of water-quality constituents in the combined sewer overflow discharges, stormwater outfalls, and streams were computed and compared. The results of the study indicate that combined sewer overflow and stormwater discharges are affecting the water quality of the streams in the Omaha area. At the Papillion Creek Basin sites, Escherichia coli densities were greater than 126 units per 100 milliliters in 99 percent of the samples (212 of 213 samples analyzed for Escherichia coli) collected during the recreational-use season from May through September (in 2006 and 2007). Escherichia coli densities in 76 percent of Missouri River samples (39 of 51 samples) were greater than 126 units per 100 milliliters in samples collected from May through September (in 2006 and 2007). None of the constituents with human health criteria for consumption of water, fish, and other aquatic organisms were detected at levels greater than the criteria in any of the samples collected during this study. Total phosphorus concentrations in water samples collected in the Papillion Creek Basin were in excess of the U.S. Environmental Protection Agency's proposed

Estimating instream constituent loads using replicate synoptic sampling, Peru Creek, Colorado

Science.gov (United States)

Runkel, Robert L.; Walton-Day, Katherine; Kimball, Briant A.; Verplanck, Philip L.; Nimick, David A.

2013-01-01

The synoptic mass balance approach is often used to evaluate constituent mass loading in streams affected by mine drainage. Spatial profiles of constituent mass load are used to identify sources of contamination and prioritize sites for remedial action. This paper presents a field scale study in which replicate synoptic sampling campaigns are used to quantify the aggregate uncertainty in constituent load that arises from (1) laboratory analyses of constituent and tracer concentrations, (2) field sampling error, and (3) temporal variation in concentration from diel constituent cycles and/or source variation. Consideration of these factors represents an advance in the application of the synoptic mass balance approach by placing error bars on estimates of constituent load and by allowing all sources of uncertainty to be quantified in aggregate; previous applications of the approach have provided only point estimates of constituent load and considered only a subset of the possible errors. Given estimates of aggregate uncertainty, site specific data and expert judgement may be used to qualitatively assess the contributions of individual factors to uncertainty. This assessment can be used to guide the collection of additional data to reduce uncertainty. Further, error bars provided by the replicate approach can aid the investigator in the interpretation of spatial loading profiles and the subsequent identification of constituent source areas within the watershed.The replicate sampling approach is applied to Peru Creek, a stream receiving acidic, metal-rich effluent from the Pennsylvania Mine. Other sources of acidity and metals within the study reach include a wetland area adjacent to the mine and tributary inflow from Cinnamon Gulch. Analysis of data collected under low-flow conditions indicates that concentrations of Al, Cd, Cu, Fe, Mn, Pb, and Zn in Peru Creek exceed aquatic life standards. Constituent loading within the study reach is dominated by effluent from the

Estimating instream constituent loads using replicate synoptic sampling, Peru Creek, Colorado

Science.gov (United States)

Runkel, Robert L.; Walton-Day, Katherine; Kimball, Briant A.; Verplanck, Philip L.; Nimick, David A.

2013-05-01

SummaryThe synoptic mass balance approach is often used to evaluate constituent mass loading in streams affected by mine drainage. Spatial profiles of constituent mass load are used to identify sources of contamination and prioritize sites for remedial action. This paper presents a field scale study in which replicate synoptic sampling campaigns are used to quantify the aggregate uncertainty in constituent load that arises from (1) laboratory analyses of constituent and tracer concentrations, (2) field sampling error, and (3) temporal variation in concentration from diel constituent cycles and/or source variation. Consideration of these factors represents an advance in the application of the synoptic mass balance approach by placing error bars on estimates of constituent load and by allowing all sources of uncertainty to be quantified in aggregate; previous applications of the approach have provided only point estimates of constituent load and considered only a subset of the possible errors. Given estimates of aggregate uncertainty, site specific data and expert judgement may be used to qualitatively assess the contributions of individual factors to uncertainty. This assessment can be used to guide the collection of additional data to reduce uncertainty. Further, error bars provided by the replicate approach can aid the investigator in the interpretation of spatial loading profiles and the subsequent identification of constituent source areas within the watershed. The replicate sampling approach is applied to Peru Creek, a stream receiving acidic, metal-rich effluent from the Pennsylvania Mine. Other sources of acidity and metals within the study reach include a wetland area adjacent to the mine and tributary inflow from Cinnamon Gulch. Analysis of data collected under low-flow conditions indicates that concentrations of Al, Cd, Cu, Fe, Mn, Pb, and Zn in Peru Creek exceed aquatic life standards. Constituent loading within the study reach is dominated by effluent

Geochemistry of Standard Mine Waters, Gunnison County, Colorado, July 2009

Science.gov (United States)

Verplanck, Philip L.; Manning, Andrew H.; Graves, Jeffrey T.; McCleskey, R. Blaine; Todorov, Todor I.; Lamothe, Paul J.

2009-01-01

In many hard-rock-mining districts water flowing from abandoned mine adits is a primary source of metals to receiving streams. Understanding the generation of adit discharge is an important step in developing remediation plans. In 2006, the U.S. Environmental Protection Agency listed the Standard Mine in the Elk Creek drainage basin near Crested Butte, Colorado as a superfund site because drainage from the Standard Mine enters Elk Creek, contributing dissolved and suspended loads of zinc, cadmium, copper, and other metals to the stream. Elk Creek flows into Coal Creek, which is a source of drinking water for the town of Crested Butte. In 2006 and 2007, the U.S. Geological Survey undertook a hydrogeologic investigation of the Standard Mine and vicinity and identified areas of the underground workings for additional work. Mine drainage, underground-water samples, and selected spring water samples were collected in July 2009 for analysis of inorganic solutes as part of a follow-up study. Water analyses are reported for mine-effluent samples from Levels 1 and 5 of the Standard Mine, underground samples from Levels 2 and 3 of the Standard Mine, two spring samples, and an Elk Creek sample. Reported analyses include field measurements (pH, specific conductance, water temperature, dissolved oxygen, and redox potential), major constituents and trace elements, and oxygen and hydrogen isotopic determinations. Overall, water samples collected in 2009 at the same sites as were collected in 2006 have similar chemical compositions. Similar to 2006, water in Level 3 did not flow out the portal but was observed to flow into open workings to lower parts of the mine. Many dissolved constituent concentrations, including calcium, magnesium, sulfate, manganese, zinc, and cadmium, in Level 3 waters substantially are lower than in Level 1 effluent. Concentrations of these dissolved constituents in water samples collected from Level 2 approach or exceed concentrations of Level 1 effluent

Identification of dissolved-constituent sources in mine-site ground water using batch mixing

Science.gov (United States)

Clark, Gregory M.; Williams, Robert S.

1991-01-01

Batch-mixing experiments were used to help identify lithologic and mineralogic sources of increased concentrations of dissolved solids in water affected by surface coal mining in northwestern Colorado. Ten overburden core samples were analyzed for mineral composition and mixed with distilled water for 90 days until mineral-water equilibrium was reached. Between one day and 90 days after initial contact, specific conductance in the sample mixtures had a median increase of 306 percent. Dissolved-solids concentrations ranged from 200 to 8,700 mg/L in water samples extracted from the mixtures after 90 days. Mass-balance simulations were conducted using the geochemical models BALANCE and WATEQF to quantify mineral-water interactions occurring in five selected sample mixtures and in water collected from a spring at a reclaimed mine site. The spring water is affected by mineral-water interactions occurring in all of the lithologic units comprising the overburden. Results of the simulations indicate that oxidation of pyrite, dissolution of dolomite, gypsum, and epsomite, and cation-exchange reactions are the primary mineral-water interactions occurring in the overburden. Three lithologic units in the overburden (a coal, a sandstone, and a shale) probably contribute most of the dissolved solids to the spring water. Water sample extracts from mixtures using core from these three units accounted for 85 percent of the total dissolved solids in the 10 sample extracts. Other lithologic units in the over-burden probably contribute smaller quantities of dissolved solids to the spring water.

Long-term behavior of the concentration of the minor constituents in the mesosphere – a model study

Directory of Open Access Journals (Sweden)

M. Grygalashvyly

2009-04-01

Full Text Available We investigate the influence the rising concentrations of methane, nitrous oxide and carbon dioxide which have occurred since the pre-industrial era, have had on the chemistry of the mesosphere. For this investigation we use our global 3-D-model COMMA-IAP which was designed for the exploration of the MLT-region and in particular the extended mesopause region. Assumptions and approximations for the trends in the Lyman-α flux (needed for the water vapor dissociation rate, methane and the water vapor mixing ratio at the hygropause are necessary to accomplish this study. To approximate the solar Lyman-α flux back to the pre-industrial time, we derived a quadratic fit using the sunspot number record which extends back to 1749 and is the only solar proxy available for the Lyman-α flux prior to 1947. We assume that methane increases with a constant growth rate from the pre-industrial era to the present. An unsolved problem for the model calculations consists of how the water vapor mixing ratio at the hygropause should be specified during this period. We assume that the hygropause was dryer during pre-industrial times than the present. As a consequence of methane oxidation, the model simulation indicates that the middle atmosphere has become more humid as a result of the rising methane concentration, but with some dependence on height and with a small time delay of few years. The solar influence on the water vapor mixing ratio is insignificant below about 80 km in summer high latitudes, but becomes increasingly more important above this altitude. The enhanced water vapor concentration increases the hydrogen radical concentration and reduces the mesospheric ozone. A second region of stronger ozone decrease is located in the vicinity of the stratopause. Increases in CO₂ concentration enhance slightly the concentration of CO in the mesosphere. However, its influence upon the chemistry is small and its main effect is connected with a cooling

Comparison of tritium concentrations in rainwater, simulated infiltrating water, and groundwater

International Nuclear Information System (INIS)

Ishii, Yoshiyuki; Saito, Masaaki; Imaizumi, Hiroshi; Kato, Norio; Kitaoka, Koichi

2014-01-01

The tritium concentration in initial groundwater(i.e., freshly infiltrating rainwater) is necessary for groundwater dating. We collected simulated infiltrating water as the initial groundwater and examined its characteristics for tritium concentration. First, in Tokyo, the tritium concentration of simulated infiltrating water was compared with that of rainwater, atmospheric moisture, groundwater, spring water, and sap water. While rainwater, atmospheric moisture, and simulated infiltrating water remarkably changed month-to-month or with every rainfall event, groundwater and spring water were nearly constant throughout the year. Second, we collected the simulated infiltrating water monthly at four sampling sites widely dispersed across Japan(i.e., Sapporo, Niigata, Tokyo, and Matsuyama) from 2004 to 2010. Sapporo and Niigata showed high tritium concentrations as compared with the relatively low concentrations in Tokyo and Matsuyama. These results indicate that we can obtain annual maximum and minimum concentrations at each site, and that we can estimate the tritium concentration in initial groundwater at each site by using a mixing model composed of these maximum and minimum concentrations. (author)

Ground-Water Quality Data in the Santa Clara River Valley Study Unit, 2007: Results from the California GAMA Program

Science.gov (United States)

Montrella, Joseph; Belitz, Kenneth

2009-01-01

and age of the sampled ground water. Quality-control samples (blanks or replicates, or samples for matrix spikes) were collected from approximately 26 percent of the wells, and the analyses of these samples were used to evaluate the quality of the data for the ground-water samples. Assessment of the quality-control results showed that the quality of the environmental data was good, with low bias and low variability, and as a result, less than 0.1 percent of the analytes detected in ground-water samples were censored. This study did not attempt to evaluate the quality of water delivered to consumers; after withdrawal from the ground, water typically is treated, disinfected, and (or) blended with other waters to maintain acceptable water quality. Regulatory thresholds apply to treated water that is delivered (or, supplied) to the consumer, not to raw ground water. However, to provide some context for the results, concentrations of constituents measured in the raw ground water were compared with regulatory and non-regulatory thresholds established by the U.S. Environmental Protection Agency (USEPA) and the California Department of Public Health (CDPH) and thresholds established for aesthetic concerns (secondary maximum contaminant levels, SMCL-CA) by CDPH. Most constituents that were detected in ground-water samples were reported at concentrations below their established health-based thresholds. VOCs, pesticides and pesticide degradates, and potential wastewater-indicator compounds were detected in about 33 percent or less of the 42 SCRV grid wells. Concentrations of all detected organic constituents were below established health-based thresholds. Perchlorate was detected in approximately 12 percent of the SCRV grid wells; all concentrations reported were below the NL-CA threshold. Additional constituents, including major ions, trace elements, and nutrients were collected at 26 wells (16 grid wells and 10 understanding wells) of the 53 wells sampled f

Reflective measurement of water concentration using millimeter wave illumination

Science.gov (United States)

Sung, Shijun; Bennett, David; Taylor, Zachary; Bajwa, Neha; Tewari, Priyamvada; Maccabi, Ashkan; Culjat, Martin; Singh, Rahul; Grundfest, Warren

2011-04-01

THz and millimeter wave technology have shown the potential to become a valuable medical imaging tool because of its sensitivity to water and safe, non-ionizing photon energy. Using the high dielectric constant of water in these frequency bands, reflectionmode THz sensing systems can be employed to measure water content in a target with high sensitivity. This phenomenology may lead to the development of clinical systems to measure the hydration state of biological targets. Such measurements may be useful in fast and convenient diagnosis of conditions whose symptoms can be characterized by changes in water concentration such as skin burns, dehydration, or chemical exposure. To explore millimeter wave sensitivity to hydration, a reflectometry system is constructed to make water concentration measurements at 100 GHz, and the minimum detectable water concentration difference is measured. This system employs a 100 GHz Gunn diode source and Golay cell detector to perform point reflectivity measurements of a wetted polypropylene towel as it dries on a mass balance. A noise limited, minimum detectable concentration difference of less than 0.5% by mass can be detected in water concentrations ranging from 70% to 80%. This sensitivity is sufficient to detect hydration changes caused by many diseases and pathologies and may be useful in the future as a diagnostic tool for the assessment of burns and other surface pathologies.

An update of hydrologic conditions and distribution of selected constituents in water, Snake River Plain aquifer and perched groundwater zones, Idaho National Laboratory, Idaho, emphasis 2006-08

Science.gov (United States)

Davis, Linda C.

2010-01-01

Since 1952, radiochemical and chemical wastewater discharged to infiltration ponds (also called percolation ponds), evaporation ponds, and disposal wells at the Idaho National Laboratory (INL) has affected water quality in the eastern Snake River Plain aquifer and perched groundwater zones underlying the INL. The U.S. Geological Survey, in cooperation with the U.S. Department of Energy, maintains groundwater monitoring networks at the INL to determine hydrologic trends, and to delineate the movement of radiochemical and chemical wastes in the aquifer and in perched groundwater zones. This report presents an analysis of water-level and water-quality data collected from aquifer and perched groundwater wells in the USGS groundwater monitoring networks during 2006-08. Water in the Snake River Plain aquifer primarily moves through fractures and interflow zones in basalt, generally flows southwestward, and eventually discharges at springs along the Snake River. The aquifer primarily is recharged from infiltration of irrigation water, infiltration of streamflow, groundwater inflow from adjoining mountain drainage basins, and infiltration of precipitation. From March-May 2005 to March-May 2008, water levels in wells generally remained constant or rose slightly in the southwestern corner of the INL. Water levels declined in the central and northern parts of the INL. The declines ranged from about 1 to 3 feet in the central part of the INL, to as much as 9 feet in the northern part of the INL. Water levels in perched groundwater wells around the Advanced Test Reactor Complex (ATRC) also declined. Detectable concentrations of radiochemical constituents in water samples from wells in the Snake River Plain aquifer at the INL generally decreased or remained constant during 2006-08. Decreases in concentrations were attributed to decreased rates of radioactive-waste disposal, radioactive decay, changes in waste-disposal methods, and dilution from recharge and underflow. In April

Water quality of the Neuse River, North Carolina - Variability, pollution loads, and long-term trends

Science.gov (United States)

Harned, Doughlas A.

1982-01-01

Interpretation of water-quality data collected by the U.S. Geological Survey for the Neuse River, North Carolina, has identified water-quality variations, charactrized the current condition of the river in reference to water-quality standards, estimated the degree of pollution caused by man, and evaluated long-term trends in concentrations of major dissolved constituents. Two sampling stations, Neuse River near Clayton (02087500) and Neuse River at Kinston (02089500) have more than 12 years of water-quality data collected during the period from 1955 to 1978. The Clayton station provides information on the upper fourth of the basin (1,129 mi 2) which includes several urbanized areas, including Raleigh, N.C., and part of Durham, N.C. The Kinston station provides information from the predominantly rural midsection of the basin (2,690 mi2). A network of temporary stations on small rural streams in the Neuse River and adjacent basins provide an estimate of baseline or es- sentially unpolluted water quality. Overall, the water quality of the Neuse River is satisfactory for most uses. However, dissolved-oxygen, iron, and manganese concentrations, pH, and bacterial concentrations often reach undesirable levels. Concentrations of cadmium, and lead also periodically peak at or above criterion levels for domestic water supply sources. Nutrient levels are generally high enough to allow rich algal growth. Sediment concentrations in the Neuse are high in comparison to pristine streams, however, the impacts of these high levels are difficult to quantify. Sediment and nutrient concentrations peak on the leading edge of flood discharges at Clayton. At Kinston, however, the discharge and sediment concentration peak almost simultaneously. Changes in algal dominance, from genera usually associated with organically enriched waters to genera that are less tolerant to organic enrichment, indicate improvement in water qualiy of the Neuse since 1973. These changes, along with a reduction

The potential effects of sodium bicarbonate, a major constituent from coalbed natural gas production, on aquatic life

Science.gov (United States)

Farag, Aïda M.; Harper, David D.

2012-01-01

The production water from coalbed natural gas (CBNG) extraction contains many constituents. The U.S. Environmental Protection Agency has established aquatic life criteria for some of these constituents, and it is therefore possible to evaluate their risk to aquatic life. However, of the major ions associated with produced waters, chloride is the only one with an established aquatic life criterion (U.S. Environmental Protection Agency, 1988). The focus of this research was NaHCO3, a compound that is a major constituent of coalbed natural gas produced waters in the Tongue and Powder River Basins. This project included laboratory experiments, field in situ experiments, a field mixing zone study, and a fishery presence/absence assessment. Though this investigation focuses on the Tongue and Powder River Basins, the information is applicable to other watersheds where sodium bicarbonate is a principle component of product water either from CBNG or from traditional or unconventional oil and gas development. These data can also be used to separate effects of saline discharges from those potentially posed by other constituents. Finally, this research effort and the additional collaboration with USGS Water Resources and Mapping, Bureau of Land Management, US Environmental Protection Agency, State of Montana, State of Wyoming, Montana State University, University of Wyoming, and others as part of a Powder River Aquatic Task Group, can be used as a model for successful approaches to studying landscapes with energy development. The laboratory acute toxicity experiments were completed with a suite of organisms, including 7 species of fish, 5 species of invertebrates, and 1 amphibian species. Experiments performed on these multiple species resulted in LC50s that ranged from 1,120 to greater than (>) 8,000 milligrams sodium bicarbonate per liter (mg NaHCO3/L) (also defined as 769 to >8,000 milligrams bicarbonate per liter (mg HCO3-/L) or total alkalinity expressed as 608 to >4

Quality of surface-water supplies in the Triangle area of North Carolina, water year 2009

Science.gov (United States)

Pfeifle, C. A.; Giorgino, M. J.; Rasmussen, R. B.

2014-01-01

Surface-water supplies are important sources of drinking water for residents in the Triangle area of North Carolina, which is located within the upper Cape Fear and Neuse River Basins. Since 1988, the U.S. Geological Survey and a consortium of governments have tracked water-quality conditions and trends in several of the area’s water-supply lakes and streams. This report summarizes data collected through this cooperative effort, known as the Triangle Area Water Supply Monitoring Project, during October 2008 through September 2009. Major findings for this period include: - Annual precipitation was approximately 20 percent below the long-term mean (average) annual precipitation. - Streamflow was below the long-term mean at the 10 project streamgages during most of the year. - More than 7,000 individual measurements of water quality were made at a total of 26 sites—15 in the Neuse River Basin and 11 in the Cape Fear River Basin. Forty-seven water-quality properties and constituents were measured. - All observations met North Carolina water-quality standards for water temperature, pH, hardness, chloride, fluoride, sulfate, nitrate, arsenic, cadmium, chromium, lead, nickel, and selenium. - North Carolina water-quality standards were exceeded one or more times for dissolved oxygen, dissolved oxygen percent saturation, chlorophyll a, mercury, copper, iron, manganese, silver, and zinc. Exceedances occurred at 23 sites—13 in the Neuse River Basin and 10 in the Cape Fear River Basin. - Stream samples collected during storm events contained elevated concentrations of 18 water-quality constituents compared to samples collected during non-storm events. - Concentrations of nitrogen and phosphorus were within ranges observed during previous years. - Five reservoirs had chlorophyll a concentrations in excess of 40 micrograms per liter at least once during 2009: Little River Reservoir, Falls Lake, Cane Creek Reservoir, University Lake, and Jordan Lake.

Concentration of Nitrate in Bottled Drinking Water in Qom, Iran

Directory of Open Access Journals (Sweden)

Mohammad Saberi Bidgoli

2013-11-01

Full Text Available Background & Aims of the Study: The global consumption of bottled water is growing with substantial growth in sales volumes on every continent. The highest growth rates are occurring in Asia and South America. Biological and chemical monitoring of these waters is necessary. The aim of current study was determination of nitrate concentration in bottled drinking water in Qom, Iran in 2012. Materials & Methods: A cross-sectional study carried out in Qom, Iran. First of all, 18 most frequent brands of bottled drinking waters were purchased in June 2012 randomly. Then concentration of nitrate was measured according to the spectrophotometric method. In next step, experiment data were analyzed by Excel Software and P value was obtained by statistical calculations. Finally data were comprised with written nitrate concentration on labels and recommended permissible values . Results: The median nitrate concentration was 2.1 mg/L with the minimum 0.8 mg/L and maximum 8.1 mg/L. In 66.7 % of the samples, the measured nitrate concentrations were less than the written nitrate concentrations and in 33.3% of samples, the nitrate concentration was higher. The statistical calculation proved the significant difference between the median of written nitrate concentration on the label and investigated nitrate concentration (P value > 0.05. Conclusions: It be concluded that the measured nitrate concentration in all of the water samples is below the recommended permissible level.

Ground-Water Flow, 2004-07, and Water Quality, 1992-2007, in McBaine Bottoms, Columbia, Missouri

Science.gov (United States)

Smith, Brenda Joyce; Richards, Joseph M.

2008-01-01

The U.S. Geological Survey, in cooperation with the city of Columbia, Missouri, and the Missouri Department of Conservation, collected ground-water quality data, surface-water quality data, and water-level data in McBaine Bottoms, southwest of Columbia. McBaine Bottoms, adjacent to the Missouri River, is the location of the municipal-supply well field for the city of Columbia, the city of Columbia wastewater-treatment wetlands, and the Missouri Department of Conservation Eagle Bluffs Conservation Area. This report describes the ground-water flow and water quality of McBaine Bottoms and provides information to better understand the interaction between treated effluent from the wetlands used on the Eagle Bluffs Conservation Area and the water in the alluvial aquifer that is pumped from the city of Columbia municipal-supply well field. Changes in major chemical constituent concentrations have been detected at several sampling sites between pre- and post-effluent application data. Analysis of post-effluent data indicates substantial changes in calcium, potassium, sodium, chloride, and sulfate concentrations in ground water. These changes became apparent shortly after the beginning of the operation of the wastewater-treatment wetland in 1994 and the formation of the Eagle Bluffs Conservation Area, which uses the treated effluent as a water source for the management of migratory water fowl. The changes have continued throughout the 15 years of sample collection. The concentrations of these major chemical constituents are on the mixing continuum between pre-effluent ground water as one end member and the treated wastewater effluent as the other end member. For monitoring wells that had changes in major chemical constituent concentrations, the relative percentage of treated effluent in the ground water, assuming chloride is conservative, ranged from 6 to 88 percent. Twenty-two monitoring wells throughout McBaine Bottoms have been affected by effluent based on chloride

Simulation of water quality for Salt Creek in northeastern Illinois

Science.gov (United States)

Melching, Charles S.; Chang, T.J.

1996-01-01

Water-quality processes in the Salt Creek watershed in northeastern Illinois were simulated with a computer model. Selected waste-load scenarios for 7-day, 10-year low-flow conditions were simulated in the stream system. The model development involved the calibration of the U.S. Environmental Protection Agency QUAL2E model to water-quality constituent concentration data collected by the Illinois Environmental Protection Agency (IEPA) for a diel survey on August 29-30, 1995, and the verification of this model with water-quality constituent concentration data collected by the IEPA for a diel survey on June 27-28, 1995. In-stream measurements of sediment oxygen demand rates and carbonaceous biochemical oxygen demand (CBOD) decay rates by the IEPA and traveltime and reaeration-rate coefficients by the U.S. Geological Survey facilitated the development of a model for simulation of water quality in the Salt Creek watershed. In general, the verification of the calibrated model increased confidence in the utility of the model for water-quality planning in the Salt Creek watershed. However, the model was adjusted to better simulate constituent concentrations measured during the June 27-28, 1995, diel survey. Two versions of the QUAL2E model were utilized to simulate dissolved oxygen (DO) concentrations in the Salt Creek watershed for selected effluent discharge and concentration scenarios for water-quality planning: (1) the QUAL2E model calibrated to the August 29-30, 1995, diel survey, and (2) the QUAL2E model adjusted to the June 27-28, 1995, diel survey. The results of these simulations indicated that the QUAL2E model adjusted to the June 27-28, 1995, diel survey simulates reliable information for water-quality planning. The results of these simulations also indicated that to maintain DO concentrations greater than 5 milligrams per liter (mg/L) throughout most of Salt Creek for 7-day, 10-year low-flow conditions, the sewage-treatment plants (STP's) must discharge

Influence of salt concentration and topographical position on water ...

African Journals Online (AJOL)

Water resource quality (WRQ) is affected by salt concentration and topographical position. Indeed, an increase in salt concentration, which decreases water availability for animal and plant nutrition, and lower altitude, which diminishes the potential for production of hydropower, negatively affects WRQ. Therefore, it is useful ...

Water quality and mass transport in four watersheds in eastern Puerto Rico: Chapter E in Water quality and landscape processes of four watersheds in eastern Puerto Rico

Science.gov (United States)

Stallard, Robert F.; Murphy, Sheila F.; Murphy, Sheila F.; Stallard, Robert F.

2012-01-01

Water quality of four small watersheds in eastern Puerto Rico has been monitored since 1991 as part of the U.S. Geological Survey's Water, Energy, and Biogeochemical Budgets program. These watersheds represent a montane, humid-tropical environment and differ in geology and land cover. Two watersheds are located on granitic rocks, and two are located on volcaniclastic rock. For each bedrock type, one watershed is covered with mature rainforest in the Luquillo Mountains, and the other watershed is undergoing reforestation after being affected by agricultural practices typical of eastern Puerto Rico. A subwatershed of the Icacos watershed, the Guabá, was also monitored to examine scaling effects. The water quality of the rivers draining forest, in the Icacos and Guabá (granitic watersheds) and Mameyes (a volcaniclastic watershed), show little contamination by human activities. The water is well oxygenated and has a nearly neutral pH, and nutrient concentrations are low. Concentrations of nutrients in the disturbed watersheds, the Cayaguás (granitic rock) and Canóvanas (volcaniclastic rock), are greater than in the forested watersheds, indicating some inputs from human activities. High in-stream productivity in the Canóvanas watershed leads to occasional oxygen and calcite supersaturation and carbon dioxide undersaturation. Suspended sediment concentrations in all watersheds are low, except during major storms. Most dissolved constituents derived from bedrock weathering or atmospheric deposition (including sodium, magnesium, calcium, silica, alkalinity, and chloride) decrease in concentration with increasing runoff, reflecting dilution from increased proportions of overland or near-surface flow. Strongly bioactive constituents (dissolved organic carbon, potassium, nitrate, ammonium ion, and phosphate) commonly display increasing concentration with increasing runoff, regardless of their ultimate origin (bedrock or atmosphere). The concentrations of many of the

Spatial and temporal variations of manganese concentrations in drinking water.

Science.gov (United States)

Barbeau, Benoit; Carrière, Annie; Bouchard, Maryse F

2011-01-01

The objective of this study was to assess the variability of manganese concentrations in drinking water (daily, seasonal, spatial) for eight communities who participated in an epidemiological study on neurotoxic effects associated with exposure to manganese in drinking water. We also assessed the performance of residential point-of-use and point-of-entry devices (POE) for reducing manganese concentrations in water. While the total Mn concentrations measured during this study were highly variable depending on the location (manganese concentration for 4 out of 5 sampling locations. The efficiency of reverse osmosis and ion exchange for total Mn removal was consistently high while activated carbon provided variable results. The four POE greensand filters investigated all increased (29 to 199%) manganese concentration, indicating deficient operation and/or maintenance practices. Manganese concentrations in the distribution system were equal or lower than at the inlet, indicating that sampling at the inlet of the distribution system is conservative. The decline in total Mn concentration was linked to higher water residence time in the distribution system.

An optical water type framework for selecting and blending retrievals from bio-optical algorithms in lakes and coastal waters

OpenAIRE

Moore, Timothy S.; Dowell, Mark D.; Bradt, Shane; Verdu, Antonio Ruiz

2014-01-01

Bio-optical models are based on relationships between the spectral remote sensing reflectance and optical properties of in-water constituents. The wavelength range where this information can be exploited changes depending on the water characteristics. In low chlorophyll-a waters, the blue/green region of the spectrum is more sensitive to changes in chlorophyll-a concentration, whereas the red/NIR region becomes more important in turbid and/or eutrophic waters. In this work we present an appro...

Summary statistics and trend analysis of water-quality data at sites in the Gila River basin, New Mexico and Arizona

Science.gov (United States)

Baldys, Stanley; Ham, L.K.; Fossum, K.D.

1995-01-01

Summary statistics and temporal trends for 19 water-chemistry constituents and for turbidity were computed for 13 study sites in the Gila River basin, Arizona and New Mexico. A nonparametric technique, the seasonal Kendall tau test for flow-adjusted data, was used to analyze temporal changes in water-chemistry data. For the 19 selected constituents and turbidity, decreasing trends in concentrations outnumbered increasing trends by more than two to one. Decreasing trends in concentrations of constituents were found for 49 data sets at the 13 study sites. Gila River at Calva and Gila River above diversions, at Gillespie Dam (eight each) had the most decreasing trends for individual sites. The largest number of decreasing trends measured for a constituent was six for dissolved lead. The next largest number of decreasing trends for a constituent was for dissolved solids and total manganese (five each). Hardness, dissolved sodium, and dissolved chloride had decreasing trends at four of the study sites. Increasing trends in concen- trations of constituents were found for 24 data sets at the 13 study sites. The largest number of increasing trends measured for a single constituent was for pH (four), dissolved sulfate (three), dissolved chromium (three) and total manganese (three). Increased concentrations of constituents generally were found in three areas in the basin-at Pinal Creek above Inspiration Dam, at sites above reservoirs, and at sites on the main stem of the Gila River from Gillespie Dam to the mouth.

Radon concentration in drinking water and water for living use and their study status

International Nuclear Information System (INIS)

Tan Chenglong

2005-01-01

Low quality water is the chief reason for resulting in decrease of human group's physique, and in early appearance of nutrition and supersession diseases. The assimilation of radon released from water by human body may cause radioactive impact to those organs such as stomach and lungs. The monitoring determination for chemical quality of drinking water in developed countries comprises as many as 350 items, and the maximum contamination level of international standards is adopted for checking the radon concentration in drinking water, However, at present, only 35 items of the chemical quality of drinking water are determined in China. The monitoring determination of radon concentration in running water of cities, in distillation water, mineral water, pure water, deep well water in country side, as well as natural surface water is of great market potential in the future. (authors)

Geochemical evidence of groundwater flow paths and the fate and transport of constituents of concern in the alluvial aquifer at Fort Wingate Depot Activity, New Mexico, 2009

Science.gov (United States)

Robertson, Andrew J.; Henry, David W.; Langman, Jeffery B.

2013-01-01

As part of an environmental investigation at Fort Wingate Depot Activity, New Mexico, the U.S. Geological Survey, in cooperation with the U.S. Army Corps of Engineers, interpreted aqueous geochemical concentrations to better understand the groundwater flow paths and the fate and transport of constituents of concern in the alluvial aquifer underlying the study area. The fine-grained nature of the alluvial matrix creates a highly heterogeneous environment, which adds to the difficulty of characterizing the flow of groundwater and the fate of aqueous constituents of concern. The analysis of the groundwater geochemical data collected in October 2009 provides evidence that is used to identify four groundwater flow paths and their extent in the aquifer and indicates the dominant attenuation processes for the constituents of concern. The extent and interaction of groundwater flow paths were delineated by the major ion concentrations and their relations to each other. Four areas of groundwater recharge to the study area were identified based on groundwater elevations, hydrogeologic characteristics, and geochemical and isotopic evidence. One source of recharge enters the study area from the saturated alluvial deposits underlying the South Fork of the Puerco River to the north of the study area. A second source of recharge is shown to originate from a leaky cistern containing production water from the San Andres-Glorieta aquifer. The other two sources of recharge are shown to enter the study area from the south: one from an arroyo valley draining an area to the south and one from hill-front recharge that passes under the reported release of perchlorate and explosive constituents. The spatial extent and interaction of groundwater originating from these various sources along identified flow paths affect the persistence and attenuation of constituents of concern. It was determined that groundwater originating in the area of a former explosives’ wash-out operation and an

Boron content of South African surface waters: prelimenary assessment for irrigation

International Nuclear Information System (INIS)

Reid, P.C.; Davies, E.

1989-01-01

Boron, a naturally occuring constituent of surface and ground water, is an essential plant nutrient. However, at relatively low concentrations, boron becomes toxic to plant growth. In order to assess the boron status in South African surface waters, the Department of Water Affairs launched a long-term boron water quality assessment programme in 1985, encompassing the analysis of water samples taken at 91 sites throughout South Africa. Results to date indicate that the boron concentration in South African surface waters varies between 0,02 to 0,33 mg l -1 . At these concentrations even the most boron sensitive crops can be grown without fear of boron toxicity. 3 refs., 1 fig., 2 tabs

Ground-water quality in the Appalachian Plateaus, Kanawha River basin, West Virginia

Science.gov (United States)

Sheets, Charlynn J.; Kozar, Mark D.

2000-01-01

Water samples collected from 30 privately-owned and small public-supply wells in the Appalachian Plateaus of the Kanawha River Basin were analyzed for a wide range of constituents, including bacteria, major ions, nutrients, trace elements, radon, pesticides, and volatile organic compounds. Concentrations of most constituents from samples analyzed did not exceed U.S. Environmental Protection Agency (USEPA) standards. Constituents that exceeded drinking-water standards in at least one sample were total coliform bacteria, Escherichia coli (E. coli), iron, manganese, and sulfate. Total coliform bacteria were present in samples from five sites, and E. coli were present at only one site. USEPA secondary maximum contaminant levels (SMCLs) were exceeded for three constituents -- sulfate exceeded the SMCL of 250 mg/L (milligrams per liter) in samples from 2 of 30 wells; iron exceeded the SMCL of 300 ?g/L (micrograms per liter) in samples from 12 of the wells, and manganese exceeded the SMCL of 50 ?g/L in samples from 17 of the wells sampled. None of the samples contained concentrations of nutrients that exceeded the USEPA maximum contaminant levels (MCLs) for these constituents. The maximum concentration of nitrate detected was only 4.1 mg/L, which is below the MCL of 10 mg/L. Concentrations of nitrate in precipitation and shallow ground water are similar, potentially indicating that precipitation may be a source of nitrate in shallow ground water in the study area. Radon concentrations exceeded the recently proposed maximum contaminant level of 300 pCi/L at 50 percent of the sites sampled. The median concentration of radon was only 290 pCi/L. Radon-222 is a naturally occurring, carcinogenic, radioactive decay product of uranium. Concentrations, however, did not exceed the alternate maximum contaminant level (AMCL) for radon of 4,000 pCi/L in any of the 30 samples. Arsenic concentrations exceeded the proposed MCL of 5?g/L at 4 of the 30 sites. No samples exceeded the

MODELING NITRATE CONCENTRATION IN GROUND WATER USING REGRESSION AND NEURAL NETWORKS

OpenAIRE

Ramasamy, Nacha; Krishnan, Palaniappa; Bernard, John C.; Ritter, William F.

2003-01-01

Nitrate concentration in ground water is a major problem in specific agricultural areas. Using regression and neural networks, this study models nitrate concentration in ground water as a function of iron concentration in ground water, season and distance of the well from a poultry house. Results from both techniques are comparable and show that the distance of the well from a poultry house has a significant effect on nitrate concentration in groundwater.

Experimental Analysis of Desalination Unit Coupled with Solar Water Lens Concentrator

Science.gov (United States)

Chaithanya, K. K.; Rajesh, V. R.; Suresh, Rahul

2016-09-01

The main problem that the world faces in this scenario is shortage of potable water. Hence this research work rivets to increase the yield of desalination system in an economical way. The integration of solar concentrator and desalination unit can project the desired yield, but the commercially available concentrated solar power technologies (CSP) are not economically viable. So this study proposes a novel method to concentrate ample amount of solar radiation in a cost effective way. Water acting as lens is a highlighted technology initiated in this work, which can be a substitute for CSP systems. And water lens can accelerate the desalination process so as to increase the yield economically. The solar irradiance passing through the water will be concentrated at a focal point, and the concentration depends on curvature of water lens. The experimental analysis of water lens makes use of transparent thin sheet, supported on a metallic structure. The Plano convex shape of water lens is developed by varying the volume of water that is being poured on the transparent thin sheet. From the experimental analysis it is inferred that, as the curvature of water lens increases, solar irradiance can be focused more accurately on to the focus and a higher water temperature is obtained inside the solar still.

Water-quality trends in the Scituate reservoir drainage area, Rhode Island, 1983-2012

Science.gov (United States)

Smith, Kirk P.

2015-01-01

The Scituate Reservoir is the primary source of drinking water for more than 60 percent of the population of Rhode Island. Water-quality and streamflow data collected at 37 surface-water monitoring stations in the Scituate Reservoir drainage area, Rhode Island, from October 2001 through September 2012, water years (WYs) 2002-12, were analyzed to determine water-quality conditions and constituent loads in the drainage area. Trends in water quality, including physical properties and concentrations of constituents, were investigated for the same period and for a longer period from October 1982 through September 2012 (WYs 1983-2012). Water samples were collected and analyzed by the Providence Water Supply Board, the agency that manages the Scituate Reservoir. Streamflow data were collected by the U.S. Geological Survey. Median values and other summary statistics for pH, color, turbidity, alkalinity, chloride, nitrite, nitrate, total coliform bacteria, Escherichia coli (E. coli), and orthophosphate were calculated for WYs 2003-12 for all 37 monitoring stations. Instantaneous loads and yields (loads per unit area) of total coliform bacteria and E. coli, chloride, nitrite, nitrate, and orthophosphate were calculated for all sampling dates during WYs 2003-12 for 23 monitoring stations with streamflow data. Values of physical properties and concentrations of constituents were compared with State and Federal water-quality standards and guidelines and were related to streamflow, land-use characteristics, varying classes of timber operations, and impervious surface areas.

Ground-water quality for Grainger County, Tennessee

Science.gov (United States)

Weaver, J.D.; Patel, A.R.; Hickey, A.C.

1994-01-01

The residents of Grainger County depend on ground water for many of their daily needs including personal consumption and crop irrigation. To address concerns associated with ground-water quality related to domestic use, the U.S. Geological Survey collected water samples from 35 wells throughout the county during the summer 1992. The water samples were analyzed to determine if pesticides, nutrients, bacteria, and other selected constituents were present in the ground water. Wells selected for the study were between 100 and 250 feet deep and yielded 10 to 50 gallons of water per minute. Laboratory analyses of the water found no organic pesticides at concentrations exceeding the primary maximum contaminant levels established by the State of Tennessee for wells used for public supply. However, fecal coliform bacteria were detected at concentrations exceeding the State's maximum contaminant level in water from 15 of the 35 wells sampled. Analyses also indicated several inorganic compounds were present in the water samples at concentrations exceeding the secondary maximum contaminant level.

Hydrologic, Water-Quality, and Meteorological Data for the Cambridge, Massachusetts, Drinking-Water Source Area, Water Year 2005

Science.gov (United States)

Smith, Kirk P.

2007-01-01

station 01104455) were generally higher than the medians of the monthly mean specific conductances for the period of record. The annual mean specific conductance for Fresh Pond Reservoir increased from 514 microsiemens per centimeter (?S/cm) in the 2004 water year to 553 ?S/cm for the 2005 water year. Water samples were collected from four tributaries during base-flow and stormflow conditions in December 2004, and July, August, and September 2005 and analyzed for suspended sediment, 6 major dissolved ions, total nitrogen, total phosphorus, 8 total metals, 18 polyaromatic hydrocarbons (PAHs), 61 pesticides and metabolites, and Escherichia coli bacteria. Concentrations for most dissolved constituents in samples of stormwater were generally lower than the concentrations observed in samples collected during base flow; however, concentrations of total phosphorus, PAHs, suspended sediment, and some total recoverable metals were substantially greater in stormwater samples. Concentrations of dissolved chloride and total recoverable manganese in water samples collected during base-flow conditions from three tributaries exceeded the U.S. Environmental Protection Agency (USEPA) secondary drinking water standards of 250 and 0.05 milligrams per liter (mg/L), respectively. Concentrations of total recoverable manganese exceeded the secondary drinking water standard in samples of stormwater from each tributary. Concentrations of total recoverable iron in water samples exceeded the (USEPA) secondary drinking water standard of 0.3 mg/L periodically in water samples collected at (USEPA) stations 01104415, 01104455, and 01104475, and consistently in all water samples collected at USGS station 01104433. Concentrations of Escherichia coli bacteria in water samples collected during base flow ranged from 4 to 1,400 colony-forming units per 100 milliliters (col/100mL). Concentrations of Escherichia coli bacteria in composite samples of stormwater ranged between 1,700 to 43,000 c

Evaluation of quality-control data collected by the U.S. Geological Survey for routine water-quality activities at the Idaho National Laboratory and vicinity, southeastern Idaho, 2002-08

Science.gov (United States)

Rattray, Gordon W.

2014-01-01

Quality-control (QC) samples were collected from 2002 through 2008 by the U.S. Geological Survey, in cooperation with the U.S. Department of Energy, to ensure data robustness by documenting the variability and bias of water-quality data collected at surface-water and groundwater sites at and near the Idaho National Laboratory. QC samples consisted of 139 replicates and 22 blanks (approximately 11 percent of the number of environmental samples collected). Measurements from replicates were used to estimate variability (from field and laboratory procedures and sample heterogeneity), as reproducibility and reliability, of water-quality measurements of radiochemical, inorganic, and organic constituents. Measurements from blanks were used to estimate the potential contamination bias of selected radiochemical and inorganic constituents in water-quality samples, with an emphasis on identifying any cross contamination of samples collected with portable sampling equipment. The reproducibility of water-quality measurements was estimated with calculations of normalized absolute difference for radiochemical constituents and relative standard deviation (RSD) for inorganic and organic constituents. The reliability of water-quality measurements was estimated with pooled RSDs for all constituents. Reproducibility was acceptable for all constituents except dissolved aluminum and total organic carbon. Pooled RSDs were equal to or less than 14 percent for all constituents except for total organic carbon, which had pooled RSDs of 70 percent for the low concentration range and 4.4 percent for the high concentration range. Source-solution and equipment blanks were measured for concentrations of tritium, strontium-90, cesium-137, sodium, chloride, sulfate, and dissolved chromium. Field blanks were measured for the concentration of iodide. No detectable concentrations were measured from the blanks except for strontium-90 in one source solution and one equipment blank collected in September

Ground-Water Quality Data in the Middle Sacramento Valley Study Unit, 2006 - Results from the California GAMA Program

Science.gov (United States)

Schmitt, Stephen J.; Fram, Miranda S.; Milby Dawson, Barbara J.; Belitz, Kenneth

2008-01-01

, replicates, laboratory matrix spikes) were collected at approximately 10 percent of the wells, and the results for these samples were used to evaluate the quality of the data for the ground-water samples. Field blanks rarely contained detectable concentrations of any constituent, suggesting that contamination was not a noticeable source of bias in the data for the ground-water samples. Differences between replicate samples were within acceptable ranges, indicating acceptably low variability. Matrix spike recoveries were within acceptable ranges for most constituents. This study did not attempt to evaluate the quality of water delivered to consumers; after withdrawal from the ground, water typically is treated, disinfected, or blended with other waters to maintain acceptable water quality. Regulatory thresholds apply to treated water that is served to the consumer, not to raw ground water. However, to provide some context for the results, concentrations of constituents measured in the raw ground water were compared with health-based thresholds established by the U.S. Environmental Protection Agency (USEPA) and California Department of Public Health (CDPH) and thresholds established for aesthetic concerns (secondary maximum contaminant levels, SMCL-CA) by CDPH. Comparisons between data collected for this study and drinking-water thresholds are for illustrative purposes only and are not indicative of compliance or noncompliance with regulatory thresholds. Most constituents that were detected in ground-water samples were found at concentrations below drinking-water thresholds. VOCs were detected in less than one-third and pesticides and pesticide degradates in just over one-half of the grid wells, and all detections of these constituents in samples from all wells of the MSACV study unit were below health-based thresholds. All detections of trace elements in samples from MSACV grid wells were below health-based thresholds, with the exceptions of arsenic and boro

Questa baseline and pre-mining ground-water quality investigation. 5. Well installation, water-level data, and surface- and ground-water geochemistry in the Straight Creek drainage basin, Red River Valley, New Mexico, 2001-03

Science.gov (United States)

Naus, Cheryl A.; McCleskey, R. Blaine; Nordstrom, D. Kirk; Donohoe, Lisa C.; Hunt, Andrew G.; Paillet, Frederick L.; Morin, Roger H.; Verplanck, Philip L.

2005-01-01

selected samplings. One set of ground-water samples was collected for helium-3/tritium and chlorofluorocarbon (CFC) age dating. Several lines of evidence indicate that surface water is the primary input to the Straight Creek ground-water system. Straight Creek streamflow and water levels in wells closest to the apex of the Straight Creek debris fan and closest to Straight Creek itself appear to respond to the same seasonal inputs. Oxygen and hydrogen isotopic compositions in Straight Creek surface water and ground water are similar, and concentrations of most dissolved constituents in most Straight Creek surface-water and shallow (debris-flow and alluvial) aquifer ground-water samples correlate strongly with sulfate (concentrations decrease linearly with sulfate in a downgradient direction). After infiltration of surface water, dilution along the flow path is the dominant mechanism controlling ground-water chemistry. However, concentrations of some constituents can be higher in ground water than can be accounted for by concentrations in Straight Creek surface water, and additional sources of these constituents must therefore be inferred. Constituents for which concentrations in ground water can be high relative to surface water include calcium, magnesium, strontium, silica, sodium, and potassium in ground water from debris-flow and alluvial aquifers and manganese, calcium, magnesium, strontium, sodium, and potassium in ground water from the bedrock aquifer. All ground water is a calcium sulfate type, often at or near gypsum saturation because of abundant gypsum in the aquifer material developed from co-existing calcite and pyrite mineralization. Calcite dissolution, the major buffering mechanism for bedrock aquifer ground water, also contributes to relatively higher calcium concentrations in some ground water. The main source of the second most abundant cation, magnesium, is probably dissolution of magnesium-rich carbonates or silicates. Strontium may also be

Ground-water surveillance at the Hanford Site for CY 1982

International Nuclear Information System (INIS)

Eddy, P.A.; Prater, L.S.; Rieger, J.T.

1983-06-01

Operations at the Hanford Site since 1944 have resulted in the discharge of large volumes of process cooling water and other waste waters to the ground. These effluents, which have reached the unconfined ground water, contain low levels of radioactive and chemical substances. The movement of these constituents in the unconfined ground water is monitored as part of the Ground-Water Surveillance Program. During 1982, 324 monitoring wells were sampled at various times for radioactive and chemical constituents. Tritium are the primary ones used to monitor the movement of the ground water. This report describes recent changes in the configuration of the tritium and nitrate plumes. The tritium plume continues to show increasing concentrations near the Columbia River. While it is mapped as having reached the Columbia River, its contribution to the river has not been distinguished from other sources at this time. The general plume configuration is much the same as in 1978, 1979, 1980, and 1981. The size of the nitrate plume appears stable. Concentrations of nitrate in the vicinity of the 100-H Area continue to be high as a result of past leaks from an evaporation facility

Measurement of radon concentration in water by means of {alpha}, {gamma} spectrometry. Radon concentration in ground and spring water in Hiroshima Prefecture

Energy Technology Data Exchange (ETDEWEB)

Shizuma, Kiyoshi [Hiroshima Univ. (Japan)

1997-02-01

Radon ({sup 222}Rn, T{sub 1/2}=3.8235{+-}0.0003d) is {alpha}-ray releasing nuclide, so that it can not be detected by {gamma}-ray measurement. But, the daughter nuclides {sup 214}Pb (T{sub 1/2}=26.8 min) and {sup 214}Bi (T{sub 1/2}=19.9 min) release {gamma}-ray, accordingly they are measured by Ge detector. Their radioactive equilibrium is kept in the closed vessel, because their half-lives are shorter than that of radon. We developed a measurement method of radon concentration by means of {gamma}-spectrometry. We applied this method to catch radon in the atmosphere by active carbon. The same principle can be applied to radon in water. Radon concentrations in the ground water were measured in 22 points in the Higashi-Hiroshima city and 82 points in the Hiroshima prefecture. The efficiencies of {gamma}-ray were determined. The radon concentration showed between 11 and 459 Bq/l and the average was 123 Bq/l. The high concentration of radon was distributed in the spring of granitic layer and higher concentration of radon were observed in the ground water of fault. (S.Y.)

A survey of natural uranium concentrations in drinking water supplies in Iran

International Nuclear Information System (INIS)

Alirezazadeh, N.; Garshasbi, N.

2003-01-01

Background: Measurement of background concentration of uranium in drinking water is very important for many reasons, specially, for human health. The uranium concentration in drinking water in many countries is a matter of concern for clinical and radioactive poisoning. Materials and methods: The uranium concentration in drinking water is determined using laser fluorimetric uranium analyzer. For this purpose after sampling, sample handling and sample preserving, sample preparation and treatment for reduction of organic matter, the concentration of uranium is measured. Results: To determine the uranium concentrations in drinking water in Iran, nearly 200 water samples were collected from all sources supplying drinking water in 21 provincial centers in the country. The wells were found to be the main source for drinking water. Uranium in the samples was measured by a laser fluorimetry technique. According to results, the concentration values found in the wells ranged from 1.0 to 10.90 μgL -1 , while nearly 95 percent of the cities had uranium concentrations in the wells at less than 4.70 μgL -1 . Surface waters showed uranium concentrations in the range of 0.75 to 2.58 μgL -1 . The daily intake of uranium from drinking water was estimated to range from 2.04 to 21.80 μgd -1 , with the mean value of 5.44 μgd -1 . Conclusion: Highest uranium mean concentration of 10.9 μgL -1 was found in Ardabil area where more studies should be done in that province in the future

Water-quality data from ground- and surface-water sites near concentrated animal feeding operations (CAFOs) and non-CAFOs in the Shenandoah Valley and eastern shore of Virginia, January-February, 2004

Science.gov (United States)

Rice, Karen C.; Monti, Michele M.; Ettinger, Matthew R.

2005-01-01

Concentrated animal feeding operations (CAFOs) result from the consolidation of small farms with animals into larger operations, leading to a higher density of animals per unit of land on CAFOs than on small farms. The density of animals and subsequent concentration of animal wastes potentially can cause contamination of nearby ground and surface waters. This report summarizes water-quality data collected from agricultural sites in the Shenandoah Valley and Eastern Shore of Virginia. Five sites, three non-CAFO and two dairy-operation CAFO sites, were sampled in the Shenandoah Valley. Four sites, one non-CAFO and three poultry-operation CAFO sites were sampled on the Eastern Shore. All samples were collected during January and February 2004. Water samples were analyzed for the following parameters and constituents: temperature, specific conductance, pH, and dissolved oxygen; concentrations of the indicator organisms Escherichia coli (E. coli) and enterococci; bacterial isolates of E. coli, enterococci, Salmonella spp., and Campylobacter spp.; sensitivity to antibiotics of E. coli, enterococci, and Salmonella spp.; arsenic, cadmium, chromium3+, copper, nickel, and mercury; hardness, biological oxygen demand, nitrate, nitrite, ammonia, ortho-phosphate, total Kjeldahl nitrogen, chemical oxygen demand, total organic carbon, and dissolved organic carbon; and 45 dissolved organic compounds, which included a suite of antibiotic compounds.Data are presented in tables 5-21 and results of analyses of replicate samples are presented in tables 22-28. A summary of the data in tables 5-8 and 18-21 is included in the report.

Ground-water flow and water quality in the Upper Floridan aquifer, southwestern Albany area, Georgia, 1998-2001

Science.gov (United States)

Warner, Debbie; Lawrence, Stephen J.

2005-01-01

During 1997, the Dougherty County Health Department sampled more than 700 wells completed in the Upper Floridan aquifer in Dougherty County, Georgia, and determined that nitrate as nitrogen (hereinafter called nitrate) concentrations were above 10 milligrams per liter (mg/L) in 12 percent of the wells. Ten mg/L is the Georgia primary drinking-water standard. The ground-water flow system is complex and poorly understood in this predominantly agricultural area. Therefore, the U.S. Geological Survey (USGS) - in cooperation with Albany Water, Gas and Light Commission - conducted a study to better define ground-water flow and water quality in the Upper Florida aquifer in the southwestern Albany area, Georgia. Ground-water levels were measured in the southwestern Albany area, Georgia, during May 1998 and March 1999 (spring), and October 1998 and September 1999 (fall). Groundwater levels measured in 75 wells open only to the Upper Floridan aquifer were used to construct potentiometric-surface maps for those four time periods. These maps show that ground water generally flows from northwest to southeast at gradients ranging from about 2 to greater than 10 feet per mile. During spring and fall 1998, ground-water levels were high and mounding of the potentiometric surface occurred in the central part of the study area, indicating a local recharge area. Water levels declined from December through February, and by March 1999 the mound in the potentiometric surface had dissipated. Of the 75 wells in the potentiometric network, 24 were selected for a water-quality network. These 24 wells and 1 spring were sampled during fall 1998 and spring 1999. Samples were analyzed for major chemical constituents, selected minor constituents, selected nutrients, and chlorofluorocarbons (CFC). Water-quality field measurements - such as water temperature, pH, specific conductance (SC), and dissolved oxygen (DO) - were taken at each well. During August 2000, a ground-water sample was collected

Fluoride Concentration of Drinking-Water of Qom, Iran

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Ahmad Reza Yari

2016-03-01

Full Text Available Background and Purpose: Fluoride is a natural element essential for human nutrition due to its benefits for dental enamel. It is well-documented that standard amounts of fluoride in drinkingwater can decrease the rate of dental caries. This study was conducted with the aim of measuring fluoride concentration of drinking-water supplies and urban distribution system in Qom, Iran. Materials and Methods: Results were subsequently compared against national and international standards. All sources of drinking-water of rural and urban areas were examined. To measure fluoride, the standard SPADNS method and a DR/4000s spectrophotometer were used. Results: Results showed that the mean of fluoride concentration in rural areas, mainly supplied with groundwater sources, was 0.41 mg/L, that of the urban distribution system 0.82 mg/L, that of Ali-Abad station 0.11 mg/L, and that of the private water desalination system 0.24 mg/L. Due to the hot climate of Qom, fluoride concentration means of all sources were lower than the permissible standards set by Iranian Standards and the WHO guidelines (except those of some of the groundwater sources and urban distribution systems. Conclusion: It seems that in most of the drinking-water sources the average fluoride concentration is not enough to prevent dental caries or strengthen dental enamel. It is concluded that Qom’s drinkingwater would require at least 0.4 mg/L to reach the minimum desirable standard.

Ground-Water Quality Data in the Owens and Indian Wells Valleys Study Unit, 2006: Results from the California GAMA Program

Science.gov (United States)

Densmore, Jill N.; Fram, Miranda S.; Belitz, Kenneth

2009-01-01

delivered to consumers. Water supplied to consumers typically is treated after withdrawal from the ground, disinfected, and blended with other waters to maintain acceptable water quality. Regulatory thresholds apply to treated water that is served to the consumer, not to raw ground water. However, to provide some context for the results, concentrations of constituents measured in the raw ground water were compared with regulatory and non-regulatory health-based thresholds established by the U.S. Environmental Protection Agency (USEPA) and California Department of Public Health (CDPH) and non-regulatory thresholds established for aesthetic concerns (secondary maximum contamination levels, SMCL-CA) by CDPH. VOCs and pesticides were detected in samples from less than one-third of the grid wells; all detections were below health-based thresholds, and most were less than one-one hundredth of threshold values. All detections of perchlorate and nutrients in samples from OWENS were below health-based thresholds. Most detections of trace elements in ground-water samples from OWENS wells were below health-based thresholds. In samples from the 53 grid wells, three constituents were detected at concentrations above USEPA maximum contaminant levels: arsenic in 5 samples, uranium in 4 samples, and fluoride in 1 sample. Two constituents were detected at concentrations above CDPH notification levels (boron in 9 samples and vanadium in 1 sample), and two were above USEPA lifetime health advisory levels (molybdenum in 3 samples and strontium in 1 sample). Most of the samples from OWENS wells had concentrations of major elements, TDS, and trace elements below the non-enforceable standards set for aesthetic concerns. Samples from nine grid wells had concentrations of manganese, iron, or TDS above the SMCL-CAs.

Beneficial reuse of FGD material in the construction of low permeability liners: Impacts on inorganic water quality constituents

Energy Technology Data Exchange (ETDEWEB)

Cheng, C.M.; Tu, W.; Zand, B.; Butalia, T.; Wolfe, W.; Walker, H. [Ohio State University, Columbus, OH (United States)

2007-05-15

In this paper, we examine the water quality impacts associated with the reuse of fixated flue gas desulfurization (FGD) material as a low permeability liner for agricultural applications. A 0.457-m-thick layer of fixated FGD material from a coal-fired power plant was utilized to create a 708 m{sup 2} swine manure pond at the Ohio Agricultural Research and Development Center Western Branch in South Charleston, Ohio. To assess the effects of the fixated FGD material liner, water quality samples were collected over a period of 5 years from the pond surface water and a sump collection system beneath the liner. Water samples collected from the sump and pond surface water met all Ohio nontoxic criteria, and in fact, generally met all national primary and secondary drinking water standards. Furthermore it was found that hazardous constituents (i.e., As, B, Cr, Cu, and Zn) and agricultural pollutants (i.e., phosphate and ammonia) were effectively retained by the FGD liner system. The retention of As, B, Cr, Cu, Zn, and ammonia was likely due to sorption to mineral components of the FGD liner, while Ca, Fe, and P retention were a result of both sorption and precipitation of Fe- and Ca-containing phosphate solids.

Review of tritiated water concentration technology

International Nuclear Information System (INIS)

Ma Hongbin

2014-01-01

In order to cooperate with the construction of the spent fuel reprocessing plant in China, the research and application status of tritiated water concentration technology at home and abroad were summarized. Some suggestions for the technology research route in China were put forward. (author)

The Effects of Filter Ventilation on Flavor Constituents in Cigarette Smoke

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Jing Y

2014-12-01

Full Text Available The deliveries of 20 added flavor constituents, total particulate matter (TPM, nicotine, ‘tar’ carbon monoxide and water in cigarette mainstream smoke were studied when filter ventilation was 0, 10%, 30%, 50% and 70%, respectively. The flavor substance test was done by addition of standard samples. The flavor constituents in cigarette smoke condensate were separated by simultaneous distillation-extraction (SDE and capillary gas chromatography (GC. The flavor constituents were identified and determined quantitatively by gas chromatography-mass spectrometry (GC-MS and GC. The flavors studied were methylpyrazine, furaldehyde, 5-methylfuraldehyde, benzaldehyde, 6-methyl-5-hepten-2-one, trimethylpyrazine, 2-acetylpyridine, phenylacetaldehyde, acetophenone, linalool, b-phenylethyl alcohol, isophorone, oxoisophorone, benzyl acetate, menthol, ethyl octanoate, b-damascenone, b-damascone, geranylacetone and b-ionone. The deliveries of TPM, nicotine, ‘tar’ carbon monoxide and water in mainstream smoke were determined according to International Standard methods. It was found that the flavor constituents and routine components in mainstream smoke decreased in different proportions as the filter ventilation increased. Carbon monoxide and ‘tar’ decreased more than nicotine. The flavor constituents with lower boiling points and lower molecular weights decreased more than those with higher boiling points and higher molecular weights. With the increase of filter ventilation, not only is the amount of smoke components reduced and the smoke taste weakened, but also the composition of smoke is modified and the quality of aroma changed slightly. These findings should be considered when developing low-‘tar’ cigarettes through the use of filter ventilation technology.

The use of stable isotopes to trace oil sands constituents

International Nuclear Information System (INIS)

Farwell, A.J.; Nero, V.; Dixon, D.G.

2002-01-01

A study was conducted to determine the biological effects of oil sands mining operations on aquatic ecosystems. The study focused on the Athabasca oil sand deposit, the largest of 4 deposits in northern Alberta. In particular, the study examined the cycling of oil sand constituents in Benthic invertebrates collected from test pits at Syncrude Canada Ltd.. The invertebrates were similar in size, but different in the quantity of process-affected water or mature fine tailings containing residual bitumen. Dragonflies and damselflies in particular, showed trends of depletion for the carbon 13 isotope and enrichment in nitrogen 15 isotope in pits where levels of process affected water was high. The depletion of carbon 13 isotope suggests that oil sand constituents assimilate into the benthic food chain. The greatest carbon 13 depletion, which was approximately 27 per cent, was found to be in test pits with high turbidity. This implies that oil sands constituents degrade microbially instead of by photosynthetic production. All benthic invertebrate group demonstrated an incremental enrichment in nitrogen 15 isotope from the control pit to the pit with greatest levels of mature fine tailings

Relationship between 222Rn concentration in soil water and degree of saturation

International Nuclear Information System (INIS)

Hamada, Hiromasa; Komae, Takami

1996-01-01

The object of the researches an analyzing downward flow to groundwater using 222 Rn concentration in water as an indicator has been saturated flow. However, when groundwater table is low, downward flow from surface is unsaturated flow. In this paper, the authors represented the relationship between 222 Rn concentration in soil water and degree of saturation, and measured the vertical distributions of 222 Rn concentrations in groundwater and 222 Rn concentration in water table in the fields. As the results, it was found that 222 Rn concentrations in the vicinity of groundwater table decreased by unsaturated downward flow. Moreover, from the variation of 222 Rn concentrations in groundwater table, it was possible to show the occurrence of the unsaturated downward flow by paddy fields irrigation, i.e., the downward flow of the soil water pushed out by irrigation water, the unsaturated percolation in the irrigation period, and the redistribution of the soil water after the release of ponding water. The degree of saturation in downward flow was calculated to be about 50% from 222 Rn concentrations in the irrigation period and in the non-irrigation period. It was deduced that the value was within reasonable range considering the difference of the hydraulic conductivities between of the upper layer and of the lower layer. These results proved that the relationship between 222 Rn concentrations in soil water and degree of saturation represented by the authors was reasonable and that the analytical method using 222 Rn concentrations in groundwater table as an indicator was useful 10 analyze the actual stale of unsaturated downward flow. (author)

Measurement of radon concentration in water with Lucas cell detector

International Nuclear Information System (INIS)

Machaj, B.; Pienkos, J.P.

2003-01-01

A method for the measurement of radon concentration in water is presented based on flushing a water sample with air in a closed loop with the Lucas cell as alpha radiation detector. The main feature of the method is washing radon away from the larger sample of water (0.75 l) to a small volume of air, approximately 0.5 l, thanks to which a high radon concentration in air and a considerable sensitivity of measurement is achieved. Basic relations and results of measurements of a model of a gauge is given. The estimated measuring sensitivity (S) is 8.5 (cpm)/(Bq/l). The random error due to the statistical fluctuations of count rate at radon concentrations 1,10, 100, 1000, 10000 Bq/l is 11, 3.6, 1.1, 0.4, 0.1% correspondingly at a counting (measuring) time of 10 min. The minimum detectable radon concentration in water is 0.11 Bq/l. (author)

Assessment of the total uranium concentration in surface and underground water samples from the Caetite region, Bahia, Brazil

International Nuclear Information System (INIS)

Silva, Julia Grasiela Batista; Geraldo, Luiz Paulo; Yamazaki, Ione Makiko

2011-01-01

At the region of Caetite, BA, it is located the largest uranium mine in exploration at present days in Brazil. During the uranium extraction process, it may be having an environmental contamination by this heavy metal due to rain water and other natural transport mechanism, with potential exposition risk to the local population. The aim of this work was to investigate the total uranium concentration in surface and underground water samples collected at the Caetite region, using the nuclear track registration technique (SSNTD) in a polycarbonate plastic. A 100 mL volume of water samples were initially treated in 10 mL of HNO 3 (PA) and concentrated by evaporation at a temperature around 80 deg C. The resulting residue was diluted to a total volume of 25 mL without pass it to a filter. About 10 μL of this solution was deposited on the plastic detector surface (around 1.0 cm 2 area) together with 5 μL of a Cyastat detergent solution (5%) and evaporated under an infrared lamp. All the resulting deposits of non volatile constituents were irradiated, together with a uranium standard sample, at the IPEN-IEA-R1 (3.5 MW) nuclear reactor for approximately 3 min. After irradiations, chemical etching of the plastic detectors was carried out at 60 deg C, for 65 min. in a NaOH (6N) solution. The fission tracks were counted scanning all the deposit area of the polycarbonate plastic detector with a system consisting of an optical microscope together with a video camera and TV monitor. The average values of uranium concentrations obtained in this work ranged from (0.95±0.19) μg.L -1 to (25.60±3.3) μg.L -1 . These results were compared to values reported in the literature for water samples from other regions and discussed in terms of safe limits recommended by WHO -World Health Organization and CONAMA - Conselho Nacional do Meio Ambiente. (author)

Assessment of the total uranium concentration in surface and underground water samples from the Caetite region, Bahia, Brazil

Energy Technology Data Exchange (ETDEWEB)

Silva, Julia Grasiela Batista; Geraldo, Luiz Paulo [Centro Universitario da Fundacao Educacional de Barretos (UNIFEB), (SP) (Brazil); Yamazaki, Ione Makiko [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

2011-07-01

At the region of Caetite, BA, it is located the largest uranium mine in exploration at present days in Brazil. During the uranium extraction process, it may be having an environmental contamination by this heavy metal due to rain water and other natural transport mechanism, with potential exposition risk to the local population. The aim of this work was to investigate the total uranium concentration in surface and underground water samples collected at the Caetite region, using the nuclear track registration technique (SSNTD) in a polycarbonate plastic. A 100 mL volume of water samples were initially treated in 10 mL of HNO{sub 3} (PA) and concentrated by evaporation at a temperature around 80 deg C. The resulting residue was diluted to a total volume of 25 mL without pass it to a filter. About 10 {mu}L of this solution was deposited on the plastic detector surface (around 1.0 cm{sup 2} area) together with 5 {mu}L of a Cyastat detergent solution (5%) and evaporated under an infrared lamp. All the resulting deposits of non volatile constituents were irradiated, together with a uranium standard sample, at the IPEN-IEA-R1 (3.5 MW) nuclear reactor for approximately 3 min. After irradiations, chemical etching of the plastic detectors was carried out at 60 deg C, for 65 min. in a NaOH (6N) solution. The fission tracks were counted scanning all the deposit area of the polycarbonate plastic detector with a system consisting of an optical microscope together with a video camera and TV monitor. The average values of uranium concentrations obtained in this work ranged from (0.95{+-}0.19) {mu}g.L{sup -1} to (25.60{+-}3.3) {mu}g.L{sup -1}. These results were compared to values reported in the literature for water samples from other regions and discussed in terms of safe limits recommended by WHO -World Health Organization and CONAMA - Conselho Nacional do Meio Ambiente. (author)

Continuous measurement of the radon concentration in water using electret ion chamber method

International Nuclear Information System (INIS)

Dua, S.K.; Hopke, P.K.

1992-10-01

A radon concentration of 300 pCi/L has been proposed by the US Environmental Protection Agency as a limit for radon dissolved in municipal drinking water supplies. There is therefore a need for a continuous monitor to insure that the daily average concentration does not exceed this limit. In order to calibrate the system, varying concentrations of radon in water have been generated by bubbling radon laden air through a dynamic flowthrough water system. The value of steady state concentration of radon in water from this system depends on the concentration of radon in air, the air bubbling rate, and the water flow rate. The measurement system has been designed and tested using a 1 L volume electret ion chamber to determine the radon in water. In this dynamic method, water flows directly through the electret ion chamber. Radon is released to the air and measured with the electret. A flow of air is maintained through the chamber to prevent the build-up of high radon concentrations and too rapid discharge of the electret. It was found that the system worked well when the air flow was induced by the application of suction. The concentration in the water was calculated from the measured concentration in air and water and air flow rates. Preliminary results suggest that the method has sufficient sensitivity to measure concentrations of radon in water with acceptable accuracy and precision

Antioxidant activities of the constituents of Picris echoides

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MILUTIN STEFANOVIC

2002-01-01

Full Text Available Some flavonoids with antioxidant properties from the aerial parts of the plant species Picris echoides (family Asteraceae were identified. Upon chromatography, the ethyl acetate extract afforded flavonoids, such as: flavone apigenin (1 and its glucoside, cosmosiin (2, as well as common plant constituents from this family, flavonol galetin (3, 3,4’,5,6,7-pentahydroxyflavone and 4,4’,6,7-tetrahydroxyaurone (4. The structure of the aurone 4 has not been described so far in the literature and presented a very rare type of aurone skeleton. The structures of the isolated compounds were determined by interpretation of their physical and spectral data. The antioxidant activities of different extracts from Picris echoides were measured by the Schaal oven test at 60ºC and by the Rancimat method at 100ºC. Water/ethanol extracts (2:8, v/v, in concentrations of 0.02 and 0.05 %, showed lower activity than commercial tocopherol (Tch. On the contrary, the purified ethyl acetate extracts showed a strong concentration-dependent antioxidant effect. The investigation demonstrated that galetin was the main flavonol from this origin. According to the results of the two methods, galetin (3 showed a two-fold better activity than did Tch and a lower activity than did butylated hydroxyanisole (BHA. The aurone 4 exhibited significantly lower antioxidant activity than did galetin at the same concentration level. Thus, the plant species P. echoides is a new and favorable source of natural lipid antioxidants.

Water-quality assessment of the Cambrian-Ordovician aquifer system in the northern Midwest, United States

Science.gov (United States)

Wilson, John T.

2012-01-01

This report provides a regional assessment of groundwater quality of the Cambrian-Ordovician aquifer system, based primarily on raw water samples collected by the NAWQA Program during 1995 through 2007. The NAWQA Program has published findings in local study-unit reports encompassing parts of the Cambrian-Ordovician aquifer system. Data collected from the aquifer system were used in national synthesis reports on selected topics such as specific water-quality constituent classes, well type, or aquifer material; however, a synthesis of groundwater quality at the principal aquifer scale has not been completed and is therefore the major purpose of this report. Water samples collected by the NAWQA Program were analyzed for various classes of characteristics including physical properties, major ions, trace elements, nutrients and dissolved organic carbon, radionuclides (tritium, radon, and radium), pesticides, and volatile organic compounds. Subsequent sections of this report provide discussions on these classes of characteristics. The assessment objectives of this report are to (1) summarize constituent concentrations and compare them to human-health benchmarks and non-health guidelines; (2) determine the geographic distribution of constituent concentrations and relate them to various factors such as confining conditions, well type, land use, and groundwater age; and (3) evaluate near-decadal-scale changes in nitrate concentrations and pesticide detections. The most recent sample collected from each well by the NAWQA Program was used for most analyses. Near-decadal-scale changes in nitrate concentrations and pesticide detections were evaluated for selected well networks by using the most recent sample from each well and comparing it to the results from a sample collected 7 or 11 years earlier. Because some of the NAWQA well networks provide a limited areal coverage of the aquifer system, data for raw water samples from other USGS sources and state agencies were included

assessment of heavy metals concentration in drinking water ...

African Journals Online (AJOL)

userpc

guidelines (WHO 2005). Findings suggest that continues water quality monitoring should be carried out to check the concentration levels of heavy metals in that area, to prevent them from been above the limit of WHO. Keywords: Atomic Absorption Spectrophotometers, Heavy Metals, Water, Kauru Local. Government Area.

Trends in major-ion constituents and properties for selected sampling sites in the Tongue and Powder River watersheds, Montana and Wyoming, based on data collected during water years 1980-2010

Science.gov (United States)

Sando, Steven K.; Vecchia, Aldo V.; Barnhart, Elliott P.; Sando, Thomas R.; Clark, Melanie L.; Lorenz, David L.

2014-01-01

The primary purpose of this report is to present information relating to flow-adjusted temporal trends in major-ion constituents and properties for 16 sampling sites in the Tongue and Powder River watersheds based on data collected during 1980–2010. In association with this primary purpose, the report presents background information on major-ion characteristics (including specific conductance, calcium, magnesium, potassium, sodium adsorption ratio, sodium, alkalinity, chloride, fluoride, dissolved sulfate, and dissolved solids) of the sampling sites and coal-bed methane (CBM) produced water (groundwater pumped from coal seams) in the site watersheds, trend analysis methods, streamflow conditions, and factors that affect trend results. The Tongue and Powder River watersheds overlie the Powder River structural basin (PRB) in northeastern Wyoming and southeastern Montana. Limited extraction of coal-bed methane (CBM) from the PRB began in the early 1990’s, and increased dramatically during the late 1990’s and early 2000’s. CBM-extraction activities produce discharges of water with high concentrations of dissolved solids (particularly sodium and bicarbonate ions) relative to most stream water in the Tongue and Powder River watersheds. Water-quality of CBM produced water is of concern because of potential effects of sodium on agricultural soils and potential effects of bicarbonate on aquatic biota. Two parametric trend-analysis methods were used in this study: the time-series model (TSM) and ordinary least squares regression (OLS) on time, streamflow, and season. The TSM was used to analyze trends for 11 of the 16 study sites. For five sites, data requirements of the TSM were not met and OLS was used to analyze trends. Two primary 10-year trend-analysis periods were selected. Trend-analysis period 1 (water years 1986–95; hereinafter referred to as period 1) was selected to represent variability in major-ion concentrations in the Tongue and Powder River

226Ra concentrations in some Illinois well waters

International Nuclear Information System (INIS)

Holtzman, R.B.; Gilkeson, R.H.

1982-01-01

226 Ra concentrations are reported for the waters from deep wells in 43 communities in Illinois. The concentrations range from 0.08 to 20.6 pCi/L. The effectiveness of additives (nitric acid or EDTA) in keeping the 226 Ra in solution in the samples is discussed

Cs-137 and Co-60 concentrations in water from the Savannah River and water-treatment plants downstream of SRP

International Nuclear Information System (INIS)

1983-01-01

In preparation for restart of L-Reactor, a comprehensive environmental sampling and analysis program was initiated in March 1983 to determine Cs-137 concentrations in off-site water downstream from Savannah River Plant (SRP). Concentrations of Co-60 also are determined in this sampling and analysis program. This report summarizes the first three months of results. Cesium-137 concentrations are reported for finished water from the Beaufort-Jasper, Port Wentworth and North Augusta water treatment plants for weekly continuous samples during April through June 1983. The very low concentrations of cesium-137 in finished water from downstream water treatment plants showed significant changes during this time. The changes in concentration occurred smoothly and correlate with changes in river flow. No changes in concentration during April through June can be attributed to L-Reactor's only cold water test which occurred June 8 and 9. No Co-60 was observed in any samples

Effects of water treatment processes used at waterworks on natural radionuclide concentrations

International Nuclear Information System (INIS)

Haemaelaeinen, K.; Vesterbacka, P.; Maekelaeinen, I.; Arvela, H.

2004-08-01

The occurrence of uranium and other natural radionuclides in waters of waterworks and the effects of the conventional water treatment processes on radionuclide concentrations were investigated. Water samples were collected from 17 waterworks. Radionuclide concentrations of the collected samples were compared to the currently valid concentrations according to the Finnish regulation, ST guide 12.3. Similarly the measured concentrations were compared to the values presented in the 98/83/EC directive and in the Commission recommendation, 2001/928/Euratom. The guidelines based on chemical toxicity of uranium were also considered. This report presents a summary of the radionuclide concentrations in waters distributed by waterworks. Short-term and logn-term temporal variation of radionuclide levels in raw water were also investigated. Waterworks selected to this study used different kinds of raw water sources and a variety of water treatment processes. Water samples were collected from 46 water catchments which used groundwater in soil, artificial groundwater or groundwater in bedrock as a source of raw water. The most common water treatment used in these catchments was alkalization. Other treatment processes used were various types of filtrations (sand, anthracite, slow sand and membrane filtration) and aeration. Four of the catchments distributed water without treatment. Sampling was carried out in co-operation with local health inspectors and waterworks staff in spring 2002. Later that autumn, monitoring samples were collected from eight catchments. The maximum value for radon, presented in ST guide 12.3, was exceeded in three water catchments that used groundwater in bedrock as a source of raw water. No exceedings were found in those water catchments that use groundwater in soil or artificial groundwater. The limits of uranium and radium calculated from the total indicative dose (98/83/EC) were not exceeded but the guidelines for lead and polonium, given in the

Rn-222 concentrations in private well water and in river water around Ningyo Toge area

Energy Technology Data Exchange (ETDEWEB)

Yunoki, Eiji [Okayama, Prefectural Inst. for Environmental Science and Public Health (Japan)

1997-02-01

The Ningyo-Toge Works of Power Reactor and Nuclear Fuel Development Corporation have started the pilot plant for uranium refining and conversion in 1984 and thereafter been producing 6-uranium fluoride, which is a raw material for an uranium concentration plant. The operation of prototype reactor has started since 1989. In this study, radioactive contamination around the works under these circumstances has been monitored in the respects of Rn concentrations in well water and river one for more than 10 years. The radioactivities of well water sampled at 4 points in this area were in a range of 0.6-82.9 Bq/l. The differences in the activities seemed to be depending on petrological properties. For the river water, the Rn concentration was determined at 13 points in the area. Seasonal changes in the Rn concentrations were not significant (p<0.05) but there were significant changes among years during 1985-1995. Further, the radioactive levels of soils collected from riverbed at 5 points were significantly different both for {sup 238}U and {sup 226}Ra, but the ratios of {sup 238}U/{sup 226}Ra were consistent. Furthermore, there was no correlation between {sup 226}Ra and {sup 222}Rn concentrations in the river water. (M.N.)

Ground-Water Quality Data in the Coachella Valley Study Unit, 2007: Results from the California GAMA Program

Science.gov (United States)

Goldrath, Dara A.; Wright, Michael T.; Belitz, Kenneth

2009-01-01

ground water. A quality-control sample (blank, replicate, or matrix spike) was collected at approximately one quarter of the wells, and the results for these samples were used to evaluate the quality of the data for the ground-water samples. Assessment of the quality-control information resulted in V-coding less than 0.1 percent of the data collected. This study did not attempt to evaluate the quality of water delivered to consumers; after withdrawal from the ground, water typically is treated, disinfected, and (or) blended with other waters to maintain acceptable water quality. Regulatory thresholds apply to treated water that is supplied to the consumer, not to raw ground water. However, to provide some context for the results, concentrations of constituents measured in the raw ground water were compared with health-based thresholds established by the U.S. Environmental Protection Agency (USEPA) and the California Department of Public Health (CDPH) and thresholds established for aesthetic purposes (secondary maximum contaminant levels, SMCL-CA) by CDPH. Most constituents detected in ground-water samples were at concentrations below drinking-water thresholds. Volatile organic compounds, pesticides, and pesticide degradates were detected in less than one-third of the grid well samples collected. All VOC and pesticide concentrations measured were below health-based thresholds. Potential waste-water indicators were detected in less than half of the wells sampled, and no detections were above health-based thresholds. Perchlorate was detected in seven grid wells; concentrations from two wells were above the CDPH maximum contaminant level (MCL-CA). Most detections of trace elements in samples collected from COA Study Unit wells were below water-quality thresholds. Exceptions include five samples of arsenic that were above the USEPA maximum contaminant level (MCL-US), two detections of boron above the CDPH notification level (NL-CA), and two detections of mol

Radon concentrations of ground waters in Aichi Prefecture

Energy Technology Data Exchange (ETDEWEB)

Ohnuma, Shoko; Kawamura, Norihisa [Aichi Prefectural Inst. of Public Health, Nagoya (Japan)

1997-02-01

Aichi Prefectural Institute of Public Health has been collecting the data concerning the spacial distribution of Rn concentration of groundwater in Aichi Prefecture and its time course changes. In this report, the data was described chiefly from 1991 and the availability of newly developed polyethylene vessel was discussed. Determination of Rn concentration was performed at a total of 104 sites within the range from the horizon to the depth of 1800 m. The measurement has been repeatedly conducted for ca. 20 years. The maximum level of Rn was 896 Bq/l and the minimum was 0.3 Bq/l for the groundwater samples collected from different springs. Correlation of Rn concentration with other chemical and physical factors for ground water was investigated and a significant correlation was found only between Rn concentration and pH ({gamma}=0.304, p<0.01). No time course changes in Rn concentration was observed except for the water sample from the site affected by some newly dug wells. In addition, the newly developed extraction vessel was shown to be available for the determination and its operability in the field was superior to the conventional glass ware. (M.N.)

Water-quality and bottom-material characteristics of Cross Lake, Caddo Parish, Louisiana, 1997-99

Science.gov (United States)

McGee, Benton D.

2004-01-01

Cross Lake is a shallow, monomictic lake that was formed in 1926 by the impoundment of Cross Bayou. The lake is the primary drinking-water supply for the City of Shreveport, Louisiana. In recent years, the lakeshore has become increasinginly urbanized. In addition, the land use of the watershed contributing runoff to Cross Lake has changed. Changes in land use and urbanization could affect the water chemistry and biology of the Lake. Water-quality data were collected at 10 sites on Cross Lake from February 1997 to February 1999. Water-column and bottom-material samples were collected. The water-column samples were collected at least four times per year. These samples included physical and chemical-related properties such as water temperature, dissolved oxygen, pH, and specific conductance; selected major inorganic ions; nutrients; minor elements; organic chemical constituents; and bacteria. Suspended-sediment samples were collected seven times during the sampling period. The bottom-material samples, which were collected once during the sampling period, were analyzed for selected minor elements and inorganic carbon. Aside from the nutrient-enriched condition of Cross Lake, the overall water-quality of Cross Lake is good. No primary Federal or State water-quality criteria were exceeded by any of the water-quality constituents analyzed for this report. Concentrations of major inorganic constituents, except iron and manganese, were low. Water from the lake is a sodium-bicarbonate type and is soft. Minor elements and organic compounds were present in low concentrations, many below detection limits. Nitrogen and phosphorus were the nutrients occurring in the highest concentrations. Nutrients were evenly distributed across the lake with no particular water-quality site indicating consistently higher or lower nutrient concentrations. No water samples analyzed for nitrate exceeded the U.S. Environmental Protection Agency's Maximum Contaminant Level of 10 milligrams per

Optimization of simultaneous ultrasonic-assisted extraction of water-soluble and fat-soluble characteristic constituents from Forsythiae Fructus Using response surface methodology and high-performance liquid chromatography.

Science.gov (United States)

Xia, Yong-Gang; Yang, Bing-You; Liang, Jun; Wang, Di; Yang, Qi; Kuang, Hai-Xue

2014-07-01

The compounds (+)-pinoresinol-β-glucoside (1) forsythiaside, (2) phillyrin (3) and phillygenin (4) were elucidated to be the characteristic constituents for quality control of Forsythiae Fructus extract by chromatographic fingerprint in 2010 edition of Chinese Pharmacopoeia due to their numerous important pharmacological actions. It is of great interest to extract these medicinally active constituents from Forsythiae Fructus simultaneously. In this study, a new ultrasound-assisted extraction (UAE) method was developed for the simultaneous extraction of biological components 1-4 in Forsythiae Fructus. The quantitative effects of extraction time, ratio of liquid to solid, extraction temperature, and methanol concentration on yield of these four important biological constituents from Forsythiae Fructus were investigated using response surface methodology with Box-Behnken design. The compounds 1-4 extracted by UAE were quantitative analysis by high-performance liquid chromatography-photodiode array detect (HPLC-PAD), and overall desirability (OD), the geometric mean of the contents of four major biological components, was used as a marker to evaluate the extraction efficiency. By solving the regression equation and analyzing 3-D plots, the optimum condition was at extraction temperature 70°C, time 60 min, ratio of liquid to solid 20, and methanol concentration 76.6%. Under these conditions, extraction yields of compounds 1-4 were 2.92 mg/g, 52.10 mg/g, 0.90 mg/g and 0.57 mg/g, respectively, which were in good agreement with the predicted OD values. In order to achieve a similar yield as UAE, soxhlet extraction required at least 6 h and maceration extraction required much longer time of 24 h. Established UAE method has been successfully applied to sample preparation for the quality control of Forsythiae Fructus. Additionally, a quadrupole time-of-flight mass spectrometry was applied to the structural confirmation of analytes from the complex matrices acquired by UAE

Results of the radon concentration survey in Sibiu county underground water

International Nuclear Information System (INIS)

Chicea, Dan; Cosma, Constantin

2002-01-01

In November 2000 a survey of radon ( 222 Rn) concentration in Sibiu county underground water was conducted. The radon concentration was measured with a A LUK 3A. The radon gas was extracted from water using the LUK VR device that works with LUK 3A. All samples were taken in 0.5 l recipients that were filled and sealed. Samples from eighteen cities and villages were taken. Special care was taken for the samples to be carefully brought to room temperature and not to be agitated or stirred before measuring the radon concentration. In measuring the radon concentration corrections like the solubility coefficient variation with temperature, the radon concentration increase in air in time and the background correction were applied. Results reveal that the underground water radon concentration is bigger in wells located in mountainous area, has an average value in wells from hilly region and is considerable lower in wells located in plain area. Another thing we noticed is that the samples taken from the city water pipe system present lower radon concentration values than the samples taken from home drilled wells. The minimum radon concentration value was found in the drinking water of Sibiu city, 1.6 Bq/l and in Sadu village, 1.965 Bq/l. The highest measured values are 28.1 Bq/l in Rasinari, a village located at the bottom of the mountains and 26.4 Bq/l, in Sibiel, a village 30 km away from the first one. These results reveal that the radon concentration values measured in Sibiu county are comparable with the measured values reported in literature and well below the maximum acceptable values. (authors)

Radionuclides, inorganic constitutents, organic compounds, and bacteria in water from selected wells and springs from the southern boundary of the Idaho National Engineering Laboratory to the Hagerman Area, Idaho, 1992

International Nuclear Information System (INIS)

Bartholomay, R.C.; Edwards, D.D.; Campbell, L.J.

1994-01-01

The U.S. Geological Survey and the Idaho Department of Water Resources, in response to a request from the U.S. Department of Energy, sampled 18 sites as part of a long-term project to monitor water quality of the Snake River Plain aquifer from the southern boundary of the Idaho National Engineering Laboratory to the Hagerman area. Water samples were collected and analyzed for selected radionuclides, inorganic constituents, organic compounds, and bacteria. The samples were collected from 13 irrigation wells, 1 domestic well, 1 spring, 2 stock wells, and 1 public supply well. Quality assurance samples also were collected and analyzed. None of the samples analyzed for radionuclides, inorganic constituents, or organic compounds exceeded the established maximum contaminant levels for drinking water. Most of the radionuclide and inorganic constituent concentrations exceeded their respective reporting levels. Most of the samples analyzed for surfactants and dissolved organic carbon had concentrations that exceeded their reporting levels. None of the samples contained reportable concentrations of purgeable organic compounds or pesticides. Total coliform bacteria was present in nine samples

Relationship between drinking water and toenail arsenic concentrations among a cohort of Nova Scotians.

Science.gov (United States)

Yu, Zhijie M; Dummer, Trevor J B; Adams, Aimee; Murimboh, John D; Parker, Louise

2014-01-01

Consumption of arsenic-contaminated drinking water is associated with increased cancer risk. The relationship between arsenic body burden, such as concentrations in human toenails, and arsenic in drinking water is not fully understood. We evaluated the relationship between arsenic concentrations in drinking water and toenail clippings among a cohort of Nova Scotians. A total of 960 men and women aged 35 to 69 years provided home drinking water and toenail clipping samples. Information on water source and treatment use and covariables was collected through questionnaires. Arsenic concentrations in drinking water and toenail clippings and anthropometric indices were measured. Private drilled water wells had higher arsenic concentrations compared with other dug wells and municipal drinking water sources (Pwater arsenic levels ≥1 μg/l, there was a significant relationship between drinking water and toenail arsenic concentrations (r=0.46, Pwater, obese individuals had significantly lower concentrations of arsenic in toenails compared with those with a normal weight. Private drilled water wells were an important source of arsenic exposure in the study population. Body weight modifies the relationship between drinking water arsenic exposure and toenail arsenic concentrations.

Steroid hormone concentrations and physiological toxicity of water ...

African Journals Online (AJOL)

Seven bioassays were used to determine oestradiol (E2), oestrone (E1) and testosterone (T) concentrations, as well as neurotoxicity, cytotoxicity and immunotoxicity, in water sampled during 2010 and 2011. Oestradiol and E1 concentrations of up to 7.2 pg ml–1 and 7.6 pg ml–1, respectively, were recorded. Testosterone ...

Streamflow gains and losses and selected water-quality observations in five subreaches of the Rio Grande/Rio Bravo del Norte from near Presidio to Langtry, Texas, Big Bend area, United States and Mexico, 2006

Science.gov (United States)

Raines, Timothy H.; Turco, Michael J.; Connor, Patrick J.; Bennett, Jeffery B.

2012-01-01

Few historical streamflow and water-quality data are available to characterize the segment of the Rio Grande/Rio Bravo del Norte (hereinafter Rio Grande) extending from near Presidio to near Langtry, Texas. The U.S. Geological Survey, in cooperation with the National Park Service and the Texas Commission on Environmental Quality, collected water-quality and streamflow data from the Rio Grande from near Presidio to near Langtry, Texas, to characterize the streamflow gain and loss and selected constituent concentrations in a 336.3-mile reach of the Rio Grande from near Presidio to near Langtry, Texas. Streamflow was measured at 38 sites and water-quality samples were collected at 20 sites along the Rio Grande in February, March, and June 2006. Streamflow gains and losses over the course of the stream were measured indirectly by computing the differences in measured streamflow between sites along the stream. Water-quality data were collected and analyzed for salinity, dissolved solids, major ions, nutrients, trace elements, and stable isotopes. Selected properties and constituents were compared to available Texas Commission on Environmental Quality general use protection criteria or screening levels. Summary statistics of selected water-quality data were computed for each of the five designated subreaches. Streamflow gain and loss and water-quality constituent concentration were compared for each subreach, rather than the entire segment because of the temporal variation in sample collection caused by controlled releases upstream. Subreach A was determined to be a losing reach, and subreaches B, C, D, and E were determined to be gaining reaches. Compared to concentrations measured in upstream subreaches, downstream subreaches exhibited evidence of dilution of selected constituent concentrations. Subreaches A and B had measured total dissolved solids, chloride, and sulfate exceeding the Texas Commission on Environmental Quality general use protection criteria

Water quality assessment of the Eastern Iowa Basins: Basic water chemistry of rivers and streams, 1996-98

Science.gov (United States)

Barnes, Kimberlee K.

2001-01-01

The U.S. Geological Survey began data-collection activities in the Eastern Iowa Basins study unit of the National Water-Quality Assessment Program in September 1995 with the purpose of determining the status and trends in water quality of water from the Wapsipinicon, Cedar, Iowa, and Skunk River basins. From March 1996 through September 1998, monthly surface-water samples were collected from 11 sites on the study's rivers and streams representing three distinct physiographic regions, the Des Moines Lobe, the Iowan Surface, the Southern Iowa Drift Plain, and one subregion, the Iowan Karst. These water samples were analyzed for basic water chemistry, including, but not limited to the following cations: sodium, potassium, magnesium, calcium, and silica; anions: chloride, fluoride, sulfate, and bicarbonate; and two metals - iron and maganese. Although none of the concentrations of the constituents exceeded health advisories or drinking-water regulations, extremely high or low concentrations could potentially affect aquatic life. Calcium, magnesium, and potassium are essential elements for both plant and animal life; manganese is an essential element in plant metabolism; and silica is important in the growth of diatom algae. Calcium had the largest median concentration of 61 milligrams per liter (mg/L) of the cations, and the largest maximum concentration of 100 mg/L. Bicarbonate had the largest median concentration of 210 mg/L of the anions, and the largest maximum concentration of 400 mg/L.

Strontium concentrations in corrosion products from residential drinking water distribution systems.

Science.gov (United States)

Gerke, Tammie L; Little, Brenda J; Luxton, Todd P; Scheckel, Kirk G; Maynard, J Barry

2013-05-21

The United States Environmental Protection Agency (US EPA) will require some U.S. drinking water distribution systems (DWDS) to monitor nonradioactive strontium (Sr(2+)) in drinking water in 2013. Iron corrosion products from four DWDS were examined to assess the potential for Sr(2+) binding and release. Average Sr(2+) concentrations in the outermost layer of the corrosion products ranged from 3 to 54 mg kg(-1) and the Sr(2+) drinking water concentrations were all ≤0.3 mg L(-1). Micro-X-ray adsorption near edge structure spectroscopy and linear combination fitting determined that Sr(2+) was principally associated with CaCO3. Sr(2+) was also detected as a surface complex associated with α-FeOOH. Iron particulates deposited on a filter inside a home had an average Sr(2+) concentration of 40.3 mg kg(-1) and the associated drinking water at a tap was 210 μg L(-1). The data suggest that elevated Sr(2+) concentrations may be associated with iron corrosion products that, if disturbed, could increase Sr(2+) concentrations above the 0.3 μg L(-1) US EPA reporting threshold. Disassociation of very small particulates could result in drinking water Sr(2+) concentrations that exceed the US EPA health reference limit (4.20 mg kg(-1) body weight).

Pollutant Concentrations in the Rime and Fog Water

Czech Academy of Sciences Publication Activity Database

Fišák, Jaroslav; Tesař, Miroslav; Fottová, D.

2008-01-01

Roč. 3, č. 1 (2008), S68-S73 ISSN 1801-5395 R&D Projects: GA AV ČR IAA3042301; GA AV ČR 1QS200420562 Institutional research plan: CEZ:AV0Z30420517; CEZ:AV0Z20600510 Keywords : fog water * rime water * pollutant concentration Subject RIV: DG - Athmosphere Sciences, Meteorology

7746 CONCENTRATIONS OF FORMALDEHYDE IN RAIN WATERS ...

African Journals Online (AJOL)

Win7Ent

2013-06-03

Jun 3, 2013 ... The chromotropic acid method described by the. National Institute for ... concentration range of the formaldehyde in the rain waters varied from month to month throughout the six ... vicinity of vegetation [3]. Formaldehyde is the ...

Drinking water quality from the aspect of element concentrations

International Nuclear Information System (INIS)

Chiba, M.; Shinohara, A.; Sekine, M.; Hiraishi, S.

2006-01-01

Drinking water in developed countries is usually treated by the water-purification system, while in developing countries untreated natural water such as well water, river water, rain water, or pond water are used. On the other hand, many kinds of mineral water bottled in plastic containers are sold as drinking water with or without gas in urban areas in many countries. Seawater under hundreds meters from the surface is also bottled and sold as drinking water with advertising good mineral balance. Various element concentrations in water samples for drinking were analyzed, and then it was considered the effects of elements on human health. (author)

Study on the TOC concentration in raw water and HAAs in Tehran's water treatment plant outlet.

Science.gov (United States)

Ghoochani, Mahboobeh; Rastkari, Noushin; Nabizadeh Nodehi, Ramin; Mahvi, Amir Hossein; Nasseri, Simin; Nazmara, Shahrokh

2013-11-12

A sampling has been undertaken to investigate the variation of haloacetic acids formation and nature organic matter through 81 samples were collected from three water treatment plant and three major rivers of Tehran Iran. Changes in the total organic matter (TOC), ultraviolet absorbance (UV254), specific ultraviolet absorbance (SUVA) were measured in raw water samples. Haloacetic acids concentrations were monitored using a new static headspace GC-ECD method without a manual pre-concentration in three water treatment plants. The average concentration of TOC and HAAs in three rivers and three water treatment plants in spring, summer and fall, were 4, 2.41 and 4.03 mg/L and 48.75, 43.79 and 51.07 μg/L respectively. Seasonal variation indicated that HAAs levels were much higher in spring and fall.

Continuous water-quality monitoring and regression analysis to estimate constituent concentrations and loads in the Red River of the North at Fargo and Grand Forks, North Dakota, 2003-12

Science.gov (United States)

Galloway, Joel M.

2014-01-01

The Red River of the North (hereafter referred to as “Red River”) Basin is an important hydrologic region where water is a valuable resource for the region’s economy. Continuous water-quality monitors have been operated by the U.S. Geological Survey, in cooperation with the North Dakota Department of Health, Minnesota Pollution Control Agency, City of Fargo, City of Moorhead, City of Grand Forks, and City of East Grand Forks at the Red River at Fargo, North Dakota, from 2003 through 2012 and at Grand Forks, N.Dak., from 2007 through 2012. The purpose of the monitoring was to provide a better understanding of the water-quality dynamics of the Red River and provide a way to track changes in water quality. Regression equations were developed that can be used to estimate concentrations and loads for dissolved solids, sulfate, chloride, nitrate plus nitrite, total phosphorus, and suspended sediment using explanatory variables such as streamflow, specific conductance, and turbidity. Specific conductance was determined to be a significant explanatory variable for estimating dissolved solids concentrations at the Red River at Fargo and Grand Forks. The regression equations provided good relations between dissolved solid concentrations and specific conductance for the Red River at Fargo and at Grand Forks, with adjusted coefficients of determination of 0.99 and 0.98, respectively. Specific conductance, log-transformed streamflow, and a seasonal component were statistically significant explanatory variables for estimating sulfate in the Red River at Fargo and Grand Forks. Regression equations provided good relations between sulfate concentrations and the explanatory variables, with adjusted coefficients of determination of 0.94 and 0.89, respectively. For the Red River at Fargo and Grand Forks, specific conductance, streamflow, and a seasonal component were statistically significant explanatory variables for estimating chloride. For the Red River at Grand Forks, a time

Hydrodynamical model with massless constituents

International Nuclear Information System (INIS)

Chiu, C.B.; Wang, K.H.

1974-01-01

Within the constituent hydrodynamical model, it is shown that the total number of constituents is conserved, if these constituents are massless and satisfy the Fermi-Dirac distribution. A simple scheme for the transition from the constituent-phase to the hadron-phase is suggested, and the hadron inclusive momentum spectra are presented for this case. This phase transition scheme predicts the average transverse momentum of meson resonances which is compatible with the data. (U.S.)

Radon concentrations in the water of Misasa area (Tottori Pref.)

Energy Technology Data Exchange (ETDEWEB)

Morishima, Hiroshige; Koga, Taeko; Inagaki, Masayo [Kinki Univ., Higashi-Osaka, Osaka (Japan); Mifune, Masaaki

1997-02-01

UNSCEAR (United Nations Scientific Committee on the Effects of Atomic Radiation) Report (1988, 1993) indicated that the internal exposure dose of absorption of radon (Rn-222) and the short-lived decay product nucleus occupied about half of 2.4 m Sv of the global average of annual dose of natural radiation source. It is said to be the largest factor of radiation dose of natural radiation. Sample collection and the method, the elution properties by the concentration of Rn-222 in water and the comparison of characteristics among the different methods are explained. The detection limit of concentration of radon in water by OPTI-FLUOR direct method using the liquid scintillator spectrometer was 1.5 Bq/l for 20 mins counting. The maximum radon concentrations determined by this method showed 1700 Bq/l of the spring water in Misasa area, 400 Bq/l of the small water supply system and well and 18 Bq/l of Mitoku river. (S.Y.)

A reconnaissance spatial and temporal assessment of methane and inorganic constituents in groundwater in bedrock aquifers, Pike County, Pennsylvania, 2012-13

Science.gov (United States)

Senior, Lisa A.

2014-01-01

Pike County in northeastern Pennsylvania is underlain by the Devonian-age Marcellus Shale and other shales, formations that have potential for natural gas development. During 2012–13, the U.S. Geological Survey in cooperation with the Pike County Conservation District conducted a reconnaissance study to assess baseline shallow groundwater quality in bedrock aquifers prior to possible shale-gas development in the county. For the spatial component of the assessment, 20 wells were sampled in summer 2012 to provide data on the occurrence of methane and other aspects of existing groundwater quality throughout the county, including concentrations of inorganic constituents commonly present at low levels in shallow, fresh groundwater but elevated in brines. For the temporal component of the assessment, 4 of the 20 wells sampled in summer 2012 were sampled monthly from July 2012 through June 2013 to provide data on seasonal variability in groundwater quality. All water samples were analyzed for major ions, nutrients, selected inorganic trace constituents (including metals and other elements), stable isotopes of water, radon-222, gross alpha- and gross beta-particle activity, dissolved gases (methane, ethane, and ethene), and, if possible, isotopic composition of methane. Additional analyses for boron and strontium isotopes, age-dating of water, and radium-226 were done on water samples collected from six wells in June 2013.

Evaluation of Chlorinated Hydrocarbon Concentrations in Tehran’s Districts Drinking Water

Directory of Open Access Journals (Sweden)

Alireza Pardakhti

2012-01-01

Full Text Available In this study Tehran’s drinking water was evaluated for the presence of chlorinated hydrocarbons during spring and summer of 2009. Chlorinated hydrocarbons are an important class of environmental pollutants that cause adverse health effects on human’s kidney, liver and central nervous systems. In this study six water districts were selected for taking drinking water samples in the city of Tehran as well as one location outside the city limits. The samples were analyzed by GC/MS using EPA method 8260. The average concentrations of 1,1-dichloroethylene, 1,2 Dichloromethane, Tetra chloromethane, Trichloroethylene and tetra chloroethylene were determined during a 7 month period and the results were 0.04ppb, 0.52ppb, 0.01ppb, 0.24ppb, 0.03ppb respectively. The highest concentration of chlorinated hydrocarbon observed in Tehran’s drinking water was Trichloroethylene and the lowest concentration was Tetra chloromethane. Districts 5 and 6 showed the highest concentrations of chlorinated hydrocarbons in the city of Tehran.

Patch testing with a new fragrance mix - reactivity to the individual constituents and chemical detection in relevant cosmetic products.

Science.gov (United States)

Frosch, Peter J; Rastogi, Suresh C; Pirker, Claudia; Brinkmeier, Thomas; Andersen, Klaus E; Bruze, Magnus; Svedman, Cecilia; Goossens, An; White, Ian R; Uter, Wolfgang; Arnau, Elena Giménez; Lepoittevin, Jean-Pierre; Johansen, Jeanne Duus; Menne, Torkil

2005-04-01

A new fragrance mix (FM II), with 6 frequently used chemicals not present in the currently used fragrance mix (FM I), was evaluated in 6 dermatological centres in Europe, as previously reported. In this publication, test results with the individual constituents and after repeated open application test (ROAT) of FM II are described. Furthermore, cosmetic products which had caused a contact dermatitis in patients were analysed for the presence of the individual constituents. In 1701 patients, the individual constituents of the medium (14%) and the highest (28%) concentration of FM II were simultaneously applied with the new mix at 3 concentrations (break-down testing for the lowest concentration of FM II (2.8%) was performed only if the mix was positive). ROAT was performed with the concentration of the FM II which had produced a positive or doubtful (+ or ?+) patch test reaction. Patients' products were analysed for the 6 target compounds by gas chromatography-mass spectrometry (GC-MS). 50 patients (2.9%) showed a positive reaction to 14% FM II and 70 patients (4.1%) to 28% FM II. 24/50 (48%) produced a positive reaction to 1 or more of the individual constituents of 14% FM II and 38/70 (54.3%) to 28% FM II, respectively. If doubtful reactions to individual constituents are included, the break-down testing was positive in 74% and 70%, respectively. Patients with a positive reaction to 14% FM II showed a higher rate of reactions to the individual constituent of the 28% FM II: 36/50 (72%). Positive reactions to individual constituents in patients negative to FM II were exceedingly rare. If doubtful reactions are regarded as negative, the sensitivity, specificity, positive predictive value and negative predictive value for the medium concentration of FM II towards at least 1 individual constituent was 92.3% (exact 95% confidence interval 74.9-99.1%), 98.4% (97.7-99.0%), 48% (33.7-62.6%) and 99.9% (99.6-"100.0%), respectively. For the high concentration, the figures

Ranking filter methods for concentrating pathogens in lake water

Science.gov (United States)

Accurately comparing filtration methods for concentrating waterborne pathogens is difficult because of two important water matrix effects on recovery measurements, the effect on PCR quantification and the effect on filter performance. Regarding the first effect, we show how to create a control water...

Impact of recharge through residual oil upon sampling of underlying ground water

International Nuclear Information System (INIS)

Wise, W.R.; Chang, Chichung; Klopp, R.A.; Bedient, P.B.

1991-01-01

At an aviation gasoline spill site in Traverse City, Michigan, historical records indicate a positive correlation between significant rainfall events and increased concentrations of slightly soluble organic compounds in the monitoring wells of the site. To investigate the recharge effect on ground water quality due to infiltrating water percolating past residual oil and into the saturated zone, an in situ infiltration experiment was performed at the site. Sampling cones were set at various depths below a circular test area, 13 feet (4 meters) in diameter. Rainfall was simulated by sprinkling the test area at a rate sufficiently low to prevent runoff. The sampling cones for soil-gas and ground water quality were installed in the unsaturated and saturated zones to observed the effects of the recharge process. Infiltrated water was determined to have transported organic constituents of the residual oil, specifically benzene, toluene, ethylbenzene, and ortho-xylene (BTEX), into the ground water beneath the water table, elevating the aqueous concentrations of these constituents in the saturated zone. Soil-gas concentrations of the organic compounds in the unsaturated zone increased with depth and time after the commencement of infiltration. Reaeration of the unconfined aquifer via the infiltrated water was observed. It is concluded that water quality measurements are directly coupled to recharge events for the sandy type of aquifer with an overlying oil phase, which was studied in this work. Ground water sampling strategies and data analysis need to reflect the effect of recharge from precipitation on shallow, unconfined aquifers where an oil phase may be present

Concentration of polycyclic aromatic hydrocarbons in water samples from different stages of treatment

Science.gov (United States)

Pogorzelec, Marta; Piekarska, Katarzyna

2017-11-01

The aim of this study was to analyze the presence and concentration of selected polycyclic aromatic hydrocarbons in water samples from different stages of treatment and to verify the usefulness of semipermeable membrane devices for analysis of drinking water. For this purpose, study was conducted for a period of 5 months. Semipermeable membrane devices were deployed in a surface water treatment plant located in Lower Silesia (Poland). To determine the effect of water treatment on concentration of PAHs, three sampling places were chosen: raw water input, stream of water just before disinfection and treated water output. After each month of sampling SPMDs were changed for fresh ones and prepared for further analysis. Concentrations of fifteen polycyclic aromatic hydrocarbons were determined by high performance liquid chromatography (HPLC). Presented study indicates that the use of semipermeable membrane devices can be an effective tool for the analysis of aquatic environment, including monitoring of drinking water, where organic micropollutants are present at very low concentrations.

Concentration of polycyclic aromatic hydrocarbons in water samples from different stages of treatment

Directory of Open Access Journals (Sweden)

Pogorzelec Marta

2017-01-01

Full Text Available The aim of this study was to analyze the presence and concentration of selected polycyclic aromatic hydrocarbons in water samples from different stages of treatment and to verify the usefulness of semipermeable membrane devices for analysis of drinking water. For this purpose, study was conducted for a period of 5 months. Semipermeable membrane devices were deployed in a surface water treatment plant located in Lower Silesia (Poland. To determine the effect of water treatment on concentration of PAHs, three sampling places were chosen: raw water input, stream of water just before disinfection and treated water output. After each month of sampling SPMDs were changed for fresh ones and prepared for further analysis. Concentrations of fifteen polycyclic aromatic hydrocarbons were determined by high performance liquid chromatography (HPLC. Presented study indicates that the use of semipermeable membrane devices can be an effective tool for the analysis of aquatic environment, including monitoring of drinking water, where organic micropollutants are present at very low concentrations.

“Nanofiltration” Enabled by Super-Absorbent Polymer Beads for Concentrating Microorganisms in Water Samples

Science.gov (United States)

Xie, Xing; Bahnemann, Janina; Wang, Siwen; Yang, Yang; Hoffmann, Michael R.

2016-01-01

Detection and quantification of pathogens in water is critical for the protection of human health and for drinking water safety and security. When the pathogen concentrations are low, large sample volumes (several liters) are needed to achieve reliable quantitative results. However, most microbial identification methods utilize relatively small sample volumes. As a consequence, a concentration step is often required to detect pathogens in natural waters. Herein, we introduce a novel water sample concentration method based on superabsorbent polymer (SAP) beads. When SAP beads swell with water, small molecules can be sorbed within the beads, but larger particles are excluded and, thus, concentrated in the residual non-sorbed water. To illustrate this approach, millimeter-sized poly(acrylamide-co-itaconic acid) (P(AM-co-IA)) beads are synthesized and successfully applied to concentrate water samples containing two model microorganisms: Escherichia coli and bacteriophage MS2. Experimental results indicate that the size of the water channel within water swollen P(AM-co-IA) hydrogel beads is on the order of several nanometers. The millimeter size coupled with a negative surface charge of the beads are shown to be critical in order to achieve high levels of concentration. This new concentration procedure is very fast, effective, scalable, and low-cost with no need for complex instrumentation. PMID:26876979

Effects of waste-disposal practices on ground-water quality at five poultry (broiler) farms in north-central Florida, 1992-93

Science.gov (United States)

Hatzell, H.H.

1995-01-01

Waste-disposal areas such as chicken-house floors, litter stockpiles, fields that receive applications of litter, and dead-chicken pits are potential sources of nitrates and other chemical constituents in downward-percolating recharge water. Broiler- farms in north-central Florida are concentrated in a region where the Upper Floridan aquifer is unconfined and susceptible to contamination. Eighteen monitoring wells installed at five sites were sampled quarterly from March 1992 through January 1993. Increases in median concentrations of constituents relative to an upgradient well were used to determine the source of the nitrate at two sites. At these sites, increases in the median concentrations of nitrate as nitrogen in ground water in the vicinity of waste-disposal areas at these sites were: 5.4 mg/L for one chicken house; 9.0 mg/L for a second chicken house; 2.0 mg/L for a fallow field that received an application of litter; and, 2.0 mg/L for a dead-chicken pit. At the three remaining sites where the direction of local ground-water flow could not be ascertained, the sources of concentrations of nitrate and other constituents could not be determined. However, median nitrate concentrations in the vicinity of waste-disposal areas at these sites were: 45.5 mg/L for a set of two chicken houses; 3.0 mg/L for a stockpile area; and 2.1 mg/L for a hayfield that received an application of litter. The nitrate concentration in ground water in the vicinity of a field that had previously received heavy applications of litter increased from 3.0 mg/L to 105 mg/L approximately 4 months after receiving an application of commercial fertilizer. Increases in concentrations of organic nitrogen in ground water in the vicinity of waste-disposal areas may be related to the decomposition of litter and subsequent movement with downward percolating recharge water.(USGS)

Evaluation of nonpoint-source contamination, Wisconsin: Land-use and Best-Management-Practices inventory, selected streamwater-quality data, urban-watershed quality assurance and quality control, constituent loads in rural streams, and snowmelt-runoff analysis, water year 1994

Science.gov (United States)

Walker, J.F.; Graczyk, D.J.; Corsi, S.R.; Owens, D.W.; Wierl, J.A.

1995-01-01

isolate contamination in the sample bottle, the automatic sampler and splitter, and the filtration system. Significant contamination caused excessive concentrations of dissolved chloride, alkalinity, and biochemical oxygen demand. The level of contamination may be large enough to affect data for water samples in which these analytes are present at low concentration. Further investigation is being done to determine the source of contamination and take measures to minimize its effect on the sampling. A preliminary regression analysis was done for the rural sites using data collected during water years 1989-93. Loads of suspended solids and total phosphorus in stormflow were regressed against various precipitation-related measures. The results indicate that, for most sites, changes in constituent load on the order of 40 to 50 percent could be detected with a statistical test. For two sites, the change would have to be 60 to 70 percent to be detected. A detailed comparison of snowmelt runoff and rainfall stormflow in urban and rural areas was done using data collected during water years 1985-93. For the rural sites where statistically significant differences were found between constituent loads in snowmelt and storm runoff, the loads of suspended solids and total phosphorus in snowmelt runoff were greater than those in storm runoff. For the urban sites where statistically significant differences were found between snowmelt and storm runoff, the loads of suspended solids and total phosphorus in storm runoff were greater than those in snowmelt runoff. The importance of including snowmelt runoff in designing and analyzing the effects of BMP's on streamwater quality, particularly in rural areas, is emphasized by these results.

Determination of potassium concentration in salt water for residual beta radioactivity measurements

International Nuclear Information System (INIS)

Suarez-Navarro, J.A.; Pujol, Ll.

2004-01-01

High interferences may arise in the determination of potassium concentration in salt water. Several analytical methods were studied to determine which method provided the most accurate measurements of potassium concentration. This study is relevant for radiation protection because the exact amount of potassium in water samples must be known for determinations of residual beta activity concentration. The fitting algorithm of the calibration curve and estimation of uncertainty in potassium determinations were also studied. The reproducibility of the proposed analytical method was tested by internal and external validation. Furthermore, the residual beta activity concentration of several Spanish seawater and brackish river water samples was determined using the proposed method

Food chain model to predict westslope cutthroat trout ovary selenium concentrations from water concentrations in the Elk Valley, BC

International Nuclear Information System (INIS)

Orr, P.; Wiramanaden, C.; Franklin, W.; Fraser, C.

2010-01-01

The 5 coal mines operated by Teck Coal Ltd. in British Columbia's Elk River watershed release selenium during weathering of mine waste rock. Since 1966, several field studies have been conducted in which selenium concentrations in biota were measured. They revealed that tissue concentrations are higher in aquatic biota sampled in lentic compared to lotic habitats of the watershed with similar water selenium concentrations. Two food chain models were developed based on the available data. The models described dietary selenium accumulation in the ovaries of lotic versus lentic westslope cutthroat trout (WCT), a valued aquatic resource in the Elk River system. The following 3 trophic transfer relationships were characterized for each model: (1) water to base of the food web, (2) base of the food web to benthic invertebrates, and (3) benthic invertebrates to WCT ovaries. The lotic and lentic models combined the resulting equations for each trophic transfer relationships to predict WCT ovary concentrations from water concentrations. The models were in very good agreement with the available data, despite fish movement and the fact that composite benthic invertebrate sample data were only an approximation of the feeding preferences of individual fish. Based on the observed rates of increase in water selenium concentrations throughout the watershed, the models predicted very small/slow increases in WCT ovary concentrations with time.

Water solar distiller productivity enhancement using concentrating solar water heater and phase change material (PCM

Directory of Open Access Journals (Sweden)

Miqdam T. Chaichan

2015-03-01

Full Text Available This paper investigates usage of thermal energy storage extracted from concentrating solar heater for water distillation. Paraffin wax selected as a suitable phase change material, and it was used for storing thermal energy in two different insulated treasurers. The paraffin wax is receiving hot water from concentrating solar dish. This solar energy stored in PCM as latent heat energy. Solar energy stored in a day time with a large quantity, and some heat retrieved for later use. Water’s temperature measured in a definite interval of time. Four cases were studied: using water as storage material with and without solar tracker. Also, PCM was as thermal storage material with and without solar tracker.The system working time was increased to about 5 h with sun tracker by concentrating dish and adding PCM to the system. The system concentrating efficiency, heating efficiency, and system productivity, has increased by about 64.07%, 112.87%, and 307.54%, respectively. The system working time increased to 3 h when PCM added without sun tracker. Also, the system concentrating efficiency increased by about 50.47%, and the system heating efficiency increased by about 41.63%. Moreover, the system productivity increased by about 180%.

Optimization of simultaneous ultrasonic-assisted extraction of water-soluble and fat-soluble characteristic constituents from Forsythiae Fructus Using response surface methodology and high-performance liquid chromatography

Science.gov (United States)

Xia, Yong-Gang; Yang, Bing-You; Liang, Jun; Wang, Di; Yang, Qi; Kuang, Hai-Xue

2014-01-01

Background: The compounds (+)-pinoresinol-β-glucoside (1) forsythiaside, (2) phillyrin (3) and phillygenin (4) were elucidated to be the characteristic constituents for quality control of Forsythiae Fructus extract by chromatographic fingerprint in 2010 edition of Chinese Pharmacopoeia due to their numerous important pharmacological actions. It is of great interest to extract these medicinally active constituents from Forsythiae Fructus simultaneously. Materials and Methods: In this study, a new ultrasound-assisted extraction (UAE) method was developed for the simultaneous extraction of biological components 1-4 in Forsythiae Fructus. The quantitative effects of extraction time, ratio of liquid to solid, extraction temperature, and methanol concentration on yield of these four important biological constituents from Forsythiae Fructus were investigated using response surface methodology with Box-Behnken design. The compounds 1-4 extracted by UAE were quantitative analysis by high-performance liquid chromatography-photodiode array detect (HPLC-PAD), and overall desirability (OD), the geometric mean of the contents of four major biological components, was used as a marker to evaluate the extraction efficiency. Results: By solving the regression equation and analyzing 3-D plots, the optimum condition was at extraction temperature 70°C, time 60 min, ratio of liquid to solid 20, and methanol concentration 76.6%. Under these conditions, extraction yields of compounds 1-4 were 2.92 mg/g, 52.10 mg/g, 0.90 mg/g and 0.57 mg/g, respectively, which were in good agreement with the predicted OD values. In order to achieve a similar yield as UAE, soxhlet extraction required at least 6 h and maceration extraction required much longer time of 24 h. Established UAE method has been successfully applied to sample preparation for the quality control of Forsythiae Fructus. Additionally, a quadrupole time-of-flight mass spectrometry was applied to the structural confirmation of analytes

Ground-Water Quality Data in the Southern Sacramento Valley, California, 2005 - Results from the California GAMA Program

Science.gov (United States)

Milby Dawson, Barbara J.; Bennett, George L.; Belitz, Kenneth

2008-01-01

) were collected at ten percent of the wells, and the results for these samples were used to evaluate the quality of the data for the ground-water samples. Assessment of the quality-control data resulted in censoring of less than 0.03 percent of the analyses of ground-water samples. This study did not evaluate the quality of water delivered to consumers; after withdrawal from the ground, water typically is treated, disinfected, and (or) blended with other waters to maintain acceptable water quality. Regulatory thresholds apply to treated water that is served to the consumer, not to raw ground water. However, to provide some context for the results, concentrations of constituents measured in the raw ground water were compared with health-based thresholds established by the U.S. Environmental Protection Agency (USEPA) and California Department of Health Services (CADHS) (Maximum Contaminant Levels [MCLs], notification levels [NLs], or lifetime health advisories [HA-Ls]) and thresholds established for aesthetic concerns (Secondary Maximum Contaminant Levels [SMCLs]). All wells were sampled for organic constituents and selected general water quality parameters; subsets of wells were sampled for inorganic constituents, nutrients, and radioactive constituents. Volatile organic compounds were detected in 49 out of 83 wells sampled and pesticides were detected in 35 out of 82 wells; all detections were below health-based thresholds, with the exception of 1 detection of 1,2,3-trichloropropane above a NL. Of the 43 wells sampled for trace elements, 27 had no detections of a trace element above a health-based threshold and 16 had at least one detection above. Of the 18 trace elements with health-based thresholds, 3 (arsenic, barium, and boron) were detected at concentrations higher an MCL. Of the 43 wells sampled for nitrate, only 1 well had a detection above the MCL. Twenty wells were sampled for radioactive constituents; only 1 (radon-222) was measured at activiti

A model for oxidizing species concentrations in boiling water reactors

International Nuclear Information System (INIS)

Sun, B.; Chexal, B.; Pathania, R.; Chun, J.; Ballinger, R.; Abdollahian, D.

1993-01-01

To evaluate and control the intergranular stress corrosion cracking of boiling water reactor (BWR) vessel internal components requires knowledge of the concentration of oxidizing species that affects the electrochemical potentials in various regions of a BWR. In a BWR flow circuit, as water flows through the radiation field, the radiolysis process and chemical reactions lead to the production of species such as oxygen, hydrogen, and hydrogen peroxide. Since chemistry measurements are difficult inside BWRs, analytical tools have been developed by Ruiz and Lin, Ibe and Uchida and Chun and Ballinger for estimating the concentration of species that provide the necessary input for water chemistry control and material protection

Ion exchange separation of low boric acid concentrations from water

International Nuclear Information System (INIS)

Kysela, J.; Brabec, J.; Peterka, F.

1975-01-01

Boric acid poisoning of the moderator of the TR-O experimental heavy water reactor was studied. The possibility is discussed of removing boric acid from heavy water by means of a strong basic anion exchanger, below the residual concentration of 0.01 mg B/l. Measurements of the usable capacities of the strong basic anion exchanger Zerollit FF showed that the penetration of boric acid during the sorption period does not exceed the value of 0.015 mg B/l. The dependence was found of capacity on the boric acid concentration in the solution. Analytical methods used to determine B in water are also described. (author)

Chromatographic method of measurement of helium concentration in underground waters for dating in hydrological questions

International Nuclear Information System (INIS)

Najman, J.

2008-04-01

Research methods which use natural environmental indicators are widely applied in hydrology. Different concentrations of indicators and their isotopic components in ground waters allow to determine the genesis of waters and are valuable source of information about the water flow dynamics. One of the significant indicator is helium. The concentration of 4 He (helium) in ground water is a fine indicator in water dating in a range from a hundreds to millions of years (Aeschbach-Hertig i in., 1999; Andrews i in., 1989; Castro i in., 2000; Zuber i in., 2007). 4 He is also used for dating young waters of age about 10 years (Solomon i in., 1996). Thesis consist the description of elaborated in IFJ PAN in Krakow chromatographic measurement method of helium concentration in ground waters in aim of dating. Chapter 1 contain short introduction about ground water dating and chapter 2 description of helium property and chosen applications of helium for example in technology and earthquake predictions. Helium sources in ground waters are described in chapter 3. Helium concentration in water after infiltration (originated from atmosphere) to the ground water system depends mainly on the helium concentration coming from the equilibration with the atmosphere increased by additional concentration from '' excess air ''. With the increasing resistance time of ground water during the flow, radiogenic, non-atmospheric component of helium dissolves also in water. In chapter 4 two measurement methods of helium concentration in ground waters were introduced: mass spectrometric and gas chromatographic method. Detailed description of elaborated chromatographic measurement method of helium concentration in ground water contain chapter 5. To verify developed method the concentration of helium in ground waters from the regions of Krakow and Busko Zdroj were measured. For this waters the concentrations of helium are known from the earlier mass spectrometric measurements. The results of

On the substantion of permissible concentrations of plutonium isotopes in the water of fresh water and sea water NPP cooling reservoirs

International Nuclear Information System (INIS)

Grachev, M.I.; Gusev, D.I.; Stepanova, V.D.

1985-01-01

Substantiation of maximum permissible concentration (PC) of plutonium isotopes ( 238 Pu, 239 Pu, 240 Pu) in fresh and sea water cooling reservoirs of NPP with fast neutron reactors is given. The main criterion when calculating permissible plutonium content in water of surface reservoirs is the requirement not to exceed the established limits for radiation doses to persons resulted from water use. Data on coefficients of plutonium concentration in sea and fresh water hydrobionts are presented as well as on plutonium PC in water of fresh and sea water cooling reservoirs and bottom sediments of sea water cooling reservoirs. It is shown that doses to critical groups of population doesn't exceed potentially hazardous levels due to plutonium intake through food chains. But the calculation being carried out further should be corrected

Radionuclide concentrations and dose assessment of cistern water and groundwater at the Marshall Islands

International Nuclear Information System (INIS)

Noshkin, V.E.; Eagle, R.J.; Wong, K.M.; Jokela, T.A.; Robison, W.L.

1981-01-01

A radiological survey was conducted from September through November of 1978 to determine the concentrations of radionuclides in the terrestrial and marine environments of 11 atolls and 2 islands in the Northern Marshall Islands. More than 70 cistern and groundwater samples were collected at the atolls; the volume of each sample was between 55 and 100 l. The concentration of 90 Sr in cistern water at most atolls is that expected from world-wide fallout in wet deposition. Except for Bikini and Rongelap, 137 Cs concentrations in cistern water are in agreement with the average predicted concentrations from wet deposition. The 239+240 Pu concentrations are everywhere less than the predicted fallout concentrations except at Rongelap, Ailinginae, and Bikini where the measured and predicted concentrations are in general agreement. During the period sampled, most groundwater concentrations of 90 Sr and 137 Cs were everywhere higher than the concentrations in cistern water. Concentrations of the transurancies in filtered groundwater solution were everywhere comparable to or less than the concentrations in cistern water. It is concluded that the concentrations of radionuclides detected during any single period may not necessarily reflect the long-term average concentrations or the concentrations that might be observed if a lined well were extended above the surface. In any case, at all atolls the 90 Sr and 137 Cs concentrations in groundwater are below the concentration guidelines for drinking water recommended by the Environmental Protection Agency. The maximum annual dose rates and the 30- and 50-y integral doses are calculated for the intake of both cistern water and groundwater for each of the atolls

Radon concentrations in ground and drinking water in the state of Chihuahua, Mexico

International Nuclear Information System (INIS)

Villalba, L.; Colmenero Sujo, L.; Montero Cabrera, M.E.; Cano Jimenez, A.; Renteria Villalobos, M.; Delgado Mendoza, C.J.; Jurado Tenorio, L.A.; Davila Rangel, I.; Herrera Peraza, E.F.

2005-01-01

This paper reports 222 Rn concentrations in ground and drinking water of nine cities of Chihuahua State, Mexico. Fifty percent of the 114 sampled wells exhibited 222 Rn concentrations exceeding 11 Bq/L, the maximum contaminant level (MCL) recommended by the USEPA. Furthermore, around 48% (123 samples) of the tap-water samples taken from 255 dwellings showed radon concentrations over the MCL. There is an apparent correlation between total dissolved solids and radon concentration in ground-water. The high levels of 222 Rn found may be entirely attributed to the nature of aquifer rocks

Radon concentrations in ground and drinking water in the state of Chihuahua, Mexico.

Science.gov (United States)

Villalba, L; Colmenero Sujo, L; Montero Cabrera, M E; Cano Jiménez, A; Rentería Villalobos, M; Delgado Mendoza, C J; Jurado Tenorio, L A; Dávila Rangel, I; Herrera Peraza, E F

2005-01-01

This paper reports (222)Rn concentrations in ground and drinking water of nine cities of Chihuahua State, Mexico. Fifty percent of the 114 sampled wells exhibited (222)Rn concentrations exceeding 11Bq/L, the maximum contaminant level (MCL) recommended by the USEPA. Furthermore, around 48% (123 samples) of the tap-water samples taken from 255 dwellings showed radon concentrations over the MCL. There is an apparent correlation between total dissolved solids and radon concentration in ground-water. The high levels of (222)Rn found may be entirely attributed to the nature of aquifer rocks.

Loads and yields of deicing compounds and total phosphorus in the Cambridge drinking-water source area, Massachusetts, water years 2009–15

Science.gov (United States)

Smith, Kirk P.

2017-09-12

The source water area for the drinking-water supply of the city of Cambridge, Massachusetts, encompasses major transportation corridors, as well as large areas of light industrial, commercial, and residential land use. Because of the large amount of roadway in the drinking-water source area, the Cambridge water supply is affected by the usage of deicing compounds and by other constituents that are flushed from such impervious areas. The U.S. Geological Survey (USGS) has monitored surface-water quality in the Cambridge Reservoir and Stony Brook Reservoir Basins, which compose the drinking-water source area, since 1997 (water year 1998) through continuous monitoring and the collection of stream-flow samples.In a study conducted by the USGS, in cooperation with the City of Cambridge Water Department, concentrations and loads of calcium (Ca), chloride (Cl), magnesium (Mg), sodium (Na), and sulfate (SO4) were estimated from continuous records of specific conductance and streamflow for streams and tributaries at 10 continuous water-quality monitoring stations. These data were used to characterize current (2015) water-quality conditions, estimate loads and yields, and describe trends in Cl and Na in the tributaries and main-stem streams in the Cambridge Reservoir and Stony Brook Reservoir Basins. These data also were used to describe how stream-water quality is related to various basin characteristics and provide information to guide future management of the drinking-water source area.Water samples from 2009–15 were analyzed for physical properties and concentrations of Ca, Cl, Mg, Na, potassium (K), SO4, and total phosphorus (TP). Values of physical properties and constituent concentrations varied widely, particularly in composite samples of stormflow from tributaries that have high percentages of constructed impervious areas. Median concentrations of Ca, Cl, Mg, Na, and K in samples collected from the tributaries in the Cambridge Reservoir Basin (27.2, 273, 4.7, 154

Analysis of gamma irradiated pepper constituents, 5

International Nuclear Information System (INIS)

Takagi, Kazuko; Okuyama, Tsuneo; Ishikawa, Toshihiro.

1988-01-01

Gamma irradiated peppers (10 krad, 100 krad, 1 Mrad) were analyzed by HPLC. The extraction method and HPLC conditions were same as the first report, that is, the extraction from pepper was performed by Automatic Air Hammer and the extracted samples were separated on a reversed phase C 8 column with a concave gradient from 0.1% trifluoro aceticacid (TFA) in water to 75% acetonitrile-0.1% TFA in water for 60 minutes and detected at 210 nm, 280 nm. It is difficult to compare with irradiated and unirradiated pepper constituents by their peak height or area. And the method of multi variant statistically analysis was introduced. The 'peak n area/peak n + 1 area' ratio was calculated by computer. Each peak area was accounted by integrator. The value of these ratio were called 'parameter'. Each chromatogram has 741 parameters calculated with 39 chromatographic peaks. And these parameters were abopted to the multi variant statiscally analysis. Comparison of constituents between irradiated pepper and unirradiated pepper was done by 741 parameters. The correlation of parameters between irradiated and unirradiated was investigated by use of computer. Some parameters of irradiated case were selected as which had no correlation with unirradiated case. That is to say these parameters were thought to be changed with gamma spectrum irradiation. By this method, Coumarin was identified as a changed component with gamma irradiation. (author)

Water-Soluble Constituents of Cudrania tricuspidata (Carr.) Bur.

Institute of Scientific and Technical Information of China (English)

Zong-Ping Zheng; Jing-Yu Liang; Li-Hong Hu

2006-01-01

In order to find new structural and biologically active compounds, the constituents of the bark of Cudrania tricuspidata (Carr.) Bur. were investigated and a new 6-p-hydroxybenzyltaxifolin glucoside, named tricusposide (compound 1), together with 16 known compounds, was isolated by solvent partition,macroporous adsorption resin AB-8, silica gel, Sephadex LH-20 chromatography. Using spectroscopic methods, the structures of the compounds were elucidated as 6-p-hydroxybenzyl taxifolin-7-O-β-D-glucoside (compound 1), dihydroquerctin-7-O-β-D-glucoside (compound 2), dihydrokaempferol-3-O-β-D-glucoside (compound 3), dihydroquercetin (compound 4), peonoside (compound 5), sphaerobioside (compound 6), quercimeritrin (compound 7), genistein (compound 8), aromadendrin (compound 9), kaempferol (compound 10), genistin (compound 11), 3,4-dihydroxystyryl alcohol (compound 12), sucrose (compound 13), 1,3,5,6-tetrahydroxyxanthone (compound 14), gericudranin E (compound 15), gericudranin C (compound 16),and orobol (compound 17). Compounds 2-6, 8, 9, 12-14, and 17 were isolated from this genus for the first time.

Evaluation of processes controlling the geochemical constituents in deep groundwater in Bangladesh: Spatial variability on arsenic and boron enrichment

International Nuclear Information System (INIS)

Halim, M.A.; Majumder, R.K.; Nessa, S.A.; Hiroshiro, Y.; Sasaki, K.; Saha, B.B.; Saepuloh, A.; Jinno, K.

2010-01-01

Forty-six deep groundwater samples from highly arsenic affected areas in Bangladesh were analyzed in order to evaluate the processes controlling geochemical constituents in the deep aquifer system. Spatial trends of solutes, geochemical modeling and principal component analysis indicate that carbonate dissolution, silicate weathering and ion exchange control the major-ion chemistry. The groundwater is dominantly of Na-Cl type brackish water. Approximately 17% of the examined groundwaters exhibit As concentrations higher than the maximum acceptable limit of 10 μg/L for drinking water. Strong correlation (R 2 = 0.67) of Fe with dissolved organic carbon (DOC) and positive saturation index of siderite suggests that the reductive dissolution of Fe-oxyhydroxide in presence of organic matter is considered to be the dominant process to release high content of Fe (median 0.31 mg/L) in the deep aquifer. In contrast, As is not correlated with Fe and DOC. Boron concentration in the 26% samples exceeds the standard limit of 500 μg/L, for water intended for human consumption. Negative relationships of B/Cl ratio with Cl and boron with Na/Ca ratio demonstrate the boron in deep groundwater is accompanied by brackish water and cation exchange within the clayey sediments.

Hydrology and water quality in 13 watersheds in Gwinnett County, Georgia, 2001–15

Science.gov (United States)

Aulenbach, Brent T.; Joiner, John K.; Painter, Jaime A.

2017-02-23

peak flow data through water year 2015, using the expected moments algorithm to fit a Pearson Type III distribution to logarithms of annual peak flows. Kendall’s tau nonparametric test was used to determine the statistical significance of trends in the annual peak flows, with none of the 13 streamgages exhibiting significant trends.A comparison of base-flow and stormflow water-quality samples indicates that turbidity and concentrations of total ammonia plus organic nitrogen, total nitrogen, total phosphorus, total organic carbon, total lead, total zinc, total suspended solids, and suspended-sediment concentrations increased with increasing discharge at all watersheds. Specific conductance decreased during stormflow at all watersheds, and total dissolved solids concentrations decreased during stormflow at a few of the watersheds. Total suspended solids and suspended-sediment concentrations typically were two orders of magnitude higher in stormflow samples, turbidities were about 1.5 orders of magnitude higher, total phosphorus and total zinc were about one order of magnitude higher, and total ammonia plus organic nitrogen, total nitrogen, total organic carbon, and total lead were about twofold higher than in base-flow samples.Seasonality and long-term trends were identified for the period water years 2001–15 for 10 constituents—total nitrogen, total nitrate plus nitrite, total phosphorus, dissolved phosphorus, total organic carbon, total suspended solids, suspended-sediment concentration, total lead, total zinc, and total dissolved solids. Seasonal patterns were present in most watersheds for all constituents except total dissolved solids, and the watersheds had fairly similar patterns of higher concentrations in the summer and lower concentrations in the winter. A linear long-term trend analysis of residual concentrations from the flow-only load estimation model (without time-trend terms) identified significant trends in 67 of the 130 constituent

Factors affecting water strider (Hemiptera: Gerridae) mercury concentrations in lotic systems

Energy Technology Data Exchange (ETDEWEB)

Jardine, T.D.; Kidd, K.A.; Cunjak, R.A.; Arp, P.A. [University of New Brunswick, St John, NB (Canada). Canadian Rivers Institute

2009-07-15

Water striders (Hemiptera: Gerridae) have been considered as a potential sentinel for mercury (Hg) contamination of freshwater ecosystems, yet little is known about factors that control Hg concentrations in this invertebrate. Striders were collected from 80 streams and rivers in New Brunswick, Canada, in August and September of 2004 through 2007 to assess the influence of factors such as diet, water chemistry, and proximity to point sources on Hg concentrations in this organism. Higher than average Hg concentrations were observed in the southwest and Grand Lake regions of the province, the latter being the location of a coal-fired power plant that is a source of Hg (similar to 100 kg annually), with elevated Hg concentrations in the lichen Old Man's Beard (Usnea spp.) in its immediate vicinity. Across all streams, pH and total organic carbon of water were relatively weak predictors of strider Hg concentrations. Female striders that were larger in body size than males had significantly lower Hg concentrations within sites, suggestive of growth dilution. There was no relationship between percent aquatic carbon in the diet and Hg concentrations in striders. For those striders feeding solely on terrestrial carbon, Hg concentrations were higher in animals occupying a higher trophic level. Mercury concentrations were highly variable in striders collected monthly over two growing seasons, suggesting short-term changes in Hg availability. These measurements highlight the importance of considering both deposition and postdepositional processes in assessing Hg bioaccumulation in this species.

Water-quality assessment of the Kentucky River basin, Kentucky; results of investigations of surface-water quality, 1987-90

Science.gov (United States)

Haag, K.H.; Garcia, Rene; Jarrett, G.L.; Porter, S.D.

1995-01-01

The U.S. Geological Survey investigated the water quality of the Kentucky River Basin in Kentucky as part of the National Water-Quality Assessment program. Data collected during 1987-90 were used to describe the spatial and temporal variability of water-quality constituents including metals and trace elements, nutrients, sediments, pesticides, dissolved oxygen, and fecal-coliform bacteria. Oil-production activities were the source of barium, bromide, chloride, magnesium, and sodium in several watersheds. High concentrations of aluminum, iron, and zinc were related to surface mining in the Eastern Coal Field Region. High concentrations of lead and zinc occurred in streambed sediments in urban areas, whereas concentrations of arsenic, strontium, and uranium were associated with natural geologic sources. Concentrations of phosphorus were significantly correlated with urban and agricultural land use. The high phosphorus content of Bluegrass Region soils was an important source of phosphorus in streams. At many sites in urban areas, most of the stream nitrogen load was attributable to wastewater-treatment-plant effluent. Average suspended-sediment concentrations were positively correlated with discharge. There was a downward trend in suspended-sediment concentrations downstream in the Kentucky River main stem during the study. The most frequently detected herbicides in water samples were atrazine, 2,4-D, alachlor, metolachlor, and dicamba. Diazinon, malathion, and parathion were the most frequently detected organophosphate insecticides in water samples. Detectable concentrations of aldrin, chlordane, DDT, DDE, dieldrin, endrin, endosulfan, heptachlor, and lindane were found in streambed-sediment samples. Dissolved-oxygen concentrations were sometimes below the minimum concentration needed to sustain aquatic life. At some sites, high concentrations of fecal-indicator bacteria were found and water samples did not meet sanitary water-quality criteria.

Concentration of arsenic in water, sediments and fish species from naturally contaminated rivers.

Science.gov (United States)

Rosso, Juan José; Schenone, Nahuel F; Pérez Carrera, Alejo; Fernández Cirelli, Alicia

2013-04-01

Arsenic (As) may occur in surface freshwater ecosystems as a consequence of both natural contamination and anthropogenic activities. In this paper, As concentrations in muscle samples of 10 fish species, sediments and surface water from three naturally contaminated rivers in a central region of Argentina are reported. The study area is one of the largest regions in the world with high As concentrations in groundwater. However, information of As in freshwater ecosystems and associated biota is scarce. An extensive spatial variability of As concentrations in water and sediments of sampled ecosystems was observed. Geochemical indices indicated that sediments ranged from mostly unpolluted to strongly polluted. The concentration of As in sediments averaged 6.58 μg/g ranging from 0.23 to 59.53 μg/g. Arsenic in sediments barely followed (r = 0.361; p = 0.118) the level of contamination of water. All rivers showed high concentrations of As in surface waters, ranging from 55 to 195 μg/L. The average concentration of As in fish was 1.76 μg/g. The level of contamination with As differed significantly between species. Moreover, the level of bioaccumulation of As in fish species related to the concentration of As in water and sediments also differed between species. Whilst some fish species seemed to be able to regulate the uptake of this metalloid, the concentration of As in the large catfish Rhamdia quelen mostly followed the concentration of As in abiotic compartments. The erratic pattern of As concentrations in fish and sediments regardless of the invariable high levels in surface waters suggests the existence of complex biogeochemical processes behind the distribution patterns of As in these naturally contaminated ecosystems.

Chemical constituents of Cordia latifolia and their nematicidal activity.

Science.gov (United States)

Begum, Sabira; Perwaiz, Sobiya; Siddiqui, Bina S; Khan, Shazia; Fayyaz, Shahina; Ramzan, Musarrat

2011-05-01

Following nematicidal activity-guided isolation studies on the fruits, bark, and leaves of Cordia latifolia, two new constituents, cordinoic acid (=11-oxours-12-ene-23,28-dioic acid; 1) and cordicilin (=2-{[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-3-[4-hydroxy-3-(stearoyloxy)phenyl]propanoic acid; 2) were isolated from the stem and leaves, respectively, together with nine known compounds, namely cordioic and cordifolic acid from the stem bark, latifolicin A-D and rosmarinic acid from the fruits, and cordinol and cordicinol from the leaves. Their structures were determined by means of spectroscopic analyses including 1D- and 2D-NMR techniques. The nematicidal activities of these constituents were determined against the root-knot nematode Meloidogyne incognita. Hundred percent mortality was caused by all of these after 72 h at a 0.125% concentration. Compound 1 and cordioic acid were most active and caused 100% mortality after 24 h at a 0.50% concentration. Furthermore, compound 2, the ester of rosemarinic acid, was found to be more active than the free acid. Copyright © 2011 Verlag Helvetica Chimica Acta AG, Zürich.

Radon concentrations in ground and drinking water in the state of Chihuahua, Mexico

Energy Technology Data Exchange (ETDEWEB)

Villalba, L. [Centro de Investigacion en Materiales Avanzados, S.C., Miguel de Cervantes 120, Complejo Industrial Chihuahua, CP 31109 Chihuahua, Chih. (Mexico); Colmenero Sujo, L. [Centro de Investigacion en Materiales Avanzados, S.C., Miguel de Cervantes 120, Complejo Industrial Chihuahua, CP 31109 Chihuahua, Chih. (Mexico); Instituto Tecnologico de Chihuahua II, Ave. de las Industrias 11101, Chihuahua, Chih. (Mexico); Montero Cabrera, M.E. [Centro de Investigacion en Materiales Avanzados, S.C., Miguel de Cervantes 120, Complejo Industrial Chihuahua, CP 31109 Chihuahua, Chih. (Mexico)]. E-mail: elena.montero@cimav.edu.mx; Cano Jimenez, A. [Centro de Investigacion en Materiales Avanzados, S.C., Miguel de Cervantes 120, Complejo Industrial Chihuahua, CP 31109 Chihuahua, Chih. (Mexico); Renteria Villalobos, M. [Centro de Investigacion en Materiales Avanzados, S.C., Miguel de Cervantes 120, Complejo Industrial Chihuahua, CP 31109 Chihuahua, Chih. (Mexico); Delgado Mendoza, C.J. [Facultad de Ciencias Quimicas, Universidad Autonoma de Chihuahua, Ciudad Universitaria S/N, Chihuahua, Chih. (Mexico); Jurado Tenorio, L.A. [Facultad de Ciencias Quimicas, Universidad Autonoma de Chihuahua, Ciudad Universitaria S/N, Chihuahua, Chih. (Mexico); Davila Rangel, I. [Centro Regional de Estudios Nucleares, Universidad Autonoma de Zacatecas, Cipres 20, Zacatecas, Zac. (Mexico); Herrera Peraza, E.F. [Centro de Investigacion en Materiales Avanzados, S.C., Miguel de Cervantes 120, Complejo Industrial Chihuahua, CP 31109 Chihuahua, Chih. (Mexico)

2005-07-01

This paper reports {sup 222}Rn concentrations in ground and drinking water of nine cities of Chihuahua State, Mexico. Fifty percent of the 114 sampled wells exhibited {sup 222}Rn concentrations exceeding 11 Bq/L, the maximum contaminant level (MCL) recommended by the USEPA. Furthermore, around 48% (123 samples) of the tap-water samples taken from 255 dwellings showed radon concentrations over the MCL. There is an apparent correlation between total dissolved solids and radon concentration in ground-water. The high levels of {sup 222}Rn found may be entirely attributed to the nature of aquifer rocks.

Regional differences in constituents of gall stones.

Science.gov (United States)

Ashok, M; Nageshwar Reddy, D; Jayanthi, V; Kalkura, S N; Vijayan, V; Gokulakrishnan, S; Nair, K G M

2005-01-01

The pathogenesis of pigment and mixed gall stone formation remains elusive. The elemental constituents of gall stones from southern states of Tamil Nadu, Kerala and Karnataka have been characterized. Our aim was to determine the elemental concentration of representative samples of pigment, mixed and cholesterol gall stones from Andhra Pradesh using proton-induced X-ray emission (PIXE) using a 3 MV horizontal pelletron accelerator. Pigment gall stones had significantly high concentrations of copper, iron and lead; chromium was absent. Except for iron all these elements were significantly low in cholesterol gall stones and intermediate levels were seen in mixed gall stones. Highest concentrations of chromium was seen in cholesterol and titanium in mixed gall stones respectively; latter similar to other southern states. Arsenic was distinctly absent in cholesterol and mixed gall stones. The study has identified differences in elemental components of the gall stones from Andhra Pradesh.

Trends in surface-water quality at selected National Stream Quality Accounting Network (NASQAN) stations, in Michigan

Science.gov (United States)

Syed, Atiq U.; Fogarty, Lisa R.

2005-01-01

To demonstrate the value of long-term, water-quality monitoring, the Michigan Department of Environmental Quality (MDEQ), in cooperation with the U.S. Geological Survey (USGS), initiated a study to evaluate potential trends in water-quality constituents for selected National Stream Quality Accounting Network (NASQAN) stations in Michigan. The goal of this study is to assist the MDEQ in evaluating the effectiveness of water-pollution control efforts and the identification of water-quality concerns. The study included a total of nine NASQAN stations in Michigan. Approximately 28 constituents were analyzed for trend tests. Station selection was based on data availability, land-use characteristics, and station priority for the MDEQ Water Chemistry Monitoring Project. Trend analyses were completed using the uncensored Seasonal Kendall Test in the computer program Estimate Trend (ESTREND), a software program for the detection of trends in water-quality data. The parameters chosen for the trend test had (1) at least a 5-year period of record (2) about 5 percent of the observations censored at a single reporting limit, and (3) 40 percent of the values within the beginning one-fifth and ending one-fifth of the selected period. In this study, a negative trend indicates a decrease in concentration of a particular constituent, which generally means an improvement in water quality; whereas a positive trend means an increase in concentration and possible degradation of water quality. The results of the study show an overall improvement in water quality at the Clinton River at Mount Clemens, Manistee River at Manistee, and Pigeon River near Caseville. The detected trend for these stations show decreases in concentrations of various constituents such as nitrogen compounds, conductance, sulfate, fecal coliform bacteria, and fecal streptococci bacteria. The negative trend may indicate an overall improvement in agricultural practices, municipal and industrial wastewater

Ecological impact of chloro-organics produced by chlorination of cooling tower waters

International Nuclear Information System (INIS)

Jolley, R.L.; Cumming, R.B.; Pitt, W.W.; Taylor, F.G.; Thompson, J.E.; Hartmann, S.J.

1977-01-01

Experimental results of the initial assessment of chlorine-containing compounds in the blowdown from cooling towers and the possible mutagenic activity of these compounds are reported. High-resolution liquid chromatographic separations were made on concentrates of the blowdown from the cooling tower at the High Flux Isotope Reactor (HFIR) and from the recirculating water system for the cooling towers at the Oak Ridge Gaseous Diffusion Plant (ORGDP), Oak Ridge, Tennessee. The chromatograms of chlorinated cooling waters contained numerous uv-absorbing and cerate-oxidizable constituents that are now being processed through a multicomponent identification procedure. Concentrates of the chlorinated waters are also being examined for mutagenic activity

An Innovative System for the Efficient and Effective Treatment of Non-Traditional Waters for Reuse in Thermoelectric Power Generation

Energy Technology Data Exchange (ETDEWEB)

John Rodgers; James Castle

2008-08-31

, chemical oxygen demand (COD), and zinc. Similar to FGD waters, produced waters contained contaminants of concern that are predominantly inorganic (arsenic, cadmium, chlorides, chromium, copper, lead, mercury, nickel, sulfide, zinc, total dissolved solids), but also contained some organics (benzene, PAHs, toluene, total organic carbon, total suspended solids, and oil and grease). Constituents of concern that may cause chemical scaling, biofouling and corrosion, such as pH, hardness and ionic strength, and nutrients (P, K, and N) may also be found in all four non-traditional waters. NPDES permits were obtained for these non-traditional waters and these permit limits are summarized in tabular format within this report. These limits were used to establish treatment goals for this research along with toxicity values for Ceriodaphnia dubia, water quality criteria established by the US EPA, irrigation standards established by the United States Department of Agriculture (USDA), and reuse standards focused on minimization of damage to the power plant by treated waters. Constructed wetland treatment systems were designed for each non-traditional water source based on published literature reviews regarding remediation of the constituents of concern, biogeochemistry of the specific contaminants, and previous research. During this study, 4 non-traditional waters, which included ash basin water, cooling water, FGD water and produced water (PW) were obtained or simulated to measure constructed wetland treatment system performance. Based on data collected from FGD experiments, pilot-scale constructed wetland treatment systems can decrease aqueous concentrations of elements of concern (As, B, Hg, N, and Se). Percent removal was specific for each element, including ranges of 40.1% to 77.7% for As, 77.6% to 97.8% for Hg, 43.9% to 88.8% for N, and no measureable removal to 84.6% for Se. Other constituents of interest in final outflow samples should have aqueous characteristics sufficient for

Effect of Pumping Strategies on Pesticide Concentrations in Water Abstraction Wells

DEFF Research Database (Denmark)

Aisopou, Angeliki; Bjerg, Poul Løgstrup; Albrechtsen, Hans-Jørgen

Pesticide use in agriculture is one of the main sources of groundwater contamination and poses an important threat to groundwater abstraction. Pesticides have been detected in 37% of Danish monitoring wells sampled, with 12 % exceeding drinking water guidelines. Field data captured in monitoring...... and pumping wells show that pesticide concentrations vary greatly in both time and space. This study aimed to use models to determine how pumping affects pesticide concentrations in drinking water wells placed in two hypothetical aquifer systems; a homogeneous layered aquifer and a layered aquifer...... in a pumping well capture zone were constructed using COMSOL Multiphysics. A series of simulations were conducted to examine the effect of pumping strategies (constant versus varying pumping rate), pesticide properties and aquifer hydrogeology on the concentration in drinking water wells. The results...

Wintertime Arctic Ocean sea water properties and primary marine aerosol concentrations

Directory of Open Access Journals (Sweden)

J. Zábori

2012-11-01

Full Text Available Sea spray aerosols are an important part of the climate system through their direct and indirect effects. Due to the diminishing sea ice, the Arctic Ocean is one of the most rapidly changing sea spray aerosol source areas. However, the influence of these changes on primary particle production is not known.

In laboratory experiments we examined the influence of Arctic Ocean water temperature, salinity, and oxygen saturation on primary particle concentration characteristics. Sea water temperature was identified as the most important of these parameters. A strong decrease in sea spray aerosol production with increasing water temperature was observed for water temperatures between −1°C and 9°C. Aerosol number concentrations decreased from at least 1400 cm⁻³ to 350 cm⁻³. In general, the aerosol number size distribution exhibited a robust shape with one mode close to dry diameter D_p 0.2 μm with approximately 45% of particles at smaller sizes. Changes in sea water temperature did not result in pronounced change of the shape of the aerosol size distribution, only in the magnitude of the concentrations. Our experiments indicate that changes in aerosol emissions are most likely linked to changes of the physical properties of sea water at low temperatures. The observed strong dependence of sea spray aerosol concentrations on sea water temperature, with a large fraction of the emitted particles in the typical cloud condensation nuclei size range, provide strong arguments for a more careful consideration of this effect in climate models.

Investigation of metal concentration in water using PIXE

International Nuclear Information System (INIS)

Prajapati, P.K.; Chakraborty, S.; Tiwary, S.S.; Majumder, C.; Sharma, H.P.; Kumar, A.; Singh, K.P.; Shivcharan; Mohanty, B.P.

2017-01-01

Availability of clean drinking water is an essential requirement for human health. The Ganga water is being widely used for drinking and irrigation purposes in many cities situated near the bank of the river, which effect the human health. Hence investigation of toxic elements of Ganga water is very important. PIXE (Particle Induce X-ray Emission) is well known and useful technique for finding out qualitative and quantitative analysis of various samples (taken from environment) and may contains about 30-50 elements together with concentration of about 1ppb. The elemental analysis depends on the inner-shell ionization process and measurement of the X-ray yield of the samples. For the present investigation, samples of Ganga water were collected from Varanasi and Allahabad

Distinction of water-soluble constituents between natural and cultured Cordyceps by capillary electrophoresis.

Science.gov (United States)

Li, S P; Song, Z H; Dong, T T X; Ji, Z N; Lo, C K; Zhu, S Q; Tsim, K W K

2004-11-01

Cordyceps is an expensive traditional Chinese medicine, which has anti-tumor activity and significant effects on the immune system. In Southeast Asia, Cordyceps is commonly sold in capsule form as a health food product. Most of these products are derived from cultured Cordyceps mycelia. Because of the price difference, some manufacturers claim their products are from natural Cordyceps. In order to distinguish among various types of Cordyceps in the market, the profiles of water-soluble constituents derived from different sources of Cordyceps were determined by capillary electrophoresis (CE). Both natural and cultured Cordyceps showed three peak clusters migrated at 5-7, 9-11 and 12-13 min, and the height and resolution of these peak clusters were rather distinct. Peak cluster at 9-11 min was identified as adenosine, guanosine and uridine, and shared a similarity between natural and cultured products. In contrast, the peak cluster at 5-7 min was characteristic of natural Cordyceps, regardless of hosts and sources. By using the peak characteristics of CE profiles of different Cordyceps samples, hierarchical clustering analysis was performed. The result shows that those samples of natural Cordyceps were grouped together distinct from the cultured and commercial products. Thus, the CE profiles could serve as fingerprints for the quality control of Cordyceps.

Constituency Orientation in Irish Politics

DEFF Research Database (Denmark)

Kusche, Isabel

2017-01-01

The constituency orientation of Irish politicians is a recurring topic in Irish political science. Its analysis has predominantly focused on TDs. This article uses a content analysis of candidate video statements in the general election 2016 in order to assess the strength of constituency...... this pattern, indicated by the weak constituency orientation in Dublin and Cork constituencies. Results also indicate differences between parties and some political statuses, while the gender of the candidates is of no relevance. Although the material does not permit a clear distinction between effects...... of political culture and short-term considerations, taken together the results indicate that localism in Irish politics matters, but in more complicated ways than usually depicted....

Quantification of Phenolic Constituents and Antioxidant Activity of Pterodon emarginatus Vogel Seeds

Directory of Open Access Journals (Sweden)

Nádia R. Barbosa

2008-04-01

Full Text Available In the present study the phenolic (Folin-Dennis and flavonoid (colorimetric assay constituents and the antioxidant activity of Pterodon emarginatus seeds were investigated in several samples prepared with different extraction procedures: essential oil (EO using a Clevenger-type apparatus; hexanic (HF, ethyl acetate (EAF, buthanolic (BF and methanolic (MF fractions using Soxhlet extraction, and extracts (1 g/extract obtained from different methods: reflux 80°C/30 min, ultrasound/30 min, static maceration/48 h and heating plate 100°C/45 min. These extracts were prepared using water or ethanol/water at 30:70 v/v, 50:50 v/v or 70:30 v/v. Antioxidant activity [2,2-diphenyl-2- picrylhydrazyl hydrate (DPPH] was tested only in the fractions obtained from Soxhlet extraction. The extract obtained from reflux using ethanol/water (70:30, v/v showed the highest phenolic constituents level. The EAF, BF and MF showed DPPH scavenging activities with IC50=163.22, 18.89 and 10.15 μg/ml, respectively.

Device for regulating light water nuclear reactors by changing the boric acid concentration in the cooling water circuit

International Nuclear Information System (INIS)

Brown, W.W.; Van der Schoot, M.R.

1980-01-01

Small changes in boric acid concentration can be carried out quickly by a combination of an ion exchanger with temperature-dependent capacity and an evaporator. No boric acid need be extracted from the circuit or added to it. However, if large changes of concentration are required, boric acid has to be added. The evaporator is then used to separate distilled water and concentrated boric acid when the cooling water is diluted. (DG) [de

Plasma concentrations of enrofloxacin in African grey parrots treated with medicated water.

Science.gov (United States)

Flammer, K; Aucoin, D P; Whitt, D A; Prus, S A

1990-01-01

Plasma concentrations of enrofloxacin were measured four times during a 7-day treatment period in African grey parrots that were fed with enrofloxacin-medicated drinking water. Water medicated at doubling doses of 0.09, 0.19, 0.38, 0.75, 1.5, and 3.0 mg/ml achieved mean concentrations (+/- SEM) of 0.10 (+/- 0.05), 0.12 (+/- 0.05), 0.12 (+/- 0.03), 0.15 (+/- 0.05), 0.30 (+/- 0.11), and 0.20 (+/- 0.06) micrograms/ml, respectively. A portion of the administered enrofloxacin was metabolized to an equipotent metabolite, ciprofloxacin. Mean ciprofloxacin concentrations paralleled enrofloxacin concentrations but were lower, ranging from 0.04 to 0.27 micrograms/ml. Acceptance of medicated water was adequate at lower doses; however, at doses of 1.5 and 3.0 mg/ml, acceptance was unsatisfactory, and mean weight loss in these groups was significantly higher than the control group. Based on the concentrations achieved in these preliminary trials and the susceptibility patterns of gram-negative bacteria isolated from psittacine birds, drinking water medicated with enrofloxacin at 0.19-0.75 mg/ml might be effective for treating highly susceptible gram-negative bacterial infections in African grey parrots.

Detailed study of selenium and other constituents in water, bottom sediment, soil, alfalfa, and biota associated with irrigation drainage in the Uncompahgre Project area and in the Grand Valley, west-central Colorado, 1991-93

Science.gov (United States)

Butler, D.L.; Wright, W.G.; Stewart, K.C.; Osmundson, B.C.; Krueger, R.P.; Crabtree, D.W.

1996-01-01

In 1985, the U.S. Department of the Interior began a program to study the effects of irrigation drainage in the Western United States. These studies were done to determine whether irrigation drainage was causing problems related to human health, water quality, and fish and wildlife resources. Results of a study in 1991-93 of irrigation drainage associated with the Uncompahgre Project area, located in the lower Gunnison River Basin, and of the Grand Valley, located along the Colorado River, are described in this report. The focus of the report is on the sources, distribution, movement, and fate of selenium in the hydrologic and biological systems and the effects on biota. Generally, other trace- constituent concentrations in water and biota were not elevated or were not at levels of concern. Soils in the Uncompahgre Project area that primarily were derived from Mancos Shale contained the highest concentrations of total and watrer-extractable selenium. Only 5 of 128\\x11alfalfa samples had selenium concentrations that exceeded a recommended dietary limit for livestock. Selenium data for soil and alfalfa indicate that irrigation might be mobilizing and redistributing selenium in the Uncompahgre Project area. Distribution of dissolved selenium in ground water is affected by the aqueous geochemical environment of the shallow ground- water system. Selenium concentrations were as high as 1,300\\x11micrograms per liter in water from shallow wells. The highest concentrations of dissolved selenium were in water from wells completed in alluvium overlying the Mancos Shale of Cretaceous age; selenium concentrations were lower in water from wells completed in Mancos Shale residuum. Selenium in the study area could be mobilized by oxidation of reduced selenium, desorption from aquifer sediments, ion exchange, and dissolution. Infiltration of irrigation water and, perhaps nitrate, provide oxidizing conditions for mobilization of selenium from alluvium and shale residuum and for

Dependency of water concentration on ethanolysis of trioleoylglycerol by lipases

DEFF Research Database (Denmark)

Piyatheerawong, W.; Iwasaki, Y; Xu, Xuebing

2004-01-01

tested (Rhizomucor miehei lipase, Burkholderia cepacia lipase and Thermomyces lanuginosus lipase) required larger amounts of free water (ca. 7-9 wt.%) for their best performance and exhibited no ethanolysis reaction at low free water concentrations. The CALB's anomalous behavior was also observed...

Study of temporal variation of radon concentrations in public drinking water supplies

International Nuclear Information System (INIS)

York, E.L.

1995-01-01

The Environmental Protection Agency (EPA) has proposed a Maximum Contaminant Level (MCL) for radon-222 in public drinking water supplies of 300 pCi/L. Proposed monitoring requirements include collecting quarterly grab samples for the first year, then annual samples for the remainder of the compliance cycle provided first year quarterly samples average below the MCL. The focus of this research was to study the temporal variation of groundwater radon concentrations to investigate how reliably one can predict an annual average radon concentration based on the results of grab samples. Using a open-quotes slow-flowclose quotes collection method and liquid scintillation analysis, biweekly water samples were taken from ten public water supply wells in North Carolina (6 month - 11 month sampling periods). Based on study results, temporal variations exist in groundwater radon concentrations. Statistical analysis performed on the data indicates that grab samples taken from each of the ten wells during the study period would exhibit groundwater radon concentrations within 30% of their average radon concentration

Ground-Water Quality Data in the Southern Sierra Study Unit, 2006 - Results from the California GAMA Program

Science.gov (United States)

Fram, Miranda S.; Belitz, Kenneth

2007-01-01

quality-control information resulted in censoring of less than 0.2 percent of the data collected for ground-water samples. This study did not attempt to evaluate the quality of water delivered to consumers; after withdrawal from the ground, water typically is treated, disinfected, or blended with other waters to maintain acceptable water quality. Regulatory thresholds apply to treated water that is served to the consumer, not to raw ground water. However, to provide some context for the results, concentrations of constituents measured in the raw ground water were compared with health-based thresholds established by the U.S. Environmental Protection Agency (USEPA) and California Department of Public Health (CDPH) and thresholds established for aesthetic concerns (secondary maximum contaminant levels, SMCL-CA) by CDPH. VOCs and pesticides were detected in less than one-third of the grid wells, and all detections in samples from SOSA wells were below health-based thresholds. All detections of trace elements and nutrients in samples from SOSA wells were below health-based thresholds, with the exception of four detections of arsenic that were above the USEPA maximum contaminant level (MCL-US) and one detection of boron that was above the CDPH notification level (NL-CA). All detections of radioactive constituents were below health-based thresholds, although four samples had activities of radon-222 above the proposed MCL-US. Most of the samples from SOSA wells had concentrations of major elements, total dissolved solids, and trace elements below the non-enforceable thresholds set for aesthetic concerns. A few samples contained iron, manganese, or total dissolved solids at concentrations above the SMCL-CA thresholds.

7 CFR 930.16 - Sales constituency.

Science.gov (United States)

2010-01-01

... Definitions § 930.16 Sales constituency. Sales constituency means a common marketing organization or brokerage... 7 Agriculture 8 2010-01-01 2010-01-01 false Sales constituency. 930.16 Section 930.16 Agriculture Regulations of the Department of Agriculture (Continued) AGRICULTURAL MARKETING SERVICE (Marketing Agreements...

Evaluation of radon concentration in well and tap waters in Bursa (Turkey)

International Nuclear Information System (INIS)

Akar Tarim, U.; Gurler, O.; Akkaya, G.; Kilic, N.; Yalcin, S.; Kaynak, G.; Gundogdu, O.

2012-01-01

222 Rn measurements in water samples collected from 27 wells and 19 taps that were supplied from the investigated wells were conducted using the AlphaGUARD PQ 2000PRO radon gas analyser at sites across several geologic formations within the city of Bursa (Turkey). The measured radon concentrations ranged from 1.46 to 53.64 Bq l -1 for well water and from 0.91 to 12.58 Bq l -1 for tap water. Of the 27 sites sampled, only 7 had radon levels above the safe limit of 11.1 Bq l -1 recommended by the USEPA. In general, all determined concentrations were well below the 100 Bq l -1 revised reference level proposed by the European Union. These values of radon concentrations in water samples are compared with those reported from other countries. Doses resulting from the consumption of these waters were calculated. The minimum and the maximum annual mean effective doses due to 222 Rn intake through water consumption were 0.02 μSv a -1 and 1.11 μSv a -1 , respectively. (authors)

Ground-Water Quality Data in the Kern County Subbasin Study Unit, 2006 - Results from the California GAMA Program

Science.gov (United States)

Shelton, Jennifer L.; Pimentel, Isabel; Fram, Miranda S.; Belitz, Kenneth

2008-01-01

the wells, and the results for these samples were used to evaluate the quality of the data from the ground-water samples. Assessment of the quality-control information resulted in censoring of less than 0.4 percent of the data collected for ground-water samples. This study did not attempt to evaluate the quality of water delivered to consumers; after withdrawal from the ground, raw ground water typically is treated, disinfected, or blended with other waters to maintain acceptable water quality. Regulatory thresholds apply, not to the raw ground water, but to treated water that is served to the consumer. However, to provide some context for the results, concentrations of constituents measured in the raw ground water were compared with health-based thresholds established by the U.S. Environmental Protection Agency (USEPA) and the California Department of Public Health (CDPH), and as well as with thresholds established for aesthetic concerns (secondary maximum contaminant levels, SMCL-CA) by CDPH. VOCs and pesticides each were detected in approximately 60 percent of the grid wells, and detections of all compounds but one were below health-based thresholds. The fumigant, 1,2-dibromo-3-chloropropane (DBCP), was detected above the USEPA maximum contaminant level (MCL-US) in one sample. Detections of most inorganic constituents were also below health-based thresholds. Constituents detected above health-based thresholds include: nitrate, (MCL-US, 2 samples), arsenic (MCL-US, 2 samples), and vanadium (California notification level, NL-CA, 1 sample). All detections of radioactive constituents were below health-based thresholds, although nine samples had activities of radon-222 above the lower proposed MCL-US. Most of the samples from KERN wells had concentrations of major elements, total dissolved solids, and trace elements below the non-enforceable thresholds set for aesthetic concerns.

Trace Elements and Physico-Chemical Quality of the Well Waters in Mahitsy, Province of Antananarivo, Madagascar

International Nuclear Information System (INIS)

Rasolofonirina, M.; Randriamanivo, L.V.; Andrianarilala, M.T.; Raoelina Andriambololona

2004-01-01

The proposed study area of Mahitsy is located in the province of Antananarivo. Only 14.38% of the population in the rural zone has access to safe drinking water. Most of human population use wells or springs as the main source of drinking water. Wells are generally less than 20 meters deep and they are not properly sealed. Well waters investigated in January 2004 have a very large range of trace constituent and chemical composition in the zone of interest. Manganese concentrations range is 8μg.L -1 -1115 μg.L -1 and concentrations of barium vary in the range of 55μg.L -1 - 4967 μg.L -1 . 67% of monitored well waters are of manganese concentration higher than 50μg.L -1 and 44% contain barium with a concentration higher than 700μg.L -1 . Total dissolved solids vary between 8 mg.L -1 and 881 mg.L -1 and well water pHs are acidic (4.28 - 5.94). Nitrate concentrations monitored in Mahitsy groundwaters show that, 54% of the well water samples exceed 50 mg.L -1 (WHO guidelines value) and 84% exceed 13.5 mg.L -1 (indicative value of human activities). The nitrate content ranges from 4 to 489 mg.L -1 . Groundwater nitrate correlates positively with chloride and potassium. That would suggest that the high content of nitrate may result from the septic tank, the cesspool and the animal wastes storage, located next to the well. However, people draw water from groundwater for domestic purposes, as the water infrastructure remains undeveloped in the studied area. The measurement of trace constituents are performed using Total Relflection X-ray Fluorescence (TXRF) analytical method and the major ions are determined by Ion Chromatograph (IC) system.

Ground-Water Quality Data in the Upper Santa Ana Watershed Study Unit, November 2006-March 2007: Results from the California GAMA Program

Science.gov (United States)

Kent, Robert; Belitz, Kenneth

2009-01-01

nitrate in the study unit. In total, nearly 400 constituents and water-quality indicators were investigated for this study. This study did not attempt to evaluate the quality of water delivered to consumers; after withdrawal from the ground, water typically is treated, disinfected, and (or) blended with other waters to maintain acceptable water quality. Regulatory thresholds apply to treated water that is served to the consumer, not to raw ground water. However, to provide some context for the results, concentrations of constituents measured in the raw ground water were compared with regulatory and non-regulatory health-based thresholds established by the U.S. Environmental Protection Agency (USEPA) and the California Department of Public Health (CDPH) and thresholds established for aesthetic concerns (secondary maximum contaminant levels, SMCL-CA) by CDPH. Volatile organic compounds (VOCs) were detected in more than 80 percent of USAW grid wells. Most VOCs detected were at concentrations far less than thresholds established for drinking water to protect human health; however, six wells had VOC concentrations above health-based thresholds. Twenty-four of the 85 VOCs investigated were detected in the study unit;11 were detected in more than 10 percent of the wells. The VOCs detected above health-based thresholds in at least one well were dibromochloropropane (DBCP), tetrachloroethene (PCE), trichloroethene (TCE), carbon tetrachloride, and 1,1-dichoroethene. Pesticide compounds were detected in more than 75 percent of the grid wells. However, of the 134 different pesticide compounds investigated, 13 were detected at concentrations greater than their respective long-term method detection limits, and only 7 compounds (all herbicides or herbicide degradates) were detected in more than 10 percent of the wells. No pesticide compound was detected above its health-based threshold, although thresholds exist for fewer than half of the pesticide compounds investigat

Concentration of radiocesium in stream water from a mountainous catchment area during rainfall events

International Nuclear Information System (INIS)

Nakamura, Kimihito; Yasutaka, Tetsuo; Hatakeyama, Masato

2012-01-01

Terrestrial and aquatic systems were contaminated with radioactive materials following the nuclear accident at Fukushima Daiichi Nuclear Power Station on 11 March, 2011. It is important that levels of radiocesium (Cs) in stream water from affected areas be monitored as this water is used for paddy irrigation and domestic water. Additionally, soil particles and organic matter from the streams are deposited in rivers, estuaries and into the ocean. Predictions suggest that Cs levels will increase during intense rainfall-runoff events. To check this prediction, we monitored temporal changes in runoff events and Cs levels in stream water from a mountainous catchment area northwest of the Fukushima plant. In March and April, 2012, the concentrations of Cs and suspended solids (SS) in stream water taken from low-level water flow were found to be 0.2–0.3 Bq/L and 2–7 mg/L, respectively. A heavy rainfall event in July 2012 resulted in an increase and subsequent decrease of both the runoff volume and SS concentration. At the beginning of the rainfall event the concentration of Cs absorbed in the SS was measured to be 23 Bq/L, this decreased gradually to 0.3 Bq/L over the course of the event. The concentration of Cs dissolved in the water was 0.1 Bq/L, this decreased only slightly during the runoff event. During a low rainfall event in September 2012 the concentration of Cs absorbed in the SS at the beginning of the rainfall event was found to be 15 Bq/L, this decreased gradually to 0.5 Bq/L as the amount of SS in the water decreased. The concentration of Cs dissolved in the water was 0.2 Bq/L, again this decreased only slightly over the course of the runoff event. The Cs levels in stream water, during rainfall-runoff events, were primary influenced by the concentration of SS. The amount of Cs dissolved in the water, on the other hand, was roughly constant at 0.1–0.2 Bq/L. The results of this study indicate that, although the concentration of Cs in stream water is below

Concentration of radiocesium in stream water from a mountainous catchment area during rainfall events

International Nuclear Information System (INIS)

Nakamura, Kimihito; Yasutaka, Tetsuo; Hatakeyama, Masato

2013-01-01

Terrestrial and aquatic systems were contaminated with radioactive materials following the nuclear accident at Fukushima Daiichi Nuclear Power Station on 11 March, 2011. It is important that levels of radiocesium (Cs) in stream water from affected areas be monitored as this water is used for paddy irrigation and domestic water. Additionally, soil particles and organic matter from the streams are deposited in rivers, estuaries and into the ocean. Predictions suggest that Cs levels will increase during intense rainfall-runoff events. To check this prediction, we monitored temporal changes in runoff events and Cs levels in stream water from a mountainous catchment area northwest of the Fukushima plant. In March and April, 2012, the concentrations of Cs and suspended solids (SS) in stream water taken from low-level water flow were found to be 0.2-0.3 Bq/L and 2-7 mg/L, respectively. A heavy rainfall event in July 2012 resulted in an increase and subsequent decrease of both the runoff volume and SS concentration. At the beginning of the rainfall event the concentration of Cs absorbed in the SS was measured to be 23 Bq/L, this decreased gradually to 0.3 Bq/L over the course of the event. The concentration of Cs dissolved in the water was 0.1 Bq/L, this decreased only slightly during the runoff event. During a low rainfall event in September 2012 the concentration of Cs absorbed in the SS at the beginning of the rainfall event was found to be 15 Bq/L, this decreased gradually to 0.5 Bq/L as the amount of SS in the water decreased. The concentration of Cs dissolved in the water was 0.2 Bq/L, again this decreased only slightly over the course of the runoff event. The Cs levels in stream water, during rainfall-runoff events, were primary influenced by the concentration of SS. The amount of Cs dissolved in the water, on the other hand, was roughly constant at 0.1-0.2 Bq/L. The results of this study indicate that, although the concentration of Cs in stream water is below the

Effect of aquatic plants on 95Zr concentration in slightly polluted water

International Nuclear Information System (INIS)

Shi Jianjun; Yang Ziyin; Chen Hui

2004-01-01

Effect of three aquatic plants (Ceratophyllum demersum, Azolla caroliniana and Eichhornia crassipes) on 95 Zr concentration in slightly polluted water was studied by using isotope tracer techniques. The results showed that the aquatic plants had strong ability of 95 Zr concentration in water. The concentration factor (CF) were from 56.78 to 112.94, so three aquatic plants were suggested be bio-indicators for 95 Zr polluted water. The specific activity of 95 Zr in water decreased with time when the aquatic plants were put in slightly 95 Zr polluted water. The descent of specific activity of 95 Zr in water was very quick during the beginning period (0-3d). The time for the specific activity reduced to 50% was only 3 days, indicating that theres aquatic plants could be used to purge slightly 95 Zr polluted water. The effect of Eichhornia crassipes on purging 95 Zr in water was the best among the three aquatic plants. The specific activity of 95 Zr in bottom clay only decreased 5% after putting aquatic plants in water, indicating that desorption of 95 Zr from bottom clay was not easy. As the bottom clay had strong ability of adsorption and fixation to 95 Zr, the effect of aquatic plant on purging 95 Zr adsorbed by bottom clay was not visible

Estimating the relation between groundwater and river water by measuring the concentration of Rn-222

Energy Technology Data Exchange (ETDEWEB)

Yoneda, Minoru; Morisawa, Shinsuke [Kyoto Univ. (Japan). Faculty of Engineering

1997-02-01

This study aimed to estimate the relationship between groundwater in shallow layer and river water by determining the concentrations of {sup 222}Rn and nitric nitrogen along with water temperature. The region around ca. 20 km along river A in a certain basin was chosen as a test area. The Rn concentration of groundwater was determined by Rn extracting with toluene and counting in liquid scintillation counter, whereas for river water, it was determined by activated charcoal passive collector method developed by the authors, by which the amount of Rn adsorbed on activated charcoal was estimated by Ge-solid state detector. In addition, water temperature and nitric nitrogen concentration were measured at various points in the test area. Thus, a distribution map of the three parameters was made on the basis of the data obtained in December, 1989. Since Rn concentration is generally higher in ground water than river water and the water temperature in December is higher in the former, it seems likely that the concentrations of Rn and nitric nitrogen would become higher in the area where ground water soaks into river water. Thus, the directions of ground water flow at the respective sites along river A were estimated from the data regarding the properties of ground water. (M.N.)

The impact of water concentration on the catalytic oxidation of ethanol on platinum electrode in concentrated phosphoric acid

Energy Technology Data Exchange (ETDEWEB)

Camargo, A.P.M.; Previdello, B.A.F.; Varela, H.; Gonzalez, E.R. [Instituto de Quimica de Sao Carlos, Universidade de Sao Paulo, C.P. 780, CEP 13560-970 Sao Carlos, SP (Brazil)

2010-01-15

The electro-oxidation of ethanol on platinum in phosphoric acid opens the door to promote the oxidation reaction at higher temperatures. However, the effect of the presence of water is not well understood. In this work, the electro-oxidation of ethanol on platinum was studied in concentrated phosphoric acid containing different concentrations of water at room temperature. The results show that effect of bulk water on the rate electro-oxidation is highest at 0.60 V and decreases for increasing potentials. This was suggested as due to the increasing formation of oxygenated species on the electrode surface with potential, which in turn is more efficient than the increase of water content in the electrolyte. Altogether, these results were interpreted as an evidence of a Langmuir-Hinshelwood step involving oxygenated species as one of the adsorbed partners. (author)

Spectral Band Characterization for Hyperspectral Monitoring of Water Quality

Science.gov (United States)

Vermillion, Stephanie C.; Raqueno, Rolando; Simmons, Rulon

2001-01-01

A method for selecting the set of spectral characteristics that provides the smallest increase in prediction error is of interest to those using hyperspectral imaging (HSI) to monitor water quality. The spectral characteristics of interest to these applications are spectral bandwidth and location. Three water quality constituents of interest that are detectable via remote sensing are chlorophyll (CHL), total suspended solids (TSS), and colored dissolved organic matter (CDOM). Hyperspectral data provides a rich source of information regarding the content and composition of these materials, but often provides more data than an analyst can manage. This study addresses the spectral characteristics need for water quality monitoring for two reasons. First, determination of the greatest contribution of these spectral characteristics would greatly improve computational ease and efficiency. Second, understanding the spectral capabilities of different spectral resolutions and specific regions is an essential part of future system development and characterization. As new systems are developed and tested, water quality managers will be asked to determine sensor specifications that provide the most accurate and efficient water quality measurements. We address these issues using data from the Airborne Visible/Infrared Imaging Spectrometer (AVIRIS) and a set of models to predict constituent concentrations.

RA-226 concentration in water samples near uranium mines and in marine fishes

International Nuclear Information System (INIS)

Porntepkasemsan, B.

1987-11-01

Radium-226 and calcium were measured in water samples from the vicinity of three uranium mines and in fish samples collected from Puget sound, Washington State. The radium content of the samples were below the maximum permissible concentration 3 pCi/L for drinking water recommended by the Public Health Service and U.S. Environmental Protection Agency. The mean value of Ra-226 in water was 0.428 pCi/L and ranged from 0.043 to 1.552 pCi/L, whereas calcium content ranged from 3.0 to 190.0 mg/L. Ra-226 concentrations and calcium content in whole fish were 0.833-20.328 pCi/kg wet wt. and 114.1-259.3 mg/g ash, respectively. Results of the study indicated that Ra-226 concentration in water was correlated with calcium concentration but that this correlation was not observed in fish sample except English sole

Water chemistry and radon concentrations of thermal springs in Bastak area, south of Persia

International Nuclear Information System (INIS)

Mirhosseini, S.M.; Moattar, F.; Karbassi, A.R.

2015-01-01

Physicochemical factors, major and some minor ions and 222 Rn concentration was measured in Todruyeh, Fotuyeh and Sanguyeh thermal balneutherapy springs in Bastak, south of Iran. Water type of these springs is Na-Cl and water-mixing phenomena seem possible in them. The average of U concentration in Fatuyeh's, Sanguyeh's and Todruyeh's water are 2.2, 1.1, 0.306 ppb, respectively, and the concentration of heavy metals such as Ag, Cd, Co, Cr, Cu, Hg, Ni, Pb, Se, Zn varies from 1 to 10 ppb. The concentration of 222 Rn in the water of Fotuyeh, Sanguyeh and Todruyeh Springs includes 125-253, 53-104, and 7.4-134.7 kBq/m 3 , respectively. Values of mean annual effective doses for inhalation from these waters are below the reference level recommended by WHO. (author)

Measurement of Rn-222 concentration in underground water in Osaka stratum group in Sennan area

International Nuclear Information System (INIS)

Fukui, Masami; Katsurayama, Kosuke

1977-01-01

The Rn-222 concentration in underground water is reported as follows, which is the result obtained when the ground inspection was carried out in the Research Reactor Institute of Kyoto University located at Kumatori area in Osaka stratum group. Underground water, at different depth, well water and rain water were taken, and the contained Rn-222 was extracted with toluene to measure by liquid scintillation technique. Rn-222 concentration in rain water was 3.5 - 8.0 pCi/l, while the concentration in well water was 130 - 250 pCi/l, and that in underground water was 240 - 313 pCi/l. The seasonal change, geographical difference and variation according to depth of Rn-222 concentration were examined. Rn-222 behavior in soil should be investigated more in detail in reference to Rn-222 dispersion, transport and equilibrium problems in soil-water system in the future. (Kobatake, H.)

Solar water disinfecting system using compound parabolic concentrating collector

Energy Technology Data Exchange (ETDEWEB)

El-Ghetany, H.H.; Saitoh, T.S. [Tohoku Univ., Sendai (Japan)

2000-05-31

Solar water disinfection is an alternative technology using solar radiation and thermal treatment to inactivate and destroy pathogenic microorganisms present in water. The Compound Parabolic Concentrating, (CPC) collector can be used as an efficient key component for solar disinfectanting system. Two types of the CPC collectors are studied, namely the transparent-tube and the Copper-tube CPC collector. It is found that after 30 minutes of exposing the water sample to solar radiation or heating it up to 65 degree C for a few minuets all the coliform bacterial present in the contaminated water sample were completely eliminated. In this article, the effect of water temperature on the disinfecting process was presented. Thermal and micro-biological measurements were also made to evaluate the system performance. (author)

Concentration of involatile salts at evaporating water surfaces

International Nuclear Information System (INIS)

Gardner, G.C.

1988-02-01

Safety cases for the PWR often need to know how much of the soluble salts in the water will evaporate with the steam during flashing and when the steam is discharged to the atmosphere. Some ideal evaporating systems to give guidance. Simple formulae are derived for the surface concentration relative to the bulk concentration. An analysis is also presented which derives a formula for the mass transfer process in the steam due to both diffusion and convection, which arises from the evaporation process. The convection process will usually dominate. (author)

Ground-Water Quality Data in the San Francisco Bay Study Unit, 2007: Results from the California GAMA Program

Science.gov (United States)

Ray, Mary C.; Kulongoski, Justin T.; Belitz, Kenneth

2009-01-01

, replicate samples, matrix spike samples) were collected for approximately one-third of the wells, and the results for these samples were used to evaluate the quality of the data for the ground-water samples. Assessment of the quality-control information from the field blanks resulted in applying 'V' codes to approximately 0.1 percent of the data collected for ground-water samples (meaning a constituent was detected in blanks as well as the corresponding environmental data). See the Appendix section 'Quality-Control-Sample Results'. This study did not attempt to evaluate the quality of water delivered to consumers; after withdrawal from the ground, water typically is treated, disinfected, and (or) blended with other waters to maintain acceptable water quality. Regulatory thresholds apply to treated water that is delivered to the consumer, not to raw ground water. However, to provide some context for the results, concentrations of constituents measured in the raw ground water were compared with regulatory and non-regulatory health-based thresholds established by the U.S. Environmental Protection Agency (USEPA) and California Department of Public Health (CDPH) and thresholds established for aesthetic concerns (secondary maximum contaminant levels, SMCL-CA) by CDPH. VOCs were detected in about one-half of the grid wells, while pesticides were detected in about one-fifth of the grid wells. Concentrations of all VOCs and pesticides detected in samples from all SFBAY wells were below health-based thresholds. No pharmaceutical compounds were detected in any SFBAY well. One potential wastewater-indicator compound, caffeine, was detected in one grid well in SFBAY. Concentrations of most trace elements and nutrients detected in samples from all SFBAY wells were below health-based thresholds. Exceptions include nitrate, detected above the USEPA maximum contaminant level (MCL-US) in 3samples; arsenic, above the USEPA maximum contaminant level (MCL-US) in 3 samples; c

Collaborative validation of a rapid method for efficient virus concentration in bottled water

DEFF Research Database (Denmark)

Schultz, Anna Charlotte; Perelle, Sylvie; Di Pasquale, Simona

2011-01-01

. Three newly developed methods, A, B and C, for virus concentration in bottled water were compared against the reference method D: (A) Convective Interaction Media (CIM) monolithic chromatography; filtration of viruses followed by (B) direct lysis of viruses on membrane; (C) concentration of viruses......Enteric viruses, including norovirus (NoV) and hepatitis A virus (HAV), have emerged as a major cause of waterborne outbreaks worldwide. Due to their low infectious doses and low concentrations in water samples, an efficient and rapid virus concentration method is required for routine control...... by ultracentrifugation; and (D) concentration of viruses by ultrafiltration, for each methods' (A, B and C) efficacy to recover 10-fold dilutions of HAV and feline calicivirus (FCV) spiked in bottles of 1.5L of mineral water. Within the tested characteristics, all the new methods showed better performance than method D...

Water-quality characteristics of urban storm runoff at selected sites in East Baton Rouge Parish, Louisiana, February 2006 through November 2009

Science.gov (United States)

Frederick, C. Paul

2011-01-01

Water samples were collected at three watersheds in East Baton Rouge Parish, Louisiana, during February 2006 through November 2009 for continued evaluation of urban storm runoff. The watersheds represented land uses characterized predominantly as established commercial, industrial, and residential. The following water-quality data are reported: physical and chemical-related properties, fecal coliform, nutrients, trace elements, and organic compounds. Results of water-quality analyses enabled calculation of event-mean concentrations and estimated annual contaminant loads and yields of storm runoff from nonpoint sources for 12 water-quality properties and constituents. Lead met or exceeded the U.S. Environmental Protection Agency Maximum Contaminant Level of 15 micrograms per liter for drinking water standards in 4 of 14 samples. Low level concentrations of mercury were detected in all 14 samples, and half were two to four times above the reporting limit of 0.02 micrograms per liter. The average dissolved phosphorus concentrations from each land use were two to four times the U.S. Environmental Protection Agency criterion of 0.05 milligrams per liter. Diazinon was detected in one sample at a concentration of 0.2 micrograms per liter. In the residential watershed, the largest at 216 acres, contaminant loads for 5 of the 12 water-quality properties and constituents were highest, with 4 of these being nutrients. The industrial watershed, 97 acres, had the highest contaminant loads for 6 of the 12 water-quality properties and constituents with 3 of these being metals, which is indicative of the type of land use. Zinc had the highest metal load (155 pounds per year) in the industrial watershed, compared to 36 pounds per year in the residential watershed, and 32 pounds per year in the established commercial watershed. The industrial watershed had the highest yields for 8 of the 12 water-quality properties and constituents, whereas the established commercial watershed had

Chemical and Hydro-Geologic Analysis of Ikogosi Warm Spring Water in Nigeria

OpenAIRE

Akinola Ikudayisi; Folasade Adeyemo; Josiah Adeyemo

2015-01-01

This study focuses on the hydro-geology and chemical constituents analysis of Ikogosi Warm Spring waters in South West Nigeria. Ikogosi warm spring is a global tourist attraction because it has both warm and cold spring sources. Water samples from the cold spring, warm spring and the meeting point were collected, analyzed and the result shows close similarity in temperature, hydrogen iron concentration (pH), alkalinity, hardness, Calcium, Magnesium, Sodium, Iron, total di...

Effect of hard and soft water on mineral concentration of food items

International Nuclear Information System (INIS)

Khan, M.H.; Hafeez, M.

2006-01-01

The present study was undertaken with special reference to the change occurs in concentration of essential elements present in food items on cooking in hard and soft water. Fourteen water and 08 vegetable samples were collected from various selected sites of Muzaffarabad city and around. The parameters such as pH, conductivity and TDS of water samples were determined. The concentration of Ca and Mg being major minerals in both water and vegetable samples were determined before and after cooking by employing AAS technique. It was found that Ca has increased in vegetable samples cooked in hard water type, while in most cases it decreased when soft water was used. Magnesium has decreased in vegetables samples after cooking with hard water types. The extraction of Mg was more pronounced when soft water was used for cooking purpose. The role of Ca and Mg in human body as essential elements has been discussed. (author)

Combining of radionuclides with constituent materials of marine algae

International Nuclear Information System (INIS)

Nakamura, Ryoichi; Nakahara, Motokazu; Ishii, Toshiaki; Ueda, Taishi; Shimizu, Chiaki.

1979-01-01

The relations between the accumulation-elimination of radionuclides and the constituent materials of marine algae were studied to determine more precisely the mechanism of the radioactive contamination of marine organisms. This will increase the information about the behavior of radionuclides in marine organisms in relation to the environmental conditions (temperature, physico-chemical state of radioisotope, and so on) and the biological conditions (feeding habits, species, and so on). Eisenia contaminated by 137 Cs and 106 Ru- 106 Rh was fractionated by solvent extraction into 6 fractions. The largest portion of 137 Cs was in the boiling water fraction; 106 Ru- 106 Rh was most extracted by 24% KOH solution. Elution patterns by Sephadex G-100 gel-filtration of samples differed largely from each other, both among the 3 kinds of radionuclides and between the 2 species of the algae. Therefore, the accumulation of the radionuclides by the marine algae was proved to be not only due to a physical absorption to the surface of the algae but also to the biological combining of the radionuclides with the constituents of the algae. Furthermore, it was found that radionuclides which combine with a few constituents of alga are not eliminated equally. This is considered to be useful for the physiological analysis of elimination curves. (author)

Uranium concentration in drinking water from small-scale water supplies in Schleswig-Holstein, Germany; Urankonzentration im Trinkwasser aus Hausbrunnen in Schleswig-Holstein

Energy Technology Data Exchange (ETDEWEB)

Ostendorp, G. [Landesamt fuer soziale Dienste, Kiel (Germany). Dezernat Umweltbezogener Gesundheitsschutz

2015-07-01

In this study the drinking water of 212 small-scale water supplies, mainly situated in areas with intensive agriculture or fruit-growing, was analysed for uranium. The median uranium concentration amounted to 0.04 μg/lL, the 95th percentile was 2.5 μg/L. The maximum level was 14 μg/L. This sample exceeded the guideline value for uranium in drinking water. The uranium concentration in small-scale water supplies was found to be slightly higher than that in central water works in Schleswig-Holstein. Water containing more than 10 mg/L nitrate showed significantly higher uranium contents. The results indicate that the uranium burden in drinking water from small wells is mainly determined by geological factors. An additional anthropogenic effect of soil management cannot be excluded. Overall uranium concentrations were low and not causing health concerns. However, in specific cases higher concentrations may occur.

Estimating an appropriate sampling frequency for monitoring ground water well contamination

International Nuclear Information System (INIS)

Tuckfield, R.C.

1994-01-01

Nearly 1,500 ground water wells at the Savannah River Site (SRS) are sampled quarterly to monitor contamination by radionuclides and other hazardous constituents from nearby waste sites. Some 10,000 water samples were collected in 1993 at a laboratory analysis cost of $10,000,000. No widely accepted statistical method has been developed, to date, for estimating a technically defensible ground water sampling frequency consistent and compliant with federal regulations. Such a method is presented here based on the concept of statistical independence among successively measured contaminant concentrations in time

Constituency Input into Budget Management.

Science.gov (United States)

Miller, Norman E.

1995-01-01

Presents techniques for ensuring constituency involvement in district- and site-level budget management. Outlines four models for securing constituent input and focuses on strategies to orchestrate the more complex model for staff and community participation. Two figures are included. (LMI)

The Association of Arsenic With Redox Conditions, Depth, and Ground-Water Age in the Glacial Aquifer System of the Northern United States

Science.gov (United States)

Thomas, Mary Ann

2007-01-01

More than 800 wells in the glacial aquifer system of the Northern United States were sampled for arsenic as part of U.S. Geological Survey National Water-Quality Assessment (NAWQA) studies during 1991-2003. Elevated arsenic concentrations (greater than or equal to 10 micrograms per liter) were detected in 9 percent of samples. Elevated arsenic concentrations were associated with strongly reducing conditions. Of the samples classified as iron reducing or sulfate reducing, arsenic concentrations were elevated in 19 percent. Of the methanogenic samples, arsenic concentrations were elevated in 45 percent. In contrast, concentrations of arsenic were elevated in only 1 percent of oxic samples. Arsenic concentrations were also related to ground-water age. Elevated arsenic concentrations were detected in 34 percent of old waters (recharged before 1953) as compared to 4 percent of young waters (recharged since 1953). For samples classified as both old and methanogenic, elevated arsenic concentrations were detected in 62 percent of samples, as compared to 1 percent for samples classified as young and oxic. Arsenic concentrations were also correlated with well depth and concentrations of several chemical constituents, including (1) constituents linked to redox processes and (2) anions or oxyanions that sorb to iron oxides. Observations from the glacial aquifer system are consistent with the idea that the predominant source of arsenic is iron oxides and the predominant mechanism for releasing arsenic to the ground water is reductive desorption or reductive dissolution. Arsenic is also released from iron oxides under oxic conditions, but on a more limited basis and at lower concentrations. Logistic regression was used to investigate the relative significance of redox, ground-water age, depth, and other water-quality constituents as indicators of elevated arsenic concentrations in the glacial aquifer system. The single variable that explained the greatest amount of variation in

Chlorophyll Detection and Mapping of Shallow Water Impoundments Using Image Spectrometry

International Nuclear Information System (INIS)

Artigas, F.; Pechmann, I.; Marti, A.; Yao, N.; Pechmann, I.

2008-01-01

There exists a common perception that chlorophyll a concentrations in tidal coastal waters are unsuitable to be captured by remote sensing techniques because of high water turbidity. In this study, we use band index measurements to separate active chlorophyll pigments from other constituents in the water. Published single- and multiband spectral indices are used to establish a relationship between algal chlorophyll concentration and reflectance data. We find an index which is suitable to map chlorophyll gradients in the impoundments, ditches, and associated waterways of the Hackensack Meadow lands (NJ, USA). The resulting images clearly depict the spatial distribution of plant pigments and their relationship with the biological conditions of the waters in the estuary. Since these biological conditions are often determined by land usage, the methods in this paper provide a simple tool to address water quality management issues in fragmented urban estuaries.

Evaluation of Background Mercury Concentrations in the SRS Groundwater System

International Nuclear Information System (INIS)

Looney, B.B.

1999-01-01

Mercury analyses associated with the A-01 Outfall have highlighted the importance of developing an understanding of mercury in the Savannah River Site groundwater system and associated surface water streams. This activity is critical based upon the fact that the EPA Ambient Water Quality Criteria (AWQC) for this constituent is 0.012mg/L, a level that is well below conventional detection limits of 0.1 to 0.2 mg/L. A first step in this process is obtained by utilizing the existing investment in groundwater mercury concentrations (20,242 records) maintained in the SRS geographical information management system (GIMS) database. Careful use of these data provides a technically defensible initial estimate for total recoverable mercury in background and contaminated SRS wells

Ground-water monitoring at the Hanford Site, January-December 1984

Energy Technology Data Exchange (ETDEWEB)

Cline, C.S.; Rieger, J.T.; Raymond, J.R.

1985-09-01

This program is designed to evaluate existing and potential pathways of exposure to radioactivity and hazardous chemicals from site operations. This document contains an evaluation of data collected during CY 1984. During 1984, 339 monitoring wells were sampled at various times for radioactive and nonradioactive constituents. Two of these constituents, specifically, tritium and nitrate, have been selected for detailed discussion in this report. Tritium and nitrate in the primary plumes originating from the 200 Areas continue to move generally eastward toward the Columbia River in the direction of ground-water flow. The movement within these plumes is indicated by changes in trends within the analytical data from the monitoring wells. No discernible impact on ground water has yet been observed from the start-up of the PUREX plant in December 1983. The shape of the present tritium plume is similar to those described in previous ground-water monitoring reports, although slight changes on the outer edges have been noted. Radiological impacts from two potential pathways for radionuclide transport in ground water to the environment are discussed in this report. The pathways are: (1) human consumption of ground water from onsite wells, and (2) seepage of ground water into the Columbia River. Concentrations of tritium in spring samples that were collected and analyzed in 1983, and in wells sampled adjacent to the Columbia River in 1984 confirmed that constituents in the ground water are entering the river via springs and subsurface flow. The primary areas where radionuclides enter the Columbia River via ground-water flow are the 100-N and 300 Areas and the shoreline adjacent to the Hanford Townsite. 44 refs., 25 figs., 11 tabs.

Successes and failures of the constituent quark model

International Nuclear Information System (INIS)

Lipkin, H.J.

1982-01-01

Our approach considers the model as a possible bridge between QCD and the experimental data and examines its predictions to see where these succeed and where they fail. We also attempt to improve the model by looking for additional simple assumptions which give better fits to the experimental data. But we avoid complicated models with too many ad hoc assumptions and too many free parameters; these can fit everything but teach us nothing. We define our constituent quark model by analogy with the constituent electron model of the atom and the constituent nucleon model of the nucleus. In the same way that an atom is assumed to consist only of constituent electrons and a central Coulomb field and a nucleus is assumed to consist only of constituent nucleons hadrons are assumed to consist only of their constituent valence quarks with no bag, no glue, no ocean, nor other constituents. Although these constituent models are oversimplified and neglect other constituents we push them as far as we can. Atomic physics has photons and vacuum polarization as well as constituent electrons, but the constituent model is adequate for calculating most features of the spectrum when finer details like the Lamb shift are neglected. 54 references

Nitrate concentrations in drainage water in marine clay areas : exploratory research of the causes of increased nitrate concentrations

NARCIS (Netherlands)

Boekel, van E.M.P.M.; Roelsma, J.; Massop, H.T.L.; Hendriks, R.F.A.; Goedhart, P.W.; Jansen, P.C.

2013-01-01

The nitrate concentrations measured in drainage water and groundwater at LMM farms (farms participating in the National Manure Policy Effects Measurement Network (LLM)) in marine clay areas have decreased with 50% since the mid-nineties. The nitrate concentrations in marine clay areas are on average

Biological processes for concentrating trace elements from uranium mine waters. Technical completion report

International Nuclear Information System (INIS)

Brierley, C.L.; Brierley, J.A.

1981-12-01

Waste water from uranium mines in the Ambrosia Lake district near Grants, New Mexico, USA, contains uranium, selenium, radium and molybdenum. The Kerr-McGee Corporation has a novel treatment process for waters from two mines to reduce the concentrations of the trace contaminants. Particulates are settled by ponding, and the waters are passed through an ion exchange resin to remove uranium; barium chloride is added to precipitate sulfate and radium from the mine waters. The mine waters are subsequently passed through three consecutive algae ponds prior to discharge. Water, sediment and biological samples were collected over a 4-year period and analyzed to assess the role of biological agents in removal of inorganic trace contaminants from the mine waters. Some of the conclusions derived from this study are: (1) The concentrations of soluble uranium, selenium and molybdenum were not diminished in the mine waters by passage through the series of impoundments which constituted the mine water treatment facility. Uranium concentrations were reduced but this was due to passage of the water through an ion exchange column. (2) The particulate concentrations of the mine water were reduced at least ten-fold by passage of the waters through the impoundments. (3) The sediments were anoxic and enriched in uranium, molybdenum and selenium. The deposition of particulates and the formation of insoluble compounds were proposed as mechanisms for sediment enrichment. (4) The predominant algae of the treatment ponds were the filamentous Spirogyra and Oscillatoria, and the benthic alga, Chara. (5) Adsorptive processes resulted in the accumulation of metals in the algae cells. (6) Stimulation of sulfate reduction by the bacteria resulted in retention of molybdenum, selenium, and uranium in sediments. 1 figure, 16 tables

Evaluation of ground-water quality in the Santa Maria Valley, California

Science.gov (United States)

Hughes, Jerry L.

1977-01-01

The quality and quantity of recharge to the Santa Maria Valley, Calif., ground-water basin from natural sources, point sources, and agriculture are expressed in terms of a hydrologic budget, a solute balance, and maps showing the distribution of select chemical constituents. Point sources includes a sugar-beet refinery, oil refineries, stockyards, golf courses, poultry farms, solid-waste landfills, and municipal and industrial wastewater-treatment facilities. Pumpage has exceeded recharge by about 10,000 acre-feet per year. The result is a declining potentiometric surface with an accumulation of solutes and an increase in nitrogen in ground water. Nitrogen concentrations have reached as much as 50 milligrams per liter. In comparison to the solutes from irrigation return, natural recharge, and rain, discharge of wastewater from municipal and industrial wastewater-treatment facilities contributes less than 10 percent. The quality of treated wastewater is often lower in select chemical constituents than the receiving water. (Woodard-USGS)

Physicochemical Properties, Contamination and Suitability of Canal Water for Irrigation, Lahore Branch Pakistan

Directory of Open Access Journals (Sweden)

Tayyaba Aftab

2011-12-01

Full Text Available The pollution status of Lahore branch canal was determined by physical, chemical and metal constituents because the water is used for irrigation of lands in and around the city. The average result of each physical, chemical and metal parameter at 12 different sites (Location-1 to Location-12 of Lahore branch canal was compared with Food and Agricultural organization (FAO. All physical and chemical parameters were within standards limit while metals concentrations were found in variable quantities in canal water samples. cadmium, copper and chromium concentration was found much higher than the permissible FAO standards.

A risk-based approach for identifying constituents of concern in oil sands process-affected water from the Athabasca Oil Sands region.

Science.gov (United States)

McQueen, Andrew D; Kinley, Ciera M; Hendrikse, Maas; Gaspari, Daniel P; Calomeni, Alyssa J; Iwinski, Kyla J; Castle, James W; Haakensen, Monique C; Peru, Kerry M; Headley, John V; Rodgers, John H

2017-04-01

Mining leases in the Athabasca Oil Sands (AOS) region produce large volumes of oil sands process-affected water (OSPW) containing constituents that limit beneficial uses and discharge into receiving systems. The aim of this research is to identify constituents of concern (COCs) in OSPW sourced from an active settling basin with the goal of providing a sound rational for developing mitigation strategies for using constructed treatment wetlands for COCs contained in OSPW. COCs were identified through several lines of evidence: 1) chemical and physical characterization of OSPW and comparisons with numeric water quality guidelines and toxicity endpoints, 2) measuring toxicity of OSPW using a taxonomic range of sentinel organisms (i.e. fish, aquatic invertebrates, and a macrophyte), 3) conducting process-based manipulations (PBMs) of OSPW to alter toxicity and inform treatment processes, and 4) discerning potential treatment pathways to mitigate ecological risks of OSPW based on identification of COCs, toxicological analyses, and PBM results. COCs identified in OSPW included organics (naphthenic acids [NAs], oil and grease [O/G]), metals/metalloids, and suspended solids. In terms of species sensitivities to undiluted OSPW, fish ≥ aquatic invertebrates > macrophytes. Bench-scale manipulations of the organic fractions of OSPW via PBMs (i.e. H 2 O 2 +UV 254 and granular activated charcoal treatments) eliminated toxicity to Ceriodaphnia dubia (7-8 d), in terms of mortality and reproduction. Results from this study provide critical information to inform mitigation strategies using passive or semi-passive treatment processes (e.g., constructed treatment wetlands) to mitigate ecological risks of OSPW to aquatic organisms. Copyright © 2017 Elsevier Ltd. All rights reserved.

Influence of hydrological regime on pore water metal concentrations in a contaminated sediment-derived soil

International Nuclear Information System (INIS)

Du Laing, G.; Vanthuyne, D.R.J.; Vandecasteele, B.; Tack, F.M.G.; Verloo, M.G.

2007-01-01

Options for wetland creation or restoration might be limited because of the presence of contaminants in the soil. The influence of hydrological management on the pore water concentrations of Cd, Cr, Cu, Fe, Mn, Ni and Zn in the upper soil layer of a contaminated overbank sedimentation zone was investigated in a greenhouse experiment. Flooding conditions led to increased Fe, Mn, Ni and Cr concentrations and decreased Cd, Cu and Zn concentrations in the pore water of the upper soil layer. Keeping the soil at field capacity resulted in a low pore water concentration of Fe, Mn and Ni while the Cd, Cu, Cr and Zn concentrations increased. Alternating hydrological conditions caused metal concentrations in the pore water to fluctuate. Formation and re-oxidation of small amounts of sulphides appeared dominant in determining the mobility of Cd, Cu, and to a lesser extent Zn, while Ni behaviour was consistent with Fe/Mn oxidation and reduction. These effects were strongly dependent on the duration of the flooded periods. The shorter the flooded periods, the better the metal concentrations could be linked to the mobility of Ca in the pore water, which is attributed to a fluctuating CO 2 pressure. - The hydrological regime is a key factor in determining the metal concentration in the pore water of a contaminated sediment-derived soil

Concentrations of 23 trace elements in ground water and surface water at and near the Idaho National Engineering Laboratory, Idaho, 1988--91

International Nuclear Information System (INIS)

Liszewski, M.J.; Mann, L.J.

1993-01-01

Analytical data for 23 trace elements are reported for ground- and surface-water samples collected at and near the Idaho National Engineering Laboratory during 1988--91. Water samples were collected from 148 wells completed in the Snake River Plain aquifer, 18 wells completed in discontinuous deep perched-water zones, and 1 well completed in an alluvial aquifer. Surface-water samples also were collected from three streams, two springs, two ponds, and one lake. Data are categorized by concentrations of total recoverable of dissolved trace elements. Concentrations of total recoverable trace elements are reported for unfiltered water samples and include results for one or more of the following: aluminum, arsenic, barium, beryllium, cadmium, chromium, cobalt, copper, iron, lead, manganese, mercury, nickel, selenium, silver, and zinc. Concentrations of dissolved trace elements are reported for water samples filtered through a nominal 0.45-micron filter and may also include bromide, fluoride, lithium, molybdenum, strontium, thallium, and vanadium. Concentrations of dissolved hexavalent chromium also are reported for many samples. The water samples were analyzed at the US Geological Survey's National Water Quality Laboratory in Arvada, Colorado. Methods used to collect the water samples and quality assurance instituted for the sampling program are described. Concentrations of chromium equaled or exceeded the maximum contaminant level at 12 ground-water quality monitoring wells. Other trace elements did not exceed their respective maximum contaminant levels

Concentrations of 23 trace elements in ground water and surface water at and near the Idaho National Engineering Laboratory, Idaho, 1988--91

Energy Technology Data Exchange (ETDEWEB)

Liszewski, M.J.; Mann, L.J.

1993-12-31

Analytical data for 23 trace elements are reported for ground- and surface-water samples collected at and near the Idaho National Engineering Laboratory during 1988--91. Water samples were collected from 148 wells completed in the Snake River Plain aquifer, 18 wells completed in discontinuous deep perched-water zones, and 1 well completed in an alluvial aquifer. Surface-water samples also were collected from three streams, two springs, two ponds, and one lake. Data are categorized by concentrations of total recoverable of dissolved trace elements. Concentrations of total recoverable trace elements are reported for unfiltered water samples and include results for one or more of the following: aluminum, arsenic, barium, beryllium, cadmium, chromium, cobalt, copper, iron, lead, manganese, mercury, nickel, selenium, silver, and zinc. Concentrations of dissolved trace elements are reported for water samples filtered through a nominal 0.45-micron filter and may also include bromide, fluoride, lithium, molybdenum, strontium, thallium, and vanadium. Concentrations of dissolved hexavalent chromium also are reported for many samples. The water samples were analyzed at the US Geological Survey`s National Water Quality Laboratory in Arvada, Colorado. Methods used to collect the water samples and quality assurance instituted for the sampling program are described. Concentrations of chromium equaled or exceeded the maximum contaminant level at 12 ground-water quality monitoring wells. Other trace elements did not exceed their respective maximum contaminant levels.

Ambient concentrations of total suspended particulate matter and its elemental constituents at the wider area of the mining facilities of TVX Hellas in Chalkidiki, Greece.

Science.gov (United States)

Gaidajis, George

2003-01-01

To assess ambient air quality at the wider area of TVX Hellas mining facilities, the Total Suspended Particulate matter (TSP) and its content in characteristic elements, i.e., As, Cd, Cu, Fe, Mn, Pb, Zn are being monitored for more than thirty months as part of the established Environmental Monitoring Program. High Volume air samplers equipped with Tissue Quartz filters were employed for the collection of TSP. Analyses were effected after digestion of the suspended particulate with an HNO3-HCl solution and determination of elemental concentrations with an Atomic Absorption Spectroscopy equipped with graphite furnace. The sampling stations were selected to record representatively the existing ambient air quality in the vicinity of the facilities and at remote sites not affected from industrial activities. Monitoring data indicated that the background TSP concentrations ranged from 5-60 microg/m3. Recorded TSP concentrations at the residential sites close to the facilities ranged between 20-100 microg/m3, indicating only a minimal influence from the mining and milling activities. Similar spatial variation was observed for the TSP constituents and specifically for Pb and Zn. To validate the monitoring procedures, a parallel sampling campaign took place with different High Volume samplers at days where low TSP concentrations were expected. The satisfactory agreement (+/- 11%) at low concentrations (50-100 microg/m3) clearly supported the reproducibility of the techniques employed specifically at the critical range of lower concentrations.

Water quality and aquatic communities of upland wetlands, Cumberland Island National Seashore, Georgia, April 1999 to July 2000

Science.gov (United States)

Frick, Elizabeth A.; Gregory, M. Brian; Calhoun, Daniel L.; Hopkins, Evelyn H.

2002-01-01

alkalinity). Fecal-coliform bacteria concentrations were measured, but not detected, in samples collected from two domestic water-supply wells. During the 12-month period from April 1999 to March 2000 when water-quality and aquatic-community samples were collected, rainfall was 12.93 inches below the 30-year average rainfall. Constituent concentrations were highly variable among the different wetlands during the study period. Rainfall and tidal surges associated with tropical storms and hurricanes substantially influenced water quantity and quality, particularly in wetland areas directly influenced by tidal surges. Although surface waters on Cumberland Island are not used as sources of drinking water, exceedances of U.S. Environmental Protection Agency primary and secondary standards for drinking water were noted for comparative purposes. A nitrate concentration of 12 milligrams per liter in one sample from Whitney outflow was the only exceedance of a maximum contaminant level. Secondary standards were exceeded in 26 surface-water samples for the following constituents: pH (10 exceedances), chloride (8), sulfate (5), total dissolved solids (4), iron (2), fluoride (1), and manganese (1). The total-dissolved-solids concentrations and the relative abundance of major ions in surface-water samples collected from wetlands on Cumberland Island provide some insight into potential sources of water and influences on water quality. Major-ion chemistries of water samples from Whitney Lake, Willow Pond, and South End Pond 3 were sodium-chloride dominated, indicating direct influence from rainwater, salt aerosol, or inundation of marine waters. The remaining wetlands sampled had low total-dissolved-solids concentrations and mixed major-ion chemistries--North Cut Pond 2A was magnesium-sodium-chloride-sulfate dominated and Lake Retta and the two beach outflows were sodium-calcium-bicarbonate-chloride dominated. The higher percent calcium and bicarbonate in some wetlands sugg

A volatile organics concentrator for use in monitoring Space Station water quality

Science.gov (United States)

Ehntholt, Daniel J.; Bodek, Itamar; Valentine, James R.; Trabanino, Rudy; Vincze, Johanna E.; Sauer, Richard L.

1990-01-01

The process used to identify, select, and design an approach to the isolation and concentration of volatile organic compounds from a water sample prior to chemical analysis in a microgravity environment is discerned. The trade analysis leading to the recommended volatile organics concentrator (VOC) concept to be tested in a breadboard device is presented. The system covers the areas of gases, volatile separation from water, and water removal/gas chromatograph/mass spectrometer interface. Five options for potential use in the VOC and GC/MS system are identified and ranked, and also nine options are presented for separation of volatiles from the water phase. Seven options for use in the water removal/GC column and MS interface are also identified and included in the overall considerations. A final overall recommendation for breadboard VOC testing is given.

Variation in predicted internal concentrations in relation to PBPK model complexity for rainbow trout

Energy Technology Data Exchange (ETDEWEB)

Salmina, E.S.; Wondrousch, D. [UFZ Department of Ecological Chemistry, Helmholtz Centre for Environmental Research, Permoserstr. 15, 04318 Leipzig (Germany); Institute for Organic Chemistry, Technical University Bergakademie Freiberg, Leipziger Str. 29, 09596 Freiberg (Germany); Kühne, R. [UFZ Department of Ecological Chemistry, Helmholtz Centre for Environmental Research, Permoserstr. 15, 04318 Leipzig (Germany); Potemkin, V.A. [Department of Chemistry, South Ural State Medical University, Vorovskogo 64, 454048, Chelyabinsk (Russian Federation); Schüürmann, G. [UFZ Department of Ecological Chemistry, Helmholtz Centre for Environmental Research, Permoserstr. 15, 04318 Leipzig (Germany); Institute for Organic Chemistry, Technical University Bergakademie Freiberg, Leipziger Str. 29, 09596 Freiberg (Germany)

2016-04-15

The present study is motivated by the increasing demand to consider internal partitioning into tissues instead of exposure concentrations for the environmental toxicity assessment. To this end, physiologically based pharmacokinetic (PBPK) models can be applied. We evaluated the variation in accuracy of PBPK model outcomes depending on tissue constituents modeled as sorptive phases and chemical distribution tendencies addressed by molecular descriptors. The model performance was examined using data from 150 experiments for 28 chemicals collected from US EPA databases. The simplest PBPK model is based on the “K{sub ow}-lipid content” approach as being traditional for environmental toxicology. The most elaborated one considers five biological sorptive phases (polar and non-polar lipids, water, albumin and the remaining proteins) and makes use of LSER (linear solvation energy relationship) parameters to describe the compound partitioning behavior. The “K{sub ow}-lipid content”-based PBPK model shows more than one order of magnitude difference in predicted and measured values for 37% of the studied exposure experiments while for the most elaborated model this happens only for 7%. It is shown that further improvements could be achieved by introducing corrections for metabolic biotransformation and compound transmission hindrance through a cellular membrane. The analysis of the interface distribution tendencies shows that polar tissue constituents, namely water, polar lipids and proteins, play an important role in the accumulation behavior of polar compounds with H-bond donating functional groups. For compounds without H-bond donating fragments preferable accumulation phases are storage lipids and water depending on compound polarity. - Highlights: • For reliable predictions, models of a certain complexity should be compared. • For reliable predictions non-lipid fish tissue constituents should be considered. • H-donor compounds preferably accumulate in water

Variation in predicted internal concentrations in relation to PBPK model complexity for rainbow trout

International Nuclear Information System (INIS)

Salmina, E.S.; Wondrousch, D.; Kühne, R.; Potemkin, V.A.; Schüürmann, G.

2016-01-01

The present study is motivated by the increasing demand to consider internal partitioning into tissues instead of exposure concentrations for the environmental toxicity assessment. To this end, physiologically based pharmacokinetic (PBPK) models can be applied. We evaluated the variation in accuracy of PBPK model outcomes depending on tissue constituents modeled as sorptive phases and chemical distribution tendencies addressed by molecular descriptors. The model performance was examined using data from 150 experiments for 28 chemicals collected from US EPA databases. The simplest PBPK model is based on the “K_o_w-lipid content” approach as being traditional for environmental toxicology. The most elaborated one considers five biological sorptive phases (polar and non-polar lipids, water, albumin and the remaining proteins) and makes use of LSER (linear solvation energy relationship) parameters to describe the compound partitioning behavior. The “K_o_w-lipid content”-based PBPK model shows more than one order of magnitude difference in predicted and measured values for 37% of the studied exposure experiments while for the most elaborated model this happens only for 7%. It is shown that further improvements could be achieved by introducing corrections for metabolic biotransformation and compound transmission hindrance through a cellular membrane. The analysis of the interface distribution tendencies shows that polar tissue constituents, namely water, polar lipids and proteins, play an important role in the accumulation behavior of polar compounds with H-bond donating functional groups. For compounds without H-bond donating fragments preferable accumulation phases are storage lipids and water depending on compound polarity. - Highlights: • For reliable predictions, models of a certain complexity should be compared. • For reliable predictions non-lipid fish tissue constituents should be considered. • H-donor compounds preferably accumulate in water, polar

Phytochemical composition and radical scavenging activities of watermelon (Citrullus lanatus seed constituents

Directory of Open Access Journals (Sweden)

O. L. Otutu

2016-01-01

Full Text Available It is a known fact that antioxidant phytochemicals in foods have many health benefits including prevention of various diseases associated with oxidative stress such as cancer, cardiovascular disease, neuro-degeneration and diabetes. Watermelon seed constituents (whole meal, shelled and shells flours were evaluated for phytochemical components and in vitro antioxidant activity to determine the potential practical applications in food and other related areas. Antioxidant activity was investigated by measuring its DPPH (2,2-diphenyl-2-picryl hydrazyl and ABTS (2, 2’-azinobis-3-ethylbenzothiozoline- 6-sulphonic acid radical scavenging ability as well as FRAP method (ferric reducing power. Quantitative estimation of the constituents showed cardiac glycosides (9.94-14.35 mg/g and saponins (11.62-32.48 mg/g as the most concentrated phytochemicals in the constituents, while alkaloids (47.2-95.8 mg/g, total phenol (5.63-8.40 mg GAE/g, flavonoids 3.51-7.76 mg QE/g. A positive radical scavenging ability of the constituents against ABTS and DPPH free radicals ranged from 0.02 to 0.04 mg Trolox equivalent /g seed flour and 39.89 to 61.11 mg ascorbic acid equivalent /g seed flour respectively. There was a considerable ferric reducing power and higher activity was observed in whole meal than shelled seeds and shells. The significant antioxidant capacities of the seed constituents underline the potential source of natural antioxidants and bioactive compounds for therapeutic purposes.

Measurement of radon concentration in ground water at Saijo sake brewery by means of γ-ray spectrometry

International Nuclear Information System (INIS)

Takenaka, Kodai; Takatori, Hiroshi; Kojima, Yasuaki; Shizuma, Kiyoshi

2008-01-01

Recently, natural water such as ground water and/or spring water of various places is popular for the environmental preservation and safety of food. Measurement of the radon concentration in ground water is important for risk estimate of drinking water and whether the water can be authorized as the mineral spring (74 Bq/L). In this work, radon concentration is ground water from eight places which were utilized for Saijo sake breweries was measured by means of γ-ray spectrometry. Radon concentration in each well was measured every month for two years. The variation in the radon concentration was investigated for seasonal variation, difference between the type of well, correlations with pH, water temperature and atmospheric temperature. The results are as follows: An average value of the radon concentration was 160 Bq/L which meant most of ground water satisfies the mineral spring standard. The radon concentration of the drilling well was higher than that of the punched well. The variation in the radon concentration shows no seasonal variations, nor depends on the water temperature, the atmospheric temperature and the pH. (author)

Preliminary study of radioactive concentration in treated sewage water

Energy Technology Data Exchange (ETDEWEB)

Elassaly, F M; Beal, A D.R. [Ministry of Health P.O. Box 1853 Dubai, (United Arab Emirates)

1995-10-01

Water from sewage treatment plant is used after processing for irrigation. Two water samples and one consolidated sludge (waste treatment products) were taken each day for period of months. Medical applications and research are the main sources of radioactivity such as Cr-51, Co-57, Ga-67, Se-75, Tc-99 m, In-111, Au-198 and Tl-201. Measurements were carried out using Hp Ge spectrometer with one liter Marinelli breaker. The maximum detected activity was 5.7 Bq.liter with a daily average of 2.4 Bq/liter for water. In the second period maximum activity was found to be 5 Bq/liter with an average daily activity 1.8 Bq/liter. The maximum activity recorded in the sludge during this period was 352 Bq/liter of which 343 Bq/liter was from I-131. The average daily activity was 162 Bq/liter. From these studies the levels of radioactivity concentration were 5 Bq/liter with an average 2 Bq/1 compared level 10 Bq/1 set for drinking water for Gcc countries. Although the sludge show higher activity of 353 Bq/liter it is kept for about year before being disposed. The maximum level for animal fodder is 300 Bq/kg for Gcc countries. These results indicate that radioactive concentration (2 Bq/liter) in the treated waste water present hazard to the public and environment. 6 figs., 4 tabs.

Studies on radon concentration in underground water samples in and around Kabini river basin

International Nuclear Information System (INIS)

Yashaswini, T.; Ningappa, C.; Niranjan, R.S.; Sannappa, J.

2017-01-01

Radon is a radioactive inert gas, a decay product of radium, causes environmental health problems like lung cancer. Radium present in the earth crest continuously releases radon into underground water. From the point view of health, the study of radon concentration level in underground water base line data is important. In the present study, radon concentration in underground water have been measured in 40 underground water samples collected in and around Kabini River of Karnataka State by using Emanometry technique. The radon concentration in the study area varies from 21.2 to 168.2Bq.l -1 with a geometrical mean value of 73.3 Bq.l -1 . The physicochemical parameters of water such as chloride, Fluoride, nitrite, sulphate, TDS are measured in the same samples in order to know about the impact of these parameters on radon concentration and their health risks to the general public. The experimental techniques and results obtained are discussed in the presentation. (author)

Determination of dew absorption by coffee plant through deuterium concentrations in leaf water

Energy Technology Data Exchange (ETDEWEB)

Leopoldo, P R [Faculdade de Ciencias Medicas e Biologicas de Botucatu (Brazil); Salati, E; Matsui, E [Centro de Energia Nuclear na Agricultura, Piracicaba (Brazil)

1975-12-01

The effect of dew falling on leaves on the water metabolism of the coffee plant (Coffea arabica) is examined. The use of natural stable isotopes variations in plant physiological studies is demonstrated. Water extracted from leaf samples is analysed by mass spectrometry. Analyses of deuterium concentrations in water extracted from plant leaves, dew and nutrient solutions are made. Determination of changes in deuterium concentration in the water of leaves from plants exposed to dew, compared with leaves not exposed to dew, is carried out. Results show that during daytime there is an enrichment in deuterium in water contained in the leaves, while at night the opposite occurs.

Determination of dew absorption by coffee plant through deuterium concentrations in leaf water

International Nuclear Information System (INIS)

Leopoldo, P.R.; Salati, E.; Matsui, E.

1975-01-01

The effect of dew falling on leaves on the water metabolism of the coffee plant (Coffea arabica) is examined. The use of natural stable isotopes variations in plant physiological studies is demonstrated. Water extracted from leaf samples is analysed by mass spectrometry. Analyses of deuterium concentrations in water extracted from plant leaves, dew and nutrient solutions are made. Determination of changes in deuterium concentration in the water of leaves from plants exposed to dew, compared with leaves not exposed to dew, is carried out. Results show that during daytime there is an enrichment in deuterium in water contained in the leaves, while at night the opposite occurs [pt

A New Electropositive Filter for Concentrating Enterovirus and Norovirus from Large Volumes of Water - MCEARD

Science.gov (United States)

The detection of enteric viruses in environmental water usually requires the concentration of viruses from large volumes of water. The 1MDS electropositive filter is commonly used for concentrating enteric viruses from water but unfortunately these filters are not cost-effective...

Use of Monte Carlo analysis in a risk-based prioritization of toxic constituents in house dust.

Science.gov (United States)

Ginsberg, Gary L; Belleggia, Giuliana

2017-12-01

Many chemicals have been detected in house dust with exposures to the general public and particularly young children of potential health concern. House dust is also an indicator of chemicals present in consumer products and the built environment that may constitute a health risk. The current analysis compiles a database of recent house dust concentrations from the United States and Canada, focusing upon semi-volatile constituents. Seven constituents from the phthalate and flame retardant categories were selected for risk-based screening and prioritization: diethylhexyl phthalate (DEHP), butyl benzyl phthalate (BBzP), diisononyl phthalate (DINP), a pentabrominated diphenyl ether congener (BDE-99), hexabromocyclododecane (HBCDD), tris(1,3-dichloro-2-propyl) phosphate (TDCIPP) and tris(2-chloroethyl) phosphate (TCEP). Monte Carlo analysis was used to represent the variability in house dust concentration as well as the uncertainty in the toxicology database in the estimation of children's exposure and risk. Constituents were prioritized based upon the percentage of the distribution of risk results for cancer and non-cancer endpoints that exceeded a hazard quotient (HQ) of 1. The greatest percent HQ exceedances were for DEHP (cancer and non-cancer), BDE-99 (non-cancer) and TDCIPP (cancer). Current uses and the potential for reducing levels of these constituents in house dust are discussed. Exposure and risk for other phthalates and flame retardants in house dust may increase if they are used to substitute for these prioritized constituents. Therefore, alternative assessment and green chemistry solutions are important elements in decreasing children's exposure to chemicals of concern in the indoor environment. Copyright © 2017 Elsevier Ltd. All rights reserved.

The influence of water potassium concentration on 137Cs excretion from fish

International Nuclear Information System (INIS)

Nasvit, O.J.

1996-01-01

Results are reported of the investigation on the peculiarities of 137 Cs release from carp (Cyprinus carpio L.) acclimatized to different potassium concentrations in water. The dynamics of radiocesium release are characterized by slow and fast components. The 137 Cs release rates observed in the experiments with different water potassium concentrations were markedly different from the point of view of middle-term radioecological predictions. 5 refs., 3 figs., 3 tabs

TREATMENT OF PRODUCED OIL AND GAS WATERS WITH SURFACTANT-MODIFIED ZEOLITE

Energy Technology Data Exchange (ETDEWEB)

Lynn E. Katz; R.S. Bowman; E.J. Sullivan

2003-11-01

Co-produced water from the oil and gas industry accounts for a significant waste stream in the United States. It is by some estimates the largest single waste stream in the country, aside from nonhazardous industrial wastes. Characteristics of produced water include high total dissolved solids content, dissolved organic constituents such as benzene and toluene, an oil and grease component, and chemicals added during the oil-production process. While most of the produced water is disposed via reinjection, some must be treated to remove organic constituents before the water is discharged. Current treatment options are successful in reducing the organic content; however, they cannot always meet the levels of current or proposed regulations for discharged water. Therefore, an efficient, cost-effective treatment technology is needed. Surfactant-modified zeolite (SMZ) has been used successfully to treat contaminated ground water for organic and inorganic constituents. In addition, the low cost of natural zeolites makes their use attractive in water-treatment applications. This report summarizes the work and results of this four-year project. We tested the effectiveness of surfactant-modified zeolite (SMZ) for removal of BTEX with batch and column experiments using waters with BTEX concentrations that are comparable to those of produced waters. The data from our experimental investigations showed that BTEX sorption to SMZ can be described by a linear isotherm model, and competitive effects between compounds were not significant. The SMZ can be readily regenerated using air stripping. We field-tested a prototype SMZ-based water treatment system at produced water treatment facilities and found that the SMZ successfully removes BTEX from produced waters as predicted by laboratory studies. When compared to other existing treatment technologies, the cost of the SMZ system is very competitive. Furthermore, the SMZ system is relatively compact, does not require the storage of

Seasonal fluctuations of organophosphate concentrations in precipitation and storm water runoff.

Science.gov (United States)

Regnery, Julia; Püttmann, Wilhelm

2010-02-01

To investigate seasonal fluctuations and trends of organophosphate (flame retardants, plasticizers) concentrations in rain and snow, precipitation samples were collected in 2007-2009 period at a densely populated urban sampling site and two sparsely populated rural sampling sites in middle Germany. In addition, storm water runoff was sampled from May 2008 to April 2009 at an urban storm water holding tank (SWHT). Samples were analyzed for tris(2-chloroethyl) phosphate (TCEP), tris(2-chloro-1-methylethyl) phosphate (TCPP), tris(1,3-dichloro-2-propyl) phosphate (TDCP), tris(2-butoxyethyl) phosphate (TBEP), tri-iso-butyl phosphate (TiBP), and tri-n-butyl phosphate (TnBP) by gas chromatography-mass spectrometry after solid phase extraction. Among the six analyzed organophosphates (OPs), TCPP dominated in all precipitation and SWHT water samples with maximum concentrations exceeding 1000ngL(-1). For all analytes, no seasonal trends were observed at the urban precipitation sampling site, although atmospheric photooxidation was expected to reduce particularly concentrations of non-chlorinated OPs during transport from urban to remote areas in summer months with higher global irradiation. In the SWHT a seasonal trend with decreasing concentrations in summer/autumn is evident for the non-chlorinated OPs due to in-lake degradation but not for the chlorinated OPs. Furthermore, an accumulation of OPs deposited in SWHTs was observed with concentrations often exceeding those observed in wet precipitation. Median concentrations of TCPP (880ngL(-1)), TDCP (13ngL(-1)) and TBEP (77ngL(-1)) at the SWHT were more than twice as high as median concentrations measured at the urban precipitation sampling site (403ngL(-1), 5ngL(-1), and 21ngL(-1) respectively).

Filter Membrane Effects on Water-Extractable Phosphorus Concentrations from Soil.

Science.gov (United States)

Norby, Jessica; Strawn, Daniel; Brooks, Erin

2018-03-01

To accurately assess P concentrations in soil extracts, standard laboratory practices for monitoring P concentrations are needed. Water-extractable P is a common analytical test to determine P availability for leaching from soils, and it is used to determine best management practices. Most P analytical tests require filtration through a filter membrane with 0.45-μm pore size to distinguish between particulate and dissolved P species. However, filter membrane type is rarely specified in method protocols, and many different types of membranes are available. In this study, three common filter membrane materials (polyether sulfone, nylon, and nitrocellulose), all with 0.45-μm pore sizes, were tested for analytical differences in total P concentrations and dissolved reactive P (DRP) concentrations in water extracts from six soils sampled from two regions. Three of the extracts from the six soil samples had different total P concentrations for all three membrane types. The other three soil extracts had significantly different total P results from at least one filter membrane type. Total P concentration differences were as great as 35%. The DRP concentrations in the extracts were dependent on filter type in five of the six soil types. Results from this research show that filter membrane type is an important parameter that affects concentrations of total P and DRP from soil extracts. Thus, membrane type should be specified in soil extraction protocols. Copyright © by the American Society of Agronomy, Crop Science Society of America, and Soil Science Society of America, Inc.

Measuring Low Concentrations of Liquid Water in Soil

Science.gov (United States)

Buehler, Martin

2009-01-01

An apparatus has been developed for measuring the low concentrations of liquid water and ice in relatively dry soil samples. Designed as a prototype of instruments for measuring the liquidwater and ice contents of Lunar and Martian soils, the apparatus could also be applied similarly to terrestrial desert soils and sands. The apparatus is a special-purpose impedance spectrometer: Its design is based on the fact that the electrical behavior of a typical soil sample is well approximated by a network of resistors and capacitors in which resistances decrease and capacitances increase (and, hence, the magnitude of impedance decreases) with increasing water content.

Validation of Passive Sampling Devices for Monitoring of Munitions Constituents in Underwater Environments

Science.gov (United States)

2017-09-01

and explosives of concern (MEC) corroding, breaching, and leaking MC into the water column (Darrach, Chutjian, and Plett, 1998; GMI, 2007; Lewis et...underwater UWMM have the potential to corrode, breach, and leak munitions constituents (MCs) such as 2,4,6-trinitrotoluene (TNT) and hexahydro-1,3,5...Wang et al., 2013), a number of challenges prevent accurate assessment of environmental exposure using traditional water , sediment, and tissue

Determination of arsenic concentration in drinking water from tubewell

International Nuclear Information System (INIS)

Molla, N.I.; Basunia, S.; Zaman, Laila; Hossain, S.M.; Miah, R.U.; Rahman, M.

1998-01-01

Arsenic contamination in drinking water from tubewells in the north-western and south-western region of Bangladesh has posed a great risk to public health. Most of the affected districts are primarily reported to have arsenic concentration in drinking water more than the permissible level, set by WHO, of 0.01 mg/L. Therefore, use of a reliable analytical technique like instrumental neutron activation analysis (INAA) for bulk sample analysis, covering a wide sampling area, has become an essential task. In this work the analytical results of forty tubewell water samples from two districts, namely Chapainawabganj and Faridpur, are reported. The concentration level of arsenic are found to be 28 to 378 μg/L. The detection limit is 3 μg/L. Tubewell samples, collected from different locations of Chapainawabganj and Faridpur municipal areas, and standard reference material NIST 1643d (water) together with primary standard of arsenic (100 μg/L) were irradiated at the TRIGA Mark-II research reactor, AERE, Savar with a nominal neutron flux about 10 12 cm -2 s -1 for one hour using the Lazy Susan facility. After irradiation, allowing a cooling time of 50-70 hours, radioactivity of the 76 As radionuclide was measured with a high resolution HPGe detector in combination with a PC based S-100 MCA master board packages. The detector was previously calibrated with a set of standard gamma ray sources. The gamma ray spectra were analyzed using gamma-software Peakgr-10 and GANAAS and manually. It has been possible to minimize the contribution of interfering 82 Br and 122 Sb radionuclides and the background of 24Na by optimizing irradiation time, cooling period and counting time. The quality of the analysis has been crossed-checked by analyzing the NIST SRM-1643b with respect to the primary standard of arsenic (100 μg/L). It is concluded that that arsenic concentration level is much higher in underground water of some areas posing serious threat to public health. However, hundred

Effects of Water Solutions on Extracting Green Tea Leaves

Directory of Open Access Journals (Sweden)

Wen-Ying Huang

2013-01-01

Full Text Available This study investigates the effects of water solutions on the antioxidant content of green tea leaf extracts. Green teas prepared with tap water and distilled water were compared with respect to four antioxidant assays: total phenol content, reducing power, DMPD assay, and trolox equivalent antioxidant capacity assay. The results indicate that green tea prepared with distilled water exhibits higher antioxidant activity than that made with tap water. The high performance liquid chromatography showed that major constituents of green tea were found in higher concentrations in tea made with distilled water than in that made with tap water. This could be due to less calcium fixation in leaves and small water clusters. Water solutions composed of less mineralisation are more effective in promoting the quality of green tea leaf extracts.

Airborne remote sensing of water constituents at Lake Constance; Flugzeuggestuetzte Fernerkundung von Wasserinhaltsstoffen im Bodensee

Energy Technology Data Exchange (ETDEWEB)

Heege, T.

2000-12-01

An inversion scheme for the retrieval of water constituents in case II waters from airborne multispectral scanner data is presented. This method includes modules for the calculation of aerosol types and contents, for the correction of sun glitter radiances and for the atmospheric correction of the image data. In 1996 extensive measurements were performed to determine the optical properties in Lake Constance. In combination with data collected through many years within a project of the German Research Foundation (SFB 248), for the first time a data set of inherent optical parameters being specific for typical substances in the Lake could be established. By means of the inversions scheme and the specific optical properties, geo-coded maps of suspended matter and chlorophyll were calculated from the multispectral airborne measurements above Lake Constance. (orig.) [German] Zur Berechnung von Wasserinhaltsstoffen aus Daten flugzeuggetragener Multispektralscanner wird ein Inversionsverfahren vorgestellt. Es beinhaltet die Bestimmung von Aerosoltypen und -konzentrationen, die bildpunktweise Korrektur von Oberflaechenreflexionen des Sonnenlichtes und die Atmosphaerenkorrektur von Fernerkundungsdaten. Zur Erfassung der optischen Groessen im Wasser wurden umfangreiche Messkampagnen am Bodensee durchgefuehrt. Zusammen mit vieljaehrigen Datensaetzen des DFG-Sonderforschungsbereichs 248 wird damit erstmalig ein vollstaendiger Satz der inhaerenten optischen stoffspezifischen Groessen fuer den Bodensee bestimmt. Zur Validation werden diese anhand von verschiedenen Modellen zur Verknuepfung der inhaerenten Streu- und Absorptionskoeffizienten mit den messbaren Groessen Extinktion und diffuse Reflexion auf Konsistenz geprueft. Aus Befliegungen mit dem Multispektralscanner Daedalus werden mit den vorgestellten Verfahren und optischen Groessen georeferenzierte Verteilungskarten von Schwebstoff und Phytoplankton-Pigmenten berechnet. (orig.)

Ground-Water Quality Data in the Coastal Los Angeles Basin Study Unit, 2006: Results from the California GAMA Program

Science.gov (United States)

Mathany, Timothy M.; Land, Michael; Belitz, Kenneth

2008-01-01

] and dissolved noble gases also were measured to help identify the sources and ages of the sampled ground water. Quality-control samples (blanks, replicates, and samples for matrix spikes) were collected at approximately one-fourth of the wells, and the results for these samples were used to evaluate the quality of the data for the ground-water samples. Field blanks rarely contained detectable concentrations of any constituent, suggesting that contamination was not a significant source of bias. Differences between replicate samples were within acceptable ranges, indicating acceptably low variability. Matrix spike recoveries were within acceptable ranges for most compounds. Assessment of the quality-control information resulted in applying ?V? codes to approximately 0.1 percent of the data collected for ground-water samples (meaning a constituent was detected in blanks as well as the corresponding environmental data). This study did not attempt to evaluate the quality of drinking water delivered to consumers; after withdrawal from the ground, water typically is treated, disinfected, and (or) blended with other waters to maintain acceptable drinking-water quality. Regulatory thresholds are applied to the treated drinking water that is served to the consumer, not to raw ground water. However, to provide some context for the results, concentrations of constituents measured in the raw ground water were compared with regulatory and non-regulatory health-based thresholds established by the U.S. Environmental Protection Agency (USEPA), California Department of Public Health (CDPH, formerly California Department of Health Services [CADHS]) and thresholds established for aesthetic concerns (secondary maximum contaminant levels, SMCL-CA) by CDPH. Comparisons between data collected for this study and drinking-water thresholds are for illustrative purposes only, and are not indicative of compliance or non-compliance with those thresholds. VOCs were detected in alm

Spatial variability of arsenic concentration in soils and plants, and its relationship with iron, manganese and phosphorus

International Nuclear Information System (INIS)

Hossain, M.B.; Jahiruddin, M.; Panaullah, G.M.; Loeppert, R.H.; Islam, M.R.; Duxbury, J.M.

2008-01-01

Spatial distribution of arsenic (As) concentrations of irrigation water, soil and plant (rice) in a shallow tube-well (STW) command area (8 ha), and their relationship with Fe, Mn and P were studied. Arsenic concentrations of water in the 110 m long irrigation channel clearly decreased with distance from the STW point, the range being 68-136 μg L -1 . Such decreasing trend was also noticed with Fe and P concentrations, but the trend for Mn concentrations was not remarkable. Concerning soil As, the concentration showed a decreasing tendency with distance from the pump. The NH 4 -oxalate extractable As contributed 36% of total As and this amount of As was associated with poorly crystalline Fe-oxides. Furthermore only 22% of total As was phosphate extractable so that most of the As was tightly retained by soil constituents and was not readily exchangeable by phosphate. Soil As (both total and extractable As) was significantly and positively correlated with rice grain As (0.296 ± 0.063 μg g -1 , n = 56). Next to drinking water, rice could be a potential source of As exposure of the people living in the As affected areas of Bangladesh. - Arsenic concentrations of irrigation water, soil and rice decreased with distance from STW point and it was related with iron and phosphorus concentrations

Determination of the radioactive concentration of 137Cs in water

International Nuclear Information System (INIS)

1986-01-01

The recently accepted standard method to determine the radioactive concentration of 137 Cs in water is based on the selective retention of cesium ions on ammonium-phosphorous-molybdate followed by the dissolution of the sorbent and the selective precipitation of cesium-hexa-chloro-platinate. The radioactive concentration is determined by the measurement of β disintegration rate of the preparate. (V.N.)

Sources of trends in water-quality data for selected streams in Texas, 1975-89 water years

Science.gov (United States)

Schertz, T.L.; Wells, F.C.; Ohe, D.J.

1994-01-01

Sources of trends in water-quality data for selected streams in Texas for the 1975-89 water years were investigated in this study. The investigation of sources was confined to distinct geographic patterns in the trend indicators for one constituent or for a group of related constituents.

Radon Concentrations in Drinking Water in Beijing City, China and Contribution to Radiation Dose

Science.gov (United States)

Wu, Yun-Yun; Ma, Yong-Zhong; Cui, Hong-Xing; Liu, Jian-Xiang; Sun, Ya-Ru; Shang, Bing; Su, Xu

2014-01-01

222Rn concentrations in drinking water samples from Beijing City, China, were determined based on a simple method for the continuous monitoring of radon using a radon-in-air monitor coupled to an air-water exchanger. A total of 89 water samples were sampled and analyzed for their 222Rn content. The observed radon levels ranged from detection limit up to 49 Bq/L. The calculated arithmetic and geometric means of radon concentrations in all measured samples were equal to 5.87 and 4.63 Bq/L, respectively. The average annual effective dose from ingestion of radon in drinking water was 2.78 μSv, and that of inhalation of water-borne radon was 28.5 μSv. It is concluded that it is not the ingestion of waterborne radon, but inhalation of the radon escaping from water that is a substantial part of the radiological hazard. Radon in water is a big concern for public health, especially for consumers who directly use well water with very high radon concentration. PMID:25350007

Radon Concentrations in Drinking Water in Beijing City, China and Contribution to Radiation Dose

Directory of Open Access Journals (Sweden)

Yun-Yun Wu

2014-10-01

Full Text Available 222Rn concentrations in drinking water samples from Beijing City, China, were determined based on a simple method for the continuous monitoring of radon using a radon-in-air monitor coupled to an air-water exchanger. A total of 89 water samples were sampled and analyzed for their 222Rn content. The observed radon levels ranged from detection limit up to 49 Bq/L. The calculated arithmetic and geometric means of radon concentrations in all measured samples were equal to 5.87 and 4.63 Bq/L, respectively. The average annual effective dose from ingestion of radon in drinking water was 2.78 μSv, and that of inhalation of water-borne radon was 28.5 μSv. It is concluded that it is not the ingestion of waterborne radon, but inhalation of the radon escaping from water that is a substantial part of the radiological hazard. Radon in water is a big concern for public health, especially for consumers who directly use well water with very high radon concentration.

A study on the radon concentrations in water in Jeddah (Saudi Arabia) and the associated health effects

International Nuclear Information System (INIS)

Tayyeb, Z.A.; Kinsara, A.R.; Farid, S.M.

1998-01-01

Several studies have shown that water-borne 222 Rn contributes to indoor air concentrations. A passive radon measurement method was employed to determine radon activity concentrations in the water of Jeddah city (Saudi Arabia). Tap water, flushing water and drinking water, including natural mineral water, artificial mineral water and distilled water, have been investigated for their radon concentrations. It is observed that the radon concentration in natural mineral water samples is the highest and that in flush water, it is the lowest. From these measurements, the corresponding annual effective dose for the stomach and the lung are determined. It is found that the annual effective dose resulting from direct consumption of water is far greater than that due to inhalation of radon emanated from tap water and flushing water. Moreover, it is also seen that the annual effective dose resulting from inhalation of radon emanated from tap water and flushing water is negligible compared to the total annual effective dose for indoor radon in Jeddah. (author)

Effects of hydrologic, biological, and environmental processes on sources and concentrations of fecal bacteria in the Cuyahoga River, with implications for management of recreational waters in Summit and Cuyahoga Counties, Ohio

Science.gov (United States)

Myers, Donna N.; Koltun, G.F.; Francy, Donna S.

1998-01-01

water. Sediments are likely to be a relatively less important source of fecal bacteria during rainfall and runoff in the middle main stem relative to bacterial loading from point sources. Numerical streamflow and transport simulation models were calibrated and verified with data collected during field studies. Of the constituents modeled, bacteria exhibited the poorest correspondence between observed and simulated values. The simulation results for a dye tracer indicated that the model reasonably reproduced the timing of dissolved constituents as well as dilution and dispersion effects. Calibrated and verified models for 1991 and 1992 data sets were used to simulate the improvements to bacteriological water quality that might result from reductions in concentrations of fecal bacteria discharged from two major sources. The model simulation resulting in the greatest improvement in bacteriological water-quality was one in which concentrations of fecal coliform bacteria and Escherichia coli were reduced by 90 percent in the Cuyahoga River at the Old Portage gaging station, and to geometric-mean bathing-water standards in the effluent of the Akron Water Pollution Control Station (BWS/90 scenario). Compared to the results of the base-simulation, when the BWS/90 scenario was applied in the 1991 model simulation, Escherichia coli concentrations were reduced 98.5 percent at Botzum, 97.5 percent at Jaite, and 91.1 percent at Independence. For 1992 model simulations, similar percent reductions in the concentrations of Escherichia coli were predicted at the three stream sites when the same reductions were applied to sources. None of the model simulations resulted in attainment of bacteriological water-quality standards.The potential benefits of source reductions to human health and recreational uses were estimated by comparing the number of illnesses per 1,000 people from concentrations of Escherichia coli associated with the BWS/90 simulation, with the base simulation, and with

Communication: Modeling of concentration dependent water diffusivity in ionic solutions: Role of intermolecular charge transfer

Energy Technology Data Exchange (ETDEWEB)

Yao, Yi; Berkowitz, Max L., E-mail: maxb@unc.edu, E-mail: ykanai@unc.edu; Kanai, Yosuke, E-mail: maxb@unc.edu, E-mail: ykanai@unc.edu [Department of Chemistry, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599 (United States)

2015-12-28

The translational diffusivity of water in solutions of alkali halide salts depends on the identity of ions, exhibiting dramatically different behavior even in solutions of similar salts of NaCl and KCl. The water diffusion coefficient decreases as the salt concentration increases in NaCl. Yet, in KCl solution, it slightly increases and remains above bulk value as salt concentration increases. Previous classical molecular dynamics simulations have failed to describe this important behavior even when polarizable models were used. Here, we show that inclusion of dynamical charge transfer among water molecules produces results in a quantitative agreement with experiments. Our results indicate that the concentration-dependent diffusivity reflects the importance of many-body effects among the water molecules in aqueous ionic solutions. Comparison with quantum mechanical calculations shows that a heterogeneous and extended distribution of charges on water molecules around the ions due to ion-water and also water-water charge transfer plays a very important role in controlling water diffusivity. Explicit inclusion of the charge transfer allows us to model accurately the difference in the concentration-dependent water diffusivity between Na{sup +} and K{sup +} ions in simulations, and it is likely to impact modeling of a wide range of systems for medical and technological applications.

Water-quality data for Smith and Bybee Lakes, Portland, Oregon, June to November, 1982

Science.gov (United States)