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Jack E. Barbash

Publications and source records attributed to Jack E. Barbash.

13 recordsLinked to original sources
USGS2018

Concentrations of nutrients at the water table beneath forage fields receiving seasonal applications of manure, Whatcom County, Washington, autumn 2011–spring 2015

The U.S. Geological Survey, in cooperation with the Whatcom Conservation District (WCD), collected groundwater-quality data for roughly 3 years (October 2011–May 2015) from near the water table beneath forage fields receiving regular seasonal applications of liquid dairy manure in Whatcom County, Washington. The work was done as part of an evaluation of WCD’s prototypical Application Risk Management (ARM) decision support system. The ARM system uses a combination of field-specific hydrology, stage of crop-growth, manure management practices, soil conditions, and precipitation forecast to evaluate the timing of manure application via a set of decision support tools (Manure Spreading Advisory, ARM Worksheet, manure application setback distances) in order to reduce the risk of contamination of surface water and groundwater. The ARM system’s effectiveness in reducing leaching of nitrate to groundwater was evaluated by monitoring nitrate concentrations in recently recharged groundwater beneath paired test plots receiving manure application scheduled using either conventional (CON) manure scheduling procedures, which utilize fixed start and end dates for manure application along with projected crop nutrient requirements or ARM manure scheduling procedures using an approach to manure application timing based on projected crop nutrient needs, field conditions, and weather forecast. Water-quality samples from the surface of the water table were collected synoptically from paired test plots (2–5 monitoring wells per test plot) at approximately monthly intervals at three different dairy field sites. Water-quality samples from near the water table were isolated from the underlying aquifer using a combination of an inflatable packer and a fine-grained sand pack encompassing the well-screen interval. Concentrations of nitrate and chloride measured at the water table beneath test plots were highly variable. Concentrations of nitrate ranged from non-detectable to 116 milligrams nitrogen per liter (mg-N/L), and chloride ranged from 1.15 to 153 mg/L. In each test plot, seasonal variations were much greater than spatial variations. Differences in nitrate concentrations in groundwater between the two treatments were inconclusive. Nitrate concentrations in groundwater at paired treatment plots (Mann Whitney, p<0.05) were significantly lower beneath the ARM treatment plot at site B, yet significantly higher beneath the ARM treatment plot at site C. Nitrate concentrations in ground water varied significantly among individual wells at each site (Kruskal-Wallis, p<0.05), indicating that leaching of nitrates from soil following manure application is spatially variable at the field scale tested regardless of manure application strategy. At all three paired test plots, average concentrations of nitrate and chloride at the water table were lowest near the end of the growing season (September) and increased rapidly with the onset of autumn rains (October–December). Under both the conventional (calendar-based) and treatment (ARM-based) manure application scheduling systems, high soil nitrate concentrations in autumn were coincident with rising groundwater levels, suggesting that nitrate and chloride were flushed from soil to groundwater by recharge from the seasonal rains. Under both treatments, concentrations of nitrate in shallow (10–25 feet) groundwater beneath forage fields receiving manure applications were greater than the nitrate drinking water standard of 10 mg-N/L in approximately 85 percent of samples. Yearly mass loading of nitrogen to the groundwater system calculated from nitrate concentrations at the water table and estimates of recharge volume ranged from 86 to 196 pounds-N per acre, which was equivalent to approximately 16–37 percent of the recommended manure application rate for projected forage production yield of 7 dry tons per acre per year. Manure nitrogen applied in the autumn, when crop nutrient needs decrease due to reduced sunlight and cooler temperatures and commensurate with ongoing mineralization of soil organic-nitrogen and increased seasonal precipitation, are more likely to exceed the immediate plant nutritional requirements and hence be flushed to groundwater than manure applications occurring near the peak of the growing season.

Washington↗
USGS2016

Transport and deposition of asbestos-rich sediment in the Sumas River, Whatcom County, Washington

Heavy sediment loads in the Sumas River of Whatcom County, Washington, increase seasonal turbidity and cause locally acute sedimentation. Most sediment in the Sumas River is derived from a deep-seated landslide of serpentinite that is located on Sumas Mountain and drained by Swift Creek, a tributary to the Sumas River. This mafic sediment contains high amounts of naturally occurring asbestiform chrysotile. A known human-health hazard, asbestiform chrysotile comprises 0.25–37 percent, by mass, of the total suspended sediment sampled from the Sumas River as part of this study, which included part of water year 2011 and all of water years 2012 and 2013. The suspended-sediment load in the Sumas River at South Pass Road, 0.6 kilometers (km) downstream of the confluence with Swift Creek, was 22,000 tonnes (t) in water year 2012 and 49,000 t in water year 2013. The suspended‑sediment load at Telegraph Road, 18.8 km downstream of the Swift Creek confluence, was 22,000 t in water year 2012 and 27,000 t in water year 2013. Although hydrologic conditions during the study were wetter than normal overall, the 2-year flood peak was only modestly exceeded in water years 2011 and 2013; runoff‑driven geomorphic disturbance to the watershed, which might have involved mass wasting from the landslide, seemed unexceptional. In water year 2012, flood peaks were modest, and the annual streamflow was normal. The fact that suspended-sediment loads in water year 2012 were equivalent at sites 0.6 and 18.8 km downstream of the sediment source indicates that the conservation of suspended‑sediment load can occur under normal hydrologic conditions. The substantial decrease in suspended-sediment load in the downstream direction in water year 2013 was attributed to either sedimentation in the intervening river reach, transfer to bedload as an alternate mode of sediment transport, or both. The sediment in the Sumas River is distinct from sediment in most other river systems because of the large percentage of asbestiform chrysotile in suspension. The suspended sediment carried by the Sumas River consists of three major components: (1) a relatively dense, largely non-flocculated material that settles rapidly out of suspension; (2) a lighter component containing relatively high proportions of flocculated material, much of it composed of asbestiform chrysotile; and (3) individual chrysotile fibers that are too small to flocculate or settle out, and remain in suspension as wash load (these fibers are on the order of microns in length and tenths of microns in diameter). Whereas the bulk density of the first (heaviest) component of suspended sediment was between 1.5 and 1.6 grams per cubic centimeter (g/cm3), the bulk density of the flocculated material was an order of magnitude lower (0.16 g/cm3), even after 24 hours of settling. Soon after immersion in water, the fresh chrysotile fibers derived from the Swift Creek landslide seem to flocculate readily into large bundles, or floccules, that exhibit settling velocities characteristic of coarse silts and fine sands (30 and 250 micrometers). In quiescent water within this river system, the floccules settle out quickly, but still leave between 2.4 and 19.5 million chrysotile fibers per liter in the clear overlying water. Consistent with the results from previous laboratory research, the amounts of asbestiform chrysotile in the water column in Swift Creek, as well as in the Sumas River close to and downstream of its confluence with Swift Creek, were determined to be directly correlated with pH. This observation offers a possible alternative to either turbidity or suspended‑sediment concentration as a surrogate for the concentration of fresh asbestiform chrysotile in suspension. Continued movement and associated erosion of the landslide through mass wasting and runoff will maintain large sediment loads in Swift Creek and in the Sumas River for the foreseeable future. Given the present channel morphology of the river system, aggradation (that is, sediment accumulation) in Swift Creek and the Sumas River are also likely to continue.

Washington↗
USGS2015

Contaminant removal by wastewater treatment plants in the Stillaguamish River Basin, Washington

Human activities in most areas of the developed world typically release nutrients, pharmaceuticals, personal care products, pesticides, and other contaminants into the environment, many of which reach freshwater ecosystems. In urbanized areas, wastewater treatment plants (WWTPs) are critical facilities for collecting and reducing the amounts of wastewater contaminants (WWCs) that ultimately discharge to rivers, coastal areas, and groundwater. Most WWTPs use multiple methods to remove contaminants from wastewater. These include physical methods to remove solid materials (primary treatment), biological and chemical methods to remove most organic matter (secondary treatment), advanced methods to reduce the concentrations of various contaminants such as nitrogen, phosphorus and (or) synthetic organic compounds (tertiary treatment), and disinfection prior to discharge (Metcalf and Eddy, Inc., 1979). This study examined the extent to which 114 organic WWCs were removed by each of three WWTPs, prior to discharge to freshwater and marine ecosystems, in a rapidly developing area in northwestern Washington State. Removal percentages for each WWC were estimated by comparing the concentrations measured in the WWTP influents with those measured in the effluents. The investigation was carried out in the 700-mi 2 Stillaguamish River Basin, the fifth largest watershed that discharges to Puget Sound (fig. 1).

Washington↗
USGS2014

Data worth and prediction uncertainty for pesticide transport and fate models in Nebraska and Maryland, United States

BACKGROUND Complex environmental models are frequently extrapolated to overcome data limitations in space and time, but quantifying data worth to such models is rarely attempted. The authors determined which field observations most informed the parameters of agricultural system models applied to field sites in Nebraska (NE) and Maryland (MD), and identified parameters and observations that most influenced prediction uncertainty. RESULTS The standard error of regression of the calibrated models was about the same at both NE (0.59) and MD (0.58), and overall reductions in prediction uncertainties of metolachlor and metolachlor ethane sulfonic acid concentrations were 98.0 and 98.6% respectively. Observation data groups reduced the prediction uncertainty by 55&ndash;90% at NE and by 28&ndash;96% at MD. Soil hydraulic parameters were well informed by the observed data at both sites, but pesticide and macropore properties had comparatively larger contributions after model calibration. CONCLUSIONS Although the observed data were sparse, they substantially reduced prediction uncertainty in unsampled regions of pesticide breakthrough curves. Nitrate evidently functioned as a surrogate for soil hydraulic data in well-drained loam soils conducive to conservative transport of nitrogen. Pesticide properties and macropore parameters could most benefit from improved characterization further to reduce model misfit and prediction uncertainty. RESULTS: The standard error of regression of the calibrated models was about the same at both NE (0.59) and MD (0.58), and overall reductions in prediction uncertainties of metolachlor and metolachlor ethane sulfonic acid concentrations were 98.0 and 98.6% respectively. Observation data groups reduced the prediction uncertainty by 55&ndash;90% at NE and by 28&ndash;96% at MD. Soil hydraulic parameters were well informed by the observed data at both sites, but pesticide and macropore properties had comparatively larger contributions after model calibration. CONCLUSIONS: Although the observed data were sparse, they substantially reduced prediction uncertainty in unsampled regions of pesticide breakthrough curves. Nitrate evidently functioned as a surrogate for soil hydraulic data in well-drained loam soils conducive to conservative transport of nitrogen. Pesticide properties and macropore parameters could most benefit from improved characterization further to reduce model misfit and prediction uncertainty.

Maryl;Nebraska↗
USGS2012

Regression models for estimating concentrations of atrazine plus deethylatrazine in shallow groundwater in agricultural areas of the United States

Tobit regression models were developed to predict the summed concentration of atrazine [6-chloro- N -ethyl- N' -(1-methylethyl)-1,3,5-triazine-2,4-diamine] and its degradate deethylatrazine [6-chloro- N -(1-methylethyl)-1,3,5,-triazine-2,4-diamine] (DEA) in shallow groundwater underlying agricultural settings across the conterminous United States. The models were developed from atrazine and DEA concentrations in samples from 1298 wells and explanatory variables that represent the source of atrazine and various aspects of the transport and fate of atrazine and DEA in the subsurface. One advantage of these newly developed models over previous national regression models is that they predict concentrations (rather than detection frequency), which can be compared with water quality benchmarks. Model results indicate that variability in the concentration of atrazine residues (atrazine plus DEA) in groundwater underlying agricultural areas is more strongly controlled by the history of atrazine use in relation to the timing of recharge (groundwater age) than by processes that control the dispersion, adsorption, or degradation of these compounds in the saturated zone. Current (1990s) atrazine use was found to be a weak explanatory variable, perhaps because it does not represent the use of atrazine at the time of recharge of the sampled groundwater and because the likelihood that these compounds will reach the water table is affected by other factors operating within the unsaturated zone, such as soil characteristics, artificial drainage, and water movement. Results show that only about 5% of agricultural areas have greater than a 10% probability of exceeding the USEPA maximum contaminant level of 3.0 &mu;g L -1 . These models are not developed for regulatory purposes but rather can be used to (i) identify areas of potential concern, (ii) provide conservative estimates of the concentrations of atrazine residues in deeper potential drinking water supplies, and (iii) set priorities among areas for future groundwater monitoring.

Journal of Environmental Quality↗
USGS2007

The geochemistry of pesticides

The mid-1970s marked a major turning point in human history, for it was at that moment that the ability of the Earth&rsquo;s ecosystems to absorb most of the biological impacts of human activities appears to have been exceeded by the magnitude of those impacts. This conclusion is based partly upon estimates of the rate of carbon dioxide emission during the combustion of fossil fuels, relative to the rate of its uptake by terrestrial ecosystems ( Loh, 2002 ). A very different threshold, however, had already been crossed several decades earlier with the birth of the modern chemical industry, which produced novel substances for which no such natural assimilative capacity existed. Among these new chemical compounds, none has posed a greater challenge to the planet&rsquo;s ecosystems than synthetic pesticides, compounds that have been intentionally released into the hydrologic system in vast quantities&mdash;several hundred million pounds of active ingredient (a.i.) per year in the United States alone ( Donaldson et al. , 2002 )&mdash;for many decades. To gauge the extent to which we are currently able to assess the environmental implications of this new development in the Earth&rsquo;s history, this chapter presents an overview of current understanding regarding the sources, transport, fate, and biological effects of pesticides, their transformation products, and selected adjuvants in the hydrologic system. (Adjuvants are the so-called inert ingredients included in commercial pesticide formulations to enhance the effectiveness of the active ingredients.)

Book chapter↗
USGS2006

Pesticides in the Nation's Streams and Ground Water, 1992–2001

This report is one of a series of publications, The Quality of Our Nation's Waters, that describe major findings of the NAWQA Program on water-quality issues of regional and national concern. This report presents evaluations of pesticides in streams and ground water based on findings for the first decadal cycle of NAWQA. 'Pesticides in the Nation's Streams and Ground Water, 1992-2001' greatly expands the analysis of pesticides presented in 'Nutrients and Pesticides,' which was the first report in the series and was based on early results from 1992 to 1995. Other reports in this series cover additional water-quality constituents of concern, such as volatile organic compounds and trace elements, as well as physical and chemical effects on aquatic ecosystems. Each report builds toward a more comprehensive understanding of regional and national water resources. The information in this series is intended primarily for those interested or involved in resource management, conservation, regulation, and policymaking at regional and national levels. In addition, the information might interest those at a local level who wish to know more about the general quality of streams and ground water in areas near where they live and how that quality compares with other areas across the Nation.

Circular↗
USGS2005

Pesticides in ground water of the United States, 1992-1996

During the first cycle of the National Water Quality Assessment (1992&ndash;1996), ground water in 20 of the nation's major hydro-logic basins was analyzed for 90 pesticide compounds (pesticides and degradates). One or more of the pesticide compounds examined were detected at 48.4% of the 2485 ground water sites sampled. However, approximately 70% of the sites where pesticides were detected, two or more pesticide compounds analyzed were present&ndash;documenting the prevalence of pesticide mixtures in ground water. The pesticide concentrations encountered were generally low, with the median total concentration (summation of concentrations for the 90 pesticide compounds) being 0.046 &mu;g/L. Pesticides were commonly detected in shallow ground water beneath both agricultural (60.4%) and urban (48.5%) areas. This is an important finding because, although agricultural activities have long been associated with pesticide contamination, urban areas have only recently been recognized as a potential source of these types of compounds. Pesticides with higher frequencies of detection were generally those with more extensive use, greater environmental persistence, and greater mobility in ground water (lower soil-water partition coefficients).

Ground Water↗
USGS2005

Evaluation of unsaturated-zone solute-transport models for studies of agricultural chemicals

Seven unsaturated-zone solute-transport models were tested with two data sets to select models for use by the Agricultural Chemical Team of the U.S. Geological Survey's National Water-Quality Assessment Program. The data sets were from a bromide tracer test near Merced, California, and an atrazine study in the White River Basin, Indiana. In this study the models are designated either as complex or simple based on the water flux algorithm. The complex models, HYDRUS2D, LEACHP, RZWQM, and VS2DT, use Richards' equation to simulate water flux and are well suited to process understanding. The simple models, CALF, GLEAMS, and PRZM, use a tipping-bucket algorithm and are more amenable to extrapolation because they require fewer input parameters. The purpose of this report is not to endorse a particular model, but to describe useful features, potential capabilities, and possible limitations that emerged from working with the model input data sets. More rigorous assessment of model applicability involves proper calibration, which was beyond the scope of this study. Uncalibrated ("cold") simulations were run using all seven models to predict the transport of bromide (Merced) and the transport and fate of atrazine and three of its transformation products (White River Basin). Among the complex models, HYDRUS2D successfully predicted both the surface retention and accumulation of bromide at depth at the Merced site, whereas RZWQM and VS2DT predicted only the latter. RZWQM predictions of atrazine were closest to observed values at the White River Basin site, where preferential flow has been observed. LEACHP predicted smaller solute concentrations than observed at both the Merced and White River Basin sites. Among the simple models, CALF predicted the highest values of atrazine and deethylatrazine at the measurement depth of 1.5 meters. CALF includes the Addiscott flow option for preferential flow, and also accepts user-specified dispersivity. PRZM underpredicted solute concentrations, probably because control of dispersion is a problem with this model. GLEAMS has a maximum simulation depth of 1.5 meters, which is limiting for mass-balance purposes because it creates a potential disconnect between unsaturated-zone transport and the water table. Of the models tested, RZWQM, HYDRUS2D, VS2DT, GLEAMS and PRZM had graphical user interfaces. Extensive documentation was available for RZWQM, HYDRUS2D, and VS2DT. RZWQM can explicitly simulate water and solute flux in macropores, and both HYDRUS2D and VS2DT can simulate water and solute flux in two dimensions. The version of RZWQM tested had a maximum simulation depth of 3 meters. The complex models simulate the formation, transport, and fate of degradates of up to three to five compounds including the parent, with the exception of VS2DT, which simulates the transport and fate of a single compound.

California, Indiana↗
USGS2004

Chloroform in the hydrologic system--sources, transport, fate, occurrence, and effects on human health and aquatic organisms

Chloroform is one of the volatile organic compounds (VOCs) detected most frequently in both ground and surface water. Because it is also one of the four trihalomethanes (THMs) produced in the highest concentrations during the chlorination of drinking water and wastewater, the frequent detection of this compound in ground and surface water of the United States is presumed to be caused primarily by the input of chlorinated water to the hydrologic system. Although anthropogenic sources of the compound are substantial, they are currently estimated to constitute only 10 percent of the total global input to the hydrologic system. Natural sources of the compound include volcanic gases, biomass burning, marine algae, and soil microorganisms. Under most conditions (except in the presence of unusually high bromide concentrations), chloroform is the THM produced in the highest concentrations during chlorination. Furthermore, in most cases where more than one THM is produced from chlorination, the relative concentrations among the different compounds usually decrease with increasing bromination (chloroform > dichlorobromomethane > chlorodibromomethane > bromoform). This phenomenon is presumed to be responsible for the common observation that when more than one THM is detected during investigations of the occurrence of these compounds in the hydrologic system, this same trend is typically observed among their relative concentrations or, for a uniform reporting limit, their relative frequencies of detection. This pattern could provide a valuable means for distinguishing between chlorinated water and other potential sources of chloroform in the environment. Chloroform has been widely detected in national, regional, and local studies of VOCs in ground, surface, source, and drinking waters. Total THM (TTHM) concentrations of the compound, however, were typically less than the Maximum Contaminant Level (MCL) of 80 ?g/L (micrograms per liter) established by the U.S. Environmental Protection Agency (USEPA) for TTHMs. In the studies that compared land-use settings, frequencies of detection of chloroform were higher beneath urban and residential areas than beneath agricultural or undeveloped areas. Because chloroform is a suspected human carcinogen, its presence in drinking water is a potential human health concern. Liver damage, however, is known to occur at chloroform exposures lower than those required to cause cancer, an observation that has been considered by the USEPA as the basis for setting a new, non-zero Maximum Contaminant Level Goal of 70 ?g/L for the compound. As part of its National Water-Quality Assessment Program, the U.S. Geological Survey has been assembling and analyzing data on the occurrence of VOCs (including chloroform) in ground and surface water on a national scale from studies conducted between 1991 and the present. This report presents a summary of current (2004) information on the uses, sources, formation, transport, fate, and occurrence of chloroform, as well as its effects on human health and aquatic organisms.

Scientific Investigations Report↗
USGS1998

Occurrence of pesticides in shallow groundwater of the United States: initial results from the National Water-Quality Assessment program

The first phase of intensive data collection for the National Water-Quality Assessment (NAWQA) was completed during 1993&minus;1995 in 20 major hydrologic basins of the United States. Groundwater land-use studies, designed to sample recently recharged groundwater (generally within 10 years) beneath specific land-use and hydrogeologic settings, are a major component of the groundwater quality as sessment for NAWQA. Pesticide results from the 41 land-use studies conducted during 1993&minus;1995 indicate that pesticides were commonly detected in shallow groundwater, having been found at 54.4% of the 1034 sites sampled in agricultural and urban settings across the United States. Pesticide concentrations were generally low, with over 95% of the detections at concentrations less than 1 &mu;g/L. Of the 46 pesticide compounds examined, 39 were detected. The compounds detected most frequently were atrazine (38.2%), deethylatrazine (34.2%), simazine (18.0%), metolachlor (14.6%), and prometon (13.9%). Statistically significant relations were observed between frequencies of detection and the use, mobility, and persistence of these compounds. Pesticides were commonly detected in both agricultural (56.4%; 813 sites) and urban (46.6%; 221 sites) settings. Frequent detections of pesticides in urban areas indicate that, as is the case with agricultural pesticide use in agricultural areas, urban and suburban pesticide use significantly contribute to pesticide occurrence in shallow groundwater. Although pesticides were detected in groundwater sampled in urban areas and all nine of the agricultural land-use categories examined, significant variations in occurrence were observed among these categories. Maximum contaminant levels (MCLs) established by the U.S. Environmental Protection Agency for drinking water were exceeded for only one pesticide (atrazine, 3 &mu;g/L) at a single location. However, MCLs have been established for only 25 of the 46 pesticide compounds examined, do not cover pesticide degradates, and, at present, do not take into account additive or synergistic effects of combinations of pesticide compounds or potential effects on nearby aquatic ecosystems.

Environmental Science & Technology↗
USGS1997

Pesticides and volatile organic compounds in shallow urban groundwater of the United States

The widespread use of pesticides and volatile organic compounds (VOCs) over the past half century has led to their detection in many hydrologic systems in the United States. However, few systematic investigations of occurrences have been carried out over multistate regions using a consistent study design. Nine urban studies of shallow groundwater have been conducted to date as part of the U.S. Geological Survey's National Water-Quality Assessment Program. Pesticide compounds were detected in 48.6% of the 208 urban wells sampled. Sixteen different pesticide compounds were detected in samples from these wells. Prometon was by far the most frequently detected pesticide compound, being found in 8 of the 9 urban studies. VOCs were detected in 53.4% of the 208 urban wells sampled, with 36 different VOC compounds being found. Measured VOC concentrations exceeded current U.S. Environmental Protection Agency drinking water regulations in 19 wells. Methyl tert -butyl ether (MTBE), a common fuel oxygenate, was the most frequently detected VOC for this study.

Book chapter↗