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At least 307 records · Page 17Linked to original sources

USGS2019

Simulation of the regional groundwater-flow system in the St. Louis River basin, Minnesota

The St. Louis River Basin (SLRB) covers 3,600 square miles in northeastern Minnesota, with headwaters in the Mesabi Range and extensive wetlands and lakes throughout the basin. To better understand the regional groundwater system in the SLRB, a two-dimensional, steady-state groundwater-flow model of the SLRB was developed by the U.S. Geological Survey, in cooperation with the Minnesota Ojibwe Bands, using the analytic-element computer code GFLOW. The parameter-estimation software suite PEST was used to obtain a best fit of the modeled to measured groundwater levels and streamflows. The calibrated regional model was locally refined to create a smaller version of the model, the central SLRB model, that was used to evaluate hydrologic effects from extensive ditching in wetlands of the central SLRB. The refinements included adding ditches that were not represented in the regional model and modifying the aquifer base elevation to be more representative of the localized area. The central SLRB model was recalibrated to better match the distribution of mapped wetlands. Two scenarios were run of the central SLRB model: one with ditches and one without ditches. The model results were compared between the two scenarios to assess the effect of ditching on the groundwater system and potential changes to hydrologic conditions that support wetlands. Calibration of the regional SRLB model resulted in average horizontal hydraulic conductivity values of 6–39 feet per day for the glacial deposits and 3–4 feet per day for the uppermost fractured bedrock in the Biwabik Iron-Formation on the Mesabi Range. Average recharge across the calibrated model was 5.9 inches per year. Linesink resistance for the routed stream network was calibrated by using resistance categories based on the mapped soil hydrologic groups. The modeled regional groundwater-flow direction was generally to the south near the Mesabi Range topographic high and south or southwest across the rest of the basin. The updated calibration of the central SLRB model resulted in average horizontal hydraulic conductivity values of 5–36 feet per day for the glacial deposits and 3 feet per day for the uppermost fractured Biwabik Iron-Formation of the Mesabi Range. Average recharge across the ditch scenarios was 4.1 inches per year. Comparison of the preditch and postditch model scenarios showed that ditching reduced the area where the modeled water table was within 1 foot of the land surface (a wetland hydrology indicator) in as much as 40,000 acres, or 37 percent, of mapped permanent wetlands in the SLRB. An increase in the depth to the water table in wetland areas has the potential to degrade wetland persistence or function.

Minnesota↗

USGS2000

Environmental setting and its relations to water quality in the Kanawha River basin

The Kanawha River and its major tributary, the New River, drain 12,233 mi2 in West Virginia, Virginia, and North Carolina. Altitude ranges from about 550 ft to more than 4,700 ft. The Kanawha River Basin is mountainous, and includes parts of three physiographic provinces, the Blue Ridge (17 percent), Valley and Ridge (23 percent), and Appalachian Plateaus (60 percent). In the Appalachian Plateaus Province, little of the land is flat, and most of the flat land is in the flood plains and terraces of streams; this has caused most development in this part of the basin to be near streams. The Blue Ridge Province is composed of crystalline rocks, and the Valley and Ridge and Appalachian Plateaus Provinces contain both carbonate and clastic rocks. Annual precipitation ranges from about 36 in. to more than 60 in., and is orographically affected, both locally and regionally. Average annual air temperature ranges from about 43ºF to about 55ºF, and varies with altitude but not physiographic province. Precipitation is greatest in the summer and least in the winter, and has the least seasonal variation in the Blue Ridge Province. In 1990, the population of the basin was about 870,000, of whom about 25 percent lived in the Charleston, W. Va. metropolitan area. About 75 million tons of coal were mined in the Kanawha River Basin in 1998. This figure represents about 45 percent of the coal mined in West Virginia, and about seven percent of the coal mined in the United States. Dominant forest types in the basin are Northern Hardwood, Oak-Pine, and Mixed Mesophytic. Agricultural land use is more common in the Valley and Ridge and Blue Ridge Provinces than in the Appalachian Plateaus Province. Cattle are the principal agricultural products of the basin. Streams in the Blue Ridge Province and Allegheny Highlands have the most runoff in the basin, and streams in the Valley and Ridge Province and the southwestern Appalachian Plateaus have the least runoff. Streamflow is greatest in the spring and least in the autumn. About 61 percent of the basin's population use surface water from public supply for their domestic needs; about 30 percent use self-supplied ground water, and about nine percent use ground water from public supply. In 1995, total withdrawal of water in the basin was about 1,130 Mgal/d. Total consumptive use was about 118 Mgal/d. Surface water in the Blue Ridge Province is usually dilute (less than 100 mg/L dissolved solids) and well aerated. Dissolved- solids concentrations in streams of the Valley and Ridge Province at low flow are typically greater (150-180 mg/L) than those in the Blue Ridge Province. The Appalachian Plateaus Province contains streams with the most dilute (less than 30 mg/L dissolved solids) and least dilute (more than 500 mg/L dissolved solids) water in the basin. Coal mining has degraded more miles of streams in the basin than any other land use. Streams that receive coal-mine drainage may be affected by sedimentation, and typically contain high concentrations of sulfate, iron, and manganese. Other major water-quality issues include inadequate domestic sewage treatment, present and historic disposal of industrial wastes, and logging, which results in the addition of sediment, nutrients, and other constituents to the water. One hundred eighteen fish species are reported from the Kanawha River system downstream from Kanawha Falls. Of these, 15 are listed as possible, probable, or known introductions. None of these fish species is endemic to the Kanawha River Basin. The New River system has only 46 native fishes, the lowest ratio of native fishes to drainage area of any river system in the eastern United States, and the second-highest proportion of endemic fish species (eight of 46) of any river system in the eastern United States.

North Carolina, Virginia, West Virginia↗

USGS2006

Watershed characteristics and pre-restoration surface-water hydrology of Minebank Run, Baltimore County, Maryland, water years 2002-04

Stream restoration efforts have been ongoing in Maryland since the early 1990s. Physical stream restoration often involves replacement of lost sediments to elevate degraded streambeds, re-establishment of riffle-pool sequences along the channel profile, planting vegetation in riparian zones, and re-constructing channel banks, point bars, flood plains, and stream-meanders. The primary goal of many restoration efforts is to re-establish geomorphic stability of the stream channel and reduce erosive energy from urban runoff. Monitoring streams prior to and after restoration could help quantify other possible benefits of stream restoration, such as improved water quality and biota. This report presents general watershed characteristics associated with the Minebank Run watershed; a small, urban watershed in the south-central section of Baltimore County, Maryland that was physically restored in phases during 1999, 2004, and 2005. The physiography, geology, hydrology, land use, soils, and pre-restoration geomorphic setting of the unrestored stream channel are discussed. The report describes a reach of Minebank Run that was selected for the purpose of collecting several types of environmental data prior to restoration, including continuous-record and partial-record stage and streamflow data, precipitation, and ground-water levels. Examples of surface-water data that were collected in and near the study reach during water years 2002 through 2004, including continuous-record streamflow, partial-record stage and discharge, and precipitation, are described. These data were used in analyses of several characteristics of surface-water hydrology in the watershed, including (1) rainfall totals, storm duration, and intensity, (2) instantaneous peak discharge and daily mean discharge, (3) stage-discharge ratings, (4) hydraulic-geometry relations, (5) water-surface slope, (6) time of concentration, (7) flood frequency, (8) flood volume, and (9) rainfall-runoff relations. Several hydrologic characteristics that are typical of urban environments were quantified by these analyses. These include (1) large ratios of peak discharge to daily mean discharge as an indicator of flashiness, (2) consistent shifting of the stage-discharge rating over short periods of time that indicates instability of the stream channel, (3) analyses of hydraulic-geometry relations that indicate mean velocities of 11 feet per second or more while the flow is contained in the stream channel, (4) discharges that are 4 to 5 times larger in Minebank Run for corresponding flood frequency recurrence intervals than in Slade Run, which is a Piedmont watershed of similar size with smaller percentages of urban development, and (5) flood waves that can travel through the stream channel at a velocity of 412 feet per minute, or 6.9 feet per second.

Maryland↗

USGS2003

Environmental impacts of petroleum production--Initial results from the Osage-Skiatook Petroleum Environmental Research Sites, Osage County, Oklahoma

Exploration for and production of petroleum have caused major detrimental impacts to soils, surface and ground waters, and the local ecosystems in the United States. These impacts arise primarily from the improper disposal of large volumes of saline water produced with oil and gas, from accidental hydrocarbon and produced water releases, and from abandoned oil wells that were not correctly sealed. It is important to understand the long-term and short-term effects of produced water and hydrocarbon releases from these sites in order to develop risk-based remediation plans. Remediation is particularly needed in aging and depleted fields where land use is changing from petroleum production to residential, agricultural or recreational uses. About 20 scientists from the USGS and other governmental agencies and academia are involved in a multidisciplinary investigation to study the transport, fate, and natural attenuation of inorganic salts, trace metals, organic compounds and radionuclides present in produced water, and their impacts at the Osage-Skiatook Petroleum Environmental Research (OSPER) "A" and "B" sites, located on the Osage Reservation in Osage County, Oklahoma. Stakeholders in the project include the Osage Nation, which holds the mineral rights, the Bureau of Indian Affairs with trust responsibility, and the Army Corps of Engineers, which owns the surface rights at these sites and manages adjacent Skiatook Lake. The 4250-hectare Skiatook Lake provides drinking water to local Tulsa suburban communities and a rural water district, and offers recreational fishing and boating opportunities to tens of thousands of visitors each year. Approximately 1.5 and 1.0 hectare of land at the OSPER "A" (depleted Lester lease) and "B" (active Branstetter lease) sites, respectively, are affected by salt scarring, tree kills, soil salinization and brine and petroleum contamination due to the leakage of produced water and associated hydrocarbons from brine pits and accidental releases from active and inactive pipes and tank batteries. The leases are typical of many depleted and aging petroleum fields in Osage County, which ranks among the top oil and gas producing counties in Oklahoma with about 39,000 wells. Oil and gas production has occurred in Osage county for over one hundred years, but current production is mainly from stripper wells (averaging ~2.8 bbl/d oil and >30 bbl/d brine) that are shallow, mostly 300-700 m in depth, and produce from several sandstones of Pennsylvanian age. Results to date show that the produced water source is a Na-Ca-Cl brine (~150,000 mg/L total dissolved solids), with relatively high concentrations of Mg, Sr, and NH4, but low SO4 and H2S. With the exception of Fe and Mn, the concentrations of trace metals are low. Results also show that some and, eventually, the bulk, of inorganic salts and some dissolved organic species in the released brine from both sites will reach Skiatook Lake. Results at the "A" site show that the salts have essentially been removed from the sandy soil which formed in a surficial layer of eolian sand, but degraded and weathered oil persists on the surface of old oil and brine pits, close to sites of old tanks, on old channels that carried oil from tanks to the oil pits and other impacted areas. Results also show a plume of high salinity water (5,000-30,600 mg/L TDS) is present at intermediate depths that extend from below the old oil and brine pits to Skiatook Lake. No liquid petroleum was found in the contaminated groundwater, but soluble petroleum byproducts, including organic acid anions and other volatile organic compounds (VOCs) are present. Results to date clearly show that significant amounts of salts from produced-water releases and petroleum hydrocarbons still remain in the soils and rocks of the impacted area after more than 60 years of natural attenuation. At the "B" site significant amounts of produced water from the two active brine pits percolate into the surficial rocks and flow towards the Skiatook Reservoir; but only minor amounts of liquid petroleum leave the brine pits and reach the Skiatook Reservoir. At both sites, results show that the chemical composition of released brines is modified further by sorption, mineral precipitation/dissolution, transpiration, volatilization and bacterially mediated oxidation/reduction reactions.

Oklahoma↗

USGS2020

Temporal and spatial variability of water quality in the San Antonio segment of the Edwards aquifer recharge zone, Texas, with an emphasis on periods of groundwater recharge, September 2017–July 2019

Ongoing urbanization on the Edwards aquifer recharge zone in the greater San Antonio area raises concern about the potential adverse effects on the public water supply from development. To address this concern, the U.S. Geological Survey, in cooperation with the City of San Antonio, studied patterns of temporal and spatial changes in water quality at selected surface-water and groundwater sites in the Edwards aquifer recharge zone, with an emphasis on changes during periods of groundwater recharge. Water-quality characteristics were continuously monitored and discrete water samples were collected at two sets of paired surface-water (stream) and groundwater (well) sites during a 2-year period (2017–19) that included relatively dry conditions and a large recharge event in September 2018 when as much as 16 inches of rain fell in parts of the study area. Continuous monitoring of water-level altitude, specific conductance, and concentrations of nitrate in two wells completed in the Edwards aquifer provided high-resolution data showing detailed changes in water quality across a broad range of hydrologic conditions. Water levels in the wells responded rapidly (within hours to days) to recharge from both small and large rainfall and runoff events; changes in groundwater quality as a consequence of the influx of surface-derived recharge were indicated by changes in values of the monitored characteristics. A broad range in measured values of the stable isotopes of water expressed as delta deuterium and delta oxygen-18 in the water samples collected from two streams (Salado and West Elm Creeks), in comparison to the tight clustering of the values of these isotopes in groundwater samples, indicates that source waters (surface waters) of widely varying chemical characteristics become homogenized within the aquifer system. Concentrations of major ions, trace ions, and nutrient concentrations in stormwater runoff indicate a combination of land-derived and rainfall-derived constituents. The distribution of concentrations of nitrogen species (nitrite, nitrate, and nitrogen in ammonia) among sampling sites transitions from a more variable distribution in stormwater runoff to a more uniform distribution in groundwater in which the dominant form is nitrate. Differences in nitrate isotopic composition and concentration in groundwater across the study area are likely controlled by the relative contributions of natural and anthropogenic nitrogen (with the anthropogenic nitrogen component including a wastewater source) and by the process of nitrification. Among all measured constituents, pesticides detected in discrete stormwater-runoff samples provided the clearest indication that urbanization was adversely affecting water quality; specifically, the more urbanized surface-water site had a greater number of detections and greater variety of detected pesticides. Though temporal variability in the numbers and types of pesticides was evident, the overall proportion of pesticides was dominated by triazine herbicides including atrazine, atrazine degradates, and simazine. The observed hydrologic responses to rainfall and corresponding changes in water quality in wells are thought to result from the direct hydrologic connectivity of surface water and unconfined groundwater; however, patterns of groundwater-quality change indicate mixing from multiple sources such as ambient groundwater, recent surface-derived recharge, and possibly inflow from other aquifers. Therefore, understanding the connection between urbanization and groundwater quality cannot be inferred from the input of stormwater runoff alone as changes related to local and regional hydrologic conditions also need to be considered. It should be noted that a single study comparing the results from two site pairs is not able to support definitive conclusions about the full effect of urbanization on surface water/groundwater quality; however, this study does provide useful insights about the spatial and temporal variability of both stormwater runoff and unconfined groundwater that are consistent with expectations based on the current conceptual model that depicts the Edwards aquifer surface-water/groundwater system as a single water resource.

Texas↗

USGS2006

Water Quality, Hydrology, and Response to Changes in Phosphorus Loading of Nagawicka Lake, a Calcareous Lake in Waukesha County, Wisconsin

Nagawicka Lake is a 986-acre, usually mesotrophic, calcareous lake in southeastern Wisconsin. Because of concern over potential water-quality degradation of the lake associated with further development in its watershed, a study was conducted by the U.S. Geological Survey from 2002 to 2006 to describe the water quality and hydrology of the lake; quantify sources of phosphorus, including those associated with urban development; and determine the effects of past and future changes in phosphorus loading on the water quality of the lake. All major water and phosphorus sources were measured directly, and minor sources were estimated to construct detailed water and phosphorus budgets for the lake. The Bark River, near-lake surface inflow, precipitation, and ground water contributed 74, 8, 12, and 6 percent of the inflow, respectively. Water leaves the lake primarily through the Bark River outlet (88 percent) or by evaporation (11 percent). The water quality of Nagawicka Lake has improved dramatically since 1980 as a result of decreasing the historical loading of phosphorus to the lake. Total input of phosphorus to the lake was about 3,000 pounds in monitoring year (MY) 2003 and 6,700 pounds in MY 2004. The largest source of phosphorus entering the lake was the Bark River, which delivered about 56 percent of the total phosphorus input, compared with about 74 percent of the total water input. The next largest contributions were from the urbanized near-lake drainage area, which disproportionately accounted for 37 percent of the total phosphorus input but only about 5 percent of the total water input. Simulations with water-quality models within the Wisconsin Lakes Modeling Suite (WiLMS) indicated the response of Nagawicka Lake to 10 phosphorus-loading scenarios. These scenarios included historical (1970s) and current (base) years (MY 2003-04) for which lake water quality and loading were known, six scenarios with percentage increases or decreases in phosphorus loading from controllable sources relative to the base years 2003-04, and two scenarios corresponding to specific management actions. Because of the lake's calcareous character, the average simulated summer concentration of total phosphorus for Nagawicka Lake was about 2 times that measured in the lake. The models likely over-predict because they do not account for coprecipitation of phosphorus and dissolved organic matter with calcite, negligible release of phosphorus from the deep sediments, and external phosphorus loading with abnormally high amounts of nonavailable phosphorus. After adjusting the simulated results for the overestimation of the models, a 50-percent reduction in phosphorus loading resulted in an average predicted phosphorus concentration of 0.008 milligrams per liter (mg/L) (a decrease of 46 percent). With a 50-percent increase in phosphorus loading, the average predicted concentration was 0.020 mg/L (an increase of 45 percent). With the changes in land use under the assumed future full development conditions, the average summer total phosphorus concentration should remain similar to that measured in MY 2003-04 (approximately 0.014 mg/L). However, if stormwater and nonpoint controls are added to achieve a 50-percent reduction in loading from the urbanized near-lake drainage area, the average summer total phosphorus concentration should decrease from the present conditions (MY 2003-04) to 0.011 mg/L. Slightly more than a 25-percent reduction in phosphorus loading from that measured in MY 2003-04 would be required for the lake to be classified as oligotrophic.

Scientific Investigations Report↗

USGS2007

Nutrient and biological conditions of selected small streams in the Edwards Plateau, central Texas, 2005-06, and implications for development of nutrient criteria

During the summers of 2005 and 2006 the U.S. Geological Survey, in cooperation with the Texas Commission on Environmental Quality, evaluated nutrient and biological conditions in small streams in parts of the Edwards Plateau of Central Texas. Land-cover analysis was used to select 15 small streams that represented a gradient of conditions with the potential to affect nutrient concentrations across the study area, which comprises two of four subregions of the Edwards Plateau ecoregion. All 15 streams were sampled for water properties, nutrients, algae, benthic invertebrates, and fish in summer 2005, and eight streams were resampled in summer 2006. Streams that did not receive wastewater effluent had relatively low nutrient concentrations and were classified as oligotrophic; streams receiving wastewater effluent had relatively high nutrient concentrations and were classified as eutrophic. Nutrient concentrations measured in the least-disturbed streams closely matched the U.S. Environmental Protection Agency nutrient criteria recommendations based on estimated reference concentrations. Nitrogen/phosphorus ratios indicated streams not affected by wastewater effluent might be limited by phosphorus concentrations. Algal indicators of nutrient condition were closely related to dissolved nitrogen concentrations and streamflow conditions. Ambient dissolved nitrogen concentrations (nitrite plus nitrate) were positively correlated with benthic algal chlorophyll-a concentrations. The correlation of benthic algal chlorophyll-a with instantaneous nitrite plus nitrate load was stronger than correlations with ambient nutrients. Increased nutrient concentrations were associated with increased macroalgae cover, wider diel dissolved oxygen ranges, and reduced diel dissolved oxygen minimums. Benthic invertebrate aquatic life use scores generally were classified as High to Exceptional in study streams despite the influence of urbanization or wastewater effluent. Reductions in aquatic life use scores appeared to be related to extremely low flow conditions and the loss of riffle habitats. Benthic invertebrate aquatic life use scores and several of the metrics used to compute composite aquatic life use scores tended to increase with increasing total nitrogen concentrations. Fish community aquatic life use scores generally were classified as High or Exceptional with the exception of a few samples collected from streams receiving wastewater effluent that were classified as Intermediate. Fish community aquatic life use scores and several fish community metrics were positively correlated with nutrient concentrations and macroalgae cover. The majority of the positive correlations among nutrient concentrations, macroalgae cover, and fish metrics were strongly influenced by relatively high nutrient concentrations. Both benthic and planktonic chlorophyll-a measures were related to nutrients, but this study indicates that benthic chlorophyll-a was the better choice for monitoring nutrient enrichment because (1) the relation between benthic chlorophyll-a and nutrients was stronger, and (2) a strong relation between benthic chlorophyll-a and nutrients persisted after removal of the sites influenced by wastewater effluent, which indicates superior ability of benthic chlorophyll-a to discriminate between conditions at lower nutrient concentrations. The transect-based algal abundance estimate technique is a useful tool for identifying eutrophic conditions, assessing nuisance algal growth, and making broad comparisons among sites, but it appears to lack the fine resolution to identify lesser degrees of nutrient enrichment. Several individual benthic invertebrate and fish metrics were correlated with nutrient conditions, but correlations were generally positive and the reverse of what would be expected when nutrient enrichment causes a proliferation of algal growth and stream degradation. However, the benthic invertebrate functional feeding group metrics showed some

Scientific Investigations Report↗

USGS2018

Nearshore sediment monitoring for the Stormwater Action Monitoring (SAM) Program, Puget Sound, western Washington

Chemicals such as metals and organics (polychlorinated biphenyl [PCBs], polybrominated diphenyl ethers [PBDEs], polycyclic aromatic hydrocarbons [PAHs], and phthalates) continue to enter Puget Sound, western Washington, from point sources (such as industrial and municipal outfalls) and combined sewer outfalls and non-point sources (such as stormwater runoff). Runoff during storm events has been identified as a major source of contamination entering Puget Sound and has been implicated in the degradation of nearshore habitats and biota. Metals, organic chemicals, and other pollutants are known to accumulate in sediments such as those present along the shoreline of Puget Sound. In addition to chemical contaminants, small plastic particles (known as microplastics), found in marine waters of Puget Sound and suspected of being in aquatic sediments, are a potential concern because they can be ingested by animals and are suspected of transporting sorbed chemicals such as PCBs and metals. The Stormwater Work Group of Puget Sound (SWG) (composed of State and municipal stormwater permittees, and other stakeholders) developed a strategy to address sediment conditions in the nearshore environment of Puget Sound. As part of this strategy, the SWG developed a regional stormwater monitoring strategy designed to inform monitoring requirements in National Pollutant Discharge Elimination System (NPDES) stormwater permits issued by the Washington State Department of Ecology (Ecology). The monitoring program is referred to as the Stormwater Action Monitoring (SAM). The overall focus of the work described in this report is to address one of the goals of SAM, which is to characterize the status, spatial extent, and quality of Puget Sound sediment chemicals in the nearshore urban areas. The nearshore urban areas are defined as areas parallel to established Urban Growth Areas (UGAs) using a spatially balanced probabilistic Generalized Random Tessellation Stratified (GRTS) sampling design. One of the benefits of the GRTS sampling design used for this study is that it allows one to efficiently extrapolate from a relatively small number of sampled nearshore sites to the entire nearshore shoreline within the 2011 defined UGA boundaries of Puget Sound. In addition to characterizing nearshore sediment chemical concentrations, this study also characterized the abundance of microplastics in the nearshore sediment. A total of 41 randomly selected sites were sampled throughout Puget Sound in summer and early autumn of 2016. All sampling sites were located at 6 feet below the Mean Lower Low Water line. The top 2–3 centimeters of sediment were collected using a boat-mounted, pre-cleaned stainless-steel box corer. All chemical samples were sieved to 2 millimeters and placed in appropriate containers for chemical analysis for PCBs, PBDEs, PAHs, phthalates, metals, total organic carbon, and grain size. Pre-sieved sediment samples were stored in glass containers for microplastic analysis. Nearshore sediment chemical concentrations were summarized using numerous statistical approaches to examine the minimum, mean, and maximum concentrations for each of the compounds analyzed and to compare the results to criteria and other nearshore and marine sediment studies. The GRTS sampling design also allowed the authors to assess the percentage of the UGA nearshore environment that did not meet established standards or criteria for each chemical analyzed. Additionally, regression and machine learning statistical analyses were used to examine relations between measured chemical concentrations, and land cover and geologic features at multiple scales within the watersheds adjacent to sampling sites. The influence of marine hydrodynamic factors on nearshore sediment chemical concentrations was statistically evaluated with nonparametric methods by assigning each sampling site to one of five nearshore drift cell types based on its location. The Puget Sound shoreline can be divided into segments, referred to as drift cells, based on the movement of sediment along the shore by waves. Each drift cell type has a unique influence on nearshore sediment transport. The nearshore sediment chemical concentrations for organics and metals generally were low, and in most cases less than Washington State criteria. The concentrations of some PAHs were greater than the criteria, but these exceedances were limited to one or two sites. The results of the probabilistic study design determined that, for the PAHs examined, 96 percent or more of the 1,344 km of shoreline represented by this study had concentrations less than any established criteria. For the remaining organics (PCBs and PBDEs), the probabilistic study design indicates that more than 98 percent of shoreline examined had concentrations less than criteria or proposed standards. For the metals, the results of the study indicate that 100 percent of the nearshore sediment had concentrations less than the criteria. The relations between sediment organic and metal concentrations, and adjacent watershed land cover and the particle size of the samples, were determined to be weakly related. Although weakly related, the particle size of the sediment in a sample typically explained more of the variation in metal concentrations than organics. While the measured watershed attributes adjacent to the sampling sites and sediment size of the samples were weakly related to chemical concentrations, they were significantly related to unique drift cells along the shoreline of Puget Sound known as drift cells. Each drift cell represents a long-term directional transport of sediment from its source to its depositional zone. Sediment chemical concentrations were significantly higher in drift cells with limited sediment movement compared to those with higher sediment transport energy. Microplastics in the nearshore sediment ranged from 0.02 to 0.65 pieces per gram of sediment, with a mean of 0.19 pieces per gram of sediment, and were dominated by small fibers (355–1,000 micrometers). Like chemical concentrations, microplastics concentrations in the nearshore sediment were poorly related to watershed land cover. Although not significantly different, microplastics concentrations generally were higher in the low energy drift cells compared to the high energy drift cells. The results of this study provide a statistically valid status assessment of current nearshore sediment chemical conditions throughout Puget Sound in those areas adjacent to defined UGAs. In addition to the study findings of relatively low concentrations of PCBs, PBDEs, PAHs, phthalates, and metals, the study design provides a statistically valid tool for evaluating changes in these compounds over time if future nearshore sediment assessments are done. Furthermore, the assessment of microplastic abundance represents the first study of its kind that can be used as a benchmark for future evaluations. The results of this study will help inform Ecology in the implementation of monitoring requirements as part of its NPDES stormwater permitting process.

Washington↗

USGS1999

Hydrogeologic framework and sampling design for an assessment of agricultural pesticides in ground water in Pennsylvania

State agencies responsible for regulating pesticides are required by the U.S. Environmental Protection Agency to develop state management plans for specific pesticides. A key part of these management plans includes assessing the potential for contamination of ground water by pesticides throughout the state. As an example of how a statewide assessment could be implemented, a plan is presented for the Commonwealth of Pennsylvania to illustrate how a hydrogeologic framework can be used as a basis for sampling areas within a state with the highest likelihood of having elevated pesticide concentrations in ground water. The framework was created by subdividing the state into 20 areas on the basis of physiography and aquifer type. Each of these 20 hydrogeologic settings is relatively homogeneous with respect to aquifer susceptibility and pesticide use—factors that would be likely to affect pesticide concentrations in ground water. Existing data on atrazine occurrence in ground water was analyzed to determine (1) which areas of the state already have sufficient samples collected to make statistical comparisons among hydrogeologic settings, and (2) the effect of factors such as land use and aquifer characteristics on pesticide occurrence. The theoretical vulnerability and the results of the data analysis were used to rank each of the 20 hydrogeologic settings on the basis of vulnerability of ground water to contamination by pesticides. Example sampling plans are presented for nine of the hydrogeologic settings that lack sufficient data to assess vulnerability to contamination. Of the highest priority areas of the state, two out of four have been adequately sampled, one of the three areas of moderate to high priority has been adequately sampled, four of the nine areas of moderate to low priority have been adequately sampled, and none of the three low priority areas have been sampled. Sampling to date has shown that, even in the most vulnerable hydrogeologic settings, pesticide concentrations in ground water rarely exceed U.S. Environmental Protection Agency Drinking Water Standards or Health Advisory Levels. Analyses of samples from 1,159 private water supplies reveal only 3 sites for which samples with concentrations of pesticides exceeded drinking-water standards. In most cases, samples with elevated concentrations could be traced to point sources at pesticide loading or mixing areas. These analyses included data from some of the most vulnerable areas of the state, indicating that it is highly unlikely that pesticide concentrations in water from wells in other areas of the state would exceed the drinking-water standards unless a point source of contamination were present. Analysis of existing data showed that water from wells in areas of the state underlain by carbonate (limestone and dolomite) bedrock, which commonly have a high percentage of corn production, was much more likely to have pesticides detected. Application of pesticides to the land surface generally has not caused concentrations of the five state priority pesticides in ground water to exceed health standards; however, this study has not evaluated the potential human health effects of mixtures of pesticides or pesticide degradation products in drinking water. This study also has not determined whether concentrations in ground water are stable, increasing, or decreasing.

Water-Resources Investigations Report↗

USGS2008

Nutrient Concentrations and Their Relations to the Biotic Integrity of Nonwadeable Rivers in Wisconsin

Excessive nutrient [phosphorus (P) and nitrogen (N)] input from point and nonpoint sources is frequently associated with degraded water quality in streams and rivers. Point-source discharges of nutrients are fairly constant and are controlled by the U.S. Environmental Protection Agency's (USEPA) National Pollutant Discharge Elimination System. To reduce inputs from nonpoint sources, agricultural performance standards and regulations for croplands and livestock operations are being proposed by various States. In addition, the USEPA is establishing regionally based nutrient criteria that can be refined by each State to determine whether actions are needed to improve water quality. More confidence in the environmental benefits of the proposed performance standards and nutrient criteria would be possible with improved understanding of the biotic responses to a range of nutrient concentrations in different environmental settings. To achieve this general goal, the U.S. Geological Survey and the Wisconsin Department of Natural Resources collected data from 282 streams and rivers throughout Wisconsin during 2001 through 2003 to: (1) describe how nutrient concentrations and biotic-community structure differ throughout the State, (2) determine which environmental characteristics are most strongly related to the distribution of nutrient concentrations and biotic-community structure, (3) determine reference conditions for water quality and biotic indices for streams and rivers in the State, (4) determine how the biotic communities in streams and rivers in different areas of the State respond to differences in nutrient concentrations, (5) determine the best regionalization scheme to describe the patterns in reference conditions and the corresponding responses in water quality and the biotic communities (primarily for smaller streams), and (6) develop algorithms to estimate nutrient concentrations in streams and rivers from a combination of biotic indices. The ultimate goal of this study is to provide the information needed to guide the development of regionally based nutrient criteria for Wisconsin streams and rivers. In this report, data collected, primarily in 2003, from 42 nonwadeable rivers are used to describe nutrient concentrations and their relations to the biotic integrity of rivers in Wisconsin. In a separate report by Robertson and others (2006a), the data collected from 240 wadeable streams are used to describe these relations in streams in Wisconsin. Reference water-quality conditions for nonwadeable rivers were found to be similar throughout Wisconsin (approximately 0.035 milligrams per liter (mg/L) for total P (TP), 0.500 mg/L for total N (TN), 4 micrograms per liter for suspended chlorophyll a (SCHL), and greater than 110 centimeters for Secchi-tube depth (SD)). For each category of the biotic community (SCHL, macroinvertebrates, and fish), a few indices were more strongly related to differences in nutrient concentrations than were others. For the indices most strongly related to nutrient concentrations, reference conditions were obtained with a regression approach, from values corresponding to the worst 75th-percentile value from a subset of minimally impacted streams (streams having reference nutrient concentrations), and from the best 25th-percentile value of all the data. Concentrations of TP and TN in nonwadeable rivers increased as the percentage of agricultural land in the basin increased; these increases resulted in increased SCHL concentrations and decreased SDs. The responses in SDs and SCHL concentrations to changes in nutrient concentrations were similar throughout most of the State except in rivers in the southeastern part, where SCHL concentrations were lower than would be expected given their nutrient concentrations. Rivers in the southeastern part of the State had high concentrations of total suspended sediment compared to the SCHL concentrations. Many biotic indices responded to increases in nu

Professional Paper↗

USGS2022

Sources and characteristics of dissolved organic carbon in the McKenzie River, Oregon, related to the formation of disinfection by-products in treated drinking water

Executive Summary This study characterized the concentration and quality of dissolved organic carbon (DOC) in the McKenzie River, a relatively undeveloped watershed in western Oregon, and its link to forming disinfection by-products (DBPs) in treated drinking water. The study aimed to identify the primary source(s) of DOC in source water for the Eugene Water & Electric Board’s (EWEB) conventional treatment plant on the McKenzie River near river mile 11, upstream of Hayden Bridge. The two classes of regulated compounds examined—trihalomethanes (THMs) and haloacetic acids (HAAs)—form when organic carbon in raw source water reacts with chlorine and (or) bromine during water treatment. The objectives of the study were to: characterize the amount and quality of DOC in the McKenzie River and select tributaries during storms; identify the most common types of carbon using UV-vis spectroscopy and other methods; evaluate optical properties for predicting DBP precursors in surface water; and identify land cover classes or vegetation types that may be important sources of organic carbon and DBP precursors in EWEB’s source water. Eleven storms were sampled synoptically in upstream-to-downstream fashion to provide a “snapshot” of water quality conditions at four sites on the McKenzie River from Frissell Bridge (6 miles downstream from Trail Bridge Reservoir) to the EWEB water treatment plant at Hayden Bridge and nine contributing tributaries. Storms included late summer and early autumn “first flush” events and late autumn, winter, and spring storms spanning a range in streamflows from 3,000 to 26,000 cubic feet per second as measured in the main stem McKenzie River at the EWEB water intake. Water samples were analyzed for DOC concentrations and optical properties (fluorescence and ultraviolet absorbance [UVA]) across a range of wavelengths to characterize the quantity and quality of dissolved organic matter (DOM) in the McKenzie River at the drinking water intake and upstream locations. Paired sets of source and finished water samples were collected at the EWEB treatment plant to identify DOC quality parameters in raw source water that might predict DBP concentrations in finished drinking water. DOC concentrations were relatively low in the McKenzie River (0.4–3 milligrams per liter [mg/L]; average 1.5 mg/L) but much higher in the tributaries. The highest DOC concentrations occurred during “first flush” storms in October 2012 and September 2013; the highest value (16 mg/L) was measured at the 52nd Street stormwater outfall. The average DOC concentration in the lower basin-tributaries was 3.8 mg/L; three middle basin tributaries—Quartz, Gate, and Haagen Creeks, which drain private forestland with less coniferous forest compared with other higher elevation tributaries— had slightly lower average DOC concentrations (2.8 mg/L). These middle-basin watersheds may be important sources of DOC and DBP precursors to the McKenzie River, even more so than the lower basin tributaries, depending on their flows (and loads). This is particularly true after the September 2020 Holiday Farm fire, which burned much of this area. DOC concentrations increased 68 percent in the McKenzie River between the uppermost reference site at Frissell Bridge and Vida; this includes drainage from Quartz Creek, Blue River Lake and Cougar Reservoir, which all contributed DOC to the main stem. In contrast, the lowermost tributaries draining most of the agricultural and urban land did not have a large effect on DOC in the McKenzie River despite their higher DOC concentrations because of their presumed relatively low streamflows and, consequently, DOC loads. Apart from the continuous flow monitors in the McKenzie River and some tributaries (Blue River and South Fork McKenzie River, and streamflow at Hayden Bridge and Vida, Camp Creek and some other locations), streamflow was not assessed during sample collection for this study. This lack of streamflow data precludes a detailed analysis of loads, which is discussed in the future studies section. All DBP concentrations in finished drinking water were less than EPA maximum contaminant levels (MCLs) of 0.080 mg/L for the four trihalomethanes (THM4) and 0.060 mg/L for five haloacetic acids (HAA5). During the 11 storm sampling events the maximum summed concentrations were about 0.040 mg/L for both THM4 and HAA5. Compliance monitoring samples, collected separately by EWEB, yielded some higher concentrations—0.046 mg/L THM4 and 0.047 HAA5—during the December 2012 storm. The corresponding benchmark quotient (BQ) values, which indicate how close a measured DBP concentration is to the MCL, were 0.58 and 0.78, respectively, for THM4 and HAA5. Compared with a similar 2007–08 McKenzie River study that did not target storm events, concentrations of THM4 and HAA5 in finished water were 68 percent and 33 percent higher, respectively, during the current study. Due to the high dilution rates in the McKenzie River main stem, many of the individual fluorescence excitation-emission measurements were low (<0.1 Raman units) and approached analytical detection limits. Parallel factor analysis (PARAFAC) resulted in a five-component model (C1–C5) that represents five unique organic fluorophores. Components C1, C2, and C3 represent DOM associated with soil-derived, humic-like, more degraded organic matter. In contrast, components C4 and C5 represent “fresher” DOM, derived from terrestrial and aquatic plants, including algae and cyanobacteria that are common in the McKenzie River and its tributaries and reservoirs. The fluorescence data and PARAFAC modeling suggest that most of the DOC in the McKenzie River originated from terrestrial sources (primarily components C1 and C2). The largest increases in DOC in the main stem occurred in the reach upstream of Vida, from inflows by Quartz Creek, Blue River, South Fork McKenzie River, and other tributaries. Concentrations of DBPs in EWEB’s finished drinking water were positively correlated with DOC concentrations in raw source water (THM4, p <0.05; HAA5, p <0.01) for paired samples collected 12−24 hours apart. DOC concentrations were significantly positively correlated ( p <0.001) with laboratory-based fluorescent dissolved organic matter (fDOM) measurements, suggesting fDOM as a useful parameter for monitoring and predicting DOC concentration in surface water and DBP concentrations in finished water. Of all the PARAFAC components in surface water, C5 had the highest correlations with DBPs in finished water (rho = 0.77–0.84, p <0.01), followed by components C1 and C2 (rho = 0.75 and 0.71, respectively, p <0.01). This C5 carbon is associated with recently produced DOM, possibly from decomposed terrestrial and aquatic vegetation. Model loadings of these three components were considerably higher in the sampled tributaries relative to the main stem McKenzie River, with most of the observed increases in the main stem apparent at Vida. This points to Quartz Creek or other tributaries in the reach between Frissell Bridge and the sampling site near Vida (South Fork McKenzie and Blue Rivers) as potentially key contributors of DOM source material that leads to the production of DBPs in treated drinking water. A limited load analysis showed that the reservoirs contributed 8–37 percent of the instantaneous DOC loads observed at Vida at the time of sampling, which suggests other sources such as Quartz Creek and other streams in the reach between Frissell Bridge and Vida are more important. Random forest analyses identified PARAFAC components C1 and C5 and fluorescence peaks A, C, M, T and N as the best predictors for HAA5 concentrations in finished drinking water, explaining 62.5 percent of the variation. The best predictors for THM4 were C1, C4 + C5, and peaks T, A, and N, which explained 33 percent of the variation. Several land cover and vegetation classes were correlated with DOC concentration and other optical measurements. The percentage of evergreen forest in each of the subwatersheds sampled was negatively correlated ( p <0.001) with DOC concentration and many optical indicators of DOM quantity: UVA 254 , fDOM, and all of the fluorescence peaks. In contrast, mixed (deciduous) forest was positively correlated ( p <0.001) with DOC, fDOM, UVA 254 , and several fluorescence peaks, demonstrating the importance of deciduous leaf fall in generating DOC and DBP precursors. The high level of human activities in the middle and lower portion of the basin—including timber harvesting and road construction on private forestland, agricultural, rural, industrial, and urban development—have resulted in the greatest loss in native coniferous and mixed deciduous forests in the basin. DOC loading from these tributaries and reservoir releases, which contain DOC from terrestrial and aquatic productivity, both enrich the McKenzie River. Concentrations of DOC increased an average of 71 percent (range 30–120 percent) in the McKenzie River between Frissell Bridge, the upstream reference site, and Vida. PARAFAC components C1, C2, and C5—which were correlated with DBPs in finished water—increased, on average, 109–136 percent (range 20–250 percent) in this same Frissell-to-Vida reach. These increases occur from input of tributaries in the middle basin such as Quartz Creek and others, as noted above. Future monitoring, field, and lab studies can improve our understanding of seasonal and spatial sources of organic carbon contributing DBP precursors to the McKenzie River and allow detection of long-term trends resulting from the recent Holiday Farm Fire, which burned 173,393 acres of forestland, including riparian areas along the main stem, and numerous structures, homes, and outbuildings in September 2020. Future studies could examine DOC fluxes and flushing of carbon from the watershed, investigate the role of precipitation amount and intensity in mobilizing carbon and sediment, and evaluate impacts to aquatic communities and human health as part of a post-fire assessment. Other areas ripe for study include evaluating the impacts of potential temperature increases on carbon sequestration and decomposition in the burned and unburned forests and identifying practices that foster sequestration of carbon in forest soils. The use of fluorescence sensors such as fDOM to monitor the concentration and composition of raw water supplies may be improved for detection of specific DBP precursors, to provide continuous and real-time information to treatment plant operators. Future studies that monitor DOM amount and quality, and DBP Formation Potential (FP), particularly during storm events, paired with streamflow measurements, as suggested above, could help identify areas that contribute high DOC loads and thus help managers identify the key areas to focus restoration activities. Other studies could examine treatment options for currently regulated DBPs and potentially unregulated compounds, including advanced biological treatments for their removal. This study was a collaboration between the U.S. Geological Survey (USGS) and EWEB in Eugene, Oregon, with additional funding provided from USGS Cooperative Matching Funds Program.

Oregon↗

USGS2004

Water and Streambed Sediment Quality, and Ecotoxicology of a Stream along the Blue Ridge Parkway, Adjacent to a Closed Landfill, near Roanoke, Virginia: 1999

A study was done of the effects of a closed landfill on the quality of water and streambed sediment and the benthic macroinvertebrate community of an unnamed stream and its tributary that flow through Blue Ridge Parkway lands in west-central Virginia. The primary water source for the tributary is a 4-inch polyvinyl chloride (PVC) pipe that protrudes from the slope at the base of the embankment bordering the landfill. An unusual expanse of precipitate was observed in the stream near the PVC pipe. Stream discharge was measured and water and streambed sediment samples were collected at a nearby reference site and at three sites downstream of the landfill in April and September 1999. Water samples were analyzed for major ions, nitrate, total and dissolved metals, total dissolved solids, total organic carbon, and volatile and semivolatile organic compounds, including organochlorine pesticides and polychlorinated biphenyls (PCBs). Streambed sediment samples were analyzed for total metals, total organic carbon, percent moisture, and volatile and semivolatile organic compounds, including organochlorine pesticides and PCBs. The benthic macroinvertebrate community within the stream channel also was sampled at the four chemical sampling sites and at one additional site in April and September. Each of the five sites was assessed for physical habitat quality. Water collected periodically at the PVC pipe discharge between November 1998 and November 1999 was used to conduct 48-hour acute and 7-day chronic toxicity tests using selected laboratory test organisms. Two 10-day chronic toxicity tests of streambed sediments collected near the discharge pipe also were conducted. Analyses showed that organic and inorganic constituents in water from beneath the landfill were discharged into the sampled tributary. In April, 79 percent of inorganic constituents detected in water had their highest concentrations at the site closest to the landfill; at the same site, 59 percent of inorganic constituents detected in streambed sediments were at their lowest concentration. The low dissolved-oxygen concentration and relatively low pH in ground water from beneath the landfill probably had a direct effect on the solubility of metals and other constituents, resulting in the high concentration of inorganic constituents in water, low concentration in sediment, and the development of the precipitate. Most constituents in water in April were progressively lower in concentration from the landfill site downstream. The highest concentrations for 59 percent of constituents detected in sediment were at the farthest downstream site, suggesting that the inorganic constituents came out of solution as the stream water was exposed to the atmosphere. In September, 52 percent of inorganic constituents detected in water were at their highest concentrations at the site nearest the landfill. Of inorganic constituents detected in streambed sediments in September, 60 percent were at their highest concentrations near the landfill. A storm that occurred a few days prior to the September sampling probably affected the preceding steady-state conditions and the distribution of constituents in sediment along the stream. Concentrations of many inorganic constituents in water remained elevated at the farthest downstream site in comparison to the reference site in April and September, indicating that concentrations did not return to background concentrations. In April and September, most of the 17 organic compounds detected in water, including volatile organic and semivolatile organic compounds, were collected in samples near the landfill, and most concentrations were below their respective reporting limits. Probably because of their volatility, few organic compounds were detected at sites downstream of that site. A total of 17 discrete organic compounds were detected in sediment samples in either April or September, including trichloroethene and tetrachloroethene along with their degrad

Water-Resources Investigations Report↗

USGS2018

Drain tiles and groundwater resources: Understanding the relations

Executive Summary Drainage for agricultural production over the past 150 years has been an integral component of human-driven change to Minnesota’s rural landscapes. Benefits of drainage Historically, poorly drained soils across much of the State would often remain saturated or flooded after spring snowmelt, preventing timely farm operations such as tilling and planting crops (Arneman, 1963). Installation of agricultural drainage, both surface ditches and subsurface drainage, accelerated transport of water off farm fields and imparted producers higher crop yields (Beauchamp, 1987; Stoner and others, 1993). Agricultural drainage offered many other benefits such as preventing crop drown out, aerating the soil profile for improved plant growth, limiting surface runoff and soil erosion, and allowing farmers better access to croplands (Fausey and others, 1987). Without agricultural drainage on much of Minnesota’s croplands, it would have been difficult to realize high enough crop yields to remain economically viable. Environmental concerns While drainage of Minnesota croplands provided the benefits mentioned above, several environmental concerns result. These include wetland loss, degradation of downstream water quality, and reduced [potential for] recharge. Early agricultural drainage efforts (pre-20th century) led to the disappearance of much of Minnesota’s natural wetlands. Increased focus on preventing or mitigating wetland loss over the last 50 years has helped curtail further losses, even as agricultural drainage proceeds. Prior to establishment of Minnesota statehood, wetlands accounted for more than 10 million acres in Minnesota, including prairie wetlands, peatlands, and forest wetlands that comprised approximately 19 percent of the total land area (Palmer, 1915; King, 1980). In 2018, only half of Minnesota’s pre-settlement wetlands remain, mostly in parts of the State that have not experienced widespread drainage, such as northern Minnesota. Water-quality monitoring has shown that agricultural drainage, in particular the practice of subsurface drainage, provides a direct flow path for nutrient (nitrogen and soluble phosphorus) losses to surface water resources. The negative consequences of agricultural drainage on surface water quality are well documented (for example, Dinnes and others, 2002; Kladivko and others, 2004; Richards and others, 2008; Rozemeijer and others, 2010; Schottler and others, 2013). Agricultural basins with a high percentage of agricultural drainage have been implicated as part of the cause of the Gulf of Mexico hypoxia zone due to excessive nitrogen export (Goolsby and Battaglin, 2001; Randall and Mulla, 2001). The connection of hydrological effects of agricultural subsurface drainage on groundwater recharge and aquifers, on the other hand, has not been well-established. Agricultural subsurface drainage intercepts infiltrating water below croplands and directly discharges the water to nearby surface waters. However, the size of the water balance shift from drained water that would have evapotranspired or run off the land to drained water that would recharge underlying aquifers has been poorly characterized (Schuh, 2008). Drain Tiles and Groundwater Given the poor accounting of subsurface drainage effects on groundwater resources, the Minnesota Ground Water Association (MGWA) deemed it imperative that we document these effects so that groundwater resources in agricultural regions with substantial drainage can be effectively managed. This white paper documents the relations of drain tiles and groundwater resources and discusses the historical significance of agricultural drainage practices, the recognized positive benefits and potential negative consequences of agricultural drainage practices, and the gaps in understanding of the connections between agricultural drainage and groundwater resources. The major messages emerged from the findings of this white paper are: Complex history. Minnesota has a long history of agricultural drainage, spanning over 150 years. Agricultural drainage, and the eventual widespread usage of subsurface drainage, can be separated into at least four distinct periods of time: (a) early drainage to get water off the land, pre-20th century; (b) the boom and bust era (1900-1945); (c) postwar resurgence of subsurface drainage and early conservation efforts (1945-1960); and, (d) emergence of the environmental movement (1960 to present). The State’s regulatory framework that both allowed for drainage and controlled its usage during these periods is complicated and has been governed by a patchwork of both State and Federal statutes. Drainage Provinces. This white paper advances the concept of tile drainage provinces to aid in the discussion of regional differences in subsurface drainage and its overall effect on groundwater resources. Built upon the concept of groundwater provinces (Minnesota Department of Natural Resources, 2001), three distinct tile drainage provinces were conceptualized: (1) the Southeastern Province; (2) the SouthCentral Province; and, (3) the Western Province. The distinct geology and the soils that developed in these regions have implications for each region’s subsurface drainage density and the potential implications for groundwater. Knowledge gaps. Several critical knowledge gaps are identified in this paper, creating opportunities for further research to improve our understanding for better managed water resources: Extent of drainage is unknown. Direct estimates of the extent of subsurface drainage do not exist in Minnesota. However, several indirect methods have been utilized to estimate subsurface drainage, from the field-scale to countylevel through the use of geographic information system (GIS) analysis and aerial photography. Based on a 2012 U.S. Geological Survey estimate of subsurface drainage extent (Nakagaki and Wieczorek, 2016), about 21% of the land area in Minnesota has some density of subsurface drainage. Effect of drainage on underlying aquifers is unknown. A basic understanding of unconfined and confined aquifers and their recharge is necessary to connect any hydrological effects from agricultural drainage to groundwater. The basic goal of subsurface drainage to efficiently drain saturated soils clearly alters the water balance in croplands. However, its overall effect on groundwater resources has been poorly characterized, and is in large part determined by the geology below drained areas and the arrangement of underlying aquifers. Water balance shifts. An improved understanding of historical water balance shifts from pre- to post-drainage periods is necessary to understand long-term implications on net groundwater recharge. Also, more direct field-scale studies and indirect modeling studies are needed to characterize water budgets for fields with subsurface drainage.

Minnesota↗

USGS1995

Water-quality characteristics of five tributaries to the Chesapeake Bay at the Fall Line, Virginia, July 1988 through June 1993

Development in the Chesapeake Bay region has adversely affected the water quality of the Bay. The general degradation in the Bay has resulted in the decline of commercial fishing industries and has reduced the area of aquatic vegetation that provides food and habitat for fish and shellfish. In order to assess the effectiveness of programs aimed at reducing the effects of excess nutrients and suspended solids on Chesapeake Bay, it is necessary to quantify the loads of these constituents into the Bay, and to evaluate the trends in water quality. This report presents the results of a study funded by the Virginia Department of Environmental Quality Chesapeake Bay and Coastal Programs and the U.S. Geological Survey, to monitor and estimate loads of selected nutrients and suspended solids discharged to Chesapeake Bay from five major tributaries in Virginia. The water-quality data and load estimates provided in this report also will be used to calibrate computer models of Chesapeake Bay. Water-quality constituents were monitored in the James and Rappahannock Rivers over a 5-year period, and in the Pamunkey, Appomattox, and Mattaponi Rivers over a 4-year period. Water-quality samples were collected from July 1, 1988 through June 30, 1993, for the James and Rappahannock Rivers; from July 1, 1989 through June 30, 1993, for the Pamunkey and Appomattox Rivers; and from September 1,1989 through June 30, 1993, for the Mattaponi River. Water-quality samples were collected on a scheduled basis and during stormflow to cover a range in discharge conditions. Monitore water-quality constituents, for which loads were estimated include total suspended solids (residue, total at 105° Celsius), dissolved nitrite-plus-nitrate nitrogen, dissolved ammonia nitrogen, total Kjeldahl nitrogen, total nitrogen, total phosphorus, dissolved orthophosphorus, total organic carbon, and dissolved silica. Organic nitrogen concentrations were calculated from measurements of ammonia and total Kjeldahl nitrogen, and organic nitrogen loads were estimated using these calculations. Other selected water-quality constituents were monitored for which loads were not calculated. Daily mean load estimates of each constituent were computed by use of a seven-parameter log-linear regression model that uses variables of time, discharge, and seasonality. Concentration of total nitrogen ranged from less than 0.14 to 3.41 mg/L (milligrams per liter), with both extreme values occurring at the Rappahannock River. Concentration of total Kjeldahl nitrogen ranged from less than 0.1 mg/L in the James, Rappahannock, and Appomattox Rivers to 3.0 mg/L in the James River. Organic nitrogen was the predominant form of nitrogen at all stations except the Rappahannock River, where nitrite plus-nitrate nitrogen was predominant, and organic nitrogen comprised the majority of the measured total Kjeldahl nitrogen at all stations, ranging from 0.01 mg/L in the Appomattox River to 2.86 mg/L in the James River. Concentration of dissolved ammonia nitrogen ranged from 0.01 mg/L in the Pamunkey River to 0.54 mg/L at the James River. Concentration of nitrite-plusnitrate nitrogen ranged from 0.02 to 1.05 mg/L in the James River. Concentrations of total phosphorus ranged from less than 0.01 mg/L in the Rappahannock and the Mattaponi Rivers to 1.4 mg/L in the James River. Dissolved orthophosphorus ranged from less than 0.01 mg/L in all five rivers to 0.51 mg/L in the James River. Total suspended solids ranged from a concentration of less than 1 mg/L in all five rivers to 844 mg/L in the Rappahannock River. Total organic carbon ranged from 1.1 mg/L in the Appomattox River to 110 mg/L in the Rappahannock River. Dissolved silica ranged from 2.4 mg/L in the James River to 18 mg/L in the Appomattox River. The James and Rappahannock Rivers had high median concentrations and large ranges in concentrations for most constituents, probably because of a greater number of point and nonpoint sources of nutrients and suspended solids, and differences in land use when compared with the other basins. A significantly higher median concentration and greater range of dissolved orthophosphorus generally occurred at the James River than in all other rivers, which primarily is due to the greater number of point sources, such as municipal waste-water treatment plants. The Rappahannock River had significantly higher median concentrations and greater ranges of dissolved nitrite-plus-nitrate nitrogen and total nitrogen than other rivers, probably derived from agricultural sources. Total organic carbon was highest in the Mattaponi and Pamunkey River Basins that contain expanses of wetlands. The Appomattox River had the highest concentration of dissolved silica. The median monthly load of total nitrogen ranged from 16,500 kg (kilogram) in the Mattaponi River to 371,000 kg in the James River. Total Kjeldahl nitrogen ranged from a median monthly load of 12,500 kg in the Mattaponi River to 205,500 kg, also in the James River. Organic nitrogen comprised the majority of the total Kjeldahl nitrogen load in all five rivers, ranging from a median monthly load of 11,251 kg in the Mattaponi River to 3,299,500 kg in the James River. The median monthly load of dissolved ammonia nitrogen was 1,130 kg in the Mattaponi River and was as much as 21,050 kg in the James River, whereas nitrite-plus-nitrate nitrogen ranged from a median monthly load of 4,065 kg in the Mattaponi River to 156,500 kg in the James River. The median monthly load of total phosphorus ranged from 1,670 kg in the Mattaponi River to 61,600 kg in the James River, whereas the median monthly load of dissolved orthophosphorus ranged from 350 kg in the Mattaponi River to 25,900 kg in the James River. Total suspended solids ranged from a median monthly load of 241,500 kg in the Mattaponi River to 20,050,000 kg in the James River. Total organic carbon ranged from a median monthly load of 167,000 kg in the Mattaponi River to 2,100,000 kg in the James River. The median monthly load of dissolved silica ranged from 209,500 kg in the Mattaponi River to 3,625,000 kg in the James River. In general, annual loads for complete years of data collection were greatest at the James River for all constituents, probably because of the much higher discharge, greater basin size, and higher rates of runoff. Yields, or computations of loads per square mile of basin area, were generally highest at the Rappahannock River for total suspended solids, total Kjeldahl nitrogen, nitrite-plusnitrate nitrogen, and total nitrogen. Dissolved orthophosphorus was the only constituent with a yield consistently greater at the James River. Yields of total phosphorus were highest for the James and Rappahannock River basins, whereas yields of dissolved ammonia nitrogen, total organic carbon, and dissolved silica were similar for all five river basins. Quality-assurance analyses that compare the results of the Virginia Division of Consolidated Laboratory Services and the U.S. Geological Survey Laboratory indicate that there are statistically significant differences between the laboratories for several constituents. Differences between laboratories were found to be caused by differences in analytical reporting limits, differences in analytical technique, or a slight bias at both laboratories. Quality-assurance data were used to address analytical technique problems, and to qualify final concentrations and loads.

Virginia↗

USGS2000

Effects of a Cattail Wetland on Water Quality of Irondequoit Creek near Rochester, New York

A 6-year (1990-96) study of the Ellison Park wetland, a 423-acre, predominantly cattail ( Typha glauca ) marsh in Monroe County, N.Y., was conducted to document the effect that this wetland has on the water quality of Irondequoit Creek, which flows through it. Irondequoit Creek drains 151 square miles of mostly urban and suburban land and is the main tributary to Irondequoit Bay on Lake Ontario. The wetland was a sink for total phosphorus and total suspended solids (28 and 47 percent removal efficiencies, respectively, over the 6-year study period). Sedimentation and vegetative filtration appear to be the primary mechanisms for the decrease in loads of these constituents. Total nitrogen loads were decreased slightly by the wetland; removal efficiencies for ammonia-plus-organic nitrogen and nitrate-plus-nitrite were 6 and 3 percent, respectively. The proportions of total phosphorus and total nitrogen constituents were altered by the wetland. Orthophosphate and ammonia nitrogen were generated within the wetland and represented 12 percent of the total phosphorus output load and 1.8 percent of total nitrogen output load, respectively. Conservative chemicals, such as chloride and sulfate, were littleaffected by the wetland. Concentrations of zinc, lead, and cadmium showed statistically significant decreases, which are attributed to sedimentation and filtration of sediment and organic matter to which these elements adsorb. Sediment samples from open-water depositional areas in the wetland contained high concentrations of (1) trace metals, including barium, manganese, strontium, zinc (each of which exceeded 200 parts per million), as well as chromium, copper, lead, and vanadium, and (2) some polycyclic aromatic hydrocarbons. Persistent organochlorine pesticides, such as chlordane, dieldrin, DDT and its degradation products (DDD and DDE), and polychlorinated biphenyls (PCB's), also were detected, but concentrations of these compounds were within the ranges often found in depositional environments in highly urbanized areas. Cattail shoots attained a maximum height of 350 centimeters, a density of more than 30 shoots per square meter, and total biomass of more than 5,600 grams per square meter (46 percent of which was in above-ground tissues during the growing season). Nitrogen and potassium were three times more abundant in above-ground tissues (2.4 and 1.5 percent by dry weight, respectively) than in below-ground tissues (0.8 and 0.5 percent, respectively). Concentrations of phosphorus, molybdenum, and manganese in above-ground tissues were similar to those in below-ground tissues, but the concentrations of all other constituents were considerably higher in below-ground tissues. Concentrations of several elements exceeded those typically found in natural wetlands; these included manganese (417 ppm, parts per million) and sodium (3,600 ppm) in above-ground tissues, and aluminum (1,540 ppm), iron (15,400 ppm), manganese (433 ppm), and sodium (10,000 ppm) in below-ground tissues. Large quantities of nutrients are assimilated by wetland vegetation during the growing season, but neither tissue production nor microbial metabolic processes appeared to play a significant role in the observed patterns of surface-water chemical input-to-output relations on a seasonal basis. Presumably, internal cycling of nutrients sequestered in the sediments and detritus, combined with a summer increase in microbially mediated chemical transformations, obscured the effects of vegetative assimilation during the summer on surface-water chemical loads. Additionally, the natural confinement of most flows within the banks of Irondequoit Creek, which resulted in passage of stormwater through the wetland with little dispersion or detention in the cattail and backwater areas, diminished the capability of the wetland to improve water quality. Additional factors that probably affected the chemical-removal efficiency of the wetland included chemical inflow loading rates, storage and release mechanisms of the sediments (sedimentation, adsorption, filtration, precipitaton, dissolution, and resuspension), and accretion and burial of organic matter. Measurements of chlorophyll_ a concentrations, and calculations of potential phosphorus concentrations, since the 1970’s indicate an improvement in the trophic state of Irondequoit Bay. Estimated average annual loads (1990-96) of selected constituents entering Irondequoit Bay indicate that, since 1980, the loads of all major forms of nitrogen have decreased, chloride loads have increased, and sulfate loads have changed little. Inputs of total phosphorus and suspended solids to the wetland have increased since 1980, possibly as a result of increased erosion by stormflows from an increasingly developed watershed. The wetland decreases the loads of these constituents, but the trends of these loads entering Irondequoit Bay cannot be reliably defined because the removal efficiencies during the two earlier study periods (1980–81 and 1984–88) are known.

Water-Resources Investigations Report↗

USGS2008

Ground-water quality data in the coastal Los Angeles Basin study unit, 2006: Results from the California GAMA Program

Ground-water quality in the approximately 860 square-mile Coastal Los Angeles Basin study unit (CLAB) was investigated from June to November of 2006 as part of the Statewide Basin Assessment Project of the Ground-Water Ambient Monitoring and Assessment (GAMA) Program. The GAMA Statewide Basin Assessment was developed in response to the Ground-Water Quality Monitoring Act of 2001, and is being conducted by the U.S. Geological Survey (USGS) in cooperation with the California State Water Resources Control Board (SWRCB). The Coastal Los Angeles Basin study was designed to provide a spatially unbiased assessment of raw ground-water quality within CLAB, as well as a statistically consistent basis for comparing water quality throughout California. Samples were collected from 69 wells in Los Angeles and Orange Counties. Fifty-five of the wells were selected using a spatially distributed, randomized grid-based method to provide statistical representation of the study area (?grid wells?). Fourteen additional wells were selected to evaluate changes in ground-water chemistry or to gain a greater understanding of the ground-water quality within a specific portion of the Coastal Los Angeles Basin study unit ('understanding wells'). Ground-water samples were analyzed for: a large number of synthetic organic constituents [volatile organic compounds (VOCs), gasoline oxygenates and their degradates, pesticides, polar pesticides, and pesticide degradates, pharmaceutical compounds, and potential wastewater-indicators]; constituents of special interest [perchlorate, N-nitrosodimethylamine (NDMA), 1,4-dioxane, and 1,2,3-trichloropropane (1,2,3-TCP)]; inorganic constituents that can occur naturally [nutrients, major and minor ions, and trace elements]; radioactive constituents [gross-alpha and gross-beta radiation, radium isotopes, and radon-222]; and microbial indicators. Naturally occurring isotopes [stable isotopic ratios of hydrogen and oxygen, and activities of tritium and carbon-14] 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

California↗

USGS2012

Hydrogeology, water chemistry, and transport processes in the zone of contribution of a public-supply well in Albuquerque, New Mexico, 2007-9

The National Water-Quality Assessment Program (NAWQA) of the U.S. Geological Survey began a series of groundwater studies in 2001 in representative aquifers across the Nation in order to increase understanding of the factors that affect transport of anthropogenic and natural contaminants (TANC) to public-supply wells. One of 10 regional-scale TANC studies was conducted in the Middle Rio Grande Basin (MRGB) in New Mexico, where a more detailed local-scale study subsequently investigated the hydrogeology, water chemistry, and factors affecting the transport of contaminants in the zone of contribution of one 363-meter (m) deep public-supply well in Albuquerque. During 2007 through 2009, samples were collected for the local-scale study from 22 monitoring wells and 3 public-supply (supply) wells for analysis of major and trace elements, arsenic speciation, nutrients, dissolved organic carbon, volatile organic compounds (VOCs), dissolved gases, stable isotopes, and tracers of young and old water. To study groundwater chemistry and ages at various depths within the aquifer, the monitoring wells were divided into three categories: (1) each shallow well was screened across the water table or had a screen midpoint within 18.3 m of the water level in the well; (2) each intermediate well had a screen midpoint between about 27.1 and 79.6 m below the water level in the well; and (3) each deep well had a screen midpoint about 185 m or more below the water level in the well. The 24-square-kilometer study area surrounding the "studied supply well" (SSW), one of the three supply wells, consists of primarily urban land within the MRGB, a deep alluvial basin with an aquifer composed of unconsolidated to moderately consolidated deposits of sand, gravel, silt, and clay. Conditions generally are unconfined, but are semiconfined at depth. Groundwater withdrawals for public supply have substantially changed the primary direction of flow from northeast to southwest under predevelopment conditions, to west to east under modern conditions. Analysis of age tracers indicates that groundwater from most sampled wells is dominated by old (pre-1950) water, ranging in mean age from about 4,000 years to more than 22,000 years, but includes a fraction of young (post-1950) recharge. Patterns in chemical and isotopic data are consistent with the conclusions that shallow groundwater in the area typically includes a fraction that evaporated prior to recharge and (or) flushed accumulated solutes out of the unsaturated zone during recharge, and that shallow groundwater has mixed to deeper parts of the aquifer, which receives recharge mainly by seepage from the Rio Grande. Among shallow and intermediate wells that produced water with a fraction of young recharge, that fraction ranged between 1.5 and 46 percent. Samples from the two deep wells had groundwater ages exceeding 18,000 years, with no fraction of young recharge. Two supply wells (including the SSW) had a fraction of young recharge, which ranged between about 3 and 11 percent, despite mean groundwater ages exceeding 10,000 years. The fraction of young recharge to the SSW varied seasonally, probably because seasonal pumping patterns affected local hydraulic gradients and (or) because of flow through the well bore when the SSW is not pumping. Well-bore flow data collected during winter (low-pumping season) indicated that about 61 percent of the water pumped from the SSW entered the well from the intermediate part of the aquifer, and that the remaining 39 percent entered from the deep part of the aquifer. Volatile organic compounds (VOCs) were detected in samples from most shallow and intermediate monitoring wells and from two of three supply wells, including the SSW. Detected VOCs were primarily chlorinated solvents or their degradation products. Many of the wells in which most of these VOCs were detected are located near known sites of solvent contamination that were targeted for sampling because trichloroethylene (TCE) and cis-1,2-dichloroethylene had been detected in the SSW, and several of these wells may have become contaminated at least partly because of enhanced vertical migration associated with the pumping of and (or) direct migration down deep well bores. Except for TCE in the sample from a shallow monitoring well, all detections of VOCs were at concentrations below Maximum Contaminant Levels (MCLs) set by the U.S. Environmental Protection Agency. Concentrations of all VOCs detected in the supply wells were less than one-tenth of the corresponding MCLs. However, the presence of VOCs in all but deep groundwater, including the detection of chloroform (a chlorination byproduct) in several shallow wells, indicates that groundwater in the study area commonly is affected by human activities, even to substantial depths. The only natural contaminant detected at concentrations near or above its MCL was arsenic, which has been detected at elevated concentrations across broad areas of the MRGB. Concentrations of arsenic, present primarily as arsenate, exceeded the MCL of 10 micrograms per liter (μg/L) in water from the two deep wells (one of which had the highest concentration, 35 μg/L), from one intermediate well, and from two supply wells, including the SSW. Water-quality and solid-phase data from this study are consistent with elevated arsenic concentrations in groundwater being related to pH-dependent desorption of arsenic from ferric oxyhydroxides in sediments in deep parts of the aquifer. Concentrations of nitrate ranged between 1.3 and 5.4 milligrams per liter (mg/L) in water from shallow wells screened across the water table, but were less than 0.9 mg/L in water from all but one deeper well. Nitrogen isotopes and chloride/bromide ratios for shallow wells were consistent with natural soil nitrogen. Nitrate concentrations and nitrogen isotopes indicated that denitrification is occurring at intermediate aquifer depths, and that the progress of the denitrification reaction typically is greatest for wells that include a fraction of groundwater associated with particular recharge sources or with known sites of contamination contributing organic compounds that can provide a carbon source for microbial respiration. Overall, hydrologic and chemical data from the study area indicate that young recharge is reaching the aquifer across broad areas and is migrating from shallow to intermediate depths of the aquifer as a result of mixing that is associated with human development of groundwater. Consequently, groundwater that human activities in the urban study area have affected is present at depths that are within the screened intervals of public-supply wells, resulting in detections of VOCs and implying greater vulnerability to anthropogenic contamination than might be assumed based on the dominantly old age of the regional groundwater. However, the fractions of old groundwater that public-supply wells produce substantially dilute the anthropogenic contaminants, while contributing natural contaminants (primarily arsenic) to the wells. Based on data from the SSW, vulnerability of public-supply wells to natural and anthropogenic contaminants in the area changes through time, including with seasonal changes in pumping stresses that alter the fractions of young and old water being contributed to wells.

New Mexico↗

USGS2002

Ground-water monitoring plan, water quality, and variability of agricultural chemicals in the Missouri River alluvial aquifer near the City of Independence, Missouri, well field, 1998-2000

A detailed ground-water sampling plan was developed and executed for 64 monitoring wells in the city of Independence well field to characterize ground-water quality in the 10-year zone of contribution. Samples were collected from monitoring wells, combined Independence well field pumpage, and the Missouri River at St. Joseph, Missouri, from 1998 through 2000. In 328 ground-water samples from the 64 monitoring wells and combined well field pumpage samples, specific conductance values ranged from 511 to 1,690 microsiemens per centimeter at 25 degrees Celsius, pH values ranged from 6.4 to 7.7, water temperature ranged from 11.3 to 23.6 degrees Celsius, and dissolved oxygen concentrations ranged from 0 to 3.3 milligrams per liter. In 12 samples from the combined well field pumpage samples, specific conductance values ranged from 558 to 856 microsiemens per centimeter at 25 degrees Celsius, pH values ranged from 6.9 to 7.7, water temperature ranged from 5.8 to 22.9 degrees Celsius, and dissolved oxygen concentrations ranged from 0 to 2.4 milligrams per liter. In 45 Missouri River samples, specific conductance values ranged from 531 to 830 microsiemens per centimeter at 25 degrees Celsius, pH ranged from 7.2 to 8.7, water temperature ranged from 0 to 30 degrees Celsius, and dissolved oxygen concentrations ranged from 5.0 to 17.6 milligrams per liter. The secondary maximum contaminant level for sulfate in drinking water was exceeded once in samples from two monitoring wells, the maximum contaminant level (MCL) for antimony was exceeded once in a sample from one monitoring well, and the MCL for barium was exceeded once in a sample from one monitoring well. The MCL for iron was exceeded in samples from all monitoring wells except two. The MCL for manganese was exceeded in all samples from monitoring wells and combined well field pumpage. Enzyme linked immunoassay methods indicate total benzene, toluene, ethyl benzene, and xylene (BTEX) was detected in samples from five wells. The highest total BTEX concentration was less than the MCL of toluene, ethyl benzene, or xylene but greater than the MCL for benzene. Total BTEX was not detected in samples from any well more than once. Atrazine was detected in samples from nine wells, and exceeded the MCL once in a sample from one well. Alachlor was detected in samples from 22 wells but the MCL was never exceeded in any sample. Samples from five wells analyzed for a large number of organic compounds indicate concentrations of volatile organic compounds did not exceed the MCL for drinking water. No semi-volatile organic compounds were detected; dieldrin was detected in one well sample, and no other pesticides, herbicides, polychlorinated biphenyls, or polychlorinated napthalenes were detected. Dissolved ammonia, dissolved nitrite plus nitrate, dissolved orthophosphorus, alachlor, and atrazine analyses were used to determine the spatial and temporal variability of agricultural chemicals in ground water. Detection frequencies for dissolved ammonia increased with well depth, decreased with depth for dissolved nitrite plus nitrate, and remained relatively constant with depth for dissolved orthophosphorus. Maximum concentrations of dissolved ammonia, dissolved nitrite plus nitrate, and dissolved orthophosphorus were largest in the shallowest wells and decreased with depth, which may indicate the land surface as the source. However, median concentrations increased with depth for dissolved ammonia, were less than the detection limit for dissolved nitrite plus nitrate, and decreased with depth for dissolved orthophosphorus. This pattern does not indicate a well-defined single source for these constituents. Dissolved orthophosphorus median concentrations were similar, but decreased slightly with depth, and may indicate the land surface as the source. Seasonal variability of dissolved ammonia, dissolved nitrite plus nitrate, and dissolved orthophosphorus concentrations is not well-defined for samples grouped by month. Individual sample results from the Missouri River and the combined Independence well field pumpage show a seasonal trend that may indicate the effect of induced recharge from the Missouri River on the well field. Individual results and samples from seven wells indicate relatively constant dissolved ammonia concentrations, low dissolved nitrite plus nitrate concentrations in all but one well, and a more well-defined seasonal variation of dissolved orthophosphorus than either dissolved ammonia or dissolved nitrite plus nitrate. Larger detection frequencies in the shallow depth intervals and the large maximum concentrations of alachlor and atrazine in the shallower wells indicate that the source of these chemicals to shallow ground water most likely is the land surface rather than induced river recharge. Seasonal variability of alachlor is not well-defined from samples grouped by month. Individual results from the combined Independence well field pumpage and samples from seven wells indicate variation in both alachlor and atrazine with time, but the degree and timing of the variation is not consistent. This inconsistency most likely is caused by varying rates of transport from the land surface to wells, different rates of degradation of both alachlor and atrazine in soil and ground water, the timing and area of application, and multiple source areas in and around the Independence well field. Alachlor and atrazine concentrations in the Missouri River at Hermann, Missouri, increased in spring, greater concentrations continued until late summer or early fall, and lower concentrations occurred in late fall and winter. Alachlor and atrazine concentrations most likely followed a similar trend in the Missouri River near the Independence well field. The lack of a seasonal trend similar to that of the Missouri River in the combined Independence well field pumpage and the monitoring wells may indicate that the source of alachlor and atrazine to ground water is the land surface rather than the Missouri River.

Missouri↗