SEARCH · Geology Reports

Results for “Physical Chemistry Chemical Physics”

Search indexed USGS publications on groundwater, aquifers, geologic maps, mineral resources and earthquakes. Explore source records by subject and place.

SourceResearch connectionFrom yearThrough year

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 55 records · Page 3Linked to original sources

USGS2009

Effects of urbanization on the chemical, physical, and biological characteristics of small Blackland Prairie streams in and near the Dallas-Fort Worth metropolitan area, Texas

In 2001, the U.S. Geological Survey National Water Quality Assessment Program began a series of studies in the contiguous United States to examine the effects of urbanization on the chemical, physical, and biological characteristics of streams. Small streams in the Texas Blackland Prairie level III ecoregion in and near the Dallas-Fort Worth metropolitan area were the focus of one of the studies. The principal objectives of the study, based on data collected in 2003-04 from 28 subbasins of the Trinity River Basin, were to (1) define a gradient of urbanization for small Blackland Prairie streams in the Trinity River Basin on the basis of a range of urban intensity indexes (UIIs) calculated using land-use/land-cover, infrastructure, and socioeconomic characteristics; (2) assess the relation between this gradient of urbanization and the chemical, physical, and biological characteristics of these streams; and (3) evaluate the type of relation (that is, linear or nonlinear, and whether there was a threshold response) of the chemical, physical, and biological characteristics of these streams to the gradient of urbanization. Of 94 water-chemistry variables and one measure of potential toxicity from a bioassay, the concentrations of two pesticides (diazinon and sima-zine) and one measure of potential toxicity (P450RGS assay) from compounds sequestered in semipermeable membrane devices were significantly positively correlated with the UII. No threshold responses to the UII for diazinon and simazine concentrations were observed over the entire range of the UII scores. The linear correlation for diazinon with the UII was significant, but the linear correlation for simazine with the UII was not. No statistically significant relations between the UII and concentrations of suspended sediment, total nitrogen, total phosphorous, or any major ions were indicated. Eleven of 59 physical variables from streamflow were significantly correlated with the UII. Temperature was not significantly correlated with the UII, and none of the physical habitat measurements were significantly correlated with the UII. Seven physical variables categorized as streamflow flashiness metrics were significantly positively correlated with the UII, two of which showed a linear but not a threshold response to the UII. Four flow-duration metrics were significantly negatively correlated with the UII, of which two showed a linear response to the UII, one showed a threshold response, and one showed neither. None of the fish metrics were significantly correlated with the UII in the Blackland Prairie streams. Two qualitative multi-habitat benthic macroinvertebrate metrics, predator richness and percentage filterer-collector richness, were significantly correlated with the UII; predator richness was negatively correlated with the UII, and percentage filterer-collector richness was positively correlated with the UII. No threshold response to the UII was observed for either metric, but both showed a significant linear response to the UII. Three richest targeted habitat (RTH) benthic macroinvertebrate metrics, Margalef's richness, predator richness, and omnivore richness were significantly negatively correlated with the UII. Margalef's richness was the only RTH metric that indicated a threshold response to the UII. The majority of unique taxa collected in the periphytic algae samples were diatoms. Six RTH periphytic algae metrics were correlated with the UII and five of the six showed no notable threshold response to the UII; but all five showed significant linear responses to the UII. Only the metric OT_VL_DP, which indicates the presence of algae that are tolerant of low dissolved oxygen conditions, showed a threshold response to the UII. Six depositional target habitat periphytic algae metrics were correlated with the UII, five of which showed no threshold response to the UII; three of the five showed significant linear responses to the UII, one showed a borderline significant

Texas↗

USGS2021

Literature review for candidate chemical control agents for nonnative crayfish

Nonnative crayfish are an immediate and pervasive threat to aquatic environments and their biodiversity. Crayfish control can be achieved by physical methods, water chemistry modification, biological methods, biocidal application, and application of crayfish physiology modifiers. The purpose of this report is to identify suitable candidates for potential control of nonnative crayfish through a comprehensive literature review. This review focuses on control methods, specifically on the available data to support registration of a crayfish pesticide. The literature search resulted in 28,058 documents, which were searched to determine if they contained information on physical, chemical, biological, and (or) biocidal approaches to control crayfish. Pesticides directly toxic to crayfish in this literature review include: pyrethroids (natural pyrethrins and synthetic), fipronil, mirex, antimycin-A, and rotenone. Some chemicals, such as diflubenzuron and emamectin benzoate, alter crayfish physiology resulting in a lower pesticide dose needed to control crayfish. Environmental damage, application rate, exposure duration, nontarget effects, environmental persistence, and registration data gaps were used as criteria to define which pesticides are potentially selective to crayfish, along with which have the greatest amount of data to support registration by the U.S. Environmental Protection Agency. Synthetic pyrethroids were identified as the most likely candidate to be developed into a crayfish pesticide. A type-2 synthetic pyrethroid, cyfluthrin, has the greatest potential for eradicating nonnative crayfish. Although other invertebrate species will be negatively affected at the concentrations required for crayfish control, compared with other pyrethroids and other potential control chemicals, cyfluthrin offers rapid ecosystem recovery due to being more selective, having fewer effects on native fish, and having a short aquatic persistence. Cyfluthrin also has few data gaps for U.S. Environmental Protection Agency registration purposes.

Open-File Report↗

USGS1891

Report of work done in the division of chemistry and physics, mainly during the fiscal year 1889-90

This bulletin, like the bulletins issued in previous years and numbered 9, 27, 42, 55, 60, and 64, contains a partial record of work completed in the chemical and physical laboratories of the Survey Turing one tiscAl year. It represents, however, only a portion of the whole work done, for various investigations, begun during the year 1859—'90, are still unfinished; many analyses are reserved for publication in other reports; and certain of the larger researches, notably the physical studies of Dr. Barns, will appear in independent form as separate bulletins. In the annual reports of the Director of the Survey a tolerably complete summary of the work done in the Division of Chemistry and Physics is always given, and such summaries, taken in connection with these bulletins, convey.a fair idea of the amount of ground actually covered.

Bulletin↗

USGS1991

Role of sediment-trace element chemistry in water-quality monitoring and the need for standard analytical methods

Multiple linear regression models calculated from readily obtainable chemical and physical parameters can explain a high percentage (70% or greater) of observed sediment trace-element variance for Cu, Zn, Pb, Cr, Ni, Co, As, Sb, Se, and Hg. Almost all the factors used in the various models fall into the category of operational definitions (e.g., grain size, surface area, and geochemical substrates such as amorphous iron and manganese oxides). Thus, the concentrations and distributions used in the various models are operationally defined, and are subject to substantial change depending on the method used to determine them. Without standardized procedures, data from different sources are not comparable, and the utility and applicability of the various models would be questionable.

Conference Paper↗

USGS2009

Effects of fire temperature on the physical and chemical characteristics of the ash from two plots of Cork oak (Quercus Suber)

Cork oak, (Quercus suber) is widely distributed in the Mediterranean region, an area subject to frequent fires. The ash produced by burning can have impacts on the soil status and water resources that can differ according to the temperature reached during fire and the characteristics of the litter, defined as the dead organic matter accumulated on the soil surface prior to the fire. The aim of this work is to determine the physical and chemical characteristics of ash produced in laboratory experiments to approximate conditions typical of fires in this region. The litter of Quercus suber collected from two different plots on the Iberian Peninsula, Mas Bassets (Catalonia) and Albufeira (Portugal), was combusted at different temperatures for 2h. We measured Mass Loss (ML per cent), ash colour and CaCO 3 content, pH, Electrical Conductivity (EC) and the major cations (Ca 2+ , Mg 2+ , K + and Na + ) released from ash slurries created by mixing ash with deionized water. The results showed that ML per cent is higher at all temperatures in Albufeira samples compared to Mas Bassets samples, except at 550??C, and the rate of loss increases faster with temperature than the Mas Bassets samples. At 150??C the ash colour is yellowish, becoming reddish at 200- 250??C and black at 300??C. Above 400??C the ash is grey/white. This thermal degradation is mostly observed in Albufeira litter. The formation of CaCO 3 was identified at a lower temperature in Albufeira litter. At temperatures <300??C, pH and EC values are lower, rising at higher temperatures, especially in Albufeira slurries. The concentration of cations at lower temperatures does not differ substantially from the unburned sample except for Mg 2+ . The cation concentration increases at medium temperatures and decrease at higher temperatures, especially the concentration of divalent cations. The monovalent cations showed a larger concentration at moderate temperatures, mainly in Albufeira ash slurries. The analysis of the Ca:Mg ratio also showed that for the same temperature, a higher severity results for Albufeira litter. Potential negative effects on soil properties are observed at medium and higher temperatures. These negative effects include a higher percentage of mass loss, meaning more soil may be exposed to erosion, higher pH values and greater cation release from ash, especially monovalalent cations (K + ,Na + ) in higher proportions than the divalent ions (Ca 2+ , Mg 2+ ), that can lead to impacts on soil physical properties like aggregate stability. Furthermore, the ions in ash may alter soil chemistry which may be detrimental to some plants thus altering the recovery of these ecosystems after fire. Low intensity prescribed fire can be a useful tool to land management in these sites, due to the reduced effects of fire temperatures on the physical and chemical properties of surface litter, and can reduce the risk of high temperature wildland fires by reducing fuel loadings. From the perspective of water resources, lower fire temperatures produce fewer impacts on the chemistry of overland flow and there is less probability that the soil surface will be eroded. Copyright ?? 2009 John Wiley & Sons, Ltd.

Land Degradation and Development↗

USGS2002

Interpretation with a Donnan-based concept of the influence of simple salt concentration on the apparent binding of divalent ions to the polyelectrolytes polystyrenesulfonate and dextran sulfate

It has been shown that the apparent enhancement of divalent metal ion binding to polyions such as polystyrenesulfonate (PSS) and dextran sulfate (DS) by decreasing the ionic strength of these mixed counterion systems (M2+, M+, X-, polyion) can be anticipated with the Donnan-based model developed by one of us (J.A.M.). Ion-exchange distribution methods have been employed to measure the removal by the polyion of trace divalent metal ion from simple salt (NaClO4)-polyion (NaPSS) mixtures. These data and polyion interaction data published earlier by Mattai and Kwak for the mixed counterion systems MgCl2-LiCl-DS and MgCl2-CsCl-DS have been shown to be amenable to rather precise analysis by this model. ?? 1985 American Chemical Society.

Journal of Physical Chemistry↗

USGS2006

Thermodynamic calculations in the system CH4-H2O and methane hydrate phase equilibria

Using the Gibbs function of reaction, equilibrium pressure, temperature conditions for the formation of methane clathrate hydrate have been calculated from the thermodynamic properties of phases in the system CH4-H 2O. The thermodynamic model accurately reproduces the published phase-equilibria data to within ??2 K of the observed equilibrium boundaries in the range 0.08-117 MPa and 190-307 K. The model also provides an estimate of the third-law entropy of methane hydrate at 273.15 K, 0.1 MPa of 56.2 J mol-1 K-1 for 1/n CH4??H 2O, where n is the hydrate number. Agreement between the calculated and published phase-equilibria data is optimized when the hydrate composition is fixed and independent of the pressure and temperature for the conditions modeled. ?? 2006 American Chemical Society.

Journal of Physical Chemistry B↗

USGS2015

Icefield-to-ocean linkages across the northern Pacific coastal temperate rainforest ecosystem

Rates of glacier mass loss in the northern Pacific coastal temperate rainforest (PCTR) are among the highest on Earth, and changes in glacier volume and extent will affect the flow regime and chemistry of coastal rivers, as well as the nearshore marine ecosystem of the Gulf of Alaska. Here we synthesize physical, chemical and biological linkages that characterize the northern PCTR ecosystem, with particular emphasis on the potential impacts of glacier change in the coastal mountain ranges on the surface–water hydrology, biogeochemistry, coastal oceanography and aquatic ecology. We also evaluate the relative importance and interplay between interannual variability and long-term trends in key physical drivers and ecological responses. To advance our knowledge of the northern PCTR, we advocate for cross-disciplinary research bridging the icefield-to-ocean ecosystem that can be paired with long-term scientific records and designed to inform decisionmakers.

Pacific coastal temperate rainforest↗

USGS1994

Physical characteristics and quality of water from selected springs and wells in the Lincoln Point-Bird Island area, Utah Lake, Utah

From February 1991 to October 1992, the U.S. Geological Survey, in cooperation with the Central Utah Water Conservancy District, investigated the hydrology of the Lincoln Point - Bird Island area in the southeast part of Utah Lake, Utah. The investigation included measurements of the discharge of selected springs and measurements of the physical and chemical characteristics of water from selected springs and wells in the LincolnPoint - Bird Island area. This report contains data for twenty-one distinct springs in the study area including two springs beneath the surface of Utah Lake at Bird Island. Data from this study, combined with data from previous studies, indicate that the location of springs in the Lincoln Point - Bird Island area probably is controlled by fractures that are the result of faulting. Measured discharge of springs in the Lincoln Point - Bird Island area ranged from less than 0.01 cubic foot per second to 0.84 cubic foot per second. Total discharge in the study area, including known unmeasured springs and seeps, is estimated to be about 5 cubic feet per second. Reported and measured temperatures of water from springs and wells in the Lincoln Point - Bird Island area ranged from 16.0 degrees Celsius to 36.5 degrees Celsius. Dissolved-solids con-centrations ranged from 444 milligrams per liter to 7,932 milligrams per liter, and pH ranged from 6.3 to 8.1. Physical and chemical characteristics of spring and well water from the west side of Lincoln Point were virtually identical to the physical and chemical characteristics of water from the submerged Bird Island springs, indicating a similar source for the water. Water chemistry, isotope analyses, and geothermometer calculations indicate deep circulation of water discharging from the springs and indicate that the source of recharge for the springs at Lincoln Point and Bird Island does not appear to be localized in the LincolnPoint - Bird Island area.

Water-Resources Investigations Report↗

USGS1996

Effect of snow and firn hydrology on the physical and chemical characteristics of glacial runoff

Near-surface processes on glaciers, including water flow over bare ice and through seasonal snow and firn, have a significant effect on the speed, volume and chemistry of water flow through the glacier. The transient nature of the seasonal snow profoundly affects the water discharge and chemistry. Water flow through snow is fairly slow compared with flow over bare ice and a thinning snowpack on a glacier decreases the delay between peak meltwater input and peak stream discharge. Furthermore, early spring melt flushes the snowpack of solutes and by mid-summer the melt water flowing into the glacier is fairly clean by comparison. The firn, a relatively constant feature of glaciers, attenuates variations in water drainage into the glacier by temporarily storing water in saturated layer. Bare ice exerts opposite influences by accentuating variations in runoff by water flowing over the ice surface. The melt of firn and ice contributes relatively clean (solute-free) water to the glacier water system.

Hydrological Processes↗

USGS2010

One-Dimensional Transport with Equilibrium Chemistry (OTEQ) - A reactive transport model for streams and rivers

OTEQ is a mathematical simulation model used to characterize the fate and transport of waterborne solutes in streams and rivers. The model is formed by coupling a solute transport model with a chemical equilibrium submodel. The solute transport model is based on OTIS, a model that considers the physical processes of advection, dispersion, lateral inflow, and transient storage. The equilibrium submodel is based on MINTEQ, a model that considers the speciation and complexation of aqueous species, acid-base reactions, precipitation/dissolution, and sorption. Within OTEQ, reactions in the water column may result in the formation of solid phases (precipitates and sorbed species) that are subject to downstream transport and settling processes. Solid phases on the streambed may also interact with the water column through dissolution and sorption/desorption reactions. Consideration of both mobile (waterborne) and immobile (streambed) solid phases requires a unique set of governing differential equations and solution techniques that are developed herein. The partial differential equations describing physical transport and the algebraic equations describing chemical equilibria are coupled using the sequential iteration approach. The model's ability to simulate pH, precipitation/dissolution, and pH-dependent sorption provides a means of evaluating the complex interactions between instream chemistry and hydrologic transport at the field scale. This report details the development and application of OTEQ. Sections of the report describe model theory, input/output specifications, model applications, and installation instructions. OTEQ may be obtained over the Internet at http://water.usgs.gov/software/OTEQ.

Techniques and Methods↗

USGS1981

Water Resources Research October 1, 1979 - September 30, 1980: Summary statements of research activities by the Water Resources Division

Research in the WRD had its beginnings in the late 1950's when the "core research" line item was added to the Congressional budget. Since this time the Federal program has grown from a "basic sciences" program to one that includes a broad spectrum of basic and applied scientific investigations. Water resources research in WRD includes the study of water in all its phases and uses the basic sciences of mathematics, chemistry, physics, biology, geology and engineering to gain a fundamental understanding of the processes that affect the movement of water and its chemical constituents through hydrologic systems. The basic knowledge and methodologies derived from water resources research are applicable not only to the solution of current problems associated with the Nation's water resources, but also to anticipated hydrologic issues.

Report↗

USGS2004

Are big basins just the sum of small catchments?

Many challenges remain in extending our understanding of how hydrologic processes within small catchments scale to larger river basins. In this study we examine how low-flow runoff varies as a function of basin scale at 11 catchments, many of which are nested, in the 176 km2 Neversink River watershed in the Catskill Mountains of New York. Topography, vegetation, soil and bedrock structure are similar across this river basin, and previous research has demonstrated the importance of deep groundwater springs for maintaining low-flow stream discharge at small scales in the basin. Therefore, we hypothesized that deep groundwater would contribute an increasing amount to low-flow discharge as basin scale increased, resulting in increased runoff. Instead, we find that, above a critical basin size of 8 to 21 km2, low-flow runoff is similar within the Neversink watershed. These findings are broadly consistent with those of a previous study that examined stream chemistry as a function of basin scale for this watershed. However, we find physical evidence of self-similarity among basins greater than 8 km2, whereas the previous study found gradual changes in stream chemistry among basins greater than 3 km 2. We believe that a better understanding of self-similarity and the subsurface flow processes that affect stream runoff will be attained through simultaneous consideration of both chemical and physical evidence. We also suggest that similar analyses of stream runoff in other basins that represent a range of spatial scales, geomorphologies and climate conditions will further elucidate the issue of scaling of hydrologic processes. Copyright ?? 2004 John Wiley & Sons, Ltd.

Hydrological Processes↗

USGS1998

Assessing sediment toxicity from navigational pools of the Upper Mississippi River using a 28-day Hyalella azteca test

To assess the extent of sediment contamination in the Upper Mississippi River (UMR) system after the flood of 1993, sediment samples were collected from 24 of the 26 navigational pools in the river and from one site in the Saint Croix River in the summer of 1994. Whole-sediment tests were conducted with the amphipod Hyalella azteca for 28 days measuring the effects on survival, growth, and sexual maturation. Amphipod survival was significantly reduced in only one sediment (13B) relative to the control and reference sediments. Body length of amphipods was significantly reduced relative to the control and reference sediments in only one sample (26C). Sexual maturation was not significantly reduced in any treatment when compared to the control and reference sediments. No significant correlations were observed between survival, growth, and maturation to either the physical or chemical characteristics of the sediment samples from the river. When highly reliable effect range medians (ERMs) were used to evaluate sediment chemistry, 47 of 49 (96%) of the samples were correctly classified as nontoxic. These results indicate that sediment samples from the Upper Mississippi River are relatively uncontaminated compared to other areas of known contamination in the United States.

Archives of Environmental Contamination and Toxico↗

USGS2005

A surficial hydrogeologic framework for the Mid-Atlantic Coastal Plain

A surficial hydrogeologic framework was developed for the Mid-Atlantic Coastal Plain, from New Jersey through North Carolina. The framework includes seven distinct hydrogeologic subregions within which the primary natural physical factors affecting the flow and chemistry of shallow ground water and small streams are relatively consistent. Within most subregions, the transport of chemicals from the land surface to ground water and streams can be described by a fairly uniform set of natural processes; some subregions include mixed hydrogeologic settings that are indistinguishable at the regional scale. The hydrogeologic framework and accompanying physiographic and geologic delineations are presented in digital and printed format. The seven hydrogeologic subregions that constitute the framework were delineated primarily on the basis of physiography and the predominant texture (typical grain size) of surficial and (where surficial sediments are particularly thin) subcropping sediments. Physiography for the Mid-Atlantic Coastal Plain was constructed by standardizing and extrapolating previously published interpretations for the Coastal Plain of South Carolina and New Jersey, based on similar work in the other States. Surficial and subcropping geology were similarly compiled from previous publications by resolving inconsistencies in nomenclature, interpretation, and scale, and interpolating across unmapped areas. A bulk sediment texture was determined for each mapped geologic unit on the basis of published descriptions. Fundamental differences among the seven hydrogeologic subregions are described on the basis of hypotheses about surficial and shallow subsurface hydrology and water chemistry in each, as well as variable land use, soils, and topography. On the regional scale, the Coastal Lowlands (Subregion 1), the Middle Coastal Plain - Fine Sediments (Subregion 3), the Middle Coastal Plain - Sands with Overlying Gravels (Subregion 4), and the Inner Coastal Plain - Upland Sands and Gravels (Subregion 5) are relatively homogeneous in terms of hydrogeology, although an examination of results from small-scale studies within the Coastal Plain demonstrates that even these areas are quite variable, locally. Moderate topographic relief and primarily permeable surficial sediments promote good drainage of the land surface in Subregion 4, for example, but drainage is commonly poor in the Coastal Lowlands (Subregion 1) due to flat topography and low elevations. Agriculture is common in both subregions, although artificial drainage is typically required to support cultivation in Subregion 1. Important physiographic differences are evident among the remaining three subregions, although sediment textures within the Middle Coastal Plain - Mixed Sediment Texture (Subregion 2), the Inner Coastal Plain - Dissected Outcrop Belt (Subregion 6), and the Alluvial and Estuarine Valleys (Subregion 7) are variable even at the regional scale.

Delaware, Maryland, New Jersey, North Carolina, Vi↗

USGS2000

Hydrogeologic setting and potential for denitrification in ground water, Coastal Plain of southern Maryland

The types and distribution of Coastal Plain sediments in the Patuxent River Basin may contribute to relatively low concentrations of nitrate (typically less than 1 milligram per liter) in stream base flow because of the chemical reduction of dissolved nitrate (denitrification) in ground water. Water chemistry data from synoptic stream base-flow surveys in the Patuxent River Basin show higher dissolved nitrate concentrations in the Piedmont than in the Coastal Plain section of the watershed. Stream base flow reflects closely the chemistry of ground water discharging from the surficial (unconfined) aquifer to the stream. Because land use in the sampled subbasins is virtually the same in each section, differences in the physical and geochemical characteristics of the surficial aquifer may explain the observed differences in water chemistry. One possible cause of lower nitrate concentrations in the Coastal Plain is denitrification within marine sediments that contain chemically reduced compounds. During denitrification, the oxygen atoms on the nitrate (N0 3 -) molecule are transferred to a reduced compound and N gas is produced. Organic carbon and ferrous iron (Fe 2+ ), derived from the dissolution of minerals such as pyrite (FeS 2 ) and glauconite (an iron aluminosilicate clay), can act as reducing substrates; these reduced chemical species are common in the marine and estuarine deposits in Southern Maryland. The spatial distribution of geologic units and their lithology (sediment type) has been used to create a map of the potential for denitrification of ground water in the surficial aquifer of the Coastal Plain in Southern Maryland.

Maryland↗

USGS2011

Understanding processes affecting mineral deposits in humid environments

Recent interdisciplinary studies by the U.S. Geological Survey have resulted in substantial progress toward understanding the influence that climate and hydrology have on the geochemical signatures of mineral deposits and the resulting mine wastes in the eastern United States. Specific areas of focus include the release, transport, and fate of acid, metals, and associated elements from inactive mines in temperate coastal areas and of metals from unmined mineral deposits in tropical to subtropical areas; the influence of climate, geology, and hydrology on remediation options for abandoned mines; and the application of radiogenic isotopes to uniquely apportion source contributions that distinguish natural from mining sources and extent of metal transport. The environmental effects of abandoned mines and unmined mineral deposits result from a complex interaction of a variety of chemical and physical factors. These include the geology of the mineral deposit, the hydrologic setting of the mineral deposit and associated mine wastes, the chemistry of waters interacting with the deposit and associated waste material, the engineering of a mine as it relates to the reactivity of mine wastes, and climate, which affects such factors as temperature and the amounts of precipitation and evapotranspiration; these factors, in turn, influence the environmental behavior of mineral deposits. The role of climate is becoming increasingly important in environmental investigations of mineral deposits because of the growing concerns about climate change.

Fact Sheet↗

USGS2018

Geochemistry and microbiology of groundwater and solids from extraction and monitoring wells and their relation to well efficiency at a Federally operated confined disposal facility, East Chicago, Indiana

In cooperation with the U.S. Army Corps of Engineers, Chicago District, the U.S. Geological Survey investigated the processes affecting water quality, geochemistry, and microbiology in representative extraction and monitoring wells at a confined disposal facility (CDF) in East Chicago, Indiana. The CDF is a 140-acre Federally-managed facility that was the former location of an oil refinery and is now used for the long-term disposal and storage of dredge material from the Indiana Harbor and Indiana Harbor Canal. Residual petroleum hydrocarbons and leachate from the CDF are contained within the facility by use of a groundwater cutoff wall. The wall consists of a soil-bentonite slurry and a gradient control system made up of an automated network of 96 extraction wells, 42 monitoring wells, and 2 ultrasonic sensors that maintain an inward hydraulic gradient at the site. The pumps in the extraction wells require vigilant maintenance and must be replaced when unable to withdraw water at a rate sufficient to maintain the required inward gradient. The wells are screened in the Calumet aquifer, a coarse-grained sand and gravel unit that extends approximately 35 feet below the land surface and is not utilized for drinking-water supply at the CDF or in the surrounding area. This study was initiated to identify the cause of decreased pump discharges and to identify potential mitigation strategies. For this study, the U.S. Geological Survey collected groundwater and solids from monitoring and extraction wells. Groundwater samples were collected during June 2014 for precautionary health screening and on four occasions during September 2014 through November 2014. Groundwater samples collected from two extraction wells during June 2014 were analyzed for concentrations of anthropogenic organic constituents. During September through November 2014, groundwater samples were collected from one additional extraction well, and samples from three monitoring wells were analyzed for concentrations of inorganic and organic constituents, dissolved gases, and bacterial abundance and diversity. Solid samples were collected during April 2014, during September 2014 through November 2014, and during November 2016. Solid samples were collected from the exterior of extraction-well pumps and as flocculent from water samples. Solid samples were collected from 10 wells, including 1 extraction well and 3 monitoring wells sampled for water quality. Solid samples were analyzed for mineralogy, solid-phase habit, geochemistry, and organic composition. The following is a list of observations that were made during this study: (1) the water quality is substantially variable among the six well locations sampled as part of this study—lower (more negative) redox values and higher concentrations of many constituents (including calcium, magnesium, sodium, and sulfate) and properties (including dissolved solids, hardness, and turbidity) were detected in sampled wells located near the extraction wells with the highest frequency of failure; (2) water-level drawdown is variable between extraction wells—wells with the greatest drawdown may pull deeper groundwater into the borehole; (3) dissolved gas results indicate reducing oxidation-reduction processes in the aquifer material that can feasibly contribute iron, carbon dioxide, and other byproducts from hydrocarbon degradation to precipitates and solids that accumulate on and impair pump operation; (4) crystalline and amorphous solid-phase minerals are precipitating in the borehole; (5) several types of bacteria are present in water pumped from extraction wells and are likely responsible for bonding mineral and microbiologic matter to the pump (and other well components); and (6) bacteria may create microenvironments that facilitate precipitation of solids or inhibit dissolution of unstable minerals once the bacteria adhere to biofilm attached to the pump. Results of the study indicate that bacteria may be accumulating and entrapping solid material on the exterior of pumps. This accumulation reduces heat transfer and water discharge from the pump and may lead to decreased efficiency or mechanical failure. Observations could not be made on the well screen, gravel pack, or surrounding geologic formation; therefore, mitigating measures in the borehole may not solve well-productivity issues. Remedies for the pump fouling problems were derived from the review and interpretation of data collected during this study and from information documented in other sources about groundwater well fouling. Potential remedies to problems associated with pump fouling at the CDF may include the following: (1) reducing attractiveness of the extraction wells for microbiological growth by modifying the chemical or physical environment of the well, (2) modifying the pump exterior to decrease microbiological adherence, (3) changing the pumping regime to control the chemistry of water entering the well from the surrounding aquifer material, (4) modifying the pumps to be less physically and thermally attractive, and (5) removing hydrocarbons from groundwater and the aquifer material surrounding the wells or adding surfactants to make them more mobile. Pilot scale testing may be necessary to identify the most effective treatment or combination of treatments.

Indiana↗