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Geochemistry of the rare earth elements in ferromanganese nodules from DOMES Site A, northern equatorial Pacific

The distribution of rare earth elements (REE) in ferromanganese nodules from DOMES Site A has been determined by instrumental neutron activation methods. The concentrations of the REE vary markedly. Low concentrations characterize samples from a depression (the valley), in which Quaternary sediments are thin or absent; high concentrations are found in samples from the surrounding abyssal hills (the highlands) where the Quaternary sediment section is relatively thick. Moreover, the valley nodules are strongly depleted in the light trivalent REE (LREE) and Ce compared with nodules from the highlands, some of the former showing negative Ce anomalies. The REE abundances in the nodules are strongly influenced by the REE abundances in coexisting bottom water. Some controls on the REE chemistry of bottom waters include: a) the more effective removal of the LREE relative to the HREE from seawater because of the greater degree of complexation of the latter elements with seawater ligands, b) the very efficient oxidative scavenging of Ce on particle surfaces in seawater, and c) the strong depletion of both Ce and the LREE in, or a larger benthic flux of the HREE into, the Antarctic Bottom Water (AABW) which flows through the valley. The distinctive REE chemistry of valley nodules is a function of their growth from geochemically evolved AABW. In contrast, the REE chemistry of highland nodules indicates growth from a local, less evolved seawater source.

Geochimica et Cosmochimica Acta↗

Denitrification in sediments from the hyporheic zone adjacent to a small forested stream

Denitrifying potentials increased with increasing distance from the stream channel. Dissolved oxygen was 100% of the concentration expected in equilibrium with the atmosphere in water obtained from monitoring wells immediately adjacent to the stream but was as low as 7% of the expected value in water 11.4 m inland. Both nitrate and dissolved organic carbon decreased over summer in wells at the base of the alder-forested slope. A 48-h injection of nitrate-amended stream water into hyporheic water 8.4 m inland stimulated nitrous oxide production in the presence of acetylene. Nitrous oxide was generated as nitrate and acetylene were co-transported to a well 13 m down-gradient. Acetylene-block experiments coupled with the chemistry data suggest that denitrification can modify the chemistry of water during passage through the hyporheic zone. -from Authors

Canadian Journal of Fisheries and Aquatic Sciences↗

A simulation-based approach for estimating premining water quality: Red Mountain Creek, Colorado

Regulatory agencies are often charged with the task of setting site-specific numeric water quality standards for impaired streams. This task is particularly difficult for streams draining highly mineralized watersheds with past mining activity. Baseline water quality data obtained prior to mining are often non-existent and application of generic water quality standards developed for unmineralized watersheds is suspect given the geology of most watersheds affected by mining. Various approaches have been used to estimate premining conditions, but none of the existing approaches rigorously consider the physical and geochemical processes that ultimately determine instream water quality. An approach based on simulation modeling is therefore proposed herein. The approach utilizes synoptic data that provide spatially-detailed profiles of concentration, streamflow, and constituent load along the study reach. This field data set is used to calibrate a reactive stream transport model that considers the suite of physical and geochemical processes that affect constituent concentrations during instream transport. A key input to the model is the quality and quantity of waters entering the study reach. This input is based on chemical analyses available from synoptic sampling and observed increases in streamflow along the study reach. Given the calibrated model, additional simulations are conducted to estimate premining conditions. In these simulations, the chemistry of mining-affected sources is replaced with the chemistry of waters that are thought to be unaffected by mining (proximal, premining analogues). The resultant simulations provide estimates of premining water quality that reflect both the reduced loads that were present prior to mining and the processes that affect these loads as they are transported downstream. This simulation-based approach is demonstrated using data from Red Mountain Creek, Colorado, a small stream draining a heavily-mined watershed. Model application to the premining problem for Red Mountain Creek is based on limited field reconnaissance and chemical analyses; additional field work and analyses may be needed to develop definitive, quantitative estimates of premining water quality.

Colorado↗

Relation of arsenic, iron, and manganese in ground water to aquifer type, bedrock lithogeochemistry, and land use in the New England coastal basins

In a study of arsenic concentrations in public-supply wells in the New England Coastal Basins, concentrations at or above 0.005 mg/L (milligrams per liter) were detected in more samples of water from wells completed in bedrock (25 percent of all samples) than in water from wells completed in stratified drift (7.5 percent of all samples). Iron and manganese were detected (at concentrations of 0.05 and 0.03 mg/L, respectively) at approximately the same frequency in water from wells in both types of aquifers. Concentrations of arsenic in public-supply wells drilled in bedrock (in the National Water-Quality Assessment Program New England Coastal Basins study unit) vary with the bedrock lithology. Broad groups of lithogeochemical units generalized from bedrock lithologic units shown on state geologic maps were used in the statistical analyses. Concentrations of arsenic in water from public-supply wells in metasedimentary bedrock units that contain slightly to moderately calcareous and calcsilicate rocks (lithogeochemical group M c ) were significantly higher than the concentrations in five other groups of bedrock units in the study unit. Arsenic was detected, at or above 0.005 mg/L, in water from 44 percent of the wells in the lithogeochemical group M c and in water from less than 28 percent of wells in the five other groups. Additionally, arsenic concentrations in ground water were the lowest in the metasedimentary rocks that are characterized as variably sulfidic (group M s ). Generally, concentrations of arsenic were low in water from bedrock wells in the felsic igneous rocks (group I f ) though locally some bedrock wells in granitic rocks are known to have ground water with high arsenic concentrations, especially in New Hampshire. The concentrations of arsenic in ground water also correlate with land-use data; significantly higher concentrations are found in areas identified as agricultural land use than in undeveloped areas. There is, however, more agricultural land in areas overlying the metasedimentary rocks of lithogeochemical groups M c and the minimally-deformed clastic sediments of group M md than in areas overlying other lithogeochemical groups. This correlation complicates the interpretation of sources of arsenic to ground water in bedrock. A test of this association revealed that relations between arsenic concentrations and the metasedimentary rocks of group M c are not weakened when data associated with agricultural land use is removed; the reverse is true, however, if the data associated with the group M c are removed from the analysis. The occurrence and variability of arsenic in water from bedrock supply wells could be related to several factors. These include (1) the distribution and chemical form of arsenic in soils and rocks that are part of the ground-water-flow system, (2) the characteristics that influence the solubility and transport of arsenic in ground water, (3) the differing degrees of vulnerability of ground-water supplies to surface contamination, and (4) the spatial associations between land use, geology, and ground-water-flow patterns. Strong relations between agricultural land use and the metasedimentary rocks of group M c complicate the interpretation of arsenic source to water in these bedrock aquifers. This is due in part to the past use of arsenical pesticides; additionally, few whole-rock geochemical data are available for the rock types in the lithogeochemical groups of aquifers that contain ground water with elevated concentrations of arsenic. Without such data, identifying specific bedrock types as arsenic sources is not possible. In southern Maine and south-central New Hampshire, and in northern Massachusetts, the few available whole-rock analyses suggest, at least for these local areas, a connection between known bedrock chemistry and ground-water arsenic levels. Although the lithogeochemical group and land-use category variables individually describe much of the variance in the concentrations of arsenic in ground water, the lithogeochemical relation is statistically stronger than the land-use relation. Low concentrations of arsenic in water from bedrock public-supply wells are associated with the metasedimentary rocks of group M s (characterized as variably sulfidic). This association could reflect a variety of factors and suggests that simple dissolution of arsenic-bearing iron phases, such as sulfides, may not explain concentrations of arsenic in water in this bedrock aquifer group. Whole-rock geochemical data and more complete water-chemistry data, as well as studies of historical variation of arsenic concentrations (time-line studies), and site-specific studies, will be critical in addressing the arsenic source issue.

New England coastal basins↗

Six years of change in Lake Nyos, Cameroon, yield clues to the past and cautions for the future

The catastrophic release of gas from Lake Nyos, Cameroon, in 1986 caused substantial but incomplete mixing of the stratified water column. The post-release evolution of water-column structure has been monitored through April 1992. Changes began immediately after the event as rainfall and inflow brought dilute fluid into the surface layer. Inflow and surface mixing have gradually deepened the chemocline. The Total Dissolved Solids (TDS) values in the upper 40 m of the water column have dropped from a few hundred mg/kg just after the release to <100 mg/kg. The chemocline is presently strongest at 50 m depth; 5 m below this, the TDS = 570 mg/kg. From 55 to 150 m depth is a gentle gradient in which TDS reaches 920 mg/kg. Little change in water-column chemistry has occurred in this depth interval since the release. Between 150 m depth and lake bottom at 210 m depth, a strong secondary chemocline has formed. Temperature, CO 2 concentration ([CO 2 ]), and TDS have all increased in the deepest layer in response to recharge by warm, mineralized water, reaching values of 25.0°C, 320 mmol/kg, and 1800 mg/kg, respectively, 1 m above lake bottom. Considering all these changes in part as a “recovery” process, it is possible to construct a model of the pre-release water column. The data indicate that the pre-release chemocline was at least 50 m deep. Above the chemocline was a dilute layer containing a seasonal thermocline; below the chemocline was probably a gradient zone(s) with correlated increases in TDS and [CO 2 ] and a secondary chemocline near lake bottom. Maximum values of TDS and [CO 2 ] calculated for pre-release bottom water are 2400 mg/kg and 430 mmol/kg, respectively, based on tritium data. From this pre-release structure, a model of the gas release is proposed that is consistent with available chemical and observational data. An important feature of the model is that disruption of the pre-existing stratification was much more extensive than previously proposed, and even the deepest water layers were involved in the event. This model is not intended to limit possible gas release mechanisms, and thus complete re-establishment of pre-1986 water-column conditions is not a prerequisite for a future release. Spontaneous instability could occur at lake bottom in <20 yr if dissolved gas pressures continue to increase in this zone by 0.5–1 bar/yr as they have for the last 6 yr.

Lake Nyos↗

Glacier-volcano interactions in the north crater of Mt. Wrangell, Alaska

Glaciological and related observations from 1961 to 2005 at the summit of Mt Wrangell (62.008 N, 144.028W; 4317 m a.s.l.), a massive glacier-covered shield volcano in south-central Alaska, show marked changes that appear to have been initiated by the Great Alaska Earthquake (MW = 9.2) of 27 March 1964. The 4 x 6 km diameter, ice-filled Summit Caldera with several post-caldera craters on its rim, comprises the summit region where annual snow accumulation is 1&ndash;2 m of water equivalent and the mean annual temperature, measured 10 m below the snow surface, is &ndash;20&deg;C. Precision surveying, aerial photogrammetry and measurements of temperature and snow accumulation were used to measure the loss of glacier ice equivalent to about 0.03 km 3 of water from the North Crater in a decade. Glacier calorimetry was used to calculate the associated heat flux, which varied within the range 20&ndash;140W m &ndash;2 ; total heat flow was in the range 20&ndash;100 MW. Seismicity data from the crater&rsquo;s rim show two distinct responses to large earthquakes at time scales from minutes to months. Chemistry of water and gas from fumaroles indicates a shallow magma heat source and seismicity data are consistent with this interpretation.

Alaska↗

Assessing sulfate reduction and methane cycling in a high salinity pore water system in the northern Gulf of Mexico

Pore waters extracted from 18 piston cores obtained on and near a salt-cored bathymetric high in Keathley Canyon lease block 151 in the northern Gulf of Mexico contain elevated concentrations of chloride (up to 838 mM) and have pore water chemical concentration profiles that exhibit extensive departures (concavity) from steady-state (linear) diffusive equilibrium with depth. Minimum ??13C dissolved inorganic carbon (DIC) values of -55.9??? to -64.8??? at the sulfate-methane transition (SMT) strongly suggest active anaerobic oxidation of methane (AOM) throughout the study region. However, the nonlinear pore water chemistry-depth profiles make it impossible to determine the vertical extent of active AOM or the potential role of alternate sulfate reduction pathways. Here we utilize the conservative (non-reactive) nature of dissolved chloride to differentiate the effects of biogeochemical activity (e.g., AOM and/or organoclastic sulfate reduction) relative to physical mixing in high salinity Keathley Canyon sediments. In most cases, the DIC and sulfate concentrations in pore waters are consistent with a conservative mixing model that uses chloride concentrations at the seafloor and the SMT as endmembers. Conservative mixing of pore water constituents implies that an undetermined physical process is primarily responsible for the nonlinearity of the pore water-depth profiles. In limited cases where the sulfate and DIC concentrations deviated from conservative mixing between the seafloor and SMT, the ??13C-DIC mixing diagrams suggest that the excess DIC is produced from a 13C-depleted source that could only be accounted for by microbial methane, the dominant form of methane identified during this study. We conclude that AOM is the most prevalent sink for sulfate and that it occurs primarily at the SMT at this Keathley Canyon site.

Marine and Petroleum Geology↗

A geochemical model of the Platanares geothermal system, Honduras

Results of exploration drilling combined with results of geologic, geophysical, and hydrogeochemical investigations have been used to construct a geochemical model of the Platanares geothermal system, Honduras. Three coreholes were drilled, two of which produced fluids from fractured Miocene andesite and altered Cretaceous to Eocene conglomerate at 450 to 680 m depth. Large volume artesian flows of 160-165??C, predominantly bicarbonate water are chemically similar to, but slightly less saline than widespread boiling hot-spring waters. The chemistry of the produced fluid is dominated by equilibrium reactions in sedimentary rocks at greater depths and higher temperatures than those measured in the wells. Chemical, isotope, and gas geothermometers indicate a deep fluid temperature of 200-245??C and reflect a relatively short residence time in the fractures feeding the wells. Chloride-enthalpy relations as well as isotopic and chemical compositions of well discharges, thermal springs, and local cold waters support a conceptual model of ascending high-temperature (minimum 225??C) parent fluid that has cooled conductively to form the 160-165??C shallow (to 680 m) fluid encountered by the wells. The hot-spring waters are formed by boiling and steam loss from more or less conductively cooled parent fluid. The more dilute boiling spring waters (Cl = ???32 mg/kg) have cooled from > 225??C to about 160??C by conduction and from 160??C to 98??C by boiling. The most concentrated boiling spring waters (Cl = 37 mg/kg) have cooled from > 225??C to about 200??C by conduction and from 200??C to 98??C by boiling. Intermediate concentrations reflect mixed cooling paths. ?? 1991.

Journal of Volcanology and Geothermal Research↗

Long-term effects of surface coal mining on ground-water levels and quality in two small watersheds in eastern Ohio

Two small watersheds in eastern Ohio that were surface mined for coal and reclaimed were studied during 1986-89. Water-level and water-quality data were compared with similar data collected during previous investigations conducted during 1976-83 to determine long-term effects of surface mining on the hydrologic system. Before mining, the watersheds were characterized by sequences of flat-lying sedimentary rocks containing two major coal seams and underclays. An aquifer was present above each of the underclays. Surface mining removed the upper aquifer, stripped the coal seam, and replaced the sediment. This created a new upper aquifer with different hydraulic and chemical characteristics. Mining did not disturb the middle aquifer. A third, deeper aquifer in each watershed was not studied. Water levels were continuously recorded in one well in each aquifer. Other wells were measured every 2 months. Water levels in the upper aquifers reached hydraulic equilibrium from 2 to 5 years after mining ceased. Water levels in the middle aquifers increased more than 5 feet during mining and reached equilibrium almost immediately thereafter. Water samples were collected from three upper-aquifer well, a seep from the upper aquifer, and the stream in each watershed. Two samples were collected in 1986 and 1987, and one each in 1988 and 1989. In both watersheds, sulfate replaced bicarbonate as the dominant upper-aquifer and surface-water anion after mining. For the upper aquifer of a watershed located in Muskingum County, water-quality data were grouped into premining and late postmining time periods (1986-89). The premining median pH and concentration of dissolved solids and sulfate were 7.6, 378 mg/L (milligrams per liter), and 41 mg/L, respectively. The premining median concentrations of iron and manganese were 10 μg/L (micrograms per liter) and 25 μg/L, respectively. The postmining median values of pH, dissolved solids, and sulfate were 6.7, 1,150 mg/L, and 560 mg/L, respectively. The postmining median concentrations of iron and manganese were 3,900 μg/L and 1,900 μg/L, respectively. For the upper aquifer of a watershed located in Jefferson County, the water-quality data were grouped into three time periods of premining, early postmining, and late postmining. The premining median pH and concentrations of dissolved solids and sulfate were 7.0, 335 mg/L, and 85 mg/L, respectively. The premining median concentrations of iron and manganese were 30 μg/L for each constituent. Late postmining median pH and concentrations of dissolved solids and sulfate were 6.7, 1,495 mg/L, and 825 mg/L, respectively. The postmining median concentrations of iron and manganese were 31 μg/L and 1,015 μg/L, respectively. Chemistry of water in the middle aquifer in each watershed underwent similar changes. In general, statistically significant increases in concentrations of dissolved constituents occurred because of surface mining. In some constituents, concentrations increased by more than an order of magnitude. The continued decrease in pH indicated that ground water had no reached geochemical equilibrium in either watershed more than 8 years after mining.

Ohio↗

The presence and distribution of polycyclic aromatic hydrocarbons and inorganic elements in water and lakebed materials and the potential for bioconcentration in biota at established sampling sites on Lake Powell, Utah and Arizona

The National Park Service is responsible for monitoring the effects of visitor use on the quality of water, lakebed material (bottom sediments), and biota, in Lake Powell, Utah and Arizona. A sampling program was begun in 2010 to assess the presence, distribution, and concentrations of organic and inorganic compounds in the water column and bottom sediment. In response to an Environmental Impact Statement regarding personal watercraft and as a continuation from previous studies by the U.S. Geological Survey and the National Park Service, Glen Canyon National Recreation Area, water samples were collected and analyzed for polycyclic aromatic hydrocarbons (PAHs) using semipermeable membrane devices and inorganic elements using a fixed-bottle sampler deployed at established monitoring sites during 2010 and 2011. Lakebed material samples were also analyzed for polycyclic aromatic hydrocarbons and inorganic elements, some of which could be harmful to aquatic biota if present at concentrations above established aquatic life criteria. Of the 44 PAH compounds analyzed, 26 individual compounds were detected above the censoring limit in the water column by semipermeable membrane devices. The highest number of compounds detected were at Lone Rock Beach, Wahweap Marina, Rainbow Bridge National Monument, and Antelope Marina which are all located in the southern part of Lake Powell where visitation and boat use is high. Because PAHs can remain near their source, the potential for bioconcentration is highest near these sites. The PAH compound found in the highest concentration was phenol (5,902 nanograms per liter), which is included in the U.S. Environmental Protection Agency’s priority pollutants list. The dissolved inorganic chemistry of water samples measured at the sampling sites in Lake Powell defined three different patterns of elements: (1) concentrations were similar between sites in the upper part of the lake near Farley Canyon downstream to Halls Crossing Marina, a distance of about 36 lake miles, (2) concentrations varied depending on the element between Halls Crossing Marina downstream to the mouth of the Escalante River, a distance of about 33 lake miles, and (3) concentrations were similar between sites from below the mouth of the Escalante River to Glen Canyon Dam, a distance of about 68 lake miles. Analysis of lakebed bottom sediment material samples detected PAH compounds at all sampling sites except at Halls Crossing Marina, Stanton Creek, and Forgotten Canyon. Twenty-four of 44 PAHs analyzed in lakebed material were detected above the reporting limit. Perylene was the most prevalent compound detected above the reporting limit in lakebed material and was detected at three sampling sites. Concentrations of perylene ranged from an estimate of 24.0 to 47.9 micrograms per kilogram (μg/kg). Fluoranthene had the highest concentration of any PAH and was detected at the Wahweap Marina with a concentration of 565 μg/kg. The highest sum of concentrations for all compounds found in lakebed material samples at one site was at the Wahweap Marina, which had concentrations five times higher than the next highest site. The three major tributaries to Lake Powell—the Colorado, Escalante, and San Juan Rivers—all showed elevated concentrations of inorganic elements in their delta sediments for most elements relative to the majority of the sediment samples taken from the lake itself. However, there were four lake sites that had concentrations for most inorganic elements that equaled or exceeded those of the tributaries. Two of these sites were at the northeast part of the lake, nearest to the Colorado River as it enters Lake Powell (Farley Canyon and Blue Notch Canyon), one was at the Escalante River below 50-Mile Canyon, and other was at Antelope Marina.

Arizona;Utah↗

Water-quality assessment of the Trinity River Basin, Texas— Ground-water quality of the Trinity, Carrizo-Wilcox, and Gulf Coast aquifers, February-August 1994

Ground-water samples were collected from wells in the outcrops of the Trinity, Carrizo-Wilcox, and Gulf Coast aquifers during February-August 1994 to determine the quality of ground water in the three major aquifers in the Trinity River Basin study unit, Texas. These samples were collected and analyzed for selected properties, nutrients, major inorganic constituents, trace elements, pesticides, dissolved organic carbon, total phenols, methylene blue active substances, and volatile organic compounds as part of the U.S. Geological Survey National Water-Quality Assessment Program. Quality-control practices included the collection and analysis of blank, duplicate, and spiked samples. Samples were collected from 12 shallow wells (150 feet or less) and from 12 deep wells (greater than 150 feet) in the Trinity aquifer, 11 shallow wells and 12 deep wells in the Carrizo-Wilcox aquifer, and 14 shallow wells and 10 deep wells in the Gulf Coast aquifer. The three aquifers had similar water chemistries-calcium was the dominant cation and bicarbonate the dominant anion. Statistical tests relating well depths to concentrations of nutrients and major inorganic constituents indicated correlations between well depth and concentrations of ammonia nitrogen, nitrite plus nitrate nitrogen, bicarbonate, sodium, and dissolved solids in the Carrizo-Wilcox aquifer and between well depth and concentrations of sulfate in the Gulf Coast aquifer. The tests indicated no significant correlations for the Trinity aquifer. Concentrations of dissolved solids were larger than the secondary maximum contaminant level of 500 milligrams per liter established for drinking water by the U.S. Environmental Protection Agency in 12 wells in the Trinity aquifer, 4 wells in the Carrizo-Wilcox aquifer, and 6 wells in the Gulf Coast aquifer. Iron concentrations were larger than the secondary maximum contaminant level of 300 micrograms per liter in at least 3 samples from each aquifer, and manganese concentrations were larger than the secondary maximum contaminant level of 50 micrograms per liter in at least 2 samples from each aquifer. The pesticides atrazine, deethylatrazine, and pp'-DDE were detected in at least one sample from each aquifer. Diazinon was detected in 11 Trinity aquifer samples and 4 Carrizo-Wilcox aquifer samples. Each aquifer had one detection of a volatile organic compound-benzene in the Trinity aquifer, trichlorofluoromethane in the Carrizo-Wilcox aquifer, and trichloromethane in the Gulf Coast aquifer.

Texas↗

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↗

Chemistry of Stream Sediments and Surface Waters in New England

Summary -- This online publication portrays regional data for pH, alkalinity, and specific conductance for stream waters and a multi-element geochemical dataset for stream sediments collected in the New England states of Connecticut, Maine, Massachusetts, New Hampshire, Rhode Island, and Vermont. A series of interpolation grid maps portray the chemistry of the stream waters and sediments in relation to bedrock geology, lithology, drainage basins, and urban areas. A series of box plots portray the statistical variation of the chemical data grouped by lithology and other features.

Open-File Report↗

Geochemistry of the Johnson River, Lake Clark National Park and Preserve, Alaska

The Johnson River Basin, located in Lake Clark National Park and Preserve, drains an area of 96 square miles. A private inholding in the upper part of the basin contains a gold deposit that may be developed in the future. To establish a natural baseline to compare potential effects on water quality if development were to occur, the upper part of the Johnson River Basin was studied from 1999 to 2001 as part of a cooperative study with the National Park Service. Two basic rock types occur within the drainage basin of the study: the Jurassic Talkeetna Formation of interbedded volcanic and volcaniclastic rocks, and the slightly younger plutonic rocks of the Aleutian-Alaska Ranges batholith. The Johnson River gold prospect reflects widespread, secondary mineralization and alteration of the Talkeetna Formation. Metals found at the prospect proper are: arsenic, cadmium, copper, gold, iron, lead, mercury, molybdenum, selenium, silver, and zinc. The Johnson River prospect is located in the East Fork Ore Creek Basin, a 0.5 square mile watershed that is a tributary to the Johnson River. Water quality data from this stream reflect the mineralization of the basin and the highest concentrations of several trace elements and major ions of the water column were found in this stream. Presently, pH in this stream is normal, indicating that there is sufficient buffering capacity. At the Johnson River streamgage, which drains approximately 25 mi2 including the East Fork Ore Creek, concentrations of these constituents are significantly lower, reflecting the runoff from Johnson Glacier and Double Glacier, which account for approximately 75 percent of the total discharge. Streambed concentrations of cadmium, lead, and zinc from East Fork Ore Creek and its receiving stream, Ore Creek, typically exceed concentrations where sediment dwelling organisms would be affected. Similar to the water column chemistry, concentrations of these elements are lower at the Johnson River streamgage, reflecting the fine sediment input from the glacier streams draining Johnson Glacier and Double Glacier. The amount of organic carbon present in the study area is relatively low and most sites indicate that some degree of toxicity is present even though these basins do not contain mineralized areas. Acid based accounting tests on rock samples in the study area indicate a neutralizing capacity in the Talkeetna Formation rocks. These results should be used with caution because similar tests were not done on rocks from narrow veins or faults that could have acid generating potential. In addition, based on field tests during the study, carbonate-bearing rocks in streambeds are armored by a carbonate-depleted shell and would not readily neutralize acidic water.

Water-Resources Investigations Report↗

Characterization of water quality in Government Highline Canal at Camp 7 Diversion and Highline Lake, Mesa County, Colorado, July 2000 through September 2003

The U.S. Geological Survey, in cooperation with the Colorado Division of Parks and Recreation, collected and analyzed water-quality data for the Government Highline Canal and Highline Lake from July 2000 through September 2003. Implementation of modernization strategies for the canal, which supplies most of the water to the lake, would decrease the amount of water spilled to Highline Lake from August through October. A reduction in spill water into Highline Lake could adversely affect the recreational uses of the lake. To address this concern and to characterize the water quality in the Government Highline Canal and Highline Lake, the U.S. Geological Survey conducted a study to evaluate limnological conditions prior to implementation of the modernization strategies. This report characterizes the water quality of inflow from the Government Canal and in Highline Lake prior to implementation of modernization strategies in the Government Canal. Flow entering the lake from the Government Canal was characterized using field properties and available chemical, sediment, and bacteria concentrations. Data collected at Highline Lake were used to characterize the seasonal stratification patterns, water-quality chemistry, bacteria populations, and phytoplankton community structure in the lake. Data used for this report were collected at one inflow site to the lake and four sites in Highline Lake. Highline Lake is a mesotrophic/eutrophic lake that has dimictic thermal stratification patterns. Samples collected in the photic zone indicated that there was little physical, chemical, or biological variability at this depth at any of the sampled sites in Highline Lake. Strong thermal and dissolved-oxygen stratification patterns were observed during summer. Dissolved-oxygen concentrations of less than 1 milligram per liter were observed during the summer. Ammonia likely was released from the bottom sediments of Highline Lake. The limiting nutrient in Highline Lake could be nitrogen or phosphorus. In general, the seasonal succession of phytoplankton was similar to that of other lakes in the temperate zone. Several types of algae associated with taste and odor issues were identified in samples, but critical concentrations were not exceeded for any listed algal group with the exception of the diatom genus Cyclotella in one sample. Bacteria concentrations were determined at the public swim beach at Highline Lake. E. coli samples were collected periodically by the USGS and weekly by the Colorado Division of Parks and Recreation. During the study period, no reported E. coli concentration exceeded the standard for natural swimming areas. Inflow water quality was characterized by samples collected at the Camp 7 check structure on the Government Canal. Inflow water temperatures reflected the seasonal patterns of the source water in the Colorado River. The water was well oxygenated. Nitrogen and phosphorus concentrations were low, and concentrations did not differ substantially from year to year or seasonally within a year. All samples had reportable numbers of fecal streptococcus. The maximum reported concentration of E. coli was reported at 77 colonies per 100 milliliters of sample. Suspended-sediment concentrations were relatively low.

Scientific Investigations Report↗

Long-term hydrologic sustainability of calcareous fens along the Glacial Lake Agassiz beach ridges, northwestern Minnesota, USA

Calcareous fens are peat-accumulating wetlands fed by calcium-rich groundwater that support several threatened species of plants that thrive in these geochemical conditions. This investigation characterized the hydrology of two calcareous fens in the Glacial Lake Agassiz beach ridge complex in northwestern Minnesota, USA. Sandy surficial beach ridge aquifers and underlying buried glacial aquifers were considered as sources of groundwater to the fen. A combination of the two sources influenced by seasonal hydrology was also considered. Synchronous hydrologic responses to rainfall events and hydraulic gradients indicate the calcareous fens are well-connected to the beach-ridge aquifers. Chemistry of water discharging to the fens is calcium-magnesium-bicarbonate type similar to the beach ridge aquifers, and distinct from buried aquifers that have significant sodium and chloride. High tritium values and oxygen isotope signatures similar to the beach ridge aquifers characterized fen water. Beach ridge aquifer complexes are relatively thin (8–10 m) and overlie thick clay/clay loam till. These beach ridges exhibit high seasonal recharge and have permanent saturated zones, providing a continual source of calcium-rich water for the fens. Electrical resistivity profiles characterized the glacial stratigraphy and highlighted the well-developed physical connection between beach ridge aquifers and calcareous fens. The results of this study allow evaluation of the potential impacts of irrigation and aggregate quarrying on calcareous fens along sand and gravel beach ridges.

Minnesota↗

Isotopic evidence for glacial meltwater recharge to the Cambrian-Ordovician aquifer, north-central United States

The chemistry of water in the Cambrian-Ordovician aquifer in six midwestern states has been studied as part of the Northern Midwest Regional Aquifer-System Analysis of the U.S. Geological Survey. Dissolved-solids concentrations generally increase perpendicular to the direction of regional groundwater flow, from less than 400 mg/liter in southeast Minnesota, southwest Wisconsin, and northeast Iowa to more than 10,000 mg/liter in northwest Missouri. Isotopic ratios of hydrogen and oxygen are significantly depleted from north to south, with an areal distribution approximately parallel to the distribution of dissolved solids. For example, ??18O in southern Iowa and northern Missouri is about 6 parts per thousand lighter than ??18O of modern recharge water in Minnesota and Wisconsin. Covariance between ??18O and ??D of the groundwater, similar to that of modern precipitation, suggests that the differences in isotopic ratios between groundwater and modern recharge water reflect meteoric signatures of water during past recharge events rather than geochemical processes such as isotopic exchange with aquifer materials. The pronounced parallelism between the distribution of isotopes and dissolved solids over large areas probably reflects largescale recharge of Pleistocene glacial meltwater into the aquifer system, which probably had a paleoflow system with a gradient from northeast to southwest rather than from northwest to southeast. ?? 1984.

Quaternary Research↗

The role of palynology in paleoecological analyses of Tertiary coals

Pollen, spores, and other plant microfossils are important constituents of Tertiary coals, both as petrographic components (the maceral sporinite) and as distinctive indicators of the nature of the depositional environment in which the coal-forming peat accumulated. Palynological analyses, which have been conducted on Tertiary coals since the 1930's, play an increasingly important role in modern paleoecological analyses of coals. Among the most important factors controlling the petrographic composition and facies characteristics of coal deposits are the types and relative abundances of plants that composed the peat. At present, wetland environments in which peat accumulates (mires) range from marshes and bogs to forested swamps; each is inhabited by distinctive plant communities. These plant communities are associated with varied conditions of climate, water depth, chemistry, and nutrient supply, and the floras can be indicative of these conditions. In the Tertiary Period, plant communities of mires were also highly diverse and specialized (especially as compared with those of the Carboniferous). The dominant species in some Paleocene mire floras were gymnosperms, but continuing a trend begun in Late Cretaceous time, angiosperms became increasingly prominent through the Tertiary. The diverse: angiosperm-dominated mire floras produced coals that vary significantly in facies and hence in quality. Such contrasts are evident in contemporaneous coals from different paleolatitudes, as well as among, coals of different ages within the Tertiary, as exemplified by selected deposits in the western United. States. The palynofloras of these coals reflect the floristic composition of the plant communities of the ancient mires.

International Journal of Coal Geology↗