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USGS2002

Water-quality and physical characteristics of streams in the Treyburn development area of Falls Lake watershed, North Carolina, 1994–98

Treyburn is a 5,400-acre planned, mixed-use development in the upper Neuse River Basin of North Carolina. The development, which began in 1986, is located in the Falls Lake watershed near three water-supply reservoirs-Lake Michie to the north, Falls Lake to the southeast, and Little River Reservoir to the west. A study began in 1988 to determine the water-quality characteristics of surface waters in and around the Treyburn development area. Data to characterize water quality at five different sites were collected from July 1994 through September 1998. Data from a previous study are available for some sites for the period 1988–93. The sites were selected to characterize water quality and quantity in and near the Treyburn development and included an undeveloped basin, a relatively small basin containing single-family residences and a golf course, a basin downstream from the western part of the development with some industrial land use, and two basins unaffected by the development where agricultural land is being converted to urban and forested land use. Suspended-sediment concentrations ranged from less than 1 to 581 milligrams per liter and were fairly uniform among the five sites. Median suspended-sediment concentrations ranged from 12 to 21 milligrams per liter. Few concentrations of metals and trace elements, except aluminum, iron, and manganese, exceeded the laboratory reporting levels or water-quality criteria. At one site, concentrations of silver exceeded both the action level and the reporting level; copper was detected at each site and exceeded the action level of 7 micrograms per liter at one site. The lowest range and median concentrations of total organic nitrogen, nitrate, ammonia, total phosphorus, and orthophosphorus occurred in the relatively undisturbed, forested site. The maximum concentration of organic nitrogen (1.97 milligrams per liter) occurred at one of the sites unaffected by the Treyburn development where agricultural land is being converted to urban land use. At all sites, ammonia concentrations ranged from less than 0.02 to 0.36 milligram per liter, and median concentrations were near the reporting level. Nitrate concentrations ranged from less than 0.05 to 0.80 milligram per liter. Phosphorus concentrations at all of the Treyburn study sites were low compared to phosphorus concentrations that typically exceed 0.1 milligram per liter at sites sampled nationally for the U.S. Geological Survey National Water-Quality Assessment Program, including the Albemarle-Pamlico study area in North Carolina. Total phosphorus concentrations ranged from less than 0.01 to 0.87 milligram per liter, and orthophosphorus concentrations ranged from less than 0.01 to 0.76 milligram per liter as phosphorus. The maximum concentrations of total phosphorus and orthophosphorus occurred at the Treyburn residential and golf-course site, likely as a result of the fertilizer applications associated with these two types of land use. Of the 119 different pesticides tested, 11 were detected in concentrations that exceeded the laboratory reporting levels, though in very low concentrations. Water samples from the residential and golf-course site contained the greatest number of pesticides (10). Five of six samples collected at this site had detectable concentrations of simazine, atrazine, and pendimethalin-all herbicides used to control weeds in crops or turf. Channel geometry was assessed at eight sites in the study area in February 1997. These sites were separated into three groups based on mean bank angle and mean channel width-to-depth ratios. Channel gradient ranged from 0.04 to 1.63 percent, and mean cross sectional area ranged from 31 to 1,227 square feet. Three macroinvertebrate samples were collected from each of 10 sites. These three samples were from areas designated as richest targeted habitats, depositional targeted habitats, and qualitative multitargeted habitats. Over 230 taxa were identified fromthese 10 sites. The North Carolina Biotic Indices ranged from 4.98 (excellent) to 6.82 (fair). River sites tended to have higher total taxa richness (91-108) than did the small, intermittent streams (49–84) or the midsize Mountain Creek (85). Intermittent streams represent fairly hostile environments for most aquatic organisms. Samples from richest targeted habitats typically were more than twice as rich as samples from depositional targeted habitats and represented from 50 to 75 percent of the taxa found at each site (mean of 62 percent). The industrial site lacked many of the mayfly taxa that were present at the undeveloped site. Mayflies are very sensitive to metals contamination, and their absence may indicate a possible problem. The supporting chemical information is not available for the industrial site, and additional study would be necessary to substantiate this possibility. The two sites with residential and golf-course land use tended to support more different types of sensitive invertebrates (that is, mayflies, stoneflies, and caddis flies) than did the forested/residential site, though the abundances of these taxa were very similar. Land-use effects were not evident based on a comparison among these sites. Indirect gradient analysis was used to determine patterns in the distribution of invertebrates and to examine the relations between these patterns and physical and chemical site characteristics determined in this study. This analysis supports the contention that the dominant factors accounting for the distribution of benthic invertebrates are associated with natural factors, such as basin size, rather than land use. Constituent loads at five study sites were calculated for nutrients, suspended sediment, and total organic carbon. The median annual total nitrogen yield ranged from 0.635 to 1.63 tons per square mile. The median annual phosphorus yield ranged from 0.046 to 0.619 ton per square mile, and the median annual orthophosphate yield ranged from 0.022 to 0.379 ton per square mile. Orthophosphate accounted for more than half of the phosphorus yield at the residential and golf-course site. The maximum suspended-sediment yield was 422 tons per square mile, and the minimum yield was 32 tons per square mile. The suspended-sediment yield at one of the sites unaffected by the Treyburn development where agricultural was being converted to urban land use was high compared to other forested basins in the Piedmont of North Carolina. Total organic carbon data sufficient for estimating loads were available at three of the five sites. Of these three sites, the undeveloped site had substantially more organic carbon yield than the other two sites. The only significant water-quality trend (alpha=0.05) was a downward trend for total nitrogen and organic nitrogen at the undeveloped site. The trend slope was small, only 0.019 milligram per liter as nitrogen or less than 9 percent of the median organic nitrogen concentration. No trend was observed for nitrite plus nitrate or for ammonia, indicating that the downward trend in total nitrogen was due only to organic nitrogen.

North Carolina↗

USGS1999

Modelling removal mechanisms of Pb, Cu, Zn and Cd in acidic groundwater during the neutralization by ambient surface and ground waters

Removal of Pb, Cu, Zn, and Cd during neutralization of acid rock drainage is examined using model simulations of field conditions and laboratory experiments involving mixing of natural drainage and surface waters or groundwaters. The simulations consider sorption onto hydrous Fe and Al oxides and particulate organic carbon, mineral precipitation, and organic and inorganic solution complexation of metals for two physical systems where newly formed oxides and particulate organic matter are either transported or retained along the chemical pathway. The calculations indicate that metal removal is a strong function of the physical system. Relative to direct discharge of ARD into streams, lower metal removals are observed where ARD enters streamwaters during the latter stages of neutralization by ambient groundwater after most of the Fe has precipitated and been retained in the soils. The mixing experiments, which represent the field simulations, also demonstrated the importance of dissolved metal to particle Fe ratios in controlling dissolved metal removal along the chemical pathway. Finally, model calculations indicate that hydrous Fe oxides and particulate organic carbon are more important than hydrous Al oxides in removing metals and that both inorganic and organic complexation must be considered when modeling metal removal from aquatic systems that are impacted by sulfide oxidation.

Environmental Science & Technology↗

USGS1996

Simulation of subsurface storage and recovery of treated effluent injected in a saline aquifer, St. Petersburg, Florida

The potential for subsurface storage and recovery of treated effluent into the uppermost producing zone (zone A) of the Upper Floridan aquifer in St. Petersburg, Florida, is being studied by the U.S. Geological Survey, in cooperation with the city of St. Petersburg and the Southwest Florida Water Management District. A measure of the success of this practice is the recovery efficiency, or the quantity of water relative to the quantity injected, that can be recovered before the water that is withdrawn fails to meet water-quality standards. The feasibility of this practice will depend upon the ability of the injected zone to receive, store, and discharge the injected fluid. A cylindrical model of ground-water flow and solute transport, incorporating available data on aquifer properties and water quality, was developed to determine the relation of recovery efficiency to various aquifer and fluid properties that could prevail in the study area. The reference case for testing was a base model considered representative of the saline aquifer underlying St. Petersburg. Parameter variations in the tests represent possible variations in aquifer conditions in the area. The model also was used to study the effect of various cyclic injection and withdrawal schemes on the recovery efficiency of the well and aquifer system. A base simulation assuming 15 days of injection of effluent at a rate of 1.0 million gallons per day and 15 days of withdrawal at a rate of 1.0 million gallons per day was used as reference to compare changes in various hydraulic and chemical parameters on recovery efficiency. A recovery efficiency of 20 percent was estimated for the base simulation. For practical ranges of hydraulic and fluid properties that could prevail in the study area, the model analysis indicates that (1) the greater the density contrast between injected and resident formation water, the lower the recovery efficiency, (2) recovery efficiency decreases significantly as dispersion increases, (3) high formation permeability favors low recovery efficiencies, and (4) porosity and anisotropy have little effect on recovery efficiencies. In several hypothetical tests, the recovery efficiency fluctuated between about 4 and 76 percent. The sensitivity of recovery efficiency to variations in the rate and duration of injection (0.25, 0.50, 1.0, and 2.0 million gallons per day) and withdrawal cycles (60, 180, and 365 days) was determined. For a given operational scheme, recovery efficiency increased as the injection and withdrawal rate is increased. Model results indicate that recovery efficiencies of between about 23 and 37 percent can be obtained for different subsurface storage and recovery schemes. Five successive injection, storage, and recovery cycles can increase the recovery efficiency to about 46 to 62 percent. There is a larger rate of increase at smaller rates than at larger rates. Over the range of variables studied, recovery efficiency improved with successive cycles, increasing rapidly during initial cycles tyhen more slowly at later cycles. The operation of a single well used for subsurface storage and recovery appears to be technically feasible under moderately favorable conditions; however, the recovery efficiency is higly dependent upon local physical and operational parameters. A combination of hydraulic, chemical, and operational parameters that minimize dispersion and buoyancy flow, maximizes recovery efficiency. Recovery efficiency was optimal where resident formation water density and permeabilities were relatively similar and low.

Water-Resources Investigations Report↗

USGS1993

Use of principal-component, correlation, and stepwise multiple-regression analyses to investigate selected physical and hydraulic properties of carbonate-rock aquifers

Correlation analysis in conjunction with principal-component and multiple-regression analyses were applied to laboratory chemical and petrographic data to assess the usefulness of these techniques in evaluating selected physical and hydraulic properties of carbonate-rock aquifers in central Pennsylvania. Correlation and principal-component analyses were used to establish relations and associations among variables, to determine dimensions of property variation of samples, and to filter the variables containing similar information. Principal-component and correlation analyses showed that porosity is related to other measured variables and that permeability is most related to porosity and grain size. Four principal components are found to be significant in explaining the variance of data. Stepwise multiple-regression analysis was used to see how well the measured variables could predict porosity and (or) permeability for this suite of rocks. The variation in permeability and porosity is not totally predicted by the other variables, but the regression is significant at the 5% significance level.

Journal of Hydrology↗

USGS2016

Climate-change signals in national atmospheric deposition program precipitation data

National Atmospheric Deposition Program (NADP)/National Trends Network precipitation type, snow-season duration, and annual timing of selected chemical wet-deposition maxima vary with latitude and longitude within a 35-year (1979–2013) data record for the contiguous United States and Alaska. From the NADP data collected within the region bounded by 35.6645°–48.782° north latitude and 124°–68° west longitude, similarities in latitudinal and longitudinal patterns of changing snow-season duration, fraction of annual precipitation recorded as snow, and the timing of chemical wet-deposition maxima, suggest that the chemical climate of the atmosphere is linked to physical changes in climate. Total annual precipitation depth has increased 4–6 % while snow season duration has decreased from approximately 7 to 21 days across most of the USA, except in higher elevation regions where it has increased by as much as 21 days. Snow-season precipitation is increasingly comprised of snow, but annually total precipitation is increasingly comprised of liquid precipitation. Meanwhile, maximum ammonium deposition occurs as much as 27 days earlier, and the maximum nitrate: sulfate concentration ratio in wet-deposition occurs approximately 10–21 days earlier in the year. The maximum crustal (calcium + magnesium + potassium) cation deposition occurs 2–35 days earlier in the year. The data suggest that these shifts in the timing of atmospheric wet deposition are linked to a warming climate, but the ecological consequences are uncertain.

Climate Dynamics↗

USGS2018

Environmental characteristics and utilization potential of metallurgical slag

Slag, an abundant byproduct from the pyrometallurgical processing of ores, can be an environmental liability or a valuable resource. The most common environmental impact of slag is from the leaching of potentially toxic elements, acidity, or alkalinity that may impact nearby soils and surface water and groundwater. Factors that influence its environmental behavior include physical characteristics, such as grain size and porosity, chemical composition with some slag being enriched in certain elements, the mineralogy and partitioning of elements in more or less reactive phases, water-slag interactions, and site conditions. Many of these same factors also influence its resource potential. For example, crystalline ferrous slag is most commonly used as construction aggregate, whereas glassy (i.e., granulated) slag is used in cement. Also, the calcium minerals found in ferrous slag result in useful applications in water treatment. In contrast, the high trace-element content of some base-metal slags makes the slags economically attractive for extraction of residual elements. An evaluation tool is used to help categorize a particular slag as an environmental hazard or valuable byproduct. Results for one type of slag, legacy steelmaking slag from the Chicago area in the USA, suggest the material has potential to be used for treating phosphate-rich or acidic waters; however, the pH and trace-element content of resulting solutions may warrant further examination.

Book chapter↗

USGS2018

Irrigated agriculture and future climate change effects on groundwater recharge, northern High Plains aquifer, USA

Understanding the controls of agriculture and climate change on recharge rates is critically important to develop appropriate sustainable management plans for groundwater resources and coupled irrigated agricultural systems. In this study, several physical (total potential ( ψ T ) time series) and chemical tracer and dating ( 3 H, Cl − , Br − , CFCs, SF 6 , and 3 H/ 3 He) methods were used to quantify diffuse recharge rates beneath two rangeland sites and irrigation recharge rates beneath two irrigated corn sites along an east-west (wet-dry) transect of the northern High Plains aquifer, Platte River Basin, central Nebraska. The field-based recharge estimates and historical climate were used to calibrate site-specific Hydrus-1D models, and irrigation requirements were estimated using the Crops Simulation Model (CROPSIM). Future model simulations were driven by an ensemble of 16 global climate models and two global warming scenarios to project a 2050 climate relative to the historical baseline 1990 climate, and simulate changes in precipitation, irrigation, evapotranspiration, and diffuse and irrigation recharge rates. Although results indicate statistical differences between the historical variables at the eastern and western sites and rangeland and irrigated sites, the low warming scenario (+1.0 °C) simulations indicate no statistical differences between 2050 and 1990. However, the high warming scenarios (+2.4 °C) indicate a 25% and 15% increase in median annual evapotranspiration and irrigation demand, and decreases in future diffuse recharge by 53% and 98% and irrigation recharge by 47% and 29% at the eastern and western sites, respectively. These results indicate an important threshold between the low and high warming scenarios that if exceeded could trigger a significant bidirectional shift in 2050 hydroclimatology and recharge gradients. The bidirectional shift is that future northern High Plains temperatures will resemble present central High Plains temperatures and future recharge rates in the east will resemble present recharge rates in the western part of the northern High Plains aquifer. The reductions in recharge rates could accelerate declining water levels if irrigation demand and other management strategies are not implemented. Findings here have important implications for future management of irrigation practices and to slow groundwater depletion in this important agricultural region.

Northern High Plains Aquifer↗

USGS1969

Micromineralogy of silver-bearing sphalerite from Flat River, Missouri

Detailed mineralogical and chemical study of sphalerite-rich lead ores from Flat River, Mo., confirms the presence of anomalous amounts of silver in the sphalerite. Although silver is closely associated with chlorine and no silver sulfide minerals were identified, geochemical considerations indicate the silver may be in the form of discrete submicron-size grains of sulfide rather than chloride. However, the close correlation between abundance variations in silver, chlorine, cadmium, iron, and minor lead suggests the possible existence of submicron-size grains of a complex chloride or oxychloride. Results from detailed chemical study of sphalerite show: (1) chlorine is present in areas containing silver and changes in abundance of both elements are similar; (2) the mole ratio of chlorine to silver varies from approximately 3:1 to 6:1 with an approximate average of 5:1 and the total content of each element varies widely between grains and within the same grain; (3) taking total silver in any analysis and calculating the amount of chlorine required for silver chloride leaves an excess of chlorine; (4) in chlorine-deficient areas the amounts of iron and cadmium substituting for zinc in the sphalerite structure vary widely; and (5) in areas containing chlorine, changes in abundance of iron and cadmium vary directly with that of chlorine. The fine-grained dusty opaque inclusions characterize sphalerite from this area; they were identified as mainly galena with lesser amounts of pyrite and cassiterite. Galena is silver-free (<0.02 weight percent Ag) and is essentially pure lead sulfide. Other sulfides identified include pyrite, a cobalt-nickel-iron sulfide of composition Co (sub 0.55) Ni (sub 0.25) Fe (sub 0.20) S (sub 2.00), and an iron-cobalt-nickel sulfide containing 22-28 weight percent Fe, 10-15 weight percent Co, and 3-5 weight percent Ni. Anomalous amounts of tin present as cassiterite are associated with the gangue minerals quartz, potash feldspar, a kaolinite-type clay, and trace amounts of cuprite. Carbonate gangue minerals include calcite, dolomite, ankerite, magnesite, and minor amounts of cerussite. Chemical analyses were made of many minerals and physical and textural relationships examined.

Missouri↗

USGS2012

Strategies for soil quality assessment using VNIR gyperspectral spectroscopy in a western Kenya Chronosequence

Visible and near-infrared reflectance spectroscopy (VNIRS) is a rapid and nondestructive method that can predict multiple soil properties simultaneously, but its application in multidimensional soil quality (SQ) assessment in the tropics still needs to be further assessed. In this study, VNIRS (350–2500 nm) was employed to analyze 227 air-dried soil samples of Ultisols from a soil chronosequence in western Kenya and assess 16 SQ indicators. Partial least squares regression (PLSR) was validated using the full-site cross-validation method by grouping samples from each farm or forest site. Most suitable models successfully predicted SQ indicators (R 2 ≥ 0.80; ratio of performance to deviation [RPD] ≥ 2.00) including soil organic matter (OM LOI ), active C, Ca, cation exchange capacity (CEC), and clay. Moderately-well predicted indicators (0.50 ≤ R 2 < 0.80; 1.40 ≤ RPD < 2.00) were water stable aggregation (WSA), Cu, silt, Mg, pH, sand, water content at permanent wilting point (Θ pwp ), and field capacity (Θ fc ). Poorly predicted indicators (R 2 < 0.50; RPD < 1.40) were EC, S, P, available water capacity (AWC), K, Zn, and penetration resistance. Combining VNIRS with selected field- and laboratory-measured SQ indicator values increased predictability. Furthermore, VNIRS showed moderate to substantial agreement in predicting interpretive SQ scores and a composite soil quality index (CSQI) especially when combined with directly measured SQ indicator values. In conclusion, VNIRS has good potential for low cost, rapid assessment of physical and biological SQ indicators but conventional soil chemical tests may need to be retained to provide comprehensive SQ assessments.

Western Kenya↗

USGS2013

Potential Environmental and Environmental-Health Implications of the SAFRR Tsunami Scenario in California: Chapter F in The SAFRR (Science Application for Risk Reduction) Tsunami Scenario

The California Tsunami Scenario models the impacts of a hypothetical, yet plausible, tsunami caused by an earthquake offshore from the Alaska Peninsula. In this chapter, we interpret plausible tsunami-related contamination, environmental impacts, potential for human exposures to contaminants and hazardous materials, and implications for remediation and recovery. Inundation-related damages to major ports, boat yards, and many marinas could release complex debris, crude oil, various fuel types and other petroleum products, some liquid bulk cargo and dry bulk cargo, and diverse other pollutants into nearby coastal marine environments and onshore in the inundation zone. Tsunami-induced erosion of contaminated harbor bottom sediments could re-expose previously sequestered metal and organic pollutants (for example, organotin or DDT). Inundation-related damage to many older buildings could produce debris containing lead paint, asbestos, pesticides, and other legacy contaminants. Intermingled household debris and externally derived debris and sediments would be left in flooded buildings. Post tsunami, mold would likely develop in inundated houses, buildings, and debris piles. Tsunamigenic fires in spilled oil, debris, cargo, vehicles, vegetation, and residential, commercial, or industrial buildings and their contents would produce potentially toxic gases and smoke, airborne ash, and residual ash/debris containing caustic alkali solids, metal toxicants, asbestos, and various organic toxicants. Inundation of and damage to wastewater treatment plants in many coastal cities could release raw sewage containing fecal solids, pathogens, and waste chemicals, as well as chemicals used to treat wastewaters. Tsunami-related physical damages, debris, and contamination could have short- and longer-term impacts on the environment and the health of coastal marine and terrestrial ecosystems. Marine habitats in intertidal zones, marshes, sloughs, and lagoons could be damaged by erosion or sedimentation, and could receive an influx of debris, metal and organic contaminants, and sewage-related pathogens. Debris and re-exposed contaminated sediments would be a source of sea- or rain-water-leachable metal and organic contaminants that could pose chronic toxicity threats to ecosystems. If human populations are successfully evacuated prior to the tsunami arrival, there would be no or limited numbers of drownings, other casualties, or related injuries, wounds, and infections. Immediately after the tsunami, human populations away from the inundation zone could be transiently exposed to airborne gases, smoke, and ash from tsunamigenic fires. Cleanup and disposal, particularly of hazardous materials, would pose substantial logistical challenges and economic costs. Given the high value of the coastal residential and commercial properties in the inundation zone, it can be postulated that there would be substantial insurance claims for environmental restoration, mold mitigation, disposal of debris that contains hazardous materials, and costs of litigation related to environmental liability. Post-tsunami cleanup, if done with appropriate mitigation (for example, dust control), personal protection, and disposal measures, would help reduce the potential for cleanup-worker and resident exposures to toxicants and pathogens in harbor waters, debris, soils, ponded waters, and buildings. A number of other steps can be taken by governments, businesses, and residents to help reduce the environmental impacts of tsunamis and to recover more quickly from these environmental impacts. For example, development of State and local policies that foster rapid assessment of potential contamination, as well as rapid decision making for disposal options should hazardous debris or sediment be identified, would help enhance recovery by speeding cleanup.

California↗

USGS1992

Ground-water-quality assessment of the central Oklahoma aquifer, Oklahoma: Hydrologic, water-quality, and quality-assurance data 1987-90

This report presents data collected from 202 wells between June 1987 and September 1990 as part of the Central Oklahoma aquifer pilot study of the National Water-Quality Assessment Program. The report describes the sampling networks, the sampling procedures, and the results of the ground-water quality and quality-assurance sample analyses. The data tables consist of information about the wells sampled and the results of the chemical analyses of ground water and quality-assurance sampling. Chemical analyses of ground-water samples in four sampling networks are presented: A geochemical network, a low-density survey bedrock network, a low-density survey alluvium and terrace deposits network, and a targeted urban network. The analyses generally included physical properties, major ions, nutrients, trace substances, radionuclides, and organic constituents. The chemical analyses of the ground-water samples are presented in five tables: (1) Physical properties and concentrations of major ions, nutrients, and trace substances; (2) concentrations of radionuclides and radioactivities; (3) carbon isotope ratios and delta values (d-values) of selected isotopes; (4) concentrations of organic constituents; and (5) organic constituents not reported in ground-water samples. The quality of the ground water sampled varied substantially. The sum of constituents (dissolved solids) concentrations ranged from 71 to 5,610 milligrams per liter, with 38 percent of the wells sampled exceeding the Secondary Maximum Contaminant Level of 500 milligrams per liter established under the Safe Drinking Water Act. Values of pH ranged from 5.7 to 9.2 units with 20 percent of the wells outside the Secondary Maximum Contaminant Level of 6.5 to 8.5 units. Nitrite plus nitrate concentrations ranged from less than 0.1 to 85 milligrams per liter with 8 percent of the wells exceeding the proposed Maximum Contaminant Level of 10 milligrams per liter. Concentrations of trace substances were highly variable, ranging from below the reporting level to concentrations over the Maximum Contaminant Levels for several constituents (arsenic, barium, cadmium, chromium, lead, and selenium). Radionuclide activities also were highly variable. Gross alpha radioactivity ranged from 0.1 to 210 picocuries per liter as 230thorium. Of the wells sampled, 20 percent exceeded the proposed Maximum Contaminant Level of 15 picocuries per liter for gross alpha radioactivity. Organic constituents were detected in 39 percent of the 170 wells sampled for organic constituents; in most cases concentrations were at or near the laboratory minimum reporting levels. Ten of the wells sampled for organic constituents had one or more constituents (chlordane, dieldrin, heptachlor epoxide, trichloroethylene, 1,1-dichloroethylene, 1,1,1-trichloroethane) at concentrations equal to or greater than the Maximum Contaminant Level or acceptable concentrations as suggested in the Environmental Protection Agency's Health Advisory Summaries. Quality-assurance sampling included duplicate samples, repeated samples, blanks, spikes, and blind samples. These samples proved to be essential in evaluating the accuracy of the data, particularly in the case of volatile organic constituents.

Oklahoma↗

USGS2011

Distribution, persistence, and hydrologic characteristics of salmon spawning habitats in clearwater side channels of the Matanuska River, southcentral Alaska

Turbid, glacially influenced rivers are often considered to be poor salmon spawning and rearing habitats and, consequently, little is known about salmon habitats that do occur within rivers of this type. To better understand salmon spawning habitats in the Matanuska River of southcentral Alaska, the distribution and characteristics of clearwater side-channel spawning habitats were determined and compared to spawning habitats in tributaries. More than 100 kilometers of clearwater side channels within the braided mainstem of the Matanuska River were mapped for 2006 from aerial images and ground-based surveys. In reaches selected for historical analysis, side channel locations shifted appreciably between 1949 and 2006, but the relative abundance of clearwater side channels was fairly stable during the same period. Geospatial analysis of side channel distribution shows side channels typically positioned along abandoned bars at the braid plain margin rather than on bars between mainstem channels, and shows a strong correlation of channel abundance with braid plain width. Physical and geomorphic characteristics of the channel and chemical character of the water measured at 19 side channel sites, 6 tributary sites, 4 spring sites, and 5 mainstem channel sites showed conditions suitable for salmon spawning in side channels and tributaries, and a correlation of side channel characteristics with the respective tributary or groundwater source water. Autumn-through-spring monitoring of intergravel water temperatures adjacent to salmon redds (nests) in three side channels and two tributaries indicate adequate accumulated thermal units for incubation and emergence of salmon in side channels and relatively low accumulated thermal units in tributaries.

Alaska↗

USGS2006

Chapter A6. Section 6.1. Temperature

Accurate temperature measurements are required for accurate determinations of important environmental parameters such as pH, specific electrical conductance, and dissolved oxygen, and to the determination of chemical reaction rates and equilibria, biological activity, and physical fluid properties. This section of the National Field Manual (NFM) describes U.S. Geological Survey (USGS) guidance and protocols for measurement of temperature in air, ground water, and surface water and calibration of the equipment used. Each chapter of the National Field Manual is published separately and revised periodically. Newly published and revised chapters will be announced on the USGS Home Page on the World Wide Web under 'New Publications of the U.S. Geological Survey.'

Techniques of Water-Resources Investigations↗

USGS1886

Report of work done in the division of chemistry and physics mainly during the fiscal year 1884-85

The present bulletin contains some of the more important results obtained in the chemical laboratory of the United States Geological Survey during the fiscal year 1884—'85. It also contains two physical papers representing work which was mainly done during previous fiscal years, but completed during the one for which this bulletin is issued. These papers are practically continuations of or supplements to Bulletin 14.

Bulletin↗

USGS1997

Adsorbed natural gas storage with activated carbons made from Illinois coals and scrap tires

Activated carbons for natural gas storage were produced from Illinois bituminous coals (IBC-102 and IBC-106) and scrap tires by physical activation with steam or CO 2 and by chemical activation with KOH, H 3 PO 4 , or ZnCl 2 . The products were characterized for N 2 -BET area, micropore volume, bulk density, pore size distribution, and volumetric methane storage capacity ( V m / V s ). V m / V s values for Illinois coal-derived carbons ranged from 54 to 83 cm 3 /cm 3 , which are 35−55% of a target value of 150 cm 3 /cm 3 . Both granular and pelletized carbons made with preoxidized Illinois coal gave higher micropore volumes and larger V m / V s values than those made without preoxidation. This confirmed that preoxidation is a desirable step in the production of carbons from caking materials. Pelletization of preoxidized IBC-106 coal, followed by steam activation, resulted in the highest V m / V s value. With roughly the same micropore volume, pelletization alone increased V m / V s of coal carbon by 10%. Tire-derived carbons had V m / V s values ranging from 44 to 53 cm 3 /cm 3 , lower than those of coal carbons due to their lower bulk densities. Pelletization of the tire carbons increased bulk density up to 160%. However, this increase was offset by a decrease in micropore volume of the pelletized materials, presumably due to the pellet binder. As a result, V m / V s values were about the same for granular and pelletized tire carbons. Compared with coal carbons, tire carbons had a higher percentage of mesopores and macropores.

Energy and Fuels↗

USGS2006

Cometary impact and amino acid survival - Chemical kinetics and thermochemistry

The Arrhenius parameters for the initiating reactions in butane thermolysis and the formation of soot, reliable to at least 3000 K, have been applied to the question of the survival of amino acids in cometary impacts on early Earth. The pressure/temperature/time course employed here was that developed in hydrocode simulations for kilometer-sized comets (Pierazzo and Chyba, 1999), with attention to the track below 3000 K where it is shown that potential stabilizing effects of high pressure become unimportant kinetically. The question of survival can then be considered without the need for assignment of activation volumes and the related uncertainties in their application to extreme conditions. The exercise shows that the characteristic times for soot formation in the interval fall well below the cooling periods for impacts ranging from fully vertical down to about 9?? above horizontal. Decarboxylation, which emerges as more rapid than soot formation below 2000-3000 K, continues further down to extremely narrow impact angles, and accordingly cometa??ry delivery of amino acids to early Earth is highly unlikely. ?? 2006 American Chemical Society.

Journal of Physical Chemistry A↗

USGS2000

Data from a thick unsaturated zone underlying Oro Grande and Sheep Creek washes in the western part of the Mojave Desert, near Victorville, San Bernardino County, California

This report presents data on the physical properties of unsaturated alluvial deposits and on the chemical and isotopic composition of soil water and soil gas collected at 12 monitoring sites in the western part of the Mojave Desert, near Victorville, California. Sites were installed using the ODEX air-hammer method. Seven sites were located in the active channels of Oro Grande and Sheep Creek Washes. The remaining five sites were located away from the active washes. Most sites were drilled to a depth of about 100 feet below land surface; two sites were drilled to the water table almost 650 feet below land surface. Drilling procedures, lithologic and geophysical data, and site construction and instrumentation are described. Core material was analyzed for water content, bulk density, water potential, particle size, and water retention. The chemical composition of leachate from almost 1,000 subsamples of cores and cuttings was determined. Water extracted from selected subsamples of cores was analyzed for tritium and the stable isotopes of oxygen and hydrogen. Water from suction-cup lysimeters and soil-gas samples also were analyzed for chemical and isotopic composition. In addition, data on the chemical and isotopic composition of bulk precipitation from five sites and on ground water from two water-table wells are reported.

California↗

USGS2008

Evolving magma storage conditions beneath Mount St. Helens inferred from chemical variations in melt inclusions from the 1980-1986 and current (2004-2006) eruptions

Major element, trace element, and volatile concentrations in 187 glassy melt inclusions and 25 groundmass glasses from the 1980-86 eruption of Mount St. Helens are presented, together with 103 analyses of touching FE-Ti oxide pairs from the same samples. These data are used to evaluate the temporal evolution of the magmatic plumbing system beneath the volcano during 1980-86 and so provide a framework in which to interpret analyses of melt inclusions from the current (2004-2006) eruption. Major and trace element concentrations of all melt inclusions lie at the high SiO 2 end of the data array defined by eruptive products of the late Quaternary age from Mount St. Helens. For several major and trace elements, the glasses define a trend that is oblique to the whole-rock trend, indicating that different mineral assemblages were responsible for the two trends. The whole-rock trend can be ascribed to differentiation of hydrous basaltic parents in a deep-seated magma reservoir, probably at depths great enough to stabilize garnet. In contrast, the glass trends were generated by closed-system crystallization of the phenocryst and microlite mineral assemblages at low pressures. The dissolved H 2 O content of the melt inclusions from 1980-86, as measured by the ion microprobe, ranges from 0 to 6.7 wt. percent, with the highest values obtained from the plinian phase of May 18, 1980. Water contents decrease with increasing SiO 2 , consistent with decompression-driven crystallization. Preliminary data for dissolved CO 2 in melt inclusions from the May 18 plinian phase from August 7, 1980, indicate that X H 2 O in a vapor phase was approximately constant at 0.80, irrespective of H 2 O content, suggestive of closed-system degassing with a high bubble fraction or gas streaming through the subvolcanic system. Temperature and f O 2 estimates for touching Fe-Ti oxides show evidence for heating during crystallization owing to release of latent heat. Consequently, magmas with the highest microlite crystallinities record the highest temperatures. Magmas also become progressively reduced during ascent and degassing, probably as a result of redox equilibria between exsolving S-bearing gases and magmas. The lowest temperature oxides have f O 2 ≈ NNO, similar to high-temperature fumarole gases from the volcano. The temperature and f O 2 of the magma tapped by the plinian phase of May 18, 1980, are 870-875°C and NNO+0.8, respectively. The dissolved volatile contents of the melt inclusions have been used to calculate sealing pressures; that is, the pressure at which chemical exchange between inclusion and matrix melt ceased. These are greatest for the May 18 plinian magma (120 to 320 MPa); lower pressures are recorded by samples of the preplinian cryptodome and by all post-May 18 magmas. Magma crystallinity, calculated from melt-inclusion Rb contents, is negatively correlated with sealing pressure, consistent with decompression crystallization. Elevated contents of Li in melt inclusions from the cryptodome and post-May 18 samples are consistent with transfer of Li in a magmatic vapor phase from deeper parts of the magma system to magma stored at shallower levels. The Li enrichment attains its maximum extent at ~150 MPa, which is ascribed to separation of a single vapor phase into H 2 O-rich gas and dense Li-rich brine at the top of the magma column. There are striking correlations between melt-inclusion chemistry and monitoring data for the 1980-86 eruption. Dissolved SO 2 contents of melt inclusions from any given event, multiplied by the mass of magma erupted during that event, correlate with the measured flux of SO 2 at the surface, suggesting that magma degassing and melt-inclusion sealing are closely related in time and space. Textural and chemical evidence indicates that melt inclusions became effectively sealed (physically or kinetically) shortly before eruption. Thus by converting pressure to depth using a density model and edifice-loading algorithm for the volcano, changing depths of magma extraction with time can be tracked and compared to the seismic record. The plinian eruption of May 18, 1980, involved magma stored 5-11 km below sea level; this is inferred to be the subvolcanic magma chamber. The preceding eruptions, including the May 18, 1980, blast, involved magma withdrawal from the cryptodome and conduit down to 5 km below sea level. Subsequent 1980 eruptions tapped magma down to depths of ≤10 km below sea level. Tapping of magma stored deeper than 2 km below sea level stopped abruptly at the end of 1980, coincident with the onset of extensive shallow seismicity and a change from explosive to effusive eruption style from 1981 to 1986. Overall, the 1980-86 eruption is consistent with the evisceration of a thin, vertically extensive body of magma extending from 5 to at least 11 km below sea level and connected to the surface by a thin conduit. In the absence of sustained high magma-supply rates from depth, decompression crystallization of magma ascending through the system leads eventually to plugging of the conduit. The current eruption of Mount St. Helens shares some similarities with the 1981-86 dome-building phase of the previous eruption, in that there is extensive shallow seismicity and extrusion of highly crystalline material in the form of a sequence of flows and spines. Melt inclusions from the current eruption have low H 2 O contents, consistent with magma extraction from shallow depths. Highly enriched Li in melt inclusions suggests that vapor transport of Li is a characteristic feature of Mount St. Helens. Melt inclusions from the current eruption have subtly different trace-element chemistry from all but one of the 1980-86 melt inclusions, with steeper rareearth-element (REE) patterns and low U, Th, and high-fieldstrength elements (HFSE), indicating addition of a new melt component to the magma system. It is anticipated that increasing involvement of the new melt component will be evident as the current eruption proceeds.

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