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USGS2022

Actionable social science can guide community level wildfire solutions. An illustration from North Central Washington, US

In this study we illustrate the value of social data compiled at the community scale to guide a local wildfire mitigation and education effort. The four contiguous fire-prone study communities in North Central Washington, US, fall within the same jurisdictional fire service boundary and within one US census block group. Across the four communities, similar attitudes toward wildfire were observed. However, significant differences were found on the measures critical to tailoring wildfire preparation and mitigation programs to the local context such as risk mitigation behaviors, reported barriers to mitigation, and communication preferences across the four communities.

Washington↗

USGS2000

Polyoxometalates from heteropoly "brown" precursors. A new structural class of mixed valence heteropolytungstates, [(XO4)W3IVW17VIO 62Hx]n-

Reduction of the α-Keggin anion [X n + O 4 W 12 O 36 ] [8 − n]− (X = H 2 2+ , B 3+ , Si 4+ ) by six electrons results in the known tungsten “brown” species [X n + O 4 (H 2 O) 3 W IV 3 W VI 9 O 33 ] [8 − n ]− in which three W atoms have been reduced from W VI to W IV , forming a metal–metal bonded triad. The W IV atoms have terminal water coordinated in place of terminal oxo groups. Additional tungstate can condense onto these water molecules in aqueous solution between pH = 4 and 6.5 to form the species reported here, [(XO 4 )W IV 3 W VI 17 O 62 H x ] y − . The boron derivative (X = B 3+ ) is more stable than the metatungstate (X = H 2 2+ ), both of which have been characterized by elemental analysis, 183 W NMR and X-ray crystal structure analysis. Eight additional tungstate groups condense in the form of a partial Keggin structure containing two triads and one dyad which is rotated 60° relative to a hypothetical α-isomer.

Journal of the Chemical Society, Dalton Transactio↗

USGS2011

Mineralogy, morphology, and textural relationships in coatings on quartz grains in sediments in a quartz-sand aquifer

Mineralogical studies of coatings on quartz grains and bulk sediments from an aquifer on Western Cape Cod, Massachusetts, USA were carried out using a variety of transmission electron microscopy (TEM) techniques. Previous studies demonstrated that coatings on quartz grains control the adsorption properties of these sediments. Samples for TEM characterization were made by a gentle mechanical grinding method and focused ion beam (FIB) milling. The former method can make abundant electron-transparent coating assemblages for comprehensive and quantitative X-ray analysis and the latter technique protects the coating texture from being destroyed. Characterization of the samples from both a pristine area and an area heavily impacted by wastewater discharge shows similar coating textures and chemical compositions. Major constituents of the coating include Al-substituted goethite and illite/chlorite clays. Goethite is aggregated into well-crystallized domains through oriented attachment resulting in increased porosity. Illite/chlorite clays with various chemical compositions were observed to be mixed with goethite aggregates and aligned sub-parallel to the associated quartz surface. The uniform spatial distribution of wastewater-derived phosphorus throughout the coating from the wastewater-contaminated site suggests that all of the coating constituents, including those adjacent to the quartz surface, are accessible to groundwater solutes. Both TEM characterization and chemical extraction results indicate there is a significantly greater amount of amorphous iron oxide in samples from wastewater discharge area compared to those from the pristine region, which might reflect the impact of redox cycling of iron under the wastewater-discharge area. Coating compositions are consistent with the moderate metal and oxy-metalloid adsorption capacities, low but significant cation exchange capacities, and control of iron(III) solubility by goethite observed in reactive transport experimental and modeling studies conducted at the site.

Massachusetts↗

USGS2007

The feasibility of applying immature yard-waste compost to remove nitrate from agricultural drainage effluents: A preliminary assessment

Nitrate is a major agricultural pollutant found in drainage waters. Immature yard-waste compost was selected as a filter media to study its feasibility for removing nitrate from drainage water. Different operation parameters were tested to examine the denitrification efficiency, including the amounts of compost packed in columns, the flow rate, and the compost storage periods. The experimental results suggested that hydraulic retention time was the major factor to determine the extent of nitrate removal, although the amount of compost packed could also contribute to the nitrate removal efficiency. The effluent nitrate concentration increased as the flow rate decreased, and the compost column reduced nitrate concentrations from 20 mg/L to less than 5 mg/L within 1.5 h. The solution pH increased at the onset of experiment because of denitrification, but stabilized at a pH of about 7.8, suggesting that the compost had a buffering capacity to maintain a suitable pH for denitrification. Storing compost under air-dried conditions may diminish the extent nitrate removed initially, but the effects were not apparent after longer applications. It appeared that immature yard-waste compost may be a suitable material to remove nitrate from tile drainage water because of its relatively large organic carbon content, high microbial activity, and buffering capacity. ?? 2006 Elsevier B.V. All rights reserved.

Journal of Hazardous Materials↗

USGS2007

Velocity control as a tool for optimal plume containment in the Equus Beds aquifer, Kansas

A ground-water-management model was developed to investigate the best management options for the containment of an oil-field-brine plume in the Equus Beds aquifer in south-central Kansas. The main purpose of the management model was to find the optimal locations and minimum rates of pumpage of a set of plume-interception wells, to successfully reverse the velocity vectors at observation wells located along the plume front, and also to satisfy freshwater demands from supply wells. The effects of the calculated minimum withdrawals from the interception wells on the migration of contaminants throughout the ground-water system were evaluated utilizing a solute-transport model. This latter analysis was carried out to ensure the containment of the plume. Whereas application of the management model to the study area achieves the management objectives, the implementation of the results is believed to be impractical and expensive. This is because a considerable amount of water must be pumped out to reverse the velocity vectors in the vicinity of the plume. In general, the proposed technique of pollutant containment may be effective when applied to aquifers having low hydraulic gradients and/or to aquifers with hazardous plumes whose containment is not subject to economic constraints.

Kansas↗

USGS1983

Relation of concealed faults to water quality and the formation of solution features in the Floridan aquifer, northeastern Florida, U.S.A.

Geological and hydrological information on the Floridan aquifer in northeastern Florida indicates that isolated occurrences of water having relatively high chloride concentration in the upper part of the aquifer may be associated with buried faults. Water having chloride concentrations of more than 700 mg l −1 occurs in the deeper zone of the aquifer at depths below ∼ 600 m below sea level in the coastal and east-central part of the study area. This deep salty water is under higher artesian pressure than water in the shallower, generally freshwater zones, but it is restricted from moving upward by relatively impermeable dolomite beds. Two buried faults with vertical displacements of 30–45 m are in areas where relatively high concentrations of chloride have been detected in water in the upper part of the aquifer. Geochemical, artesian pressure, and water temperature data show that the source of the relatively high concentrations of chloride in water in the upper part of the aquifer is from the deeper zone. This indicates that the faults may have breached the dolomite confining beds and allowed the upward movement of salty water from the deeper zone. The upward movement of mineralized water along the faults may also have formed some of the solution features found in the aquifer near the faults. In this area, freshwater in the upper part of the aquifer is normally saturated with respect to calcite and dolomite. However, water from wells tapping the upper part of the aquifer near the faults is not fully saturated suggesting that the mixing of deep mineralized water with shallower freshwater produces a mixture that is not saturated with respect to these minerals and allows for the dissolution of limestone in the aquifer near the faults. Dissolution of limestone may also be occurring at the freshwater-saltwater interface in the deeper zones of the aquifer.

Florida↗

USGS1990

Modelling streamwater chemistry as a mixture of soilwater end-members - An application to the Panola Mountain catchment, Georgia, U.S.A.

Streamwater chemistry at Panola Mountain research catchment, Georgia, U.S.A., is explained as a mixture of representative soilwater solutions that are considered to be temporally invariant to a first approximation. The selection of three end-members from all sampled soil waters is evaluated by comparing the observed and predicted streamwater concentration of six solutes (alkalinity, sulfate, sodium, magnesium, calcium and dissolved silica), which are assumed to mix conservatively, and by assessing the consistency of the implied hydrograph separation with the hydrological mechanisms that are believed to be operating in this catchment. The percentage of variation in the streamwater solute concentrations explained by the end-member mixing analysis (EMMA) ranges from 82 to >97%, and the hydrograph separation is, intuitively, physically reasonable. If the correct end-members have been identified, the streamwater chemical response to different levels of acidic deposition can be predicted by examining the change in each end-member under different loads; no hydrological model is required. If a traditional hydrochemical model, which is driven by rainfall quantity and quality, is desired, this analysis provides an indication of the model structure that would be necessary to reproduce both streamwater and soilwater chemistry.

Georgia↗

USGS2010

Source and fate of inorganic solutes in the Gibbon River, Yellowstone National Park, Wyoming, USA. II. Trace element chemistry

The Gibbon River in Yellowstone National Park receives inflows from several geothermal areas, and consequently the concentrations of many trace elements are elevated compared to rivers in non-geothermal watersheds. Water samples and discharge measurements were obtained from the Gibbon River and its major tributaries near Norris Geyser Basin under the low-flow conditions of September 2006 allowing for the identification of solute sources and their downstream fate. Norris Geyser Basin, and in particular Tantalus Creek, is the largest source of many trace elements (Al, As, B, Ba, Br, Cs, Hg, Li, Sb, Tl, W, and REEs) to the Gibbon River. The Chocolate Pots area is a major source of Fe and Mn, and the lower Gibbon River near Terrace Spring is the major source of Be and Mo. Some of the elevated trace elements are aquatic health concerns (As, Sb, and Hg) and knowing their fate is important. Most solutes in the Gibbon River, including As and Sb, behave conservatively or are minimally attenuated over 29 km of fluvial transport. Some small attenuation of Al, Fe, Hg, and REEs occurs but primarily there is a transformation from the dissolved state to suspended particles, with most of these elements still being transported to the Madison River. Dissolved Hg and REEs loads decrease where the particulate Fe increases, suggesting sorption onto suspended particulate material. Attenuation from the water column is substantial for Mn, with little formation of Mn as suspended particulates.

Wyoming↗

USGS1998

Comparing sea-ice sediment load with Beaufort Sea shelf deposits: Is entrainment selective?

Modern dispersal of sea-ice-rafted debris (IRD) is important for the Arctic Ocean sediment budget from sources to sinks. Sediment entrainment occurs mainly through the action of small ice crystals (frazil) attaching to sedimentary particles in shallow water, a mechanism that could be selective. The principal source for entrainment of IRD by suspension freezing into the Beaufort Gyre, western Arctic Ocean, is the adjacent shallow (<30 m) shelf, here called the source surface. The texture, clay-mineral composition, coarse sand (<250 micrometers) lithology, and carbon and carbonate content of IRD in the Beaufort Gyre were compared to sediments from the probable source surface, in order to determine whether preferential entrainment occurs with any of these sediment parameters. IRD is generally much finer grained than the source surface, showing that silt- and clay-size particles are preferentially entrained by frazil ice, although anchor ice can locally incorporate very high percentages of sand and coarser clasts. The coarsest IRD is also the most poorly sorted. The clay mineralogy of the <2 micrometer IRD fraction is very similar to that of the source surface, indicating no selective entrainment within the clay fraction. The lithology of sand in IRD also matches that of the source surface, although the number of coarse grains is too small (<100) in most samples for a statistically meaningful count. The average organic-carbon content of IRD is three times higher than that of the source surface, but we attribute this to summer algal growth on ice floes rather than to selective entrainment. A relatively low carbonate content in IRD may be because much of the carbonate in the source is of silt size while about 50% of the IRD measured is clay size. The low carbonate content may also reflect solution under acidic summer conditions on sea ice. Selective export of silt- and clay-size particles by ice rafting from the shallow shelf with time should lead to the formation of a slightly coarser lag, even though some of the dirty ice drops its sediment load in the entrainment area. Further mineralogical and lithological analysis on IRD promises to become a useful tool for the study of sediment dispersal paths by drift ice in the Arctic today and in the past, and also for the study of sources of anthropogenic pollutants found in sea ice.

Beaufort Sea shelf↗

USGS2007

Research activities at U.S. Government agencies in subsurface reactive transport modeling

The fate of contaminants in the environment is controlled by both chemical reactions and transport phenomena in the subsurface. Our ability to understand the significance of these processes over time requires an accurate conceptual model that incorporates the various mechanisms of coupled chemical and physical processes. Adsorption, desorption, ion exchange, precipitation, dissolution, growth, solid solution, redox, microbial activity, and other processes are often incorporated into reactive transport models for the prediction of contaminant fate and transport. U.S. federal agencies use such models to evaluate contaminant transport and provide guidance to decision makers and regulators for treatment issues. We provide summaries of selected research projects and programs to demonstrate the level of activity in various applications and to present examples of recent advances in subsurface reactive transport modeling.

Vadose Zone Journal↗

USGS2004

Field investigation into unsaturated flow and transport in a fault: Model analyses

Results of a fault test performed in the unsaturated zone of Yucca Mountain, Nevada, were analyzed using a three-dimensional numerical model. The fault was explicitly represented as a discrete feature and the surrounding rock was treated as a dual-continuum (fracture-matrix) system. Model calibration against seepage and water-travel-velocity data suggests that lithophysal cavities connected to fractures can considerably enhance the effective fracture porosity and therefore retard water flow in fractures. Comparisons between simulation results and tracer concentration data also indicate that matrix diffusion is an important mechanism for solute transport in unsaturated fractured rock. We found that an increased fault-matrix and fracture-matrix interface areas were needed to match the observed tracer data, which is consistent with previous studies. The study results suggest that the current site-scale model for the unsaturated zone of Yucca Mountain may underestimate radionuclide transport time within the unsaturated zone, because an increased fracture-matrix interface area and the increased effective fracture porosity arising from lithophysal cavities are not considered in the current site-scale model. ?? 2004 Published by Elsevier B.V.

Journal of Contaminant Hydrology↗

USGS1983

Gas-film coefficients for streams

Equations for predicting the gas-film coefficient for the volatilization of organic solutes from streams are developed. The film coefficient is a function of windspeed and water temperature. The dependence of the coefficient on windspeed is determined from published information on the evaporation of water from a canal. The dependence of the coefficient on temperature is determined from laboratory studies on the evaporation of water. Procedures for adjusting the coefficients for different organic solutes are based on the molecular diffusion coefficient and the molecular weight. The molecular weight procedure is easiest to use because of the availability of molecular weights. However, the theoretical basis of the procedure is questionable. The diffusion coefficient procedure is supported by considerable data. Questions, however, remain regarding the exact dependence of the film coefficint on the diffusion coefficient. It is suggested that the diffusion coefficient procedure with a 0.68-power dependence be used when precise estimate of the gas-film coefficient are needed and that the molecular weight procedure be used when only approximate estimates are needed.

Journal of Environmental Engineering↗

USGS1986

Transport of chloride ion in a water-unsaturated soil exhibiting anion exclusion

Miscible displacement techniques were used to create Cl - concentration profiles in unsaturated laboratory columns of Delhi sand (Typic Xeropsamments), each having a nearly uniform water content. The three steady flow rates used resulted in three different, average water contents. Chloride concentrations near the top of the column were smaller and penetration of Cl - in the column was deeper than expected assuming that Cl - is a noninteracting solute. Such observations indicate the presence of anion exclusion. This interpretation is further substantiated by chloride and tritium breakthrough curves obtained from a saturated column of the same soil. The saturated experiments show that tritium occupies the entire measured pore volume of the column, but that Cl - is restricted to a smaller pore volume. The formulation of the conventional convection-dispersion theory for solute transport in soil which includes anion exclusion resulted in model calculations that fitted the unsaturated Cl - concentration profiles quite well. The dispersion coefficients obtained for the unsaturated profiles increase with water velocity and are lower than those previously reported for comparable water velocities in the same but saturated soil. The dispersivity of the unsaturated soil is also smaller than that reported for the saturated soil. For the experimental conditions used, the effective Cl - exclusion volume was found to be independent of water content and velocity and occupied about ten percent of the unsaturated water content.

Soil Science Society of America Journal↗

USGS1999

Diagenesis of lower Cretaceous pelagic carbonates, North Atlantic: Paleoceanographic signals obscured

The stable isotope and minor element geochemistry of Neocomian (Lower Cretaceous) pelagic carbonates of the North Atlantic Basin (Deep Sea Drilling Project Sites 105, 367, 387, 391, and 603) was examined to develop a diagenetic model for pelagic limestones. In particular, we hoped to test the fidelity of whole-rock geochemical records as paleoceanographic indicators for pelagic deposits of pre-Aptian age, in which individual microfossils are not available for analysis. Data indicate that in addition to depth of burial, rhythmic variations in primary carbonate content have strongly controlled diagenetic patterns and associated geochemical signatures in these Neocomian sequences. Samples become increasingly depleted in Sr and 18O with increasing CaCO3 content. Within individual sedimentary sections, substantial decreases in Sr/Ca ratios and ??18O values are evident over a range of 4 to 98% CaCO3. However, even over a relatively narrow range of 50 to 98% CaCO3 a 2.5%c variation in ??18O values and a change of a factor of 1.7 in Sr/Ca ratios are observed. Carbon isotope compositions do not vary as extensively with CaCO3 content, but carbonate-rich intervals tend to be relatively depleted in 13C. Petrographic analysis reveals that these geochemical patterns are related to the transfer of CaCO3 from carbonate-poor intervals (calcareous shales and marlstones) to adjacent carbonate-rich intervals (limestones) during burial compaction and pressure solution. This process results in the addition of diagenetic cement to carbonate-rich intervals to produce a bulk composition that is relatively depleted in Sr and 18O and, at the same time, enables the retention of more-or-less primary carbonate that is relatively enriched in Sr and 18O in adjacent carbonate-poor intervals. Thus, although cyclic variations in CaCO3 content are primary in the Neocomian sequences examined, measured variations in Sr/Ca ratios and ??18O values are not and, as such, do not provide reliable proxies for past variations in climate, oceanographic conditions, or global ice volume.

Journal of Foraminiferal Research↗

USGS1967

The ternary system K2SO4 MgSO4 CaSO4

Melting and subsolidus relations in the system K 2 SO 4 MgSO 4 CaSO 4 were studied using heating-cooling curves, differential thermal analysis, optics, X-ray diffraction at room and high temperatures and by quenching techniques. Previous investigators were unable to study the binary MgSO 4 CaSO 4 system and the adjacent area in the ternary system because of the decomposition of MgSO 4 and CaSO 4 at high temperatures. This problem was partly overcome by a novel sealed-tube quenching method, by hydrothermal synthesis, and by long-time heating in the solidus. As a result of this study, we found: (1) a new compound, CaSO 4 ·3MgSO 4 (m.p. 1201°C) with a field extending into the ternary system; (2) a high temperature form of MgSO 4 with a sluggishly reversible inversion. An X-ray diffraction pattern for this polymorphic form is given; (3) the inversion of β-CaSO 4 (anhydrite) to α-CaSO 4 at 1195°C, in agreement with grahmann ; (1) (4) the melting point of MgSO 4 is 1136°C and that of CaSO 4 is 1462°C (using sealed tube methods to prevent decomposition of the sulphates); (5) calcium langbeinite (K 2 SO 4 ·2CaSO 4 ) is the only compound in the K 2 SO 4 CaSO 4 binary system. This resolved discrepancies in the results of previous investigators; (6) a continuous solid solution series between congruently melting K 2 SOP 4 ·2MgSO 4 (langbeinite) and incongruently melting K 2 SO 4 ·2CaSO 4 (calcium langbeinite); (7) the liquidus in the ternary system consists of primary phase fields of K 2 SO 4 , MgSO 4 , CaSO 4 , langbeinite-calcium langbeinite solid solution, and CaSO 4 ·3MgSO 4 . The CaSO 4 field extends over a large portion of the system. Previously reported fields for the compounds (K 2 SO 4 ·MgSO 4 ·nCaSO 4 ), K 2 SO 4 ·3CaSO 4 and K 2 SO 4 ·CaSO 4 were not found; (8) a minimum in the ternary system at: 740°C, 25% MgSO 4 , 6% CaSO 4 , 69% K 2 SO 4 ; and ternary eutectics at 882°C, 49% MgSO 4 , 19% CaSO 4 , 32% K 2 SO 4 ; and 880°, 67·5% MgSO 4 , 5% CaSO 4 , 27·5% K 2 SO 4 .

Journal of Inorganic and Nuclear Chemistry↗

USGS1977

Feasibility and technology for making remote measurements of solutes in water

An indepth evaluation of the available technology in the field of laser-Raman spectroscopy indicates that a TV-type detector, a single monochromator with a holographic grating, an entrance slit filter blocking the Rayleigh light, and a pulsed laser coupled to signal averaging electronics is the best combination of commercial equipment that is presently available for building a remote water-quality sensor. The resultant sensor would be capable of measuring oxyanions in water at concentrations from 10 to 50 milligrams per liter at distances from ground level to 30 meters above the sample. The main interferences would be ambient light, bioluminescence, and natural fluorescence, all of which are minimized when taking advantage of the signal generating and readout capability contained in this equipment package.

Journal of Research of the U.S. Geological Survey↗

USGS2010

Assessment of basin-scale hydrologic impacts of CO2 sequestration, Illinois basin

Idealized, basin-scale sharp-interface models of CO2 injection were constructed for the Illinois basin. Porosity and permeability were decreased with depth within the Mount Simon Formation. Eau Claire confining unit porosity and permeability were kept fixed. We used 726 injection wells located near 42 power plants to deliver 80 million metric tons of CO2/year. After 100 years of continuous injection, deviatoric fluid pressures varied between 5.6 and 18 MPa across central and southern part of the Illinois basin. Maximum deviatoric pressure reached about 50% of lithostatic levels to the south. The pressure disturbance (>0.03 MPa) propagated 10-25 km away from the injection wells resulting in significant well-well pressure interference. These findings are consistent with single-phase analytical solutions of injection. The radial footprint of the CO2 plume at each well was only 0.5-2 km after 100 years of injection. Net lateral brine displacement was insignificant due to increasing radial distance from injection well and leakage across the Eau Claire confining unit. On geologic time scales CO2 would migrate northward at a rate of about 6 m/1000 years. Because of paleo-seismic events in this region (M5.5-M7.5), care should be taken to avoid high pore pressures in the southern Illinois basin. ?? 2010 Elsevier Ltd.

International Journal of Greenhouse Gas Control↗

USGS1983

Comparison of analytical methods for the determination of silica in geothermal waters

The silica concentration of 26 Guatemalan geothermal waters were analyzed colorimetrically (spectrophotometrically) and by atomic absorption. Results by the atomic absorption method were less affected by polymerization and precipitation of silica from supersaturated solutions. Shaking the samples prior to analysis improves the accuracy of the atomic absorption results. The advantages of colorimetric analysis over atomic absorption are better sensitivity and precision. However, for accurate colorimetric results, geothermal samples must be sufficiently diluted in the field, which ensures that no further polymerization occurs and that amorphous silica that may be present will redissolve. If the samples are not diluted in the field they should be diluted in the laboratory and left standing for at least a month to allow the silica to redissolve. If analyzed immediately the diluted samples should be made alkaline and heated overnight in a 90?? oven. ?? 1983.

Journal of Volcanology and Geothermal Research↗