Results for “Nature Based Solutions” — Page 6

USGS2021

Review: “Jacob’s Zoo”— How using Jacob’s method for aquifer testing leads to more intuitive understanding of aquifer characteristics

The interpretation of aquifer responses to pumping tests is an important tool for assessing aquifer geometry and properties, which are critical in the assessment of water resources or in environmental remediation. However, the responses of aquifers, measured by time-drawdown relationships in monitoring wells, are nonunique solutions that are affected by many factors. Jacob’s Zoo is a collection of graphical interpretations that allows students and practitioners to develop an intuitive feel for how natural hydrogeological systems work, and develop a set of skills that provide a better understanding of aquifer properties far beyond interpretation of pumping tests. Jacob’s Zoo, based on the work of Jacob (1950), fosters a deeper understanding, although few practitioners realize the full utility of the method. Jacob CE (1950) Flow of groundwater, In: Rouse H (ed) Engineering Hydraulics, Wiley, New York. P 321–386.

Hydrogeology Journal↗

USGS2016

Arctic Research Plan: FY2017-2021

The United States is an Arctic nation—Americans depend on the Arctic for biodiversity and climate regulation and for natural resources. America’s Arctic—Alaska—is at the forefront of rapid climate, environmental, and socio-economic changes that are testing the resilience and sustainability of communities and ecosystems. Research to increase fundamental understanding of these changes is needed to inform sound, science-based decision- and policy-making and to develop appropriate solutions for Alaska and the Arctic region as a whole. Created by an Act of Congress in 1984, and since 2010 a subcommittee of the National Science and Technology Council (NSTC) in the Executive Office of the President, the Interagency Arctic Research Policy Committee (IARPC) plays a critical role in advancing scientific knowledge and understanding of the changing Arctic and its impacts far beyond the boundaries of the Arctic. Comprising 14 Federal agencies, offices, and departments, IARPC is responsible for the implementation of a 5-year Arctic Research Plan in consultation with the U.S. Arctic Research Commission, the Governor of the State of Alaska, residents of the Arctic, the private sector, and public interest groups.

Report↗

USGS2010

Speciation and equilibrium relations of soluble aluminum in a headwater stream at base flow and during rain events

In a small watershed in the Shenandoah National Park, Virginia, the short-term dynamics of soluble aluminum in stream water sampled during rain events differed significantly from stream water sampled during base flow conditions. Three fractions of dissolved aluminum were measured. The inorganic monomeric fraction made up approximately two thirds of the total reactive aluminum at base flow, followed by the acid-soluble and organic monomeric fractions, respectively. Equilibrium modeling showed that hydroxide complexes were the most abundant form of inorganic monomeric aluminum followed by fluoride, free aluminum ion, and sulfate. The activity of inorganic monomeric aluminum at base flow appears to be in equilibrium with an Al(OH) 3 phase with solubility intermediate between microcrystalline gibbsite and natural gibbsite. During two rain events, the concentration of all three aluminum fractions increased significantly. Available chemical evidence indicates that acidic soil water was the primary source of dissolved aluminum. As flow increased, the Al(OH) 3 saturation index in the stream water increased significantly. The primary cause of the transient increase in the Al(OH) 3 saturation index appears to have been the neutralization of excess H + added by soil water through reaction with stream water HCO 3 − at a more rapid rate than excess inorganic monomeric aluminum could be removed from solution by hydroxide mineral precipitation. A soil water/stream water mixing model was developed based on measured changes of stream water alkalinity, silica concentration, and charge imbalance during the rain events. Model results indicate that a small amount of soil water (3–11%) was present in the stream at peak stage.

Virginia↗

USGS2018

Evaluation of biodiversity data portals based on requirement analysis

In recent years, concern about the misuse of natural resources has been increasing. It is essential to know in detail the biodiversity of an ecosystem to understand and analyze the impact of human activities on nature, as well as to promote the economic growth of a country. To achieve these goals, public and private institutions are aggregating and sharing biological data around the world by means of biodiversity data portals. The main purpose of those portals is to provide a set of tools that help users and institutions catalog, analyze, and publish raw data about different species in a manner that is open and freely available to any interested party. Normally the process of choosing the best software solution is not straightforward. This paper proposes a methodology to evaluate a collection of data portals to establish a clear and consistent selection process that analyzes a collection of requirements and research purposes. The proposed approach is based on three strategies: the use of software engineering techniques to identify the desired group of features to be available in the data portal; the application of the Kano Satisfaction Model to score each requirement according to a preset weight of importance; and the use of tree-maps to visualize the requirements based on their implementation priority, to establish a portal deployment road-map. The proposed methodology is broadly applicable to portal analyses for many communities of practice.

Ecological Informatics↗

USGS2022

Seismic monitoring solutions for buildings

This chapter introduces seismic monitoring of structural systems for buildings and begins with a historical background of this topic in the United States. After providing the historical context, the chapter reviews common seismic instrumentation issues such as utilization of data, code versus extensive instrumentation, free-field instrumentation, record synchronization requirements and more. Recent developments in damage detection is examined including damage detection based on changes in natural frequencies, permanent deformations, and interstory drift. Finally, applications in Europe, the Middle East, and Japan of seismic monitoring of structural systems for buildings are discussed.

Book chapter↗

USGS2005

Chemical weathering rates of a soil chronosequence on granitic alluvium: III. Hydrochemical evolution and contemporary solute fluxes and rates

Although long-term changes in solid-state compositions of soil chronosequences have been extensively investigated, this study presents the first detailed description of the concurrent hydrochemical evolution and contemporary weathering rates in such sequences. The most direct linkage between weathering and hydrology over 3 million years of soil development in the Merced chronosequence in Central California relates decreasing permeability and increasing hydrologic heterogeneity to the development of secondary argillic horizons and silica duripans. In a highly permeable, younger soil (40 kyr old), pore water solutes reflect seasonal to decadal-scale variations in rainfall and evapotranspiration (ET). This climate signal is strongly damped in less permeable older soils (250 to 600 kyr old) where solutes increasingly reflect weathering inputs modified by heterogeneous flow. Elemental balances in the soils are described in terms of solid state, exchange and pore water reservoirs and input/output fluxes from precipitation, ET, biomass, solute discharge and weathering. Solute mineral nutrients are strongly dependent on biomass variations as evidenced by an apparent negative K weathering flux reflecting aggradation by grassland plants. The ratios of solute Na to other base cations progressively increase with soil age. Discharge fluxes of Na and Si, when integrated over geologic time, are comparable to solid-state mass losses in the soils, implying similar past weathering conditions. Similarities in solute and sorbed Ca/Mg ratios reflect short-term equilibrium with the exchange reservoir. Long-term consistency in solute ratios, when contrasted against progressive decreases in solid-state Ca/Mg, requires an additional Ca source, probably from dry deposition. Amorphous silica precipitates from thermodynamically-saturated pore waters during periods of high evapotranspiration and result in the formation of duripans in the oldest soils. The degree of feldspar and secondary gibbsite and kaolinite saturation varies both spatially and temporally due to the seasonality of plant-respired CO 2 and a decrease in organically complexed Al. In deeper pore waters, K-feldspar is in equilibrium and plagioclase is about an order of magnitude undersaturated. Hydrologic heterogeneity produces a range of weathering gradients that are constrained by solute distributions and matrix and macropore flow regimes. Plagioclase weathering rates, based on precipitation-corrected Na gradients, vary between 3 and 7 × 10 −16 mol m −2 s −1 . These rates are similar to previously determined solid-state rates but are several orders of magnitude slower than for experimental plagioclase dissolution indicating strong inhibitions to natural weathering, partly due to near-equilibrium weathering reactions.

Geochimica et Cosmochimica Acta↗

USGS1992

Seasonal dynamics of groundwater-lake interactions at Doñana National Park, Spain

The hydrologic and solute budgets of a lake can be strongly influenced by transient groundwater flow. Several shallow interdunal lakes in southwest Spain are in close hydraulic connection with the shallow ground water. Two permanent lakes and one intermittent lake have chloride concentrations that differ by almost an order of magnitude. A two-dimensional solute-transport model, modified to simulate transient groundwater-lake interaction, suggests that the rising water table during the wet season leads to local flow reversals toward the lakes. Response of the individual lakes, however, varies depending on the lake's position in the regional flow system. The most dilute lake is a flow-through lake during the entire year; the through flow is driven by regional groundwater flow. The other permanent lake, which has a higher solute concentration, undergoes seasonal groundwater flow reversals at its downgradient end, resulting in complex seepage patterns and higher solute concentrations in the ground water near the lake. The solute concentration of the intermittent lake is influenced more strongly by the seasonal wetting and drying cycle than by the regional flow system. Although evaporation is the major process affecting the concentration of conservative solutes in the lakes, geochemical and biochemical reactions influence the concentration of nonconservative solutes. Probable reactions in the lakes include biological uptake of solutes and calcite precipitation; probable reactions as lake water seeps into the aquifer are sulfate reduction and calcite dissolution. Seepage reversals can result in water composition that appears inconsistent with predictions based on head measurements because, under transient flow conditions, the flow direction at any instant may not satisfactorily depict the source of the water. Understanding the dynamic nature of groundwater-lake interaction aids in the interpretation of hydrologic and chemical relations between the lakes and the ground water.

Journal of Hydrology↗

USGS2010

Groundwater transport of strontium 90 in a glacial outwash environment

As part of the investigation of groundwater contamination at a uranium-scrap recovery plant at Wood River Junction, Rhode Island, laboratory experiments led to the development of a model for predicting the transport of strontium 90 in glacial outwash sediments based on an approximate mechanism for ion exchange. The multicomponent system was simplified to two components by regarding all exchangeable cations other than strontium 90 as a single component. The binary ion-exchange parameter was a function of the variable, total ion concentration. A one-dimensional solute transport model was formulated to evaluate the time necessary for natural groundwater flow to remove the strontium 90 contamination plume from the groundwater system to the Pawcatuck River. The finite difference transport equations were solved sequentially for total ion concentrations, then strontium 90 concentrations. Clay-free quartz and feldspar sands at the study site have little potential for strontium 90 sorption, and high calcium, magnesium, and sodium concentrations compete for the few ion exchange sites. As the total ion concentration plume moves out of the system, ion exchange of strontium 90 increases, reducing the strontium 90 concentration in the groundwater. Cleanout times predicted using the binary ion exchange mechanism were about two thirds of those predicted using a constant distribution coefficient. It is suggested that this type of model can simulate solute transport more realistically in many groundwater systems where the total ion concentration is not constant.

Rhode Island↗

USGS2018

The 1952 Kern County, California earthquake: A case study of issues in the analysis of historical intensity data for estimation of source parameters

Seismic intensity data based on first-hand accounts of shaking give valuable insight into historical and early instrumental earthquakes. Comparing an observed intensity distribution to intensity-prediction models based on modern calibration events allows the magnitude to be estimated for many historic earthquakes. Magnitude estimates can also potentially be refined for earthquakes for which limited instrumental data are available. However, the complicated nature of macroseismic data and the methods used to collect and interpret the data introduce significant uncertainties. In this paper, we illustrate these challenges and possible solutions using the 1952 Kern County, California, earthquake as a case study. Published estimates of its magnitude vary from M W 7.2–7.5, making it possibly the second largest in California during the 20th century. We considered over 1100 first-hand reports of shaking, supplemented with other data, and inferred the magnitude in several ways using intensity prediction equations, yielding a preferred intensity magnitude M I 7.2 ± 0.2, where the uncertainty reflects our judgement. The revised intensity distribution reveals stronger shaking on the hanging wall, south of the surface expression of the White Wolf fault, than on the footwall. Characterizing the magnitude and shaking distribution of this early instrumental earthquake can help improve estimation of the seismic hazard of the region. Such reinterpreted intensities for historic earthquakes, combined with U.S. Geological Survey (USGS) Did You Feel It? data for more recent events, can be used to produce a uniform shaking dataset with which earthquake hazard map performance can be assessed.

California↗

USGS2008

GSTARS computer models and their applications, part I: theoretical development

GSTARS is a series of computer models developed by the U.S. Bureau of Reclamation for alluvial river and reservoir sedimentation studies while the authors were employed by that agency. The first version of GSTARS was released in 1986 using Fortran IV for mainframe computers. GSTARS 2.0 was released in 1998 for personal computer application with most of the code in the original GSTARS revised, improved, and expanded using Fortran IV/77. GSTARS 2.1 is an improved and revised GSTARS 2.0 with graphical user interface. The unique features of all GSTARS models are the conjunctive use of the stream tube concept and of the minimum stream power theory. The application of minimum stream power theory allows the determination of optimum channel geometry with variable channel width and cross-sectional shape. The use of the stream tube concept enables the simulation of river hydraulics using one-dimensional numerical solutions to obtain a semi-two- dimensional presentation of the hydraulic conditions along and across an alluvial channel. According to the stream tube concept, no water or sediment particles can cross the walls of stream tubes, which is valid for many natural rivers. At and near sharp bends, however, sediment particles may cross the boundaries of stream tubes. GSTARS3, based on FORTRAN 90/95, addresses this phenomenon and further expands the capabilities of GSTARS 2.1 for cohesive and non-cohesive sediment transport in rivers and reservoirs. This paper presents the concepts, methods, and techniques used to develop the GSTARS series of computer models, especially GSTARS3. ?? 2008 International Research and Training Centre on Erosion and Sedimentation and the World Association for Sedimentation and Erosion Research.

International Journal of Sediment Research↗

USGS2003

Sequestration of phosphorus by acid mine drainage floc

Solubilization and transport of phosphorus (P) to the water environment is a critical environmental issue. Flocs resulting from neutralizing acid mine drainage (AMD) were tested as a possible low-cost amendment to reduce the loss of soluble P from agricultural fields and animal wastewater. Flocs were prepared by neutralizing natural and synthetic solutions of AMD with limestone, lime, ammonium hydroxide, and sodium hydroxide. Phosphorus sequestration was tested in three distinct environments: water, soil, and manure storage basins. In water, flocs prepared from AMD adsorbed 10 to 20 g P kg −1 dry floc in equilibrium with 1 mg L −1 soluble P. Similar results were observed for both Fe-based and Al-based synthetic flocs. A local soil sample adsorbed about 0.1 g P kg −1 , about two orders of magnitude less. The AMD-derived flocs were mixed with a high-P soil at 5 to 80 g floc kg −1 soil, followed by water and acid (Mehlich-1) extractions. All flocs performed similarly. About 70% of the water-extractable P was sequestered by the floc when applied at a rate of 20 g floc kg −1 soil, whereas plant-available P only decreased by about 30%. Under anaerobic conditions simulating manure storage basins, all AMD flocs reduced soluble P by greater than 95% at a rate of 0.2 g floc g −1 rainbow trout ( Oncorhynchus mykiss ) manure. These findings indicate that AMD flocs could be an effective agent for preventing soluble P losses from soil and manure to the water environment, while at the same time decreasing the costs associated with AMD treatment.

Journal of Environmental Quality↗

USGS1961

Geologic summary of the Appalachian Basin, with reference to the subsurface disposal of radioactive waste solutions

The Appalachian basin is an elongate depression in the crystalline basement complex which contains a great volume of predominantly sedimentary stratified rocks. As defined in this paper it extends from the Adirondack Mountains in New York to central Alabama. From east to west it extends from the west flank of the Blue Ridge Mountains to the crest of the Findlay and Cincinnati arches and the Nashville dome. It encompasses an area of about 207,000 square miles, including all of West Virginia and parts of New York, New Jersey, Pennsylvania, Ohio, Maryland, Virginia, Kentucky, Tennessee, North Carolina, Georgia, and Alabama. The stratified rocks that occupy the basin constitute a wedge-shaped mass whose axis of greatest thickness lies close to and parallel to the east edge of the basin. The maximum thickness of stratified rocks preserved in any one part of the basin today is between 35,000 and 40,000 feet. The volume of the sedimentary rocks is approximately 510,000 cubic miles and of volcanic rocks is a few thousand cubic miles. The sedimentary rocks are predominantly Paleozoic in age, whereas the volcanic rocks are predominantly Late Precambrian. On the basis of gross lithology the stratified rocks overlying the crystalline basement complex can be divided into nine vertically sequential units, which are designated "sequences" in this report. The boundaries between contiguous sequences do not necessarily coincide with the commonly recognized boundaries between systems or series. All sequences are grossly wedge shaped, being thickest along the eastern margin of the basin and thinnest along the western margin. The lowermost unit the Late Precambrian stratified sequence is present only along part of the eastern margin of the basin, where it lies unconformably on the basement complex. It consists largely of volcanic tuffs and flows but contains some interbedded sedimentary rocks. The Late Precambrian sequence is overlain by the Early Cambrian clastic sequence. Where the older sequence is absent, the Early Cambrian sequence rests on the basement complex. Interbedded fine- to coarse-grained noncarbonate detrital rocks comprise the bulk of the sequence, but some volcanic and carbonate rocks are included. Next above is the Cambrian-Ordovician carbonate sequence which consists largely of limestone and dolomite. Some quartzose sandstone is present in the lower part in the western half of the basin, and much shale is present in the upper part in the southeast part of the basin. The next higher sequence is the Late Ordovician clastic sequence, which consists largely of shale, siltstone, and sandstone. Coarse-grained light-gray to red rocks are common in the sequence along the eastern side of the basin, whereas fine-grained dark-gray to black calcareous rocks are common along the west side. The Late Ordovician clastic sequence is overlain unconformably in many places by the Early Silurian clastic sequence. The latter comprises a relatively thin wedge of coarse-grained clastic rocks. Some of the most prolific oil- and gas-producing sandstones in the Appalachian basin are included. Among these are the "Clinton" sands of Ohio, the Medina Sandstones of New York and Pennsylvania, and the Keefer or "Big Six" Sandstone of West Virginia and Kentucky. Conformably overlying the Early Silurian clastic sequence is the Silurian-Devonian carbonate sequence, which consists predominantly of limestone and dolomite. It also contains a salt-bearing unit in the north-central part of the basin and a thick wedge of coarse-grained red beds in the northeastern part. The sequence is absent in much of the southern part of the basin. Large volumes of gas and much oil are obtained from some of its rocks, especially from the Oriskany Sandstone and the Huntersville Ghert. The Silurian-Devonian carbonate sequence is abruptly overlain by the Devonian clastic sequence a thick succession of interbedded shale, mudrock, siltstone, and sandstone. Colors range from predominantly purple and red in the northeastern part of the basin to predominantly dark gray and black in the southwestern part. Many rocks in the upper part contain hydrocarbons in commercial quantities. The next higher sequence is a heterogeneous succession that comprises most rocks of Mississippian age in the basin. It is composed largely of fine-grained to very coarse-grained noncalcareous clastic rocks in the northern half of the basin, and largely of carbonate rocks in the southern part. Large quantities of oil and gas are produced from the sequence. The youngest sequence consists of coarse-grained clastic rocks largely of Pennsylvanian age. In the center of the basin a relatively small volume of lithologically similar rocks of Permian age are included. The sequence has been intensively mined for coal throughout most of its extent. The waste-disposal possibilities of the stratified rocks in the Appalachian basin are considered in terms of the following: 1) gross lithology of the sequences; 2) general lithology of the rock units composing the sequences; and 3) the structural attitudes of the sequences in different parts of the basin. The degree of exploitation of economically significant mineral* resources is considered briefly where such exploitation may affect waste-disposal possibilities. Hydrologic aspects are not in general considered. Based largely on consideration of the above geologic factors the following types of reservoirs associated with particular geologic environments offer some prospects for the disposal of radioactive waste solutions. They are: 1) artificially created cavities in thick salt beds; 2) artificially fractured thin lenticular sandstone bodies isolated in shale or mudrock sequences; 3) portions of thick noncarbonate clastic sequences possessing appreciable natural porosity and permeability; 4) thin clastic units (with natural or artificially created openings) in the plate of a thrust fault overlain by impermeable strata. Considered in its entirety the Late Ordovician clastic sequence appears to have a greater number of favorable geologic factors for waste-disposal purposes than the others. The Early Silurian clastic sequence, the Silurian-Devonian carbonate sequence, and the Devonian clastic sequence offer fewer possibilities. The Late Precambrian stratified sequence, Early Cambrian, and the Cambrian-Ordovician carbonate sequence offer few possibilities. The Mississippian and Pennsylvanian sequences appear to be generally unsuitable.

Appalachian Basin↗

USGS1961

Geologic summary of the Appalachian basin, with reference to the subsurface disposal of radioactive waste solutions

The Appalachian basin is an elongate depression in the crystalline basement complex which contains a great volume of predominantly sedimentary stratified rocks. As defined in this paper it extends from the Adirondack Mountains in New York to central Alabama. From east to west it extends from the west flank of the Blue Ridge Mountains to the crest of the Findlay and Cincinnati arches and the Nashville dome. It encompasses an area of about 207,000 square miles, including all of West Virginia and parts of New York, New Jersey, Pennsylvania, Ohio, Maryland, Virginia, Kentucky, Tennessee, North Carolina, Georgia, and Alabama. The stratified rocks that occupy the basin constitute a wedge-shaped mass whose axis of greatest thickness lies close to and parallel to the east edge of the basin. The maximum thickness of stratified rocks preserved in any one part of the basin today is between 35,000 and 40,000 feet. The volume of the sedimentary rocks is approximately 510,000 cubic miles and of volcanic rocks is a few thousand cubic miles. The sedimentary rocks are predominantly Paleozoic in age, whereas the volcanic rocks are predominantly Late Precambrian. On the basis of gross lithology the stratified rocks overlying the crystalline basement complex can be divided into nine vertically sequential units, which are designated "sequences" in this report. The boundaries between contiguous sequences do not necessarily coincide with the commonly recognized boundaries between systems or series. All sequences are grossly wedge shaped, being thickest along the eastern margin of the basin and thinnest along the western margin. The lowermost unit the Late Precambrian stratified sequence is present only along part of the eastern margin of the basin, where it lies unconformably on the basement complex. It consists largely of volcanic tuffs and flows but contains some interbedded sedimentary rocks. The Late Precambrian sequence is overlain by the Early Cambrian clastic sequence. Where the older sequence is absent, the Early Cambrian sequence rests on the basement complex. Interbedded fine- to coarse-grained noncarbonate detrital rocks comprise the bulk of the sequence, but some volcanic and carbonate rocks are included. Next above is the Cambrian-Ordovician carbonate sequence which consists largely of limestone and dolomite. Some quartzose sandstone is present in the lower part in the western half of the basin, and much shale is present in the upper part in the southeast part of the basin. The next higher sequence is the Late Ordovician clastic sequence, which consists largely of shale, siltstone, and sandstone. Coarse-grained light-gray to red rocks are common in the sequence along the eastern side of the basin, whereas fine-grained dark-gray to black calcareous rocks are common along the west side. The Late Ordovician clastic sequence is overlain unconformably in many places by the Early Silurian clastic sequence. The latter comprises a relatively thin wedge of coarse-grained clastic rocks. Some of the most prolific oil- and gas-producing sandstones in the Appalachian basin are included. Among these are the "Clinton" sands of Ohio, the Medina Sandstones of New York and Pennsylvania, and the Keefer or "Big Six" Sandstone of West Virginia and Kentucky. Conformably overlying the Early Silurian clastic sequence is the Silurian-Devonian carbonate sequence, which consists predominantly of limestone and dolomite. It also contains a salt-bearing unit in the north-central part of the basin and a thick wedge of coarse-grained red beds in the northeastern part. The sequence is absent in much of the southern part of the basin. Large volumes of gas and much oil are obtained from some of its rocks, especially from the Oriskany Sandstone and the Huntersville Ghert. The Silurian-Devonian carbonate sequence is abruptly overlain by the Devonian clastic sequence a thick succession of interbedded shale, mudrock, siltstone, and sandstone. Colors range from predominantly purple and red in the northeastern part of the basin to predominantly dark gray and black in the southwestern part. Many rocks in the upper part contain hydrocarbons in commercial quantities. The next higher sequence is a heterogeneous succession that comprises most rocks of Mississippian age in the basin. It is composed largely of fine-grained to very coarse-grained noncalcareous clastic rocks in the northern half of the basin, and largely of carbonate rocks in the southern part. Large quantities of oil and gas are produced from the sequence. The youngest sequence consists of coarse-grained clastic rocks largely of Pennsylvanian age. In the center of the basin a relatively small volume of lithologically similar rocks of Permian age are included. The sequence has been intensively mined for coal throughout most of its extent. The waste-disposal possibilities of the stratified rocks in the Appalachian basin are considered in terms of the following: 1) gross lithology of the sequences; 2) general lithology of the rock units composing the sequences; and 3) the structural attitudes of the sequences in different parts of the basin. The degree of exploitation of economically significant mineral* resources is considered briefly where such exploitation may affect waste-disposal possibilities. Hydrologic aspects are not in general considered. Based largely on consideration of the above geologic factors the following types of reservoirs associated with particular geologic environments offer some prospects for the disposal of radioactive waste solutions. They are: 1) artificially created cavities in thick salt beds; 2) artificially fractured thin lenticular sandstone bodies isolated in shale or mudrock sequences; 3) portions of thick noncarbonate clastic sequences possessing appreciable natural porosity and permeability; 4) thin clastic units (with natural or artificially created openings) in the plate of a thrust fault overlain by impermeable strata. Considered in its entirety the Late Ordovician clastic sequence appears to have a greater number of favorable geologic factors for waste-disposal purposes than the others. The Early Silurian clastic sequence, the Silurian-Devonian carbonate sequence, and the Devonian clastic sequence offer fewer possibilities. The Late Precambrian stratified sequence, Early Cambrian, and the Cambrian-Ordovician carbonate sequence offer few possibilities. The Mississippian and Pennsylvanian sequences appear to be generally unsuitable.

Appalachian Basin↗

USGS2005

Evaluation of volatilization as a natural attenuation pathway for MTBE

Volatilization and diffusion through the unsaturated zone can be an important pathway for natural attenuation remediation of methyl tert-butyl ether (MTBE) at gasoline spill sites. The significance of this pathway depends primarily on the distribution of immiscible product within the unsaturated zone and the relative magnitude of aqueous-phase advection (ground water recharge) to gaseous-phase diffusion. At a gasoline spill site in Laurel Bay, South Carolina, rates of MTBE volatilization from ground water downgradient from the source are estimated by analyzing the distribution of MTBE in the unsaturated zone above a solute plume. Volatilization rates of MTBE from ground water determined by transport modeling ranged from 0.0020 to 0.0042 g m- 2 /year, depending on the assumed rate of ground water recharge. Although diffusive conditions at the Laurel Bay site are favorable for volatilization, mass loss of MTBE is insignificant over the length (230 m) of the solute plume. Based on this analysis, significant volatilization of MTBE from ground water downgradient from source areas at other sites is not likely. In contrast, model results indicate that volatilization coupled with diffusion to the atmosphere could be a significant mass loss pathway for MTBE in source areas where residual product resides above the capillary zone. Although not documented, mass loss of MTBE at the Laurel Bay site due to volatilization and diffusion to the atmosphere are predicted to be two to three times greater than mass loading of MTBE to ground water due to dissolution and recharge. This result would imply that volatilization in the source zone may be the critical natural attenuation pathway for MTBE at gasoline spill sites, especially when considering capillary zone limitations on volatilization of MTBE from ground water and the relative recalcitrance of MTBE to biodegradation.

Groundwater↗

USGS2021

Profiling lunar dust dissolution in aqueous environments: The design concept

Published studies and internal NASA reports indicate that when native lunar dust is suspended in an aqueous solution a variety of metal and other ions are released. This release has implications for future lunar missions, ranging from effects on mission hardware, effects on life support systems, possible direct effects on human health, and effects on research experiments such as plant growth experiments, space biology experiments and any activities that may involve the use of water sourced from the lunar poles. Furthermore, such contaminants could become concentrated or chemically altered to a more hazardous form during a variety of lunar mission activities, including everything from space suit cleaning to lunar industrial materials extraction. The exact profile of the release of ions from lunar dust and the nature of the partially dissolved particles has not been explored. Any model of this dissolution must be based on an understanding of the unique micromorphology of lunar dust, including its glassy nature, agglutinate features, high surface area and the presence of small deposits of elemental iron (nanophase iron) located near the surface of the grain particles. Dust has a very high surface area available for interaction with water. For this reason, on first exposure to water, an immediate pulsed release of ions could occur, with more prolonged release taking place over months or years. The few studies that have been conducted previously have been limited in both the time scales examined and in the selection of ions that were measured. The proposed investigation is a comprehensive materials science investigation, using the most modern analytical tools to catalogue all metals given off from lunar dust in various aqueous solutions and their time profiles of release from the very short term to the very long term. The product of the proposed study will be a comprehensive database determined from NASA curated samples collected from the Apollo landing sites that can be applied to research in both living systems and non-living systems on the moon. The methods developed in the proposed study will also establish standards for analysis of lunar dust samples returned from future manned missions (Artemis and others) and future robotic missions. The knowledge gained from this basic materials science investigation will have broad impact on the design of engineered human safety and health systems.

Acta Astronautica↗

USGS1995

The stability of hydrogen ion and specific conductance in filtered wet-deposition samples stored at ambient temperatures

Separate experiments by the U.S. Geological Survey (USGS) and the Illinois State Water Survey Central Analytical Laboratory (CAL) independently assessed the stability of hydrogen ion and specific conductance in filtered wet-deposition samples stored at ambient temperatures. The USGS experiment represented a test of sample stability under a diverse range of conditions, whereas the CAL experiment was a controlled test of sample stability. In the experiment by the USGS, a statistically significant (?? = 0.05) relation between [H+] and time was found for the composited filtered, natural, wet-deposition solution when all reported values are included in the analysis. However, if two outlying pH values most likely representing measurement error are excluded from the analysis, the change in [H+] over time was not statistically significant. In the experiment by the CAL, randomly selected samples were reanalyzed between July 1984 and February 1991. The original analysis and reanalysis pairs revealed that [H+] differences, although very small, were statistically different from zero, whereas specific-conductance differences were not. Nevertheless, the results of the CAL reanalysis project indicate there appears to be no consistent, chemically significant degradation in sample integrity with regard to [H+] and specific conductance while samples are stored at room temperature at the CAL. Based on the results of the CAL and USGS studies, short-term (45-60 day) stability of [H+] and specific conductance in natural filtered wet-deposition samples that are shipped and stored unchilled at ambient temperatures was satisfactory.

Water, Air, & Soil Pollution↗

USGS2000

Empirical assessment of fish introductions in a subtropical wetland: An evaluation of contrasting views

We summarized data from eight quantitative fish surveys conducted in southern Florida to evaluate the distribution and relative abundance of introduced fishes across a variety of habitats. These surveys encompassed marsh and canal habitats throughout most of the Everglades region, including the mangrove fringe of Florida Bay. Two studies provided systematically collected density information over a 20-year period, and documented the first local appearance of four introduced fishes based on their repeated absence in prior surveys. Those species displayed a pattern of rapid population growth followed by decline, then persistence at lower densities. Estuarine areas in the southern Everglades, characterized by natural tidal creeks surrounded by mangrove-dominated marshes, and canals held the largest introduced-fish populations. Introduced fishes were also common, at times exceeding 50% of the fish community, in solution holes that serve as dry-season refuges in short-hydroperiod rockland habitats of the eastern Everglades. Wet prairies and alligator ponds distant from canals generally held few individuals of introduced fishes. These patterns suggest that the introduced fishes in southern Florida at present may not be well-adapted to persist in freshwater marshes of the Everglades, possibly because of an interaction of periodic cold-temperature stress and hydrologic fluctuation. Our analyses indicated low densities of these fishes in central or northern Everglades wet-prairie communities, and, in the absence of experimental data, little evidence of biotic effects in this spatially extensive habitat. There is no guarantee that this condition will be maintained, especially under the cumulative effects of future invasions or environmental change.

Biological Invasions↗

USGS2007

Evasion of added isotopic mercury from a northern temperate lake

Isotopically enriched Hg (90% 202Hg) was added to a small lake in Ontario, Canada, at a rate equivalent to approximately threefold the annual direct atmospheric deposition rate that is typical of the northeastern United States. The Hg spike was thoroughly mixed into the epilimnion in nine separate events at two-week intervals throughout the summer growing season for three consecutive years. We measured concentrations of spike and ambient dissolved gaseous Hg (DGM) concentrations in surface water and the rate of volatilization of Hg from the lake on four separate, week-long sampling periods using floating dynamic flux chambers. The relationship between empirically measured rates of spike-Hg evasion were evaluated as functions of DGM concentration, wind velocity, and solar illumination. No individual environmental variable proved to be a strong predictor of the evasion flux. The DGM-normalized flux (expressed as the mass transfer coefficient, k) varied with wind velocity in a manner consistent with existing models of evasion of volatile solutes from natural waters but was higher than model estimates at low wind velocity. The empirical data were used to construct a description of evasion flux as a function of total dissolved Hg, wind, and solar illumination. That model was then applied to data for three summers for the experiment to generate estimates of Hg re-emission from the lake surface to the atmosphere. Based on ratios of spike Hg to ambient Hg in DGM and dissolved total Hg pools, ratios of DGM to total Hg in spike and ambient Hg pools, and flux estimates of spike and ambient Hg, we concluded that the added Hg spike was chemically indistinguishable from the ambient Hg in its behavior. Approximately 45% of Hg added to the lake over the summer was lost via volatilization.

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