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USGS1990

Variations of electric resistance and H2 and Rn emissions of concrete blocks under increasing uniaxial compression

Electric resistance and emissions of hydrogen and radon isotopes of concrete (which is somewhat similar to fault-zone materials) under increasing uniaxial compression were continuously monitored to check whether they show any pre- and post-failure changes that may correspond to similar changes reported for earthquakes. The results show that all these parameters generally begin to increase when the applied stresses reach 20% to 90% of the corresponding failure stresses, probably due to the occurrence and growth of dilatant microcracks in the specimens. The prefailure changes have different patterns for different specimens, probably because of differences in spatial and temporal distributions of the microcracks. The resistance shows large co-failure increases, and the gas emissions show large post-failure increases. The post-failure increase of radon persists longer and stays at a higher level than that of hydrogen, suggesting a difference in the emission mechanisms for these two kinds of gases. The H2 increase may be mainly due to chemical reaction at the crack surfaces while they are fresh, whereas the Rn increases may be mainly the result of the increased emanation area of such surfaces. The results suggest that monitoring of resistivity and gas emissions may be useful for predicting earthquakes and failures of concrete structures. ?? 1990 Birkha??user Verlag.

Pure and Applied Geophysics PAGEOPH↗

USGS2003

Review of Selected References and Data sets on Ambient Ground- and Surface-Water Quality in the Metedeconk River, Toms River, and Kettle Creek Basins, New Jersey, 1980-2001

Surface water and ground water from unconfined aquifers are the primary sources of drinking water for much of the population, about 391,000, in the Metedeconk River, Toms River, and Kettle Creek watersheds in the New Jersey Coastal Plain. The quality of these sources of drinking water is a concern because they are vulnerable to contamination. Indications of the occurrence, distribution, and likely sources and transport mechanisms of certain contaminants were obtained from 48 selected reports and 2 selected data sets on water quality in or near the watersheds (1980-2001). These indications are described and briefly summarized in this report. The findings of studies on ground-water quality indicate that shallow ground water within the study area generally meets primary drinking-water standards, with notable exceptions. Volatile organic compounds, mercury, arsenic, radionuclides, nitrate, and coliform bacteria have been detected in shallow ground water in some areas at levels that exceed Federal and State drinking-water standards. For example, results of analyses of untreated samples collected from more than 13,000 private wells during 1983-99 indicated that concentrations of volatile organic compounds in samples from 7.3 percent of the wells exceeded at least 1 of 11 drinking-water standards, according to records maintained by the Ocean County Health Department. In cases of exceedances, however, water treatment, well replacement, and (or) retesting assured that applicable drinking-water standards were being met at the tap. Reported concentrations of the pesticide chlordane in some areas exceeded the drinking-water standard; few data are available on the occurrence of other pesticides. Studies of nearby areas, however, indicate that pesticide concentrations generally could be expected to be below drinking-water standards. The combination of low pH and low dissolved solids in many areas results in shallow ground water that is highly corrosive and, if untreated, able to leach trace elements and release asbestos fibers from plumbing materials. Reported concentrations of nitrate, volatile organic compounds, trace elements, and pesticides in samples from the monitored mainstem and tributary streams within the study area generally are below maximum contaminant levels for drinking water or below detection limits. Results of studies in other areas indicate that pesticide concentrations in surface water could be considerably higher during high flows soon after the application of pesticides to crops than during low flows. Fecal coliform bacteria counts in streams vary considerably. Concentrations or counts of these classes of surface-water-quality constituents likely are functions of the intensity and type of upstream development. Results of limited monitoring for radionuclide concentrations reported by the Brick Township Municipal Utilities Authority of the Metedeconk River indicate that radionuclide concentrations or activities do not exceed maximum contaminant levels for drinking water. As a consequence of organic matter in surface water, the formati ultraviolet absorbance in samples from the Metedeconk River and the Toms River exceeded the alternative compliance criteria for source water (2.0 milligrams per liter for total organic carbon and 0.02 absorbance units-liters per milligram-centimeter for specific ultraviolet absorbance) with respect to treatment requirements for preventing elevated concentrations of disinfection by-products in treated water. Water-quality and treatment issues associated with use of ground and surface water for potable supply in the study area are related to human activities and naturally occurring factors. Additional monitoring and analysis of ground and surface water would be needed to determine conclusively the occurrence and distribution of some contaminants and the relative importance of various potential contaminant sources, transport and attenuation mechanisms, and transport pathways.

Water-Resources Investigations Report↗

USGS2018

Uptake and distribution of organo-iodine in deep-sea corals

Understanding iodine concentration, transport, and bioavailability is essential in evaluating iodine's impact to the environment and its effectiveness as an environmental biogeotracer. While iodine and its radionuclides have proven to be important tracers in geologic and biologic studies, little is known about transport of this element to the deep sea and subsequent uptake in deep-sea coral habitats. Results presented here on deep-sea black coral iodine speciation and iodine isotope variability provides key information on iodine behavior in natural and anthropogenic environments, and its geochemical pathway in the Gulf of Mexico. Organo-iodine is the dominant iodine species in the black corals, demonstrating that binding of iodine to organic matter plays an important role in the transport and transfer of iodine to the deep-sea corals. The identification of growth bands captured in high-resolution scanning electron images (SEM) with synchronous peaks in iodine variability suggest that riverine delivery of terrestrial-derived organo-iodine is the most plausible explanation to account for annual periodicity in the deep-sea coral geochemistry. Whereas previous studies have suggested the presence of annual growth rings in deep-sea corals, this present study provides a mechanism to explain the formation of annual growth bands. Furthermore, deep-sea coral ages based on iodine peak counts agree well with those ages derived from radiocarbon ( 14 C) measurements. These results hold promise for developing chronologies independent of 14 C dating, which is an essential component in constraining reservoir ages and using radiocarbon as a tracer of ocean circulation. Furthermore, the presence of enriched 129 I/ 127 I ratios during the most recent period of skeleton growth is linked to nuclear weapons testing during the 1960s. The sensitivity of the coral skeleton to record changes in surface water 129 I composition provides further evidence that iodine composition and isotope variability captured in proteinaceous deep-sea corals is a promising geochronometer as well as an emerging tracer for continental material flux.

Journal of Environmental Radioactivity↗

USGS1982

Leaching characteristics of ash from the May 18, 1980, eruption of Mount St. Helens Volcano, Washington

Leaching of freshly erupted air-fall ash, unaffected by rain, from the May 18, 1.980,eruption of Mount St. Helens volcano, Washington, shows that Ca 2+, Na+, Mg+, SO4 2-, and Cl- are the predominant chemical species released on first exposure of the ash to water. Extremely high correlation of Ca with SO4 and Na with Cl in water leachates suggests the presence of CaSO4 and NaCl salts on the ash. The amount of water soluble material on ash increases with distance from source and with the weight fraction of small (less than 63 micrometers) ash particles of high-surface area. This suggests that surface reactions such as adsorption are responsible for concentrating the soluble material. CaSO4, NaCl, and other salts are probably formed as microscopic crystals in the high-temperature core of the eruption column and are then adsorbed by silicate ash particles. The environmentally important elements Zn, Cu, Cd, F, Pb, and Ba are released by a water leach in concentrations which could pose short-term hazards to some forms of aquatic life. However, calculated concentrations are based on a water-to-ash ratio of 4:1 or less, which is probably an underestimation of the regionally operative ratio. A subsequent leach of ash by warm alkaline solution shows dramatic increases in the amount of dissolved SiO2, U, and V, which are probably caused by increased dissolution of the glassy component of ash. Glass dissolution by alkaline ground water is a mechanism for providing these three elements to sedimentary traps where they may co-accumulate as uraniferous silica or U-V minerals. Leaching characteristics of ash from Mount St. Helens are comparable to characteristics of ash of similar composition from volcanoes in Guatemala. Ashes from each locality show similar ions predominating for a given leachate and similar fractions of a particular element in the ash removed on contact with the leach solution.

Open-File Report↗

USGS1984

A review of crust and upper mantle structure studies of the Snake River Plain-Yellowstone volcanic system: A major lithospheric anomaly in the western U.S.A.

The Snake River Plain-Yellowstone volcanic system is one of the largest, basaltic, volcanic field in the world. Here, there is clear evidence for northeasterly progression of rhyolitic volcanism with its present position in Yellowstone. Many theories have been advanced for the origin of the Snake River Plain-Yellowstone system. Yellowstone and Eastern Snake River Plain have been studied intensively using various geophysical techniques. Some sparse geophysical data are available for the Western Snake River Plain as well. Teleseismic data show the presence of a large anomalous body with low P- and S-wave velocities in the crust and upper mantle under the Yellowstone caldera. A similar body in which compressional wave velocity is lower than in the surrounding rock is present under the Eastern Snake River Plain. No data on upper mantle anomalies are available for the Western Snake River Plain. Detailed seismic refraction data for the Eastern Snake River Plain show strong lateral heterogeneities and suggest thinning of the granitic crust from below by mafic intrusion. Available data for the Western Snake River Plain also show similar thinning of the upper crust and its replacement by mafic material. The seismic refraction results in Yellowstone show no evidence of the low-velocity anomalies in the lower crust suggested by teleseismic P-delay data and interpreted as due to extensive partial melting. However, the seismic refraction models indicate lower-than-normal velocities and strong lateral inhomogeneities in the upper crust. Particularly obvious in the refraction data are two regions of very low seismic velocities near the Mallard Eake and Sour Creek resurgent domes in the Yellowstone caldera. The low-velocity body near the Sour Creek resurgent dome is interpreted as partially molten rock. Together with other geophysical and thermal data, the seismic results indicate that a sub-lithospheric thermal anomaly is responsible for the time-progressive volcanism along the Eastern Snake River Plain. However, the exact mechanism responsible for the volcanism and details of magma storage and migration are not yet fully understood.

California, Idaho, Montana, Nevada, Oregon, Washin↗

USGS1995

Graphical and PC-software analysis of volcano eruption precursors according to the Materials Failure Forecast Method (FFM)

The Materials Failure Forecasting Method for volcanic eruptions (FFM) analyses the rate of precursory phenomena. Time of eruption onset is derived from the time of “failure” implied by accelerating rate of deformation. The approach attempts to fit data, Ω, to the differential relationship Ω Ω ¨ = A Ω ˙ "> ¨ = AΩ˙ , where the dot superscript represents the time derivative, and the data Ω may be any of several parameters describing the accelerating deformation or energy release of the volcanic system. Rate coefficients, A and α, may be derived from appropriate data sets to provide an estimate of time to “failure”. As the method is still an experimental technique, it should be used with appropriate judgment during times of volcanic crisis. Limitations of the approach are identified and discussed. Several kinds of eruption precursory phenomena, all simulating accelerating creep during the mechanical deformation of the system, can be used with FFM. Among these are tilt data, slope-distance measurements, crater fault movements and seismicity. The use of seismic coda, seismic amplitude-derived energy release and time-integrated amplitudes or coda lengths are examined. Usage of cumulative coda length directly has some practical advantages to more rigorously derived parameters, and RSAM and SSAM technologies appear to be well suited to real-time applications. One graphical and four numerical techniques of applying FFM are discussed. The graphical technique is based on an inverse representation of rate versus time. For α = 2, the inverse rate plot is linear; it is concave upward for α < 2 and concave downward for α > 2. The eruption time is found by simple extrapolation of the data set toward the time axis. Three numerical techniques are based on linear least-squares fits to linearized data sets. The “linearized least-squares technique” is most robust and is expected to be the most practical numerical technique. This technique is based on an iterative linearization of the given rate-time series. The hindsight technique is disadvantaged by a bias favouring a too early eruption time in foresight applications. The “log rate versus log acceleration technique”, utilizing a logarithmic representation of the fundamental differential equation, is disadvantaged by large data scatter after interpolation of accelerations. One further numerical technique, a nonlinear least-squares fit to rate data, requires special and more complex software. PC-oriented computer codes were developed for data manipulation, application of the three linearizing numerical methods, and curve fitting. Separate software is required for graphing purposes. All three linearizing techniques facilitate an eruption window based on a data envelope according to the linear least-squares fit, at a specific level of confidence, and an estimated rate at time of failure.

Journal of Volcanology and Geothermal Research↗

USGS1951

Geologic history of sea water: An attempt to state the problem

Paleontology and biochemistry together may yield fairly definite information, eventually, about the paleochemistry of sea water and atmosphere. Several less conclusive lines of evidence now available suggest that the composition of both sea water and atmosphere may have varied somewhat during the past; but the geologic record indicates that these variations have probably been within relatively narrow limits. A primary problem is how conditions could have remained so nearly constant for so long. It is clear, even from inadequate data on the quantities and compositions of ancient sediments, that the more volatile materials—H 2 O, CO 2 , Cl, N, and S— are much too abundant in the present atmosphere, hydrosphere, and biosphere and in ancient sediments to be explained, like the commoner rock-forming oxides, as the products of rock weathering alone. If the earth were once entirely gaseous or molten, these “excess” volatiles may be residual from a primitive atmosphere. But if so, certain corollaries should follow about the quantity of water dissolved in the molten earth and the expected chemical effects of a highly acid, primitive ocean. These corollaries appear to be contradicted by the geologic record, and doubt is therefore cast on this hypothesis of a dense primitive atmosphere. It seems more probable that only a small fraction of the total “excess” volatiles was ever present at one time in the early atmosphere and ocean. Carbon plays a significant part in the chemistry of sea water and in the realm of living matter. The amount now buried as carbonates and organic carbon in sedimentary rocks is about 600 times as great as that in today's atmosphere, hydrosphere, and biosphere. If only 1/100 of this buried carbon were suddenly added to the present atmosphere and ocean, many species of marine organisms would probably be exterminated. Furthermore, unless CO 2 is being added continuously to the atmosphere-ocean system from some source other than rock weathering, the present rate of its subtraction by sedimentation would, in only a few million years, cause brucite to take the place of calcite as a common marine sediment. Apparently, the geologic record shows no evidence of such simultaneous extinctions of many species nor such deposits of brucite. Evidently the amount of CO 2 in the atmosphere and ocean has remained relatively constant throughout much of the geologic past. This calls for some source of gradual and continuous supply, over and above that from rock weathering and from the metamorphism of older sedimentary rocks. A clue to this source is afforded by the relative amounts of the different “excess” volatiles. These are similar to the relative amounts of the same materials in gases escaping from volcanoes, fumaroles, and hot springs and in gases occluded in igneous rocks. Conceivably, therefore, the hydrosphere and atmosphere may have come almost entirely from such plutonic gases. During the crystallization of magmas, volatiles such as H 2 O and CO 2 accumulate in the remaining melt and are largely expelled as part of the final fractions. Volcanic eruptions and lava flows have brought volatiles to the earth's surface throughout the geologic past; but intrusive rocks are probably a much more adequate source of the constituents of the atmosphere and hydrosphere. Judged by the thermal springs of the United States, hot springs (carrying only 1 per cent or less of juvenile matter) may be the principal channels by which the “excess” volatiles have escaped from cooling magmas below. This mechanism fails to account for a continuous supply of volatiles unless it also provides for a continuous generation of new, volatile-rich magmas. Possibly such local magmas form by a continuous process of selective fusion of subcrustal rocks, to a depth of several hundred kilometers below the more mobile areas of the crust. This would imply that the volume of the ocean has grown with time. On this point, geologic evidence permits differences of interpretation; the record admittedly does not prove, but it seems consistent with, an increasing growth of the continental masses and a progressive sinking of oceanic basins. Perhaps something like the following mechanism could account for a continuous escape of volatiles to the earth's surface and a relatively uniform composition of sea water through much of geologic time: (1) selective fusion of lower-melting fractions from deep-seated, nearly anhydrous rocks beneath the unstable continental margins and geosynclines; (2) rise of these selected fractions (as granitic and hydrous magmas) and their slow crystallization nearer the surface; (3) essentially continuous isostatic readjustment between the differentiating continental masses and adjacent ocean basins; and (4) renewed erosion and sedimentation, with resulting instability of continental margins and mountainous areas and a new round of selective fusion below.

Geological Society of America Bulletin↗

USGS1994

Fate and pathways of injection-well effluent in the Florida Keys

Twenty-four wells (21 locations) were core drilled into the limestone beneath the Keys, reef tract, and outer reefs to determine if sewage effluents injected in Class V wells onshore are reaching offshore reef areas via underground flow. These wells were fitted with PVC casings and well screens and were sampled every three months for a period of one year. Analyses showed consistent hypersalinity in most wells and a marked increase in nitrogen (as ammonia) in offshore ground water. Other forms of nitrogen (NO 2 and NO 3 ) and phosphorous were not particularly elevated in offshore ground water but were above the levels found in surface marine water. The highest levels of nitrogen (NO 2 and NO 3 ) and phosphorous were in shallow onshore ground waters. Sources for the nutrients in the shallow onshore ground water consist of septic tanks and cesspools (@ 24,000 and 5,000 in the Florida Keys, respectively), agricultural fertilizers, and natural vegetation. Ammonia concentrations were low in shallow ground waters beneath the Florida Keys, probably because of oxidizing conditions. Tidal pumping is particularly active, especially nearshore. Hydraulic heads sufficient to elevate well water as much as 7 cm above sea level during falling tides were detected in all nearshore wells. During rising tides, the situation was reversed and water flowed into the wells. Tidal pumping implies considerable water movement both in and out of the upper few meters of limestone. Tidal pumping is a likely mechanism for mixing and transferring nutrient-rich ground water into the overlying marine waters. Although tidal pumping should cause rather complete mixing and dilution of any freshwater-based effluents entering the limestone via the more than 600 disposal wells in the Florida Keys, the ground waters in the 30- to 40-ft-depth range (9-12 m) nevertheless remained slightly hypersaline relative to sea water throughout the year. Fecal coliform and fecal streptococcal bacteria were associated with three Lower Keys offshore wells and two shallow onshore wells at Key Largo. On occasions, these bacteria were detected farther offshore, once in a well 4 miles off Key Largo. The bacterial analyses for Key Largo (both onshore and offshore) are supported by two independent bacteriological researchers using more sophisticated methods than the standard 100-ml membrane-filter method used in this study. Fecal bacteria can serve as tracers; thus, we conclude their presence is possible evidence for offshore transport of ground waters originating on Key Largo. Elevated nutrients (ammonia) and slightly elevated dissolved total phosphorous in offshore ground waters, however, cannot be tied to onshore sources with existing data. Rock analyses of material from our cores do not prove or disprove the hypothesis that limestone beneath the Keys or reef tract is serving as a sink for phosphorus or other nutrients. The data, however, do not rule out phosphorus uptake by limestone adjacent to disposal sources. For the purposes of this study, monitoring wells were not positioned sufficiently close to injection wells to determine if uptake of phosphorous is taking place. Ground waters were found to contain more dissolved solids than could be accounted for if hypersalinity resulted from simple evaporation of sea water. These data indicate that ground waters in the vicinity of our wells are dissolving solids from the rock rather than precipitating material within the rock framework; however, as mentioned above, our wells were not positioned sufficiently close to disposal wells to determine if localized uptake is occurring. Examination of rock cores from these wells revealed a general distribution of reef- and grainstone-facies belts. The Upper and Middle Keys are composed of a thin coral reef facies that extends only a few hundred feet seaward of the Keys. Reef facies give way to mudstone facies within a few yards of shore on the Florida Bay side of the Keys. On the seaward side of the Keys, beneath Hawk Channel and White Bank, the Pleistocene limestone is a mixed grainstone, packstone, and wackstone facies. Corals are rare or absent. The Pleistocene limestone beneath the outer reefs 4 to 5 miles offshore, however, consists of reef facies with the same coral fauna as that found on Key Largo. This pattern of two major reef-facies belts separated by a 2- to 4-mile-wide belt of grainstone facies may have as yet undetermined effects on groundwater circulation beneath the Florida reef tract. Grainstone is approximately an order of magnitude less permeable than the coralline Key Largo Limestone facies. The Q3 surface, a major subsurface unconformity thought to form an effective confining zone elsewhere in south Florida, was not detected in wells drilled more than 1 mile from shore. This unconformity, however, was detected in all wells drilled on or near the Keys. What was found to be a more effective and widespread confining layer is the Holocene sediment deposited on the Pleistocene limestone during the past 6,000 to 7,000 years. These relatively impermeable sediments are extensive, forming a belt up to 5 miles wide beginning about 0.5 mile offshore. Holocene sediments generally consist of low-permeability lime mud just above the Pleistocene surface, overlain by more permeable carbonate sands and reefs. Leakage of ground water by tidal pumping is not likely to occur through lime-mud-dominated areas such as Hawk Channel but is likely to occur through isolated porous and permeable Holocene reefs situated on Pleistocene limestone highs, and in places where Holocene sediment does not cover the limestone bedrock. Leakage is therefore limited to 1) a shallow-water 0.5-mile-wide nearshore belt of exposed Key Largo Limestone, 2) Holocene patch reefs, which grow on mud-free topographic rock highs, and 3) along the seaward side of the outermost reef in 35 to 65 ft (10-20 m) of water, where Holocene reef and sediment accumulations are thin or absent. This study did not address direct measurements of lateral groundwater movement or a hydrologic mechanism for transporting hypersaline ground water away from the Florida Keys. More recent work, however (Halley et al., 1994), shows that sea level in Florida Bay is higher than on the Atlantic side of the Keys more than 50% of the time. Higher sea level on the bay side of the Keys provides a potential for groundwater flow toward the Atlantic most of the time. Use of tracers (dyes or harmless bacteriological tracers) injected into the center of tightly spaced clusters of monitoring wells is a simple way to ascertain the net direction and rate of groundwater movement. Knowing the direction and rate of groundwater movement is needed for prediction and modeling efforts in the future

Florida↗

USGS2014

Investigating organic matter in Fanno Creek, Oregon, Part 2 of 3: sources, sinks, and transport of organic matter with fine sediment

Organic matter (OM) is abundant in Fanno Creek, Oregon, USA, and has been tied to a variety of water-quality concerns, including periods of low dissolved oxygen downstream in the Tualatin River, Oregon. The key sources of OM in Fanno Creek and other Tualatin River tributaries have not been fully identified, although isotopic analyses from previous studies indicated a predominantly terrestrial source. This study investigates the role of fine sediment erosion and deposition (mechanisms and spatial patterns) in relation to OM transport. Geomorphic mapping within the Fanno Creek floodplain shows that a large portion (approximately 70%) of the banks are eroding or subject to erosion, likely as a result of the imbalance caused by anthropogenic alteration. Field measurements of long- and short-term bank erosion average 4.2 cm/year and average measurements of deposition for the watershed are 4.8 cm/year. The balance between average annual erosion and deposition indicates an export of 3,250 metric tons (tonnes, t) of fine sediment to the Tualatin River—about twice the average annual export of 1,880 t of sediment at a location 2.4 km from the creek’s mouth calculated from suspended sediment load regressions from continuous turbidity data and suspended sediment samples. Carbon content from field samples of bank material, combined with fine sediment export rates, indicates that about 29–67 t of carbon, or about 49–116 t of OM, from bank sediment may be exported to the Tualatin River from Fanno Creek annually, an estimate that is a lower bound because it does not account for the mass wasting of organic-rich O and A soil horizons that enter the stream.

Oregon↗

USGS2011

Arsenic, metals, and nutrients in runoff from two detention basins to Raccoon Creek, New Jersey Coastal Plain, 2008

Arsenic (As) concentrations in the waters of Raccoon Creek in southern New Jersey commonly exceed the State\'s Surface Water Quality Standard (SWQS) for freshwater of 0.017 microgram per liter (mu or ug/L). In order to assess contributions of As from residential runoff to the creek, samples of runoff water were collected from a detention basin in each of two residential developments underlain by different geologic formations and at the outlets of those basins. Samples of streamwater also were collected from Raccoon Creek adjacent to the developments. The samples were analyzed to determine concentrations of As, selected metals, organic carbon, and nutrients. Soil samples in and downgradient from the basins also were collected and analyzed. Concentrations of As in unfiltered water samples of runoff from the basin underlain by glauconitic clays generally were higher (up to 4.35 mu or ug/L) than in runoff from the basin underlain by predominantly quartz sands and silts (up to 2.68 mu or ug/L). Chromium (Cr) concentrations also were higher in runoff from the basin underlain by glauconitic clays than in runoff from the basin underlain by quartz sand and silt. In addition, Cr concentrations were higher in the glauconitic soils than in the quartz-rich soils. Metals such as aluminum (Al), iron (Fe), lead (Pb), and manganese (Mn) in the runoff and in the streamwater were mostly in particulate form. Arsenic, most metals, and phosphorus (P) however, were mostly in dissolved form in runoff but in particulate form in the streamwater. Total organic carbon concentrations in the runoff ranged from about 10 to nearly 16 milligrams per liter (mg/L). Given such levels of organic carbon and strong correlations between concentrations of some metals and organic carbon, it may be that many of the metals were complexed with dissolved organic carbon and transported in that form in the runoff. Although underlying geologic materials and soils appear to be major contributors of As to the streamwater, As also could have been contributed from lead arsenate pesticide residues. The residential development underlain by quartz-rich sediments formerly had been an orchard where such pesticides may have been used. The substantial inputs of As to runoff at this site may be attributable to this former land use, although Pb concentrations were about the same in runoff from both sites. The streamwater at both sites, however, contained Pb concentrations well above those in runoff, indicating that there are additional inputs of Pb, perhaps from roadside soils, upstream from the two sampling sites in this study. Positive relations between concentrations of As and some metals with dissolved organic carbon in runoff and streamwater indicate that complexation with organic carbon may provide a mechanism by which these constituents can be transported. Sorption of As, Pb, and P to Fe hydroxides may be indicated by the observed positive relation of particulate As, Pb, and P to particulate Fe, however, representing an additional mechanism for transport of these constituents.

New Jersey↗

USGS2005

Sorption of aromatic organic pollutants to grasses from water

The influence of plant lipids on the equilibrium sorption of three aromatic solutes from water was studied. The plant-water sorption isotherms of benzene, 1,2-dichlorobenzene, and phenanthrene were measured over a large range of solute concentrations using sealed vessels containing water, dried plant material, and solute. The plant materials studied include the shoots of annual rye, tall fescue, red fescue, and spinach as well as the roots of annual rye. Seven out of eight sorption isotherms were linear with no evidence of competitive effects between the solutes. For a given plant type, the sorption coefficient increased with decreasing solute water solubility. For a given solute, sorption increased with increasing plant lipid content. The estimated lipid-water partition coefficients of individual solutes were found to be significantly greater than the corresponding octanol-water partition coefficients. This indicates that plant lipids are a more effective partition solvent than octanol for the studied aromatic compounds. As expected, the solute lipid-water partition coefficients were log-linearly related to the respective water solubilities. For the compounds studied, partitioning into the lipids is believed to be the primary sorption mechanism. ?? 2005 American Chemical Society.

Environmental Science & Technology↗

USGS1961

Graphic and algebraic solutions of the discordant lead-uranium age problem

Uranium-bearing minerals that give lead-uranium and lead—lead ages that are essentially in agreement, i.e. concordant, generally are considered to have had a relatively simple geologic history and to have been unaltered since their deposition. The concordant ages obtained on such materials are, therefore, assumed to approach closely the actual age of the minerals. Many uranium-bearing samples, particularly uranium ores, give the following discordant age sequences; Pb 206 U 238 < Pb 207 U 235 ⪡ Pb 207 Pb 206 "> Pb 206 U 238 <Pb 207 U 235 ⪡Pb 207 Pb 206 or, less frequently, Pb 207 Pb 206 ⪡ Pb 207 U 235 < Pb 206 U 238 "> Pb 207 Pb 206 ⪡Pb 207 U 235 <Pb 206 U 238 . These discordant age sequences have been attributed most often to uncertainties in the common lead correction, selective loss of radio-active daughter products, loss or gain of lead or uranium, or contamination by an older generation of radiogenic lead. The evaluation of discordant lead isotope age data may be separated into two operations. The first operation, with which this paper is concerned, is mechanical in nature and involves the calculation of the different possible concordant ages corresponding to the various processes assumed to have produced the discordant ages. The second operation is more difficult to define and requires, in part, some personal judgement. It includes a synthesis of the possible concordant age solutions with other independent geologic and isotopic evidence. The concordant age ultimately chosen as most acceptable should be consistent not only with the known events in the geologic history of the area, the age relations of the enclosing rocks, and the mineralogic and paragenetic evidence, but also with other independent age measurements and the isotopic data obtained on the lead in related or associated non-radioactive minerals. The calculation of the possible concordant ages from discordant age data has been greatly simplified by Wetherill's graphical method of plotting the mole ratios of radiogenic Pb 206 U 238 "> Pb 206 U 238 ( N 206 N 238 "> N 206 N 238 ) vs. radiogenic Pb 207 U 235 "> Pb 207 U 235 ( N 207 N 235 "> N 207 N 235 ) after correcting for the contaminating common Pb 206 and Pb 207 . The linear relationships noted in this graphical procedure have been extended to plots of the mole ratios of total Pb 206 U 238 "> Pb 206 U 238 ( t N 206 N 238 "> t N 206 N 238 ) vs. total Pb 207 U 235 "> Pb 207 U 235 ( t N 207 N 235 "> t N 207 N 235 ). This modification permits the calculation of concordant ages for unaltered samples using only the Pb 207 Pb 206 "> Pb 207 Pb 206 ratio of the contaminating common lead. If isotopic data are available for two samples of the same age, x and y , from the same or related deposits or outcrops, graphs of the normalized difference ratios [ ( N 206 N 204 )x − ( N 206 N 204 )y ( N 238 N 204 )x −( N 238 N 204 )y ] vs. [ ( N 207 N 204 )x − ( N 207 N 204 )y ( N 235 N 204 )x −( N 235 N 204 )y ] "> [(N 206 N 204 )x − (N 206 N 204 )y(N 238 N 204 )x −(N 238 N 204 )y] vs. [(N 207 N 204 )x − (N 207 N 204 )y(N 235 N 204 )x −(N 235 N 204 )y] can give concordant ages corrected for unknown amounts of a common lead with an unknown Pb 207 / Pb 206 ratio. (If thorium is absent the difference ratios may be normalized with the more abundant index isotope, Pb 208 .) Similar plots of tho normalized, difference ratios for three genetically related samples ( x − y ) and( x − z ), will give concordant ages corrected, in addition, for either one unknown period of past alteration or initial contamination by an older generation of radiogenic lead of unknown Pb 207 /Pb 206 ratio. Practical numerical solutions for many of tho concordant age calculations are not currently available. However, the algebraic equivalents of these new graphical methods give equations which may be programmed for computing machines. For geologically probable parameters the equations of higher order have two positive real roots that rapidly converge on the exact concordant ages corrected for original radiogenic lead and for loss or gain of lead or uranium. Modifications of these general age equations expanded only to the second degree have been derived for use with desk calculators. These graphical and algebraic methods clearly suggest both the type and minimum number of samples necessary for adequate mathematical analysis of discordant lead isotope age data. This mathematical treatment also makes it clear that discordant lead isotope data alone cannot provide the basis for the choice of one of the possible concordant age solutions. The new equations, in particular, provide an incentive to improve our physical constants, analytical techniques and sampling methods in order that we may derive all of the useful geologic information that is available in a comprehensive lead isotope age study.

Geochimica et Cosmochimica Acta↗

USGS2015

Mechanisms and timescales of generating eruptible rhyolitic magmas at Yellowstone caldera from zircon and sanidine geochronology and geochemistry

We constrain the physical nature of the magma reservoir and the mechanisms of rhyolite generation at Yellowstone caldera via detailed characterization of zircon and sanidine crystals hosted in three rhyolites erupted during the (ca. 170 – 70 ka) Central Plateau Member eruptive episode – the most recent post-caldera magmatism at Yellowstone. We present 238U-230Th crystallization ages and trace-element compositions of the interiors and surfaces (i.e., unpolished rims) of individual zircon crystals from each rhyolite. We compare these zircon data to 238U- 230Th crystallization ages of bulk sanidine separates coupled with chemical and isotopic data from single sanidine crystals. Zircon age and trace-element data demonstrate that the magma reservoir that sourced the Central Plateau Member rhyolites was long-lived (150 – 250 kyr) and genetically related to the preceding episode of magmatism, which occurred ca. 256 ka. The interiors of most zircons in each rhyolite were inherited from unerupted material related to older stages of Central Plateau Member magmatism or the preceding late Upper Basin Member magmatism (i.e., are antecrysts). Conversely, most zircon surfaces crystallized near the time of eruption from their host liquids (i.e., are autocrystic). The repeated recycling of zircon interiors from older stages of magmatism demonstrates that sequentially erupted Central Plateau Member rhyolites are genetically related. Sanidine separates from each rhyolite yield 238U-230Th crystallization ages at or near the eruption age of their host magmas, coeval with the coexisting zircon surfaces, but are younger than the coexisting zircon interiors. Chemical and isotopic data from single sanidine crystals demonstrate that the sanidines in each rhyolite are in equilibrium with their host melts, which considered along with their near-eruption crystallization ages suggests that nearly all CPM sanidines are autocrystic. The paucity of antecrystic sanidine crystals relative to antecrystic zircons require a model where eruptible rhyolites are generated by extracting melt and zircons from a long-lived mush of immobile crystal-rich magma. In this process the larger sanidine crystals remain trapped in the locked crystal network. The extracted melts (plus antecrystic zircon) amalgamate into a liquid dominated (i.e., eruptible) magma body that is maintained as a physically distinct entity relative to the bulk of the long-lived crystal mush. Zircon surfaces and sanidines in each rhyolite crystallize after melt extraction/amalgamation and their ages constrain the residence time of eruptible magmas at Yellowstone. Residence times of the large volume rhyolites (~40 – 70 km3) are ≤ 1 kyr (conservatively < 6 kyr), which suggests that large volumes of rhyolite can be generated rapidly by extracting melt from a crystal mush. Because the lifespan of the crystal mush that sourced the Central Plateau Member rhyolites is two orders of magnitude longer than the residence time of eruptible magma bodies within the reservoir, it is apparent that the Yellowstone magma reservoir spends most of its time in a largely-crystalline (i.e., uneruptible) state, similar to the present-day magma reservoir, and that eruptible magma bodies are ephemeral features.

Idaho, Wyoming↗

USGS1968

On the maintenance of anomalous fluid pressures: II. Source layer at depth

Physico-chemical mechanisms have been suggested to account for anomalous fluid pressures in the geologic environment which require a fluid source at depth. The persistence of anomalous pressure is a problem that involves nonsteady fluid flow. The hydrodynamics and particular boundary conditions control the time rate of pressure change and its maintenance. A series of mathematical solutions germane to the maintenance of anomalous pressure caused by the injection of fluids into the system from a source layer are presented. The phase change, gypsum to anhydrite plus water, is used as an example of a fluid source at depth. The thermodynamics of the gypsum-dehydration reaction indicates that conversion will probably occur at shallow depths and produce fluid at a constant rate. The dehydration of montmorillonite will also produce fluids at a constant rate under geologic conditions where the reaction can occur. If horizons of material of low permeability are missing or scarce, it is doubtful that anomalous pore pressures can be maintained for more than a geologic instant. The creation and continuation of anomalous pressure depend largely upon the hydraulic conductivity and, to a lesser extent, upon the specific storage of clay layers within the system. © 1968, The Geological Society of America, Inc.

Geological Society of America Bulletin↗

USGS1949

Distribution of uranium in the Florida phosphate field

Land-pebble phosphate, hard-rock phosphate, and river-pebble phosphate are the three types of phosphatic rock found in Florida. This report is concerned primarily with the land-pebble deposits, the only type which contains a significant amount of uranium. The most productive part of the land-pebble district is in Polk and Hillsborough Counties, in the west-central part of the Florida peninsula. Phosphate occurs in both the Hawthorn formation of lower middle Miocene age and the Bone Valley formation of Pliocene age. The phosphate in the Bone Valley is generally of higher grade, probably as the result of mechanical reworking and further precipitation during submergence in Pliocene time. In a few places, leached parts of the Hawthorn formation are also of minable grade. , Pleistocene terrace deposits and beach sands unconformably overlie the Bone Valley. In Polk and Hillsborough Counties, the high-grade part of the land-pebble phosphate district, uranium occurs principally in the Bone Valley formation and is concentrated in the upper part of the formation, which has been leached by ground water. The maximum tenor found to date is 0.1 percent uranium. The basal member of the Bone Valley has a maximum grade of .02 percent uranium, and averages about .01 percent uranium. Fresh, unweathered Hawthorn formation has little or no uranium, but leached Hawthorn, rich in P 2 O 5 , contains a maximum of 0.01 percent uranium. The Pleistocene sands have no uranium except where they contain reworked phosphatic material from the Bone Valley formation. South of the high- grade district, in Manatee and Hardee Counties, the Bone Valley, Hawthorn, and Pleistocene formations contain only very minor amounts of uranium. The uranium in the land-pebble deposits was probably syngenetic in origin. Subsequent leaching of soluble material has resulted in residual enrichment of uranium. The uranium seems to be associated with the phosphate mineral.

Florida↗

USGS2007

Methane gas hydrate effect on sediment acoustic and strength properties

To improve our understanding of the interaction of methane gas hydrate with host sediment, we studied: (1) the effects of gas hydrate and ice on acoustic velocity in different sediment types, (2) effect of different hydrate formation mechanisms on measured acoustic properties (3) dependence of shear strength on pore space contents, and (4) pore pressure effects during undrained shear. A wide range in acoustic p-wave velocities (V p ) were measured in coarse-grained sediment for different pore space occupants. V p ranged from less than 1 km/s for gas-charged sediment to 1.77–1.94 km/s for water-saturated sediment, 2.91–4.00 km/s for sediment with varying degrees of hydrate saturation, and 3.88–4.33 km/s for frozen sediment. V p measured in fine-grained sediment containing gas hydrate was substantially lower (1.97 km/s). Acoustic models based on measured V p indicate that hydrate which formed in high gas flux environments can cement coarse-grained sediment, whereas hydrate formed from methane dissolved in the pore fluid may not. The presence of gas hydrate and other solid pore-filling material, such as ice, increased the sediment shear strength. The magnitude of that increase is related to the amount of hydrate in the pore space and cementation characteristics between the hydrate and sediment grains. We have found, that for consolidation stresses associated with the upper several hundred meters of sub-bottom depth, pore pressures decreased during shear in coarse-grained sediment containing gas hydrate, whereas pore pressure in fine-grained sediment typically increased during shear. The presence of free gas in pore spaces damped pore pressure response during shear and reduced the strengthening effect of gas hydrate in sands.

Journal of Petroleum Science and Engineering↗

USGS2009

Anatomy of the dead sea transform from lithospheric to microscopic scale

Fault zones are the locations where motion of tectonic plates, often associated with earthquakes, is accommodated. Despite a rapid increase in the understanding of faults in the last decades, our knowledge of their geometry, petrophysical properties, and controlling processes remains incomplete. The central questions addressed here in our study of the Dead Sea Transform (DST) in the Middle East are as follows: (1) What are the structure and kinematics of a large fault zone? (2) What controls its structure and kinematics? (3) How does the DST compare to other plate boundary fault zones? The DST has accommodated a total of 105 km of leftlateral transform motion between the African and Arabian plates since early Miocene (???20 Ma). The DST segment between the Dead Sea and the Red Sea, called the Arava/ Araba Fault (AF), is studied here using a multidisciplinary and multiscale approach from the ??m to the plate tectonic scale. We observe that under the DST a narrow, subvertical zone cuts through crust and lithosphere. First, from west to east the crustal thickness increases smoothly from 26 to 39 km, and a subhorizontal lower crustal reflector is detected east of the AF. Second, several faults exist in the upper crust in a 40 km wide zone centered on the AF, but none have kilometer-size zones of decreased seismic velocities or zones of high electrical conductivities in the upper crust expected for large damage zones. Third, the AF is the main branch of the DST system, even though it has accommodated only a part (up to 60 km) of the overall 105 km of sinistral plate motion. Fourth, the AF acts as a barrier to fluids to a depth of 4 km, and the lithology changes abruptly across it. Fifth, in the top few hundred meters of the AF a locally transpressional regime is observed in a 100-300 m wide zone of deformed and displaced material, bordered by subparallel faults forming a positive flower structure. Other segments of the AF have a transtensional character with small pull-aparts along them. The damage zones of the individual faults are only 5-20 m wide at this depth range. Sixth, two areas on the AF show mesoscale to microscale faulting and veining in limestone sequences with faulting depths between 2 and 5 km. Seventh, fluids in the AF are carried downward into the fault zone. Only a minor fraction of fluids is derived from ascending hydrothermal fluids. However, we found that on the kilometer scale the AF does not act as an important fluid conduit. Most of these findings are corroborated using thermomechanical modeling where shear deformation in the upper crust is localized in one or two major faults; at larger depth, shear deformation occurs in a 20-40 km wide zone with a mechanically weak decoupling zone extending subvertically through the entire lithosphere. Copyright 2009 by the American Geophysical Union.

Reviews of Geophysics↗

USGS2010

Isotopic composition and origin of indigenous natural perchlorate and co-occurring nitrate in the southwestern United States

Perchlorate (ClO 4 − ) has been detected widely in groundwater and soils of the southwestern United States. Much of this ClO 4 − appears to be natural, and it may have accumulated largely through wet and dry atmospheric deposition. This study evaluates the isotopic composition of natural ClO 4 − indigenous to the southwestern U.S. Stable isotope ratios were measured in ClO 4 − (δ 18 O, Δ 17 O, δ 37 Cl) and associated NO 3 − (δ 18 O, Δ 17 O, δ 15 N) in groundwater from the southern High Plains (SHP) of Texas and New Mexico and the Middle Rio Grande Basin (MRGB) in New Mexico, from unsaturated subsoil in the SHP, and from NO 3 − -rich surface caliche deposits near Death Valley, California. The data indicate natural ClO 4 − in the southwestern U.S. has a wide range of isotopic compositions that are distinct from those reported previously for natural ClO 4 − from the Atacama Desert of Chile as well as all known synthetic ClO 4 − . ClO 4 − in Death Valley caliche has a range of high Δ 17 O values (+8.6 to +18.4 ‰), overlapping and extending the Atacama range, indicating at least partial atmospheric formation via reaction with ozone (O 3 ). However, the Death Valley δ 37 Cl values (−3.1 to −0.8 ‰) and δ 18 O values (+2.9 to +26.1‰) are higher than those of Atacama ClO 4 − . In contrast, ClO 4 − from western Texas and New Mexico has much lower Δ 17 O (+0.3 to +1.3‰), with relatively high δ 37 Cl (+3.4 to +5.1 ‰) and δ 18 O (+0.5 to +4.8 ‰), indicating either that this material was not primarily generated with O 3 as a reactant or that the ClO 4 − was affected by postdepositional O isotope exchange. High Δ 17 O values in ClO 4 − (Atacama and Death Valley) are associated with high Δ 17 O values in NO 3 − , indicating that both compounds preserve characteristics of O 3 -related atmospheric production in hyper-arid settings, whereas both compounds have low Δ 17 O values in less arid settings. Although Δ 17 O variations in terrestrial NO 3 − can be attributed to mixing of atmospheric (high Δ 17 O) and biogenic (low Δ 17 O) NO 3 − , variations in Δ 17 O of terrestrial ClO 4 − are not readily explained in the same way. This study provides important new constraints for identifying natural sources of ClO 4 − in different environments by multicomponent isotopic characteristics, while presenting the possibilities of divergent ClO 4 − formation mechanisms and(or) ClO 4 − isotopic exchange in biologically active environments.

Environmental Science & Technology↗