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At least 379 records · Page 21Linked to original sources

Crystallization history of Kilauea Iki lava lake as seen in drill core recovered in 1967-1979

Kilauea Iki lava lake formed during the 1959 summit eruption, one of the most picritic eruptions of Kilauea Volcano in the twentieth century. Since 1959 the 110 to 122 m thick lake has cooled slowly, developing steadily thickening upper and lower crusts, with a lens of more molten lava in between. Recent coring dates, with maximum depths reached in the center of the lake, are: 1967 (26.5 m). 1975 (44.2 m), 1976 (46.0 m) and 1979 (52.7 m). These depths define the base of the upper crust at the time of drilling. The bulk of the core consists of a gray, olivine-phyric basalt matrix, which locally contains coarser-grained diabasic segregation veins. The most important megascopic variation in the matrix rock is its variation in olivine content. The upper 15 m of crust is very olivine-rich. Abundance and average size of olivine decrease irregularly downward to 23 m; between 23 and 40 m the rock contains 5-10% of small olivine phenocrysts. Below 40 m. olivine content and average grainsize rise sharply. Olivine contents remain high (20-45%, by volume) throughout the lower crust, except for a narrow (< 6 m) olivine depleted zone near the basalt contact. Petrographically the olivine phenocrysts in Kilauea Iki can be divided into two types. Type 1 phenocrysts are large (1-12 mm long), with irregular blocky outlines, and often contain kink bands. Type 2 crystals are relatively small (0.5-2 mm in length), euhedral and undeformed. The variations in olivine content of the matrix rock are almost entirely variations in the amount of type 1 olivines. Sharp mineral layering of any sort is rare in Kilauea Iki. However, the depth range 41-52 m is marked by the frequent occurrence of steeply dipping (70??-90??) bands or bodies of slightly vuggy olivine-rich rock locally capped with a small cupola of segregation-vein material. In thin section there is clear evidence for relative movement of melt and crystals within these structures. The segregation veins occur only in the upper crust. The most widely distributed (occurring from 4.5-59.4 m) are thin veins (most < 5 cm thick), which cut the core at moderate angles and appear to have been derived from the immediately adjacent wall-rock by filter pressing. There is also a series of thicker (0.1-1.5 m) segregation veins, which recur every 2-3 m, between 20 and 52 m. These have subhorizontal contacts and appear, from similarities in thickness and spacing, to correlate between drill holes as much as 100 m apart. These large veins are not derived from the adjacent wallrock: their mechanism of formation is still problematical. The total thickness of segregation veins in Kilauea Iki is 3-6 m in the central part of the lake, corresponding to 6-11% of the upper crust. Whole-rock compositions for Kilauea Iki fall into two groups: the matrix rock ranges from 20-7.5% MgO, while the segregation veins all contain between 6.0 and 4.5% MgO. There are no whole-rock compositions of intermediate MgO content. Samples from < 12 m show eruption-controlled chemistry. Below that depth, matrix rock compositions have higher Al2O3, TiO2 and alkalies, and lower CaO and FeO, at a given MgO content than do the eruption pumices. The probable causes of this are assimilation of low-melting components from foundered crust, plus removal of olivine, plus removal of minor augite, for rocks with MgO contents of < 8.0%. Given the observed rate of growth of the upper crust, one can infer that significant removal of the type 1 olivine phenocrysts from the upper part of the lake began in 1963 and ceased sometime prior to 1972. The process. probably gravitative settling, appears to have been inhibited earlier by gas streaming from the lower part of the lens of melt. The olivine cumulate zone, which extends into the upper crust, contains relatively few (25-40%) olivine crystals, few of which actually touch each other. The diffuseness of the cumulate zone raises the possibility that the crystals were coated with a relatively visous boundary layer

Bulletin Volcanologique↗

Modelling root reinforcement in shallow forest soils

A hypothesis used to explain the relationship between timber harvesting and landslides is that tree roots add mechanical support to soil, thus increasing soil strength. Upon harvest, the tree roots decay which reduces soil strength and increases the risk of management -induced landslides. The technical literature does not adequately support this hypothesis. Soil strength values attributed to root reinforcement that are in the technical literature are such that forested sites can't fail and all high risk, harvested sites must fail. Both unstable forested sites and stable harvested sites exist, in abundance, in the real world thus, the literature does not adequately describe the real world. An analytical model was developed to calculate soil strength increase due to root reinforcement. Conceptually, the model is composed of a reinforcing element with high tensile strength, i.e. a conifer root, embedded in a material with little tensile strength, i.e. a soil. As the soil fails and deforms, the reinforcing element also deforms and stretches. The lateral deformation of the reinforcing element is treated analytically as a laterally loaded pile in a flexible foundation and the axial deformation is treated as an axially loaded pile. The governing differential equations are solved using finite-difference approximation techniques. The root reinforcement model was tested by comparing the final shape of steel and aluminum rods, parachute cord, wooden dowels, and pine roots in direct shear with predicted shapes from the output of the root reinforcement model. The comparisons were generally satisfactory, were best for parachute cord and wooden dowels, and were poorest for steel and aluminum rods. A parameter study was performed on the root reinforcement model which showed reinforced soil strength increased with increasing root diameter and soil depth. Output from the root reinforcement model showed a strain incompatibility between large and small diameter roots. The peak increase in soil strength attributed to roots was controlled by the small (<4mm) diameter root fraction. These results were used to calculate the effect of timber harvesting on a small, approximately 7.6 m 3 (10 yd 3 ), hypothetical landslide in a shallow, cohesionless, forest soil. The root reinforcement model predicted a post-harvest reduction in soil strength of 14 and 19 percent for a soil with and without 5 kPa (105 lbs/ft 2 ) of cohesion, respectively.

Thesis↗

Use of OSL dating to establish the stratigraphic framework of Quaternary eolian sediments, Anton scarp upper trench, Northeastern Colorado High Plains, USA

This paper contains the results of the optically stimulated luminescence (OSL) dating used to establish stratigraphic ages and relationships of eolian sediments in a trench in northeastern Colorado, USA. This trench was located in the upper face of the Anton scarp, a major topographic lineament trending NW-SE for a distance of 135 km, in anticipation of intersecting near-surface faulting. The trench was 180 m long, 4.5-6.0 m deep, and exposed 22 m of stratigraphic section, most of which dipped gently west and was truncated by gulley channeling at the face of the scarp. No direct evidence of faulting was found in the upper trench. The stratigraphy from the trench was described, mapped and dated using OSL on quartz and potassium feldspar, and 14 C obtained from woody material. OSL dating identified two upper loess units as Peoria Loess and Gilman Canyon Loess, deposited between 16 and 30 ka ago. The bottom layers of the trench were substantially older, giving OSL ages in excess of 100 ka. These older ages are interpreted as underestimates, owing to saturation of the fast component of OSL. Using OSL and 14 C dating, we can constrain the erosion and down cutting of the scarp face as occurring between 16 and 5.7 ka. As the trenching investigation continues in other parts of the scarp face, the results of this preliminary study will be of importance in relating the ages of the strata that underlie different parts of the scarp, and in determining whether Quaternary faulting was a mechanism that contributed to the formation of this regional geomorphic feature.

Quaternary International↗

The Mars 2020 Perseverance rover mast camera zoom (Mastcam-Z) multispectral, stereoscopic imaging investigation

Mastcam-Z is a multispectral, stereoscopic imaging investigation on the Mars 2020 mission’s Perseverance rover. Mastcam-Z consists of a pair of focusable, 4:1 zoomable cameras that provide broadband red/green/blue and narrowband 400-1000 nm color imaging with fields of view from 25.6° × 19.2° (26 mm focal length at 283 μrad/pixel) to 6.2° × 4.6° (110 mm focal length at 67.4 μrad/pixel). The cameras can resolve (≥ 5 pixels) ∼0.7 mm features at 2 m and ∼3.3 cm features at 100 m distance. Mastcam-Z shares significant heritage with the Mastcam instruments on the Mars Science Laboratory Curiosity rover. Each Mastcam-Z camera consists of zoom, focus, and filter wheel mechanisms and a 1648 × 1214 pixel charge-coupled device detector and electronics. The two Mastcam-Z cameras are mounted with a 24.4 cm stereo baseline and 2.3° total toe-in on a camera plate ∼2 m above the surface on the rover’s Remote Sensing Mast, which provides azimuth and elevation actuation. A separate digital electronics assembly inside the rover provides power, data processing and storage, and the interface to the rover computer. Primary and secondary Mastcam-Z calibration targets mounted on the rover top deck enable tactical reflectance calibration. Mastcam-Z multispectral, stereo, and panoramic images will be used to provide detailed morphology, topography, and geologic context along the rover’s traverse; constrain mineralogic, photometric, and physical properties of surface materials; monitor and characterize atmospheric and astronomical phenomena; and document the rover’s sample extraction and caching locations. Mastcam-Z images will also provide key engineering information to support sample selection and other rover driving and tool/instrument operations decisions.

Space Science Reviews↗

Breaching the levee of a channel on the Mississippi Fan

GLORIA images of the youngest channel on the Mississippi Fan indicate that it has not been a stable feature, but instead has shifted its course several times. A detailed study of a site of channel shifting found a complex stratigraphy that resulted from one episode of channel avulsion. The channel avulsion appears to have been initiated by a large mass flow that choked the channel below the point where the levee was breached and additionally spilled a large volume of material through the breach in the levee onto the adjacent fan. Subsequent flows were redirected through this breach in the levee and built a channel-levee complex over the mass movement deposits. A second phase of mass movement resulted from another large mass flow that came down the channel and triggered the collapse of part of the newly developed levee. In this case, locally derived levee sediment was mixed with allochthonous sediment from farther up the fan and was spread northward from the levee. This localized study suggests that fan stratigraphy is complex and variable at several scales, not just at the scale resolved in seismic stratigraphic studies (Weimer 1989) and that large mass flows capable of choking the channel system have been an important mechanism in redirecting sedimentation on the Mississippi Fan.

Mississippi Fan↗

Mechanisms for chemostatic behavior in catchments: implications for CO 2 consumption by mineral weathering

Concentrations of weathering products in streams often show relatively little variation compared to changes in discharge, both at event and annual scales. In this study, several hypothesized mechanisms for this “chemostatic behavior” were evaluated, and the potential for those mechanisms to influence relations between climate, weathering fluxes, and CO 2 consumption via mineral weathering was assessed. Data from Loch Vale, an alpine catchment in the Colorado Rocky Mountains, indicates that cation exchange and seasonal precipitation and dissolution of amorphous or poorly crystalline aluminosilicates are important processes that help regulate solute concentrations in the stream; however, those processes have no direct effect on CO 2 consumption in catchments. Hydrograph separation analyses indicate that old water stored in the subsurface over the winter accounts for about one-quarter of annual streamflow, and almost one-half of annual fluxes of Na and SiO 2 in the stream; thus, flushing of old water by new water (snowmelt) is an important component of chemostatic behavior. Hydrologic flushing of subsurface materials further induces chemostatic behavior by reducing mineral saturation indices and increasing reactive mineral surface area, which stimulate mineral weathering rates. CO 2 consumption by carbonic acid mediated mineral weathering was quantified using mass-balance calculations; results indicated that silicate mineral weathering was responsible for approximately two-thirds of annual CO 2 consumption, and carbonate weathering was responsible for the remaining one-third. CO 2 consumption was strongly dependent on annual precipitation and temperature; these relations were captured in a simple statistical model that accounted for 71% of the annual variation in CO 2 consumption via mineral weathering in Loch Vale.

Colorado↗

Biodiversity and Habitat Markets—Policy, Economic, and Ecological implications of Market-Based Conservation

This report is a primer on market-like and market-based mechanisms designed to conserve biodiversity and habitat. The types of markets and market-based approaches that were implemented or are emerging to benefit biodiversity and habitat in the United States are examined. The central approaches considered in this report include payments for ecosystem services, conservation banks, habitat exchanges, and eco-labels. Based on literature reviews and input from experts and practitioners, the report characterizes each market-based approach including policy context and structure; the theoretical basis for applying market-based approaches; the ecological effectiveness of practices and tools for measuring performance; and the future outlook for biodiversity and habitat markets. This report draws from previous research and serves as a summary of pertinent information associated with biodiversity and habitat markets while providing references to materials that go into greater detail on specific topics.

Circular↗

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↗

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↗

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↗

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↗

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↗

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 &#x3A9; &#xA8; = A &#x3A9; &#x2D9; "> ¨ = 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↗

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↗

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↗

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&mdash;about twice the average annual export of 1,880 t of sediment at a location 2.4 km from the creek&rsquo;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&ndash;67 t of carbon, or about 49&ndash;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↗

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↗

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↗