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Spectra of altered rocks in the visible and near infrared

Visible and near-infrared (0.35 to 2.5 mu m) bidirectional reflection spectra were recorded for a suite of well-characterized hydrothermally altered rock samples. The spectra typically display well-defined bands caused by both electronic and vibrational processes in the individual mineral constituents.Electronic transitions in the iron-bearing constituent minerals produce diagnostic minima near 0.43, 0.65, 0.85, and 0.93 mu m. Vibrational transitions in clay and water-bearing mineral constituents typically produce characteristic single or multiple features over limited spectral ranges near 1.4, 1.75, 1.9, 2.2, and 2.35 mu m. The most abundant feature-producing minerals present in these rocks are hematite, goethite, and alunite, while others frequently present are jarosite, kaolinite, potassium micas, pyrophyllite, montmorillonite, diaspore, and gypsum.This study shows that visible-near infrared spectrometry is a reliable and rapid technique for detecting and identifying clay minerals and alunite in rocks. Because these minerals are important constituents of altered rocks, the feasibility of using the visible and near infrared for detecting altered rocks by remote-sensing techniques is indicated. The spectral region near 2.2 mu m is particularly important for this purpose.

Nevada↗

Near-infrared spectra of West Shasta gossans compared with true and false gossans from Australia and Saudi Arabia

The near-infrared spectra of a suite of outcrop samples of massive sulfide gossans and false gossans representing three different weathering environments were measured and studied with X-ray, scanning electron microscope, and energy dispersive X-ray. Gossans that formed in a humid tropical environment are represented by samples from the Mt. Isa area, Queensland, Australia, and gossans that formed in an arid environment are represented by samples from several locations in Saudi Arabia. The gossans of the West Shasta massive sulfide district in California represent a weathering environment intermediate between these two extremes.On the basis of these spectral measurements, true gossans after massive sulfide deposits have spectra in the 800 to 2,500 nanometer (nm) region that are distinctly different from the spectra of false gossans. In the humid tropical environment, highly leached, newly formed kaolin minerals in the gossan cause spectral differences at about 1,400 to 2,200 nm. In the arid environment, true gossans preserve talc and minor mica from the massive sulfide deposit; these minerals are not observed in false gossans. These minerals result in spectral differences in the 2,200- to 2,300-nm region. In addition, true gossans generally have goethite spectral bands at about 900 nm as opposed to hematite spectral bands at about 850 nm for the false gossans.False gossans are not known in the West Shasta district; however, the gossan at the largest deposit, Iron Mountain, is a true gossan that has the distinctive spectral features of goethite at about 900 nm and diaspore in the 1,400- to 2,500-nm region. The other gossans also have the spectral features of goethite, but they contain a less leached mixture of kaolinite plus illite and have distinctive spectral features in the 1,400- to 2,500-nm region. These spectral differences define two groups of West Shasta gossans--inner gossans in large deposits and outer gossans at the margins of large deposits and in lesser massive sulfide deposits.

Economic Geology↗

A method for the concentration of fine-grained rutile (TiO2) from sediment and sedimentary rocks by chemical leaching

Quaternary marine sediment in the Gulf of Maine basins contains 0.7 to 1.0 wt percent TiO 2 (determined by X-ray fluorescence spectrometry). Most of this TiO 2 exists in the form of silt-size rutile crystals that are visible by using the petrographic microscope with transmitted light (Valentine and Commeau, 1990). The identification of rutile was confirmed by using a scanning electron microscope (SEM) equipped with an energy-dispersive X-ray spectrometer (EDS) system. To quantify the amount of TiO 2 in the sediment contributed by rutile and its polymorphs, anatase and brookite, it was necessary to eliminate as many of the other minerals as possible, especially titanium-bearing minerals such as ilmenite, ilmenomagnetite, biotite, hornblende, oyroxene, and sphene. We accomplished this by developing a method of chemical dissolution that removed the bulk of the raw material and left the TiO 2 minerals intact. Many methods using acids and bases have been developed over the years to dissolve rocks, minerals, and sediments for chemical analysis or to concentrate specific minerals (Dolcater et al., 1970; Church, 1971; Campbell, 1973, and the references cited therein). The method developed by Raman and Jackson (1965) to concentrate rutile and anatase in soils and sediments requires digesting the sample in concentrated hydrofluoric acid (HF) for 24 hours. However, Campbell (1973) found that digestion in HF for more than 2 hours results in a loss of anatase. The method of Dolcater et al. (1970) for concentrating titanium as a free oxide requires the use of hydrofluotitanic acid (H 2 TiF 6 ), which is difficult to find on the commercial market. The acid can be prepared by the reaction of concentrated HF (48%) with an excess of TiO 2 , but the procedure requires 36 hours to complete and should be attempted with caution because it is highly exothermic. Jackson (1979) provides a detailed method for digesting soils, but many of the recommended pretreatment steps employ sodium compounds such as sodium bicarbonate (NaHCO 3 ), sodium citrate (Na 3 C 6 H 5 O 7 -2H 2 O), and sodium dithionate (Na 2 S 2 O 4 ), which are used for the removal of calcium carbonate, iron oxides, and phosphates. In combining the methods of Dolcater and Jackson, sodium compounds must be thoroughly washed from the sample because they form sodium fluotitanate (Na 2 TiF 6 ) in the presence of hydrofluotitanic acid (Fig. 1K). French and Adams (1973) described an inexpensive method for decomposing silicates by HF digestion in polypropylene containers. Their technique was effective for a wide variety of rock types. However, it did not address the problem caused by the precipitation of insoluble fluorides, nor did it outline a procedure to concentrate any residue that remained. As no one method gave the results we required, we modified procedures described in the literature and developed a process that removes 96 to 98 wt percent of the raw sample material. The residue is composed of rutile and minor amounts of micro- and cryptocrystalline TiO 2 (Fig. 1A-J), barite (Fig. 1L), elemental carbon (coal), and insoluble fluorides (Fig. 1J). The fluorides precipitate during the decomposition of siliceous material in hydrofluoric acid (e.g., MgF 2 and MgAlF 5 -2.7H 2 O; Lanmyhr and Kringstad, 1966). Most of the sample analyzed by the method described were marine muds collected from the Gulf of Maine (Valentine and Commeau, 1990). The silt and clay fraction (up to 99 wt% of the sediment) is composed of clay minerals (chiefly illite-mica and chlorite), silt-size quartz and feldspar, and small crystals (2-12 um) of rutile and hematite. The bulk sediment samples contained an average of 2 to 3 wt percent CaCO 3 . Tiher samples analyzed include red and gray Carboniferous and Triassic sandstones and siltstones exposed around the Bay of Fundy region and Paleozoic sandstones, siltstones, and shales from northern Maine and New Brunswick. These rocks are probable sources for the fine-grained rutile found in the Gulf of Maine.

Economic Geology↗

Origin and significance of tourmaline-rich rocks in the Broken Hill district, Australia

Tourmaline-rich rocks are widespread minor lithologies within the Early Proterozoic Willyama Supergroup in the Broken Hill district, Australia. Tourmaline concentrations occur in strata-bound and local stratiform tourmalinites, clastic metasedimentary rocks, quartz-gahnite lode rocks, stratiform Pb-Zn-Ag sulfide ores, garnet quartzites, strata-bound scheelite deposits, quartz-tourmaline nodules, discordant quartz veins, and granitic pegmatites. Most of the tourmaline-rich rocks are within the Broken Hill Group that hosts the main Pb-Zn-Ag ores.At the Globe mine along the northeast end of the main lodes, tourmalinites are closely associated with Pb-Zn-Ag mineralization and in places are interbedded with Mn-rich garnet quartzites. Galena and other ore minerals occur locally in the cores of recrystallized tourmaline grains in these tourmalinites, indicating that tourmaline and sulfides were present together prior to deformation and high-grade metamorphism. Electron microprobe analyses of tourmalines intergrown with Fe sulfides at the Globe mine show Mg-rich compositions relative to tourmalines in sulfide-free assemblages from the same area, suggesting early (premetamorphic) introduction of boron and Mg enrichment of tourmaline by sulfide-silicate reactions during metamorphism.Combined field and geochemical data indicate that the district tourmalinites represent normal clastic sediments that were metasomatically altered by boron-rich hydrothermal fluids at or below the sediment-water interface. Whole-rock chemical analyses of 33 tourmaline-rich rocks show linear trends of data for major and trace elements that closely resemble the trends observed for unmineralized elastic metasedimentary rocks of the district. Average Fe/Al, Mg/Al, Na/Al, and Ti/Al molar ratios of the tourmaline-rich rocks and clastic metasediments are very similar; the average K/Al molar ratio of the tourmaline-rich rocks is significantly lower than that of the clastic metasediments, reflecting the loss of K during tourmalinite formation. Chondrite-normalized patterns of rare earth elements (REE) in the quartz-rich tourmalinites are generally similar to those of the clastic metasediments, except for minor depletions of light REE; local positive and negative Ce anomalies suggest tourmalinite formation in the presence of seawater or a seawater-derived pore fluid. The geochemical data imply relative immobility of Al, Ti, Cr, and heavy REE during hydrothermal alteration and later metamorphism. Boron isotope analyses of 52 tourmaline separates show a total range of delta 11 B values from -26.8 to -17.0 per mil. Fine-grained, euhedral, nonpoikilitic tourmalines from tourmalinites in the andalusite-muscovite zone in the northern part of the district (e.g., Black Prince mine) have delta 11 B values from -21 to -17 per mil, whereas coarse granoblastic and poikilo-blastic tourmalines from the sillimanite and two-pyroxene granulite zones in the southern part of the district (e.g., Globe mine) have delta 11 B values of-24 to -19 per mil. Tourmalines in strongly retrogressed tourmalinites have delta 11 B values from about -27 to -20 per mil. The observed variations in delta 11 B are consistent with prograde and retrograde metamorphic fractionation of boron isotopes, in which the fluid phase is preferentially enriched in the heavier isotope ( 11 B). Premetamorphic hydrothermal fluids that deposited the Black Prince tourmalinites had delta 11 B values of-8 to -5 per mil at 200 degrees to 300 degrees C, suggesting a boron source from nonmarine evaporite borates.Tourmalinites in the Broken Hill district apparently formed by the same submarine hydrothermal processes as the main Pb-Zn-Ag lodes and the siliceous ferromanganese protoliths of the garnet quartzites. In our model, the hydrothermal system(s) acquired abundant boron by leaching evaporitic borates within the Thackaringa Group, the stratigraphic sequence that underlies the Broken Hill Group and most of the tourmaline concentrations. We suggest that evaporites of the Thackaringa Group provided a source of readily extractable boron for formation of the tourmalinites and also the source of the fluoride, sulfur, and perhaps the carbonate in the main lodes; such evaporites may have been critical for increased metal chloride complexing and transport necessary for deposition of the high-grade Pb-Zn-Ag ores. The Broken Hill deposit may have formed contemporaneously with the Mount Isa and McArthur River Pb-Zn-Ag deposits in similar evaporite-bearing sequences during widespread Early Proterozoic continental rifting.

Economic Geology↗

Applied geochemistry, geology and mineralogy of the northernmost Carlin trend, Nevada

Investigations in the northernmost Carlin trend were undertaken to advance understanding of the geochemical signatures and genesis of precious metal deposits in the trend . Two fundamental geologic relationships near the trend significantly affect regional geochemical distributions: a remarkably intact lower Paleozoic stratigraphic sequence of siliceous rocks in the upper plate of the middle Paleozoic Roberts Mountains thrust, and the widespread repetition of rocks high in the upper plate during late Paleozoic thrusting that thickens the cover above mineralized rock in the lower plate. A compilation of previously published chemical analyses of 440 stream sediment samples and 115 rocks from two 7 1/2-minute quadrangles, as well as new chemical analyses of approximately 1,000 drill core samples in a 1,514 m (4,970 ft) hole through the Rodeo Creek deposit were used to construct three-dimensional element distribution models that highlight metal zonation in the mineralized systems. The Rodeo Creek deposit comprises deep Ag base-metal ± Au-mineralized rock below the Roberts Mountains thrust and contains an unusually high Ag/Au ratio greater than 30. Stacked geochemical halos related to the deposit are confined to the lower plate of the Roberts Mountains thrust and include two horizons of Hg, Cu, and Zn anomalies-as much as 180 m above the deposit-that mostly result from mercurian sphalerite. Extremely subtle indications of mineralization in the upper plate of the Roberts Mountains thrust above the deposit include arsenopyrite overgrowths on small pyrite crystals in 50- to 75-μm-wide clay-carbonate veinlets that lack alteration halos, arsenical rims on small disseminated crystal of recrystallized diagenetic pyrite, and partial replacement of diagenetic pyrite by tennantite. Some of these minerals contain anomalously high Au. However, these As-(Au)-bearing rocks most likely represent another locus of largely untested mineralized rock rather than distal halos related to either the Rodeo Creek or the nearby Dee and Storm gold deposits. Application of micromineralogic techniques helped to identify mineral assemblages that are specific to mineralization and provided an empirical foundation for interpretations of geochemical halos in the Carlin trend . District-scale geochemical patterns of several elements in stream sediments and surface rocks coincide with the northernmost Carlin trend and can be used to explore for Carlin -type deposits. Concentrations of elevated As and Sb in stream sediments (as much as 54 ppm As) have northwest-elongate lobate patterns that clearly outline the trend across a width of approximately 4 km. Arsenic contents of exposed rocks (as much as 90 ppm As) strongly correlate with As contents of derivative stream sediments, and rock contents of Sb show a somewhat lesser but nonetheless strong and similar correspondence. Factor analysis of stream-sediment data shows that those factor scores that are correlated with As, Sb, Au, and Pb also are high along the trend and suggest that mineralized rocks may be present. Although As was not detected by scanning electron microscope-energy dispersive spectrometer (SEM-EDS) studies in heavy mineral concentrates of high-As stream sediments in the Carlin trend , X-ray absorption near-edge spectra (XANES) of selected light fractions of stream sediment samples indicate that Al-bearing phases, such as gibbsite, amorphous Al oxyhydroxides, or aluminosilicate clay minerals host most of the As(V). The best fit, visually and in terms of the lowest residual, was obtained by a model compound of As(V) sorbed to gibbsite. Thus, most As in stream sediments derived from altered rock within the Carlin trend apparently is contained in light fractions. The geochemical character of young, unconsolidated, postmineral deposits that cover mineralized rocks on the Carlin trend partly results from mineralized sources along the trend . Concentration of As in the Miocene Carlin Formation shows an exceptionally well developed progressive increase to about 30 ppm As as altered rock surrounding the trend is approached. Mineralized and/or altered rock fragments probably have been shed directly into the sedimentary basin of the Carlin Formation, and migration of As, now fixed as As(V), also may have occurred in the supergene environment after material was recycled out of the Carlin Formation and into present-day gulleys.

Nevada↗

Steeply dipping heaving bedrock, Colorado: Part 2 - Mineralogical and engineering properties

This paper describes the mineralogical and engineering properties of steeply dipping, differentially heaving bedrock, which has caused severe damage near the Denver area. Several field sites in heave-prone areas have been characterized using high sample densities, numerous testing methodologies, and thousands of sample tests. Hydrometer testing shows that the strata range from siltstone to claystone (33 to 66 percent clay) with occasional bentonite seams (53 to 98 percent clay mixed with calcite). From X-ray diffraction analyses, the claystone contains varying proportions of illite-smectite and discrete (pure) smectite, and the bentonite contains discrete smectite. Accessory minerals include pyrite, gypsum, calcite, and oxidized iron compounds. The dominant exchangeable cation is Ca2+, except where gypsum is prevalent, and Mg2+ and Na1+ are elevated. Scanning electron microscope analyses show that the clay fabric is deformed and porous and that pyrite is absent within the weathered zone. Unified Soil Classification for the claystone varies from CL to CH, and the bentonite is CH to MH. Average moisture content values are 17 percent for claystone and 32 percent for bentonite, and these are typically 0 to 5 percent lower than the plastic limit. Swell-consolidation and suction testing shows a full range of swelling potentials from low to very high. These findings confirm that type I (bed-parallel, symmetrical to asymmetrical) heave features are strongly associated with changes in bedrock composition and mineralogy. Composition changes are not necessarily a factor for type II (bed-parallel to bed-oblique, strongly asymmetrical) heave features, which are associated with movements along subsurface shear zones.

Environmental & Engineering Geoscience↗

Hydraulic modeling for lahar hazards at cascades volcanoes

The National Weather Service flood routing model DAMBRK is able to closely replicate field-documented stages of historic and prehistoric lahars from Mt. Rainier, Washington, and Mt. Hood, Oregon. Modeled time-of-travel of flow waves are generally consistent with documented lahar travel-times from other volcanoes around the world. The model adequately replicates a range of lahars and debris flows, including the 230 million km3 Electron lahar from Mt. Rainier, as well as a 10 m3 debris flow generated in a large outdoor experimental flume. The model is used to simulate a hypothetical lahar with a volume of 50 million m3 down the East Fork Hood River from Mt. Hood, Oregon. Although a flow such as this is thought to be possible in the Hood River valley, no field evidence exists on which to base a hazards assessment. DAMBRK seems likely to be usable in many volcanic settings to estimate discharge, velocity, and inundation areas of lahars when input hydrographs and energy-loss coefficients can be reasonably estimated.

Environmental & Engineering Geoscience↗

Biostratigraphy and paleoenvironment of Miocene- Pliocene hemipelagic limestone: Kingshill Seaway, St. Croix, US Virgin Islands.

The Kingshill Limestone and younger carbonate rocks constitute the central portion of St. Croix, forming the remains of an ancient seaway that was flanked by emergent highlands. The seaway has been filled with thick epipelagic sediments alternating with carbonate turbidites and ash falls and capped with shallow-water reefal and terrigenous debris. Planktonic foraminifera indicate that ages of these rocks range sequentially in a SW direction from the middle Miocene to lower Pliocene. Scanning electron micrographs illustrate 42 species and subspecies of pelagic foraminifera and 13 selected paleoenvironmentally significant aberrant forms.-from Author

Journal of Foraminiferal Research↗

Paleocene to Middle Miocene planktic foraminifera of the southwestern Salisbury Embayment, Virginia and Maryland: biostratigraphy, allostratigraphy, and sequence stratigraphy

The Paleocene to Middle Miocene sedimentary fill of the southwestern Salisbury Embayment contains a fragmental depositional record, interrupted by numerous local diastems and regional unconformities. Using planktic foraminiferal biostratigraphy, 15 unconformity-bounded depositional units have been identified, assigned to six formations and seven alloformations previously recognized in the embayment. The units correlate with second- and third-order sequences of the Exxon sequence stratigraphy model, and include transgressive and highstand systems tracts. Alloformation, formation, and sequence boundaries are marked by abrupt, scoured, burrowed, erosional surfaces, which display lag deposits, biostratigraphic gaps, and intense reworking of microfossils above and below the boundaries. Paleocene deposits represent the upper parts of upper Pleocene Biochronozones P4 and P5, and rest uncomformably on Cretaceous sedimentary beds of various ages (Maastrichtian to Albian). Lower Eocene deposits represent parts of Biochronozones P6 and P9. Middle Eocene strata represent mainly parts of Biochronozones P11, P12, and P14. Upper Eocene sediments include parts of Biochronozones P15, P16, and P17. Oligocene deposits encompass parts of Biochronozones. N4b to N7 undifferentiated, P21a, and, perhaps, N4a. Lower Miocene deposits encompass parts of Biochronozones N4b to N7 undifferentiated. Middle Miocene strata represent mainly parts of Biochronorones N8, N9, and N10. Nine plates of scanning electron micrographs illustrate the principal planktic foraminifera used to establish the biostratigraphic framework. Two new informal formine of Praeterenuitella praegemma Li, 1987, are introduced.

Journal of Foraminiferal Research↗

Mid-Pliocene planktic foraminifer assemblage of the North Atlantic Ocean

The US Geological Survey Pliocene Research, Interpretation and Synoptic Mapping (PRISM) North Atlantic faunal data set provides a unique, temporally constrained perspective to document and evaluate the quantitative geographic distribution of key mid-Pliocene taxa. Planktic foraminifer census data from within the PRISM time slab (3.29 to 2.97 Ma) at thirteen sites in the North Atlantic Ocean have been analyzed. We have compiled Scanning Electron Micrographs for an atlas of mid-Pliocene assemblages from the North Atlantic with descriptions of each taxon to document the taxonomic concepts that accompany the PRISM data. In mid-Pliocene assemblages, the geographic distributions of extant taxa are similar to their present day distributions, although some are extended to the north. We use the distribution of extinct taxa to assess previous assumptions regarding environmental preferences.

Micropaleontology↗

Design and application of an electromagnetic vibrator seismic source

Vibrational seismic sources frequently provide a higher-frequency seismic wavelet (and therefore better resolution) than other sources, and can provide a superior signal-to-noise ratio in many settings. However, they are often prohibitively expensive for lower-budget shallow surveys. In order to address this problem, I designed and built a simple but effective vibrator source for about one thousand dollars. The "EMvibe" is an inexpensive electromagnetic vibrator that can be built with easy-to-machine parts and off-the-shelf electronics. It can repeatably produce pulse and frequency-sweep signals in the range of 5 to 650 Hz, and provides sufficient energy for recording at offsets up to 20 m. Analysis of frequency spectra show that the EMvibe provides a broader frequency range than the sledgehammer at offsets up to ??? 10 m in data collected at a site with soft sediments in the upper several meters. The EMvibe offers a high-resolution alternative to the sledgehammer for shallow surveys. It is well-suited to teaching applications, and to surveys requiring a precisely-repeatable source signature.

Journal of Environmental & Engineering Geophysics↗

Oxidation and mobilization of selenium by nitrate in irrigation drainage

Selenium (Se) can be oxidized by nitrate (NO − 3 ) from irrigation on Cretaceous marine shale in western Colorado. Dissolved Se concentrations are positively correlated with dissolved NO − 3 concentrations in surface water and ground water samples from irrigated areas. Redox conditions dominate in the mobilization of Se in marine shale hydrogeologic settings; dissolved Se concentrations increase with increasing platinum-electrode potentials. Theoretical calculations for the oxidation of Se by NO − 3 and oxygen show favorable Gibbs free energies for the oxidation of Se by NO − 3 , indicating NO − 3 can act as an electron acceptor for the oxidation of Se. Laboratory batch experiments were performed by adding Mancos Shale samples to zero-dissolved-oxygen water containing 0, 5, 50, and 100 mg/L NO − 3 as N (mg N/L). Samples were incubated in airtight bottles at 25°C for 188 d; samples collected from the batch experiment bottles show increased Se concentrations over time with increased NO − 3 concentrations. Pseudo first-order rate constants for NO − 3 oxidation of Se ranged from 0.0007 to 0.0048/d for 0 to 100 mg N/L NO − 3 concentrations, respectively. Management of N fertilizer applications in Cretaceous shale settings might help to control the oxidation and mobilization of Se and other trace constituents into the environment.

Journal of Environmental Quality↗

Transport and fate of nitrate in a glacial outwash aquifer in relation to ground water age, land use practices, and redox processes

A combination of ground water modeling, chemical and dissolved gas analyses, and chlorofluorocarbon age dating of water was used to determine the relation between changes in agricultural practices, and NO − 3 concentrations in ground water of a glacial outwash aquifer in west-central Minnesota. The results revealed a redox zonation throughout the saturated zone with oxygen reduction occurring near the water table, NO − 3 reduction immediately below it, and then a large zone of ferric iron reduction, with a small area of sulfate (SO 2− 4 ) reduction and methanogenesis (CH 4 ) near the end of the transect. Analytical and NETPATH modeling results supported the hypothesis that organic carbon served as the electron donor for the redox reactions. Denitrification rates were quite small, 0.005 to 0.047 mmol NO − 3 yr −1 , and were limited by the small amounts of organic carbon, 0.01 to 1.45%. In spite of the organic carbon limitation, denitrification was virtually complete because residence time is sufficient to allow even slow processes to reach completion. Ground water sample ages showed that maximum residence times were on the order of 50 to 70 yr. Reconstructed NO − 3 concentrations, estimated from measured NO − 3 and dissolved N gas showed that NO − 3 concentrations have been increasing in the aquifer since the 1940s, and have been above the 714 μmol L −1 maximum contaminant level at most sites since the mid- to late-1960s. This increase in NO − 3 has been accompanied by a corresponding increase in agricultural use of fertilizer, identified as the major source of NO − 3 to the aquifer.

Minnesota↗

Transport and fate of nitrate at the ground-water/surface-water interface

Although numerous studies of hyporheic exchange and denitrification have been conducted in pristine, high-gradient streams, few studies of this type have been conducted in nutrient-rich, low-gradient streams. This is a particularly important subject given the interest in nitrogen (N) inputs to the Gulf of Mexico and other eutrophic aquatic systems. A combination of hydrologic, mineralogical, chemical, dissolved gas, and isotopic data were used to determine the processes controlling transport and fate of NO 3 − in streambeds at five sites across the USA. Water samples were collected from streambeds at depths ranging from 0.3 to 3 m at three to five points across the stream and in two to five separate transects. Residence times of water ranging from 0.28 to 34.7 d m −1 in the streambeds of N-rich watersheds played an important role in allowing denitrification to decrease NO 3 − concentrations. Where potential electron donors were limited and residence times were short, denitrification was limited. Consequently, in spite of reducing conditions at some sites, NO 3 − was transported into the stream. At two of the five study sites, NO 3 − in surface water infiltrated the streambeds and concentrations decreased, supporting current models that NO 3 − would be retained in N-rich streams. At the other three study sites, hydrogeologic controls limited or prevented infiltration of surface water into the streambed, and ground-water discharge contributed to NO 3 − loads. Our results also show that in these low hydrologic-gradient systems, storm and other high-flow events can be important factors for increasing surface-water movement into streambeds.

Journal of Environmental Quality↗

Miscellaneous methods for measuring matric or water potential

A variety of techniques to measure matric potential or water potential in the laboratory and in the field are described in this section. The techniques described herein require equilibration of some medium whose matric or water potential can be determined from previous calibration or can be measured directly. Under equilibrium conditions the matric or water potential of the medium is equal to that of the soil. The techniques can be divided into: (i) those that measure matric potential and (ii) those that measure water potential (sum of matric and osmotic potentials). Matric potential is determined when the sensor matrix is in direct contact with the soil, so salts are free to diffuse in or out of the sensor matrix, and the equilibrium measurement therefore reflects matric forces acting on the water. Water potential is determined when the sensor is separated from the soil by a vapor gap, so salts are not free to move in or out of the sensor, and the equilibrium measurement reflects the sum of the matric and osmotic forces acting on the water. Seven different techniques are described in this section. Those that measure matric potential include (i) heat dissipation sensors, (ii) electrical resistance sensors, (iii) frequency domain and time domain sensors, and (iv) electro-optical switches. A method that can be used to measure matric potential or water potential is the (v) filter paper method. Techniques that measure water potential include (vi) the Dew Point Potentiameter (Decagon Devices, Inc., Pullman, WA1) (water activity meter) and (vii) vapor equilibration. The first four techniques are electronically based methods for measuring matric potential. Heat dissipation sensors and electrical resistance sensors infer matric potential from previously determined calibration relations between sensor heat dissipation or electrical resistance and matric potential. Frequency-domain and timedomain matric potential sensors measure water content, which is related to matric potential of the sensor through calibration. Electro-optical switches measure changes in light transmission through thin, nylon filters as they absorb or desorb water in response to changes in matric potential. Heat dissipation sensors and electrical resistance sensors are used primarily in the field to provide information on matric potential. Frequency domain matric potential sensors are new and have not been widely used. Time domain matric potential sensors and electro-optical switches are new and have not been commercialized. For the fifth technique, filter paper is used as the standard matrix. The filter paper technique measures matric potential when the filter paper is in direct contact with soil or water potential when separated from soil by a vapor gap. The Dew Point Potentiameter calculates water potential from the measured dew point and sample temperature. The vapor equilibration technique involves equilibration of soil samples with salt solutions of known osmotic potential. The filter paper, Dew Point Potentiameter, and vapor equilibration techniques are generally used in the laboratory to measure water potential of disturbed field samples or to measure water potential for water retention functions.

Soil Science Society of America Book Series↗

Improved method for measuring water imbibition rates on low-permeability porous media

Existing methods for measuring water imbibition rates are inadequate when imbibition rates are small (e.g., clay soils and many igneous rocks). We developed an improved laboratory method for performing imbibition measurements on soil or rock cores with a wide range of hydraulic properties. Core specimens are suspended from an electronic strain gauge (load cell) in a closed chamber while maintaining the lower end of the core in contact with a free water surface in a constant water level reservoir. The upper end of the core is open to the atmosphere. During imbibition, mass increase of the core is recorded continuously by a datalogger that converts the load cell voltage signal into mass units using a calibration curve. Computer automation allows imbibition rate measurement on as many as eight cores simultaneously and independently. Performance of each component of the imbibition apparatus was evaluated using a set of rock cores (2.5 cm in diameter and 2–5 cm in length) from a signle lithostratigraphic unit composed of non-to-moderately welded ash-flow tuff (a glass-rich pyroclastic rock partially fused by heat and pressure) with porosities ranging from 0.094 to 0.533 m 3 m -3 . Reproducibility of sample handling and testing procedures was demonstrated using replicate measurements. Precision and accuracy of load cell measurements were assessed using mass balance calculations and indicated agreement within a few tenths of a percent of total mass. Computed values of sorptivity, S , ranged from 8.83 × 10 -6 to 4.55 × 10 -4 m s -0.5 . The developed method should prove useful for measuring imbibition rates on a wide range of porous materials.

Soil Science Society of America Journal↗

Phosphate reactivity in long-term poultry litter-amended southern Delaware sandy soils

Eutrophication caused by dissolved P from poultry litter (PL)-amended agricultural soils has been a serious environmental concern in the Delaware-Maryland-Virginia Peninsula (Delmarva), USA. To evaluate state and federal nutrient management strategies for reducing the environmental impact of soluble P from long-term PL-amended Delaware (DE) soils, we investigated (i) inorganic P speciation; (ii) P adsorption capacity; and (iii) the extent of P desorption. Although the electron microprobe (EMP) analyses showed a strong correlation between P and Al/Fe, crystalline Al/Fe-P precipitates were not detected by x-ray diffraction (XRD). Instead, the inorganic P fractionation analyses showed high levels of oxalate extractable P, Al, and Fe fractions (615-858, 1215-1478, and 337-752 mg kg-1, respectively), which were susceptible to slow release during the long-term (30-d) P desorption experiments at a moderately acidic soil pHwater. The labile P in the short-term (24-h) desorption studies was significantly associated with oxalate and F extractable Fe and Al, respectively. This was evident in an 80% reduction maximum in total desorbable P from NH4 oxalate/F pretreated soils. In the adsorption experiments, P was strongly retained in soils at near targeted pH of lime (???6.0), but P adsorption gradually decreased with decreasing pH near the soil pHwater (???5.0). The overall findings suggest that P losses from the can be suppressed by an increase in the P retention capacity of soils via (i) an increase in the number of lime applications to maintain soil pHwater at near targeted pH values, and/or (ii) alum/iron sulfate amendments to provide additional Al- and Fe-based adsorbents. ?? Soil Science Society of America.

Soil Science Society of America Journal↗

Biologic origin of iron nodules in a marine terrace chronosequence, Santa Cruz, California

The distribution, chemistry, and morphology of Fe nodules were studied in a marine terrace soil chronosequence northwest of Santa Cruz, California. The Fe nodules are found at depths <1 m on all terraces. The nodules consisted of soil mineral grains cemented by Fe oxides. The nodules varied in size from 0.5 to 25 mm in diameter. Nodules did not occur in the underlying regolith. The Fe-oxide mineralogy of the nodules was typically goethite; however, a subset of nodules consisted of maghemite. There was a slight transformation to hematite with time. The abundance of soil Fe nodules increased with terrace age on the five terraces studied (aged 65,000-226,000 yr). Scanning electron microscopy (SEM) revealed Fe-oxide-containing fungal hyphae throughout the nodules, including organic structures incorporating fine-grained Fe oxides. The fine-grained nature of the Fe oxides was substantiated by M??ssbauer spectroscopy. Our microscopic observations led to the hypothesis that the nodules in the Santa Cruz terrace soils are precipitated by fungi, perhaps as a strategy to sequester primary mineral grains for nutrient extraction. The fungal structures are fixed by the seasonal wetting and dry cycles and rounded through bioturbation. The organic structures are compacted by the degradation of fungal C with time. ?? Soil Science Society of America. All rights reserved.

Soil Science Society of America Journal↗