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At least 757 records · Page 42Linked to original sources
USGS1977

Ore transport and deposition in the Red Sea geothermal system: a geochemical model

Thermodynamic calculation of distribution of dissolved aqueous species in the Red Sea geothermal brine provides a model of ore transport and deposition in good agreement with observed accumulations of base metal sulfides, anhydrite, and barite. The Red Sea brine is recirculated seawater that acquires high salinity by low-temperature interaction with Miocene evaporites and is subsequently heated to temperatures in excess of 200°C by interaction with recent rift zone intrusive rocks. At temperatures up to 250°C, NaSO − 4 and MgSO 0 4 are the dominant sulfur-bearing species. H 2 S forms by inorganic sulfate reduction at the higher temperatures but is maintained at a uniform concentration of about 2 ppm by the strength of the sulfate complexes. Chloride complexes solubilize metals at the higher temperatures, and thus sulfide and metals are carried together into the Atlantis II Deep. Below 150°C, the brine becomes supersaturated with respect to chalcopyrite, sphalerite, galena, and iron monosulfide due to chloride-complex dissociation. Sulfide precipitation rates, based on the rate of brine influx, are in good agreement with measured sedimentation rates. Anhydrite precipitates as crystalline fissure infillings from high-temperature inflowing brine. Barite forms from partial oxidation of sulfides at the interface between the lower hot brine and the transitional brine layer.

Geochimica et Cosmochimica Acta↗
USGS1983

An interpretation of carbon and sulfur relationships in Black Sea sediments as indicators of environments of deposition

Syngenetic iron sulfides in sediments are formed from dissolved sulfide resulting from sulfate reduction and catabolism of organic matter by anaerobic bacteria. It has been shown that in recent marine sediments deposited below oxygenated waters there is a constant relationship between reduced sulfur and organic carbon which is generally independent of the environment of deposition. Reexamination of data from recent sediments from euxinic marine environments ( e.g. , the Black Sea) also shows a linear relationship between carbon and sulfur, but the slope is variable and the line intercepts the S axis at a value between 1 and 2 percent S. It is proposed that the positive S intercept is due to watercolumn microbial reduction of sulfate using metabolizable small organic molecules and the sulfide formed is precipitated and accumulates at the sediment-water interface. The variation in slope and intercept of the C to S plots for several cores and for different stratigraphic zones for the Black Sea can be interpreted in relation to thickness of the aqueous sulfide layer or thinness of the oxygen containing layer and to deposition rate, but also may be influenced by availability of iron, and perhaps the type of organic matter (Leventhal, 1979).

Geochimica et Cosmochimica Acta↗
USGS1991

An AEM-TEM study of weathering and diagenesis, Abert Lake, Oregon: II. Diagenetic modification of the sedimentary assemblage

This paper compares the mineralogy and chemistry of clay minerals in sediments from various depths and positions in Abert Lake and surrounding playa with those of the weathered materials entering the lake in order to reveal the nature and extent of post-depositional mineralogical modification. Analytical electron microscope (AEM) data from individual clay particles reveal that each sample is comprised of a highly inhomogeneous smectite assemblage. The thin clay flakes (commonly less than 10 nm wide) display a complete range in octahedral sheet compositions from nearly dioctahedral to nearly trioctahedral. The very abundant Mg-rich lake smectites with an estimated composition K 0.29 (Al 0.23 -Mg 2.16 Fe 0.30 )Si 3.80 Al 0.20 O 10 (OH) 2 are not formed by weathering. This confirms the importance of diagenetic Mg uptake. Lattice-fringe imaging failed to reveal distinct brucite-like or vermiculite-like layers, suggesting that interstratifications of this type are rare or absent. Siliceous coatings on clay particles (identified by silica excess in smectite analyses) seem to favor topotactic overgrowth of stevensite rather than addition of brucite-like layers to the dioctahedral nuclei. The growth of K-stevensite dilutes the Al content of the crystal, and thus the increasing diagenetic modification reduces rather than supplements its illite component. Smectite compositions within individual samples were highly variable, yet source-related characteristics such as the abundance of Fe-rich smectite were apparent. Little evidence for systematic K or Mg enrichment with depth was identified in samples from depths of down to 16 feet below the sediment-water interface. The most magnesian assemblages are associated both with weathering sources of Mg-rich smectite and playa environments subjected to repeated wetting and drying cycles. Thus, the observations suggest that clay compositions primarily reflect changes in lake levels, brine composition, and source characteristics, rather than time and depth/compaction effects. Other diagenetic reactions in the sediment include recrystallization of Na-rich silica gel and diatom fragments. Abundant, submicron-sized, untwinned, euhedral crystals of K-feldspar are interpreted to be authigenic in origin.

Geochimica et Cosmochimica Acta↗
USGS1993

Surface chemistry of ferrihydrite: Part 1. EXAFS studies of the geometry of coprecipitated and adsorbed arsenate

EXAFS spectra were collected on both the As and Fe K-edges from samples of two-line ferrihydrite with adsorbed (ADS) and coprecipitated (CPT) arsenate prepared over a range of conditions and arsenate surface coverages. Spectra also were collected for arsenate adsorbed on the surfaces of three FeOOH crystalline polymorphs, α (goethite), β (akaganeite), and γ (lepidocrocite), and as a free ion in aqueous: solution. Analyses of the As EXAFS show clear evidence for inner sphere bidentate (bridging) arsenate complexes on the ferrihydrite surface and on the surfaces of the crystalline FeOOH polymorphs. The bridging arsenate is attached to adjacent apices of edge-sharing Fe oxyhydroxyl octahedra. The arsenic-iron distance at the interface ( 3.28 ±0.01 A ̊ "> 3.28 ±0.01Å ) is close to that expected for this geometry on the FeOOH polymorph surfaces, but is slightly shorter on the ferrihydrite surfaces ( 3.25 ± 0.02 A ̊ "> 3.25 ± 0.02Å ). Mono-dentate arsenate linkages ( 3.60 ± 0.03 A ̊ "> 3.60 ± 0.03Å ) also occur on the ferrihydrite, but are not generally observed on the crystalline FeOOH polymorphs. The proportion of monodentate bonds appears largest for adsorption samples with the smallest As Fe "> AsFe molar ratio. In all cases the arsenate tetrahedral complex is relatively undistorted with As-O bonds of 1.66 ± 0.01 A ̊ "> 1.66 ± 0.01Å . Precipitation of arsenate or scorodite-like phases was not observed for any samples, all of which were prepared at a pH value of 8. The Fe EXAFS results confirm that the Fe-Fe correlations in the ferrihydrite are progressively disrupted in the CPT samples as the As Fe "> AsFe ratio is increased. Coherent crystallite size is probably no more than 10 Å in diameter and no Fe oxyhydroxyl octahedra corner-sharing linkages (as would be present in FeOOH polymorphs) are observed at the largest As Fe "> AsFe ratios. Comparison of the number and type of Fe-Fe neighbors with the topological constraints imposed by the arsenate saturation limit in the CPT samples (about 0.7 As Fe "> AsFe ) indicates ferrihydrite units consisting mainly of Fe oxyhydroxyl octahedra arranged in short dioctahedral chains with minimal interchain linking by octahedra corners. This is consistent with an enlarged surface area and a larger proportion of sites for bidentate arsenate bonding in CPT samples as compared to the ADS samples, which saturate with arsenate at lower As Fe "> AsFe ratios. The latter samples have larger crystallite sizes and a definite proportion of ferric octahedra sharing corners. The ratio of corner-sharing to edge-sharing Fe oxyhydroxyl octahedra in the ADS samples, and CPT samples with small As loadings, is very similar to what would be present in very small particles of goethite or akaganeite. The difference in the polymeric structure of ADS and CPT samples at higher As Fe "> AsFe ratios is due to strong arsenate bidentate adsorption that poisons the surface of particles of ferrihydrite precipitated in the presence of substantial arsenate, limiting their normal crystallization, and preventing further Fe-O-Fe polymerization. If the arsenate is applied after precipitation much less adsorption occurs since polymerization has already progressed. In both ADS and CPT samples, Fe-O-Fe polymerization increases with age, though at different rates for each type of sample.

Geochimica et Cosmochimica Acta↗
USGS1994

Re-Os isotopic evidence for an enriched-mantle source for the Noril'sk-type, ore-bearing intrusions, Siberia

Magmatic Cu-Ni sulfide ores and spatially associated ultramafic and mafic rocks from the Noril'sk I, Talnakh, and Kharaelakh intrusions are examined for Re-Os isotopic systematics. Neodymium and lead isotopic data also are reported for the ultramafic and mafic rocks. The Re-Os data for most samples indicate closed-system behavior since the ca. 250 Ma igneous crystallization age of the intrusions. There are small but significant differences in the initial osmium isotopic compositions of samples from the three intrusions. Ores from the Noril'sk I intrusion have γ Os values that vary from +0.4 to +8.8, but average +5.8. Ores from the Talnakh intrusion have γ Os values that range from +6.7 to +8.2, averaging +7.7. Ores from the Kharaelakh intrusion have γ Os values that range from +7.8 to +12.9, with an average value of +10.4. The osmium isotopic compositions of the ore samples from the Main Kharaelakh orebody exhibit minimal overlap with those for the Noril'sk I and Talnakh intrusions, indicating that these Kharaelakh ores were derived from a more radiogenic source of osmium than the other ores. Combined osmium and lead data for major orebodies in the three intrusions plot in three distinct fields, indicating derivation of osmium and lead from at least three isotopically distinct sources. Some of the variation in lead isotopic compositions may be the result of minor lower-crustal contamination. However, in contrast to most other isotopic and trace element data, Os-Pb variations are generally inconsistent with significant crustal contamination or interaction with the subcontinental lithosphere. Thus, the osmium and lead isotopic compositions of these intrusions probably reflect quite closely the compositions of their mantle source, and suggest that these two isotope systems were insensitive to lithospheric interaction. Ultramafic and mafic rocks have osmium and lead isotopic compositions that range only slightly beyond the compositions of the ores. These rocks also have relatively uniform ϵ Nd values that range only from −0.8 to + 1.1. This limited variation in neodymium isotopic composition may reflect the characteristics of the mantle sources of the rocks, or it may indicate that somehow similar proportions of crust contaminated the parental melts. The osmium, lead, and neodymium isotopic data for these rocks most closely resemble the mantle sources of certain ocean island basalts (OIB), such as some Hawaiian basalts. Hence, these data are consistent with derivation of primary melts from a mantle source similar to that of some types of hotspot activity. The long-term Re/Os enrichment of this and similar mantle sources, relative to chondritic upper mantle, may reflect 1. incorporation of recycled oceanic crust into the source more than 1 Ga ago, 2. derivation from a mantle plume that originated at the outer core-lower mantle interface, or 3. persistence of primordial stratification of rhenium and osmium in the mantle.

Siberia↗
USGS1994

Composition and origin of hydrothermal ironstones from central Pacific seamounts

Ironstones recovered from five Late Cretaceous seamounts in the central Pacific region probably formed during late-stage edifice-building volcanism. Ironstones are dense and compact with the appearance of brown chert. The ironstones are characterized by a goethite mineralogy with FeOOH contents up to 88%, extreme fractionation of Fe and Mn, low trace-element and rare earth element abundances, low Co Zn "> CoZn ratios, and isotopic equilibration temperatures of about 20–45 °C. These characteristics indicate that the ironstones formed from hydrothermal fluids. Ironstones probably formed below the seawater-seafloor interface, as indicated by their occurrence as a proximal hydrothermal deposit, presence of primary goethite cement, pervasive replacement of rocks by goethite, and absence of interbedded pyro-clastic beds.

Geochimica et Cosmochimica Acta↗
USGS1995

Pb2+ and Zn2+ adsorption by a natural aluminum- and iron-bearing surface coating on an aquifer sand

Pb 2+ and Zn 2+ adsorption was studied in batch experiments with material collected from a shallow, unconfined aquifer of glacial outwash sand and gravel in Falmouth, Massachusetts, USA. The aquifer solids contain primarily quartz (95% w/w), with minor amounts of alkali feldspars and ferromagnetic minerals. Pb 2+ and Zn 2+ adsorption experiments with various grain size and mineral fractions of the aquifer solids showed that (1) Zn 2+ adsorption was independent of grain size, but Pb 2+ was preferentially adsorbed by the <64 μm size fraction and (2) Pb 2+ adsorption decreased after removal of the paramagnetic, Fe-bearing mineral fraction, but Zn 2+ adsorption was unaffected. Pb 2+ and Zn 2+ adsorption on mineral separates from the aquifer material compared with metal adsorption on a purified quartz powder indicated that adsorption of both metal ions was dominated by coatings on the quartz fraction of the sediment. Characterization of the coatings by AES, SEM-EDS, and TOF-SIMS demonstrated that the natural quartz grains were extensively coated with Al- and Fe-bearing minerals of variable composition. Thin sections of quartz grains examined by TEM showed that the coatings contained both polycrystalline regions and single mineral crystals. The coating thickness varied from <10 nm up to 30 μm. The coatings were mostly resistant to dissolution by an extraction protocol designed to dissolve noncrystalline phases. The effect on metal adsorption of dissolving surface coatings from the sediment by chemical extraction was also measured. A hydroxylamine-HC] extraction designed to dissolve crystalline Fe oxide phases decreased Pb 2+ and Zn 2+ adsorption relative to untreated sediment (extracted Fe/Al ∼ 1), but Pb 2+ and Zn 2+ adsorption were not appreciably changed after sediment was extracted with dithionite-citrate (extracted Fe/Al ∼ 5). Overall, the results suggest that Pb 2+ preferred to form complexes with iron hydroxyl sites, while aluminol sites were more important for Zn 2+ adsorption. However, a definitive understanding of adsorption reactions in groundwaters will require detailed studies of the extensive coatings formed at mineral-water interfaces by chemical weathering processes.

Geochimica et Cosmochimica Acta↗
USGS1991

Application of uphole data from petroleum seismic surveys to groundwater investigations, Abu Dhabi (United Arab Emirates)

Velocity data from uphole surveys were used to map the water table and the contact at the base dune sand/top alluvium as part of a joint National Drilling Company-United States Geological Survey Ground Water Research Project in the Emirate of Abu Dhabi. During 1981–1983, a reconnaissance seismic survey was conducted for petroleum exploration in the eastern region of Abu Dhabi. Approximately 2800 kilometers of seismic data, consisting of 92 lines, were acquired in the 2500 km 2 concession area near Al Ain. Uphole surveys were conducted about 2 km apart along each seismic line, and were used to calculate weathering corrections required to further process in the seismic data. Approximately 1300 uphole surveys were completed in the concession area between March 1981 and June 1983. Reinterpretation of the velocity profiles derived from the uphole surveys provided data for determining the following subsurface layers, listed in descending order: (1) a surficial, unconsolidated weathering layer with a velocity from 300 to 450 m/s; (2) surficial dune sand, from 750 to 900 m/s; (3) unsaturated, unconsolidated alluvium, from 1000 to 1300 m/s; and (4) saturated, unconsolidated alluvium, from 1900 to 2200 m/s. Two interfaces—the water table and the base dune sand/top alluvium — were identified and mapped from boundaries between these velocity layers. Although the regional water table can fluctuate naturally as much as 3 m per year in this area and the water-table determinations from the uphole data span a 27-month period, an extremely consistent and interpretable water-table map was derived from the uphole data throughout the entire concession area. In the northern part of the area, unconfined groundwater moves northward and northwestward toward the Arabian Gulf; and in the central and southern parts of the area, groundwater moves westward away from the Oman Mountains. In the extreme southern area east of Jabal Hafit, groundwater moves southward into Oman. The map of the base dune sand/top alluvium suggests a buried paleodrainage network trending westward to southwestward away from the Oman Mountains. These paleodrainages, now buried by dune sand, probably contain alluvial fill and are logical targets for groundwater exploration.

Geoexploration↗
USGS1984

Heating of a fully saturated Darcian half-space: Pressure generation, fluid expulsion, and phase change

Analytical solutions are developed for the pressurization, expansion, and flow of one- and two-phase liquids during heating of fully saturated and hydraulically open Darcian half-spaces subjected to a step rise in temperature at its surface. For silicate materials, advective transfer is commonly unimportant in the liquid region; this is not always the case in the vapor region. Volume change is commonly more important than heat of vaporization in determining the position of the liquid-vapor interface, assuring that the temperatures cannot be determined independently of pressures. Pressure increases reach a maximum near the leading edge of the thermal front and penetrate well into the isothermal region of the body. Mass flux is insensitive to the hydraulic properties of the half-space.

International Journal of Heat and Mass Transfer↗
USGS1972

Mass spectrometric analysis of organic compounds, water and volatile constituents in the atmosphere and surface of Mars: The Viking Mars Lander

An experiment centering around a mass spectrometer is described, which is aimed at the identification of organic substances present in the top 10 cm of the surface of Mars and an analysis of the atmosphere for major and minor constituents as well as isotopic abundances. In addition, an indication of the abundance of water in the surface and some information concerning the mineralogy can be obtained by monitoring the gases produced upon heating the soil sample. The organic material will simply be expelled by heating to 150°, 300°, and 500° into the carrier gas stream of a gas chromatograph interfaced to the mass spectrometer or by slowly heating the sample in direct communication with the spectrometer. It is planned to analyze a total of up to nine soil samples in order to study diurnal and seasonal variations. The system is designed to give useful data even for minor constituents if the total of organics should be as low as 5ppm. The spectrometer covers the mass range of 12–200 with adequate resolution. The results of these experiments, which are deliberately designed to cover a wide spectrum of possibilities independent of terrestrial models, are expected to produce a good picture of the planet's organic chemistry and its possible biological significance as well as allow conclusions regarding the history of the planet's atmosphere.

Icarus↗
USGS1978

Formation of lunar basin rings

The origin of the multiple concentric rings that characterize lunar impact basins, and the probable depth and diameter of the transient crater have been widely debated. As an alternative to prevailing “megaterrace” hypotheses, we propose that the outer scarps or mountain rings that delineate the topographic rims of basins—the Cordilleran at Orientale, the Apennine at Imbrium, and the Altai at Nectaris—define the transient cavities, enlarged relatively little by slumping, and thus are analogous to the rim crests of craters like Copernicus; inner rings are uplifted rims of craters nested within the transient cavity. The magnitude of slumping that occurs on all scarps is insufficient to produce major inner rings from the outer. These conclusions are based largely on the observed gradational sequence in lunar central uplifts:. from simple peaks through somewhat annular clusters of peaks, peak and ring combinations and double ring basins, culminating in multiring structures that may also include peaks. In contrast, belts of slump terraces are not gradational with inner rings. Terrestrial analogs suggest two possible mechanisms for producing rings. In some cases, peaks may expand into rings as material is ejected from their cores, as apparently occurred at Gosses Bluff, Australia. A second process, differential excavation of lithologically diverse layers, has produced nested experimental craters and is, we suspect, instrumental in the formation of terrestrial ringed impact craters. Peak expansion could produce double-ring structures in homogeneous materials, but differential excavation is probably required to produce multiring and peak-in-ring configurations in large lunar impact structures. Our interpretation of the representative lunar multiring basin Orientale is consistent with formation of three rings in three layers detected seismically in part of the Moon—the Cordillera (basin-bounding) ring in the upper crust, the composite Montes Rook ring in the underlying, more coherent “heald” crust, and an innermost, 320-km ring at the crust-mantle interface. Depth-diameter ratios of 1 10 to 1 15 "> 110 to 115 are consistent with this interpretation and suggest that volumes of transient cavities and hence of basin ejecta may be considerably greater than commonly assumed.

Icarus↗
USGS1983

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

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

Florida↗
USGS1990

Simulation of dispersion in layered coastal aquifer systems

A density-dependent solute-transport formulation is used to examine ground-water flow in layered coastal aquifers. The numerical experiments indicate that although the transition zone may be thought of as an impermeable 'sharp' interface with freshwater flow parallel to the transition zone in homogeneous aquifers, this is not the case for layered systems. Freshwater can discharge through the transition zone in the confining units. Further, for the best simulation of layered coastal aquifer systems, either a flow-direction-dependent dispersion formulation is required, or the dispersivities must change spatially to reflect the tight thin confining unit.

Journal of Hydrology↗
USGS1991

Geochemistry of dissolved inorganic carbon in a Coastal Plain aquifer. 1. Sulfate from confining beds as an oxidant in microbial CO2 production

A primary source of dissolved inorganic carbon (DIC) in the Black Creek aquifer of South Carolina is carbon dioxide produced by microbially mediated oxidation of sedimentary organic matter. Groundwater chemistry data indicate, however, that the available mass of inorganic electron acceptors (oxygen, Fe(III), and sulfate) and observed methane production is inadequate to account for observed CO 2 production. Although sulfate concentrations are low (approximately 0.05–0.10 mM) in aquifer water throughout the flow system, sulfate concentrations are greater in confining-bed pore water (0.4–20 mM). The distribution of culturable sulfate-reducing bacteria in these sediments suggests that this concentration gradient is maintained by greater sulfate-reducing activity in sands than in clays. Calculations based on Fick's Law indicate that possible rates of sulfate diffusion to aquifer sediments are sufficient to explain observed rates of CO 2 production (about 10 −5 mmoll −1 year −1 ), thus eliminating the apparent electron-acceptor deficit. Furthermore, concentrations of dissolved hydrogen in aquifer water are in the range characteristic of sulfate reduction (2–6 nM), which provides independent evidence that sulfate reduction is the predominant terminal electron-accepting process in this system. The observed accumulation of pyrite- and calcite-cemented sandstones at sand-clay interfaces is direct physical evidence that these processes have been continuing over the history of these sediments.

Journal of Hydrology↗
USGS1992

Electromagnetic methods for mapping freshwater lenses on Micronesian atoll islands

The overall shape of freshwater lenses can be determined by applying electromagnetic methods and inverse layered-earth modeling to the mapping of atoll island freshwater lenses. Conductivity profiles were run across the width of the inhabited islands at Mwoakilloa, Pingelap, and Sapwuahfik atolls of the Pohnpei State, Federated States of Micronesia using a dual-loop, frequency-domain, electromagnetic profiling system. Six values of apparent conductivity were recorded at each sounding station and were used to interpret layer conductivities and/or thicknesses. A three-layer model that includes the unsaturated, freshwater, and saltwater zones was used to simulate apparent-conductivity data measured in the field. Interpreted results were compared with chloride-concentration data from monitoring wells and indicate that the interface between freshwater and saltwater layers, defined from electromagnetic data, is located in the upper part of the transition zone, where the chloride-concentration profile shows a rapid increase with depth. The electromagnetic method can be used to interpret the thickness of the freshwater between monitoring wells, but can not be used to interpret the thickness of freshwater from monitoring wells to the margin of an island.

Journal of Hydrology↗
USGS1990

Inorganic geochemistry of surface sediments of the Ebro shelf and slope, northwestern Mediterranean

Distributions of major, minor, and trace elements in surface sediment of the continental shelf and upper slope of the northeastern Spanish continental margin reflect the influences of discharge from the Ebro River and changes in eustatic sea levels. Multivariate factor analysis of sediment geochemistry was used to identify five groupings of samples (factors) on the shelf and slope. The first factor is an aluminosilicate factor that represents detrital clastic material. The second factor is a highly variable amount of excess SiO 2 and probably represents a quartz residuum originating from winnowing of relict detrital sediments. A carbonate factor (Factor 3) has no positive correlation with other geochemical parameters but is associated with the sand-size fraction. The carbonate in these sediments consists of a mixture of biogenic calcite and angular to subangular detrital grains. Organic carbon is associated with the aluminosilicate factor (Factor 1) but also factors out by itself (Factor 4); this suggests that there may be two sources of organic matter, terrestrial and marine. The fifth factor comprises upper slope sediments that contain high concentrations of manganese. The most likely explanation for these high manganese concentrations is precipitation of Mn oxyhydroxides at the interface between Mn-rich, oxygen-deficient, intermediate waters and oxygenated surface waters.

Marine Geology↗
USGS1990

Instantaneous and daily values of the surface energy balance over agricultural fields using remote sensing and a reference field in an arid environment

Remotely sensed surface temperature and reflectance in the visible and near infrared wavebands along with ancilliary meteorological data provide the capability of computing three of the four surface energy balance components (i.e., net radiation, soil heat flux, and sensible heat flux) at different spatial and temporal scales. As a result, under nonadvective conditions, this enables the estimation of the remaining term (i.e., the latent heat flux). One of the practical applications with this approach is to produce evapotranspiration (ET) maps for agricultural regions which consist of an array of fields containing different crops at varying stages of growth and soil moisture conditions. Such a situation exists in the semiarid southwest at the University of Arizona Maricopa Agricultural Center, south of Phoenix. For one day (14 June 1987), surface temperature and reflectance measurements from an aircraft 150 m above ground level (agl) were acquired over fields from zero to nearly full cover at four times between 1000 MST and 1130 MST. The diurnal pattern of the surface energy balance was measured over four fields, which included alfalfa at 60% cover, furrowed cotton at 20% and 30% cover, and partially plowed what stubble. Instantaneous and daily values of ET were estimated for a representative area around each flux site with an energy balance model that relies on a reference ET. This reference value was determined with remotely sensed data and several meteorological inputs. The reference ET was adjusted to account for the different surface conditions in the other fields using only remotely sensed variables. A comparison with the flux measurements suggests the model has difficulties with partial canopy conditions, especially related to the estimation of the sensible heat flux. The resulting errors for instantaneous ET were on the order of 100 W m −2 and for daily values of order 2 mm day −1 . These findings suggest future research should involve development of methods to account for the variability of meteorological parameters brought about by changes in surface conditions and improvements in the modeling of sensible heat transfer across the surface—atmosphere interface for partial canopy conditions using remote sensing information.

Remote Sensing of Environment↗
USGS1991

Effect of phosphorus deficiency on spectral reflectance and morphology of soybean plants

Soybean plants were grown in hydroponic solutions having three concentration levels of phosphorus. Spectral reflectance changes included higher reflectance in the green and yellow portions of the electromagnetic spectrum in phosphorus-deficient plants and a difference in position of the long wavelength edge (the red edge) of the chlorophyll absorption band centered near 0.68 ??m. Plants having the least phosphorus in the growing medium did not show the normal shift of the red edge to longer wavelength which occurs as leaves mature. Shoot and root biomass were significantly lower in the phosphorus-deficient plants. These results are consistent with those obtained when soybean plants are dosed with elevated concentrations of metallic elements. We hypothesize that nutrient imbalances or anomalous metal concentrations in the soil set up physiological conditions at the soil/root interface that are responsible for the reflectance differences observed in laboratory and field studies of plants growing in substrates enriched in metallic elements.

Remote Sensing of Environment↗