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Chapters 4 and 5 provide a variety of examples of how ASTER and MODIS land science applications are predicated on the availability of consistent and quality data. This chapter portrays a narrative of how those data come to exist at two different data centers, which manage them.
In this unique volume, renowned experts discuss the applications of fractals in petroleum research-offering an excellent introduction to the subject. Contributions cover a broad spectrum of applications from petroleum exploration to production. Papers also illustrate how fractal geometry can quantify the spatial heterogeneity of different aspects of geology and how this information can be used to improve exploration and production results.
The Puu Oo eruption of Kilauea Volcano in Hawaii is one of its largest and most compositionally varied historical eruptions. The mineral and whole-rock compositions of the Puu Oo lavas indicate that there were three compositionally distinct magmas involved in the eruption. Two of these magmas were differentiated (<6.8 wt% MgO) and were apparently stored in the rift zone prior to the eruption. A third, more mafic magma (9-10 wt% MgO) was probably intruded as a dike from Kilauea's summit reservoir just before the start of the eruption. Its intrusion forced the other two magmas to mix, forming a hybrid that erupted during the first three eruptive episodes from a fissure system of vents. A new hybrid was erupted during episode 3 from the vent where Puu Oo later formed. The composition of the lava erupted from this vent became progressively more mafic over the next 21 months, although significant compositional variation occurred within some eruptive episodes. The intra-episode compositional variation was probably due to crystal fractionation in the shallow (0.0-2.9 km), dike-shaped (i.e. high surface area/volume ratio) and open-topped Puu Oo magma reservoir. The long-term compositional variation was controlled largely by mixing the early hybrid with the later, more mafic magma. The percentage of mafic magma in the erupted lava increased progressively to 100% by episode 30 (about two years after the eruption started). Three separate magma reservoirs were involved in the Puu Oo eruption. The two deeper reservoirs (3-4 km) recharged the shallow (0.4-2.9 km) Puu Oo reservoir. Recharge of the shallow reservoir occurred rapidly during an eruption indicating that these reservoirs were well connected. The connection with the early hybrid magma body was cut off before episode 30. Subsequently, only mafic magma from the summit reservoir has recharged the Puu Oo reservoir. ?? 1992 Springer-Verlag.
A number of mixed valence iron oxides and silicates (e.g., magnetite, ilvaite) exhibit thermally induced electron delocalization between adjacent Fe 2+ and Fe 3+ ions and optically induced electronic transitions which are assigned to Fe 2+ →Fe 3+ intervalence charge transfer. In this paper, the mechanism of electron delocalization (i.e., polarons versus itinerant electrons) and the nature of optically induced intervalence charge-transfer in minerals are investigated using molecular orbital theory. SCF-Xα-SW molecular orbital calculations were done for several mixed-valence (Fe 2 O 10 ) 15− clusters corresponding to edgesharing Fe 2+ and Fe 3+ coordination polyhedra. A spinunrestricted formalism was used so that the effect of ferromagnetic versus antiferromagnetic coupling of adjacent Fe 2+ and Fe 3+ cations could be determined. The molecular orbital results can be related to the polaron theory of solid state physics and the perturbation theory formalism used by Robin and Day (1967) and others to describe electron transfer in mixed valence compounds. Intervalence charge-transfer results from the overlap of Fe(3d) orbitals across the shared edges of adjacent FeO 6 polyhedra to give weak Fe-Fe bonds. Electron delocalization, however, requires that adjacent Fe cations be ferromagnetically coupled. Antiferromagnetic coupling results in distinguishable Fe 2+ and Fe 3+ cations. Electronic transitions between the Fe-Fe bonding and Fe-Fe antibonding orbitals results in the optically-induced intervalence charge transfer bands observed in the electronic spectra of mixed valence minerals. Such transitions are predicted to be polarized along the metal-metal bond direction, in agreement with experimental observations.
A molecular orbital description, based on Xα-Scattered wave calculations on a (FeTiO 10 ) 14− cluster, is given for Fe 2+ → Ti 4+ charge transfer transitions in minerals. The calculated energy for the lowest Fe 2+ → Ti 4+ metal-metal charge transfer transition is 18040 cm −1 in reasonable agreement with energies observed in the optical spectra of Fe-Ti oxides and silicates. As in the case of Fe 2+ → Fe 3+ charge transfer in mixed-valence iron oxides and silicates, Fe 2+ → Ti 4+ charge transfer is associated with Fe-Ti bonding across shared polyhedral edges. Such bonding results from the overlap of the Fe( t 2 g ) and Ti( t 2 g ) 3 d orbitals.
Eighty samples of submarine basaltic lava were sampled from an 8 km segment of the floor and walls of the inner rift valley of the Mid-Atlantic Ridge during the French American Mid-Ocean Undersea Study (project Famous). The samples were collected from outcrops and talus slopes by the three submersibles: Alvin, Archimede, and Cyana at water depths of about 2600 meters. The early formed mineral content of the pillow lavas' glassy margins enables classification of the rocks into 5 types: (1) olivine basalt, (2) picritic basalt, (3) plagioclase-olivine-pyroxene basalt, (4) aphyric basalt, and (5) plagioclase-rich basalt. Chemical and mineralogical study indicates that at least 4 types are directly interrelated and that types (1) and (2) are higher-temperature, primitive lavas, and types (3) and (4) are lower-temperature, differentiated lavas derived from the primitive ones by crystal-liquid differentiation. The plagioclase-rich basalts also have a chemical composition of their glass comparable to that of the most differentiated basalts (types 3 and 4) but they differ in their greater amount of early formed plagioclase (12–35%). In general, the mineralogical variation across the rift valley shows an assymetrical distribution of the major basalt types. Despite the mineralogical diversity of the early formed crystals, the chemistry of the basalt glasses indicates a symmetrical and a gradual compositional change across the rift valley. Based primarily on their chemistry, the rock types 1 and 2 occupy an axial zone 1.1 km wide and make up the central volcanic hills. Differentiated lavas (types 3, 4) occupy the margins and walls of the inner rift valley and also occur near the center of the rift valley between the central hills. FeO/MgO ratios of olivine and coexisting melt indicate that the average temperature of eruption was 40 ° C higher for the primitive melts (types 1 and 2). Aside from major elements trends, the higher temperature character of the primitive basalts is shown by their common content of chrome spinel. The thickness of manganese oxide and palagonite on glassy lava provide an estimate of age. In a general fashion the relative age of the various volcanic events follow the compositional zoning observed in the explored area. Most of the youngest samples are olivine basalt of the axial hills. Most older samples occur in the margins of the rift valley (West and N.E. part of explored area) but are significantly younger than the spreading age of the crust on which they are erupted. Intermediate lava types occur mainly east of the rift valley axis and in other areas where plagioclase—olivine—pyroxene basalt and aphyric basalt are present. The above relations indicate that the diverse lava types were erupted from a shallow, zoned magma chamber from fissures distributed over the width of the inner rift valley and elongate parallel to it. Differentiation was accomplished by cooling and crystallization of plagioclase, olivine, and clinopyroxene toward the margins of the chamber. The centrally located hills were built by the piling up of frequent eruption of mainly primitive lavas which also are the youngest flows. In contrast smaller and less frequent eruptions of more differentiated lavas were exposed on both sides of the rift valley axis.
The chemical composition of snowmelt, groundwater, and streamwater was monitored during the spring of 1991 and 1992 in a 200-ha subalpine catchment on the western flank of the Rocky Mountains near Steamboat Springs, Colorado. Most of the snowmelt occurred during a one-month period annually that began in mid-May 1991 and mid-April 1992. The average water quality characteristics of individual sampling sites (meltwater, streamwater, and groundwater) were similar in 1991 and 1992. The major ions in meltwater were differentially eluted from the snowpack, and meltwater was dominated by Ca2+, SO4/2-, and NO3/-. Groundwater and streamwater were dominated by weathering products, including Ca2+, HCO3/- (measured as alkalinity), and SiO2, and their concentrations decreased as snowmelt progressed. One well had extremely high NO3/- concentrations, which were balanced by Ca2+ concentrations. For this well, hydrogen ion was hypothesized to be generated from nitrification in overlying soils, and subsequently exchanged with other cations, particularly Ca2+. Solute concentrations in streamwater also decreased as snowmelt progressed. Variations in groundwater levels and solute concentrations indicate thai most of the meltwater traveled through the surficial materials. A mass balance for 1992 indicated that the watershed retained H+, NH4/+, NO3/-, SO4/2- and Cl- and was the primary source of base cations and other weathering products. Proportionally more SO4/2- was deposited with the unusually high summer rainfall in 1992 compared to that released from snowmelt, whereas NO3/- was higher in snowmelt and Cl- was the same. The sum of snowmelt and rainfall could account for greater than 90% of the H+ and NH4/+ retained by the watershed and greater than 50% of the NO3/-.The chemical composition of snowmelt, groundwater, and streamwater was monitored during the spring of 1991 and 1992 in a 200-ha subalpine catchment on the western flank of the Rocky Mountains near Steamboat Springs, Colorado. The major ions in meltwater were differentially eluted from the snowpack, and meltwater was dominated by Ca2+, SO42-, and NO3-. Groundwater and streamwater were dominated by weathering products and their concentrations decreased as snowmelt progressed. Solute concentrations in streamwater also decreased as snowmelt progressed. A mass balance for 1992 showed that the watershed retained H+, NH4+, NO3-, SO42- and Cl- and was the primary source of base cations and other weathering products.
Microthermometric investigations of silicate-melt inclusions and electron microprobe analyses were conducted on experimentally homogenized silicate-melt inclusions and on the host clinopyroxenes from 4 scoria samples of different layers from the Mt. Somma-Vesuvius medieval eruption (Formazione di Terzigno, 893 A.D.). The temperature of homogenization, considered the minimum trapping temperature, ranges from 1190 to 1260 ± 5 °C for all clinopyroxene-hosted silicate melt inclusions. The major and minor-element compositional trends shown by Terzigno scoria and matrix glass chemical analysis are largely compatible with fractional crystallization of clinopyroxene and Fe-Ti oxides. Sulfur contents of the homogenized silicate-melt inclusions in clinopyroxene phenocrysts compared with that in the host scoria show that S has been significantly degassed in the erupted products; whereas, Cl has about the same abundance in the inclusions and in host scoria. Fluorine is low (infrequently up to 800 ppm) in the silicate-melt inclusions compared to 2400 ppm in the bulk scoria. Electron microprobe analyses of silicate-melt inclusions show that they have primitive magma compositions (Mg# = 75-91). The composition of the host clinopyroxene phenocrysts varies from typical plinian-related (Mg#≥85) to non plinian related (Mg#≤85). The mixed source of the host clinopyroxenes and primitive nature of the silicate-melt inclusions implies that these phenocrysts, in part, may be residual and/or have a polygenetic origin. The similar variation trends of major and minor-elements between homogenized silicate-melt inclusions from the Terzigno scoria, and silicate-melt inclusions in olivine and diopside phenocrysts from plinian eruptions ( Marianelli et al., 1995) suggest that the trapped inclusions represent melts similar to those that supplied the plinian and sub-plinian magma chambers. These geochemical characteristics suggest that the Vesuvius magmatic system retained a vestige of the most recent plinian event.
No abstract available.
The Hanford Nuclear Reservation in south central Washington was claimed by the federal government as a site for the production of plutonium. During the course of production and operation of the facilities at Hanford, radionuclides and chromium were discharged directly into the river and also contaminated the groundwater. This study was designed to assess the effects of chromium (Cr) on Chinook salmon (Oncorhynchus tshawytscha) fertilization under exposure conditions similar to those of the Hanford Reach of the Columbia River. Chinook salmon gametes were exposed to aqueous Cr concentrations ranging from 0 to 266 μg Cr l−1. The current ambient water-quality criteria (AWQC) established for the protection of aquatic life (United States Environmental Protection Agency [USEPA] 1986) is 11 μg Cr l−1. Cr has been measured in pore water from bottom sediments of the Columbia River at concentrations >600 μg Cr l−1. Under exposure conditions designed to closely mimic events that occur in the river, the fertilization of Chinook salmon eggs was not affected by concentrations of Cr ranging from 11 to 266 μg Cr l−1. Data suggest that the instantaneous nature of fertilization likely limits the potential effects of Cr on fertilization success. As a result, the current AWQC of 11 μg Cr l−1 is most likely protective of Chinook salmon fertilization.
[No abstract available]
Lakes are dominant landforms in the National Petroleum Reserve Alaska (NPRA) as well as important social and ecological resources. Of recent importance is the management of these freshwater ecosystems because lakes deeper than maximum ice thickness provide an important and often sole source of liquid water for aquatic biota, villages, and industry during winter. To better understand seasonal and annual hydrodynamics in the context of lake morphometry, we analyzed lakes in two adjacent areas where winter water use is expected to increase in the near future because of industrial expansion. Landsat Thematic Mapper and Enhanced Thematic Mapper Plus imagery acquired between 1985 and 2007 were analyzed and compared with climate data to understand interannual variability. Measured changes in lake area extent varied by 0.6% and were significantly correlated to total precipitation in the preceding 12 months (p < 0.05). Using this relation, the modeled lake area extent from 1985 to 2007 showed no long-term trends. In addition, high-resolution aerial photography, bathymetric surveys, water-level monitoring, and lake-ice thickness measurements and growth models were used to better understand seasonal hydrodynamics, surface area-to-volume relations, winter water availability, and more permanent changes related to geomorphic change. Together, these results describe how lakes vary seasonally and annually in two critical areas of the NPRA and provide simple models to help better predict variation in lake-water supply. Our findings suggest that both overestimation and underestimation of actual available winter water volume may occur regularly, and this understanding may help better inform management strategies as future resource use expands in the NPRA. ?? 2008 Springer Science+Business Media, LLC.
Multibeam bathymetric data and seismic-reflection profiles collected in eastern Long Island Sound and western Block Island Sound reveal previously unrecognized glacial features and modern bedforms. Glacial features include an ice-sculptured bedrock surface, a newly identified recessional moraine, exposed glaciolacustrine sediments, and remnants of stagnant-ice-contact deposits. Modern bedforms include fields of transverse sand waves, barchanoid waves, giant scour depressions, and pockmarks. Bedform asymmetry and scour around obstructions indicate that net sediment transport is westward across the northern part of the study area near Fishers Island, and eastward across the southern part near Great Gull Island.
Across the distances spanned by large rivers, there are important differences in catchment characteristics, tributary inputs, and river morphology that may cause longitudinal changes in nutrient, chlorophyll, and suspended solids concentrations. We investigated longitudinal and seasonal patterns in the Upper Mississippi River (UMR) using long-term data (1994-2005) from five study reaches that spanned 1300 km of the UMR. Lake Pepin, a natural lake in the most upstream study reach, had a clear effect on suspended material in the river. Suspended solids and total phosphorus (TP) concentrations were substantially lower downstream of the lake and percent organic material (OM%) in suspension was higher. Below L. Pepin, mean total and organic suspended solids (TSS, OSS) and TP increased downriver and exhibited approximately log-linear relationships with catchment area, whereas OM% declined substantially downriver. Despite the downriver increase in TSS and OSS, concentrations similar to those above L. Pepin do not occur until ~370 km downriver indicating the extent of the influence of L. Pepin on the UMR. Chlorophyll concentrations were lower in the most downstream study reach, likely reflecting the shorter residence time and poor light climate, but there was not a consistent longitudinal decline in chlorophyll across the study reaches. Dissolved silica (DSi), DSi:TN, and DSi:TP declined downriver suggesting that DSi uptake and sedimentation by river phytoplankton may be reducing DSi transport in the river, and indicating that the eutrophication of the river may contribute to a reduction of DSi export to the Gulf of Mexico. ?? 2010 US Government: USGS.
Allan Hills 85085 is a unique chondrite with affinities to the Al Rais-Renazzo clan of carbonaceous chondrites. Its constituents are less than 50 μm in mean size. Chondrules and microchondrules of all textures are present; nonporphyritic chondrules are unusually abundant. The mean compositions of porphyritic, nonporphyritic and barred olivine chondrules resemble those in ordinary chondrites except that they are depleted in volatile elements. Ca-, Al-rich inclusions are abundant and largely free of nebular alteration; they comprise types similar to those in CM and CO chondrites, as well as unique types. Calcium dialuminate occurs in several inclusions. Metal, silicate and sulfide compositions are close to those in CM-CO chondrites and Al Rais and Renazzo. C1-chondrite clasts and metal-rich “reduced” clasts are present, but opaque matrix is absent. Siderophile abundances in ALH85085 are extremely high (e.g., Fe/Si= 1.7 × solar), and volatiles are depleted (e.g., Na/Si= 0.25 × solar, S/Si= 0.03 × solar). Nonvolatile lithophile abundances are similar to those in Al Rais, Renazzo, and CM and CO chondrites.
The rate of Cd2+ sorption by a calcareous aquifer sand was characterized by two reaction steps, with the first step reaching completion in 24 hours. The second step proceeded at a slow and nearly constant rate for at least seven days. The first step includes a fast adsorption reaction which is followed by diffusive transport into either a disordered surface film of hydrated calcium carbonate or into pore spaces. After 24 hours the rate of Cd2+ sorption was constant and controlled by the rate of surface coprecipitation, as a solid solution of CdCO3 in CaCO3 formed in recrystallizing material. Desorption of Cd2+ from the sand was slow. Clean grains of primary minerals, e.g. quartz and aluminosilicates. sorbed much less Cd2+ than grains which had surface patches of secondary minerals, e.g. carbonates, iron and manganese oxides. Calcite grains sorbed the greatest amount of Cd2+ on a weight-normalized basis despite the greater abundance of quartz. A method is illustrated for determining empirical binding constants for trace metals at in situ pH values without introducing the experimental problem of supersaturation. The binding constants are useful for solute transport models which include a computation of aqueous speciation.