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Comparing activated alumina with indigenous laterite and bauxite as potential sorbents for removing fluoride from drinking water in Ghana

Fluoride is considered beneficial to teeth and bones when consumed in low concentrations, but at elevated concentrations it can cause dental and skeletal fluorosis. Most fluoride-related health problems occur in poor, rural communities of the developing world where groundwater fluoride concentrations are high and the primary sources of drinking water are from community hand-pump borehole drilled wells. One solution to drinking high fluoride water is to attach a simple de-fluoridation filter to the hand-pump; and indigenous materials have been recommended as low-cost sorbents for use in these filters. In an effort to develop an effective, inexpensive, and low-maintenance de-fluoridation filter for a high fluoride region in rural northern Ghana, this study conducted batch fluoride adsorption experiments and potentiometric titrations to investigate the effectiveness of indigenous laterite and bauxite as sorbents for fluoride removal. It also determined the physical and chemical properties of each sorbent. Their properties and the experimental results, including fluoride adsorption capacity, were then compared to those of activated alumina, which has been identified as a good sorbent for removing fluoride from drinking water. The results indicate that, of the three sorbents, bauxite has the highest fluoride adsorption capacity per unit area, but is limited by a low specific surface area. When considering fluoride adsorption per unit weight, activated alumina has the highest fluoride adsorption capacity because of its high specific surface area. Activated alumina also adsorbs fluoride well in a wider pH range than bauxite, and particularly laterite. The differences in adsorption capacity are largely due to surface area, pore size, and mineralogy of the sorbent.

Applied Geochemistry

The influence of ozone on atmospheric emissions of gaseous elemental mercury and reactive gaseous mercury from substrates

Experiments were performed to investigate the effect of ozone (O 3) on mercury (Hg) emission from a variety of Hg-bearing substrates. Substrates with Hg(II) as the dominant Hg phase exhibited a 1.7 to 51-fold increase in elemental Hg (Hgo) flux and a 1.3 to 8.6-fold increase in reactive gaseous mercury (RGM) flux in the presence of O3-enriched clean (50 ppb O3; 8 substrates) and ambient air (up to ???70 ppb O3; 6 substrates), relative to clean air (oxidant and Hg free air). In contrast, Hgo fluxes from two artificially Hgo-amended substrates decreased by more than 75% during exposure to O3-enriched clean air relative to clean air. Reactive gaseous mercury emissions from Hg o-amended substrates increased immediately after exposure to O 3 but then decreased rapidly. These experimental results demonstrate that O3 is very important in controlling Hg emissions from substrates. The chemical mechanisms that produced these trends are not known but potentially involve heterogenous reactions between O3, the substrate, and Hg. Our experiments suggest they are not homogenous gas-phase reactions. Comparison of the influence of O3 versus light on increasing Hgo emissions from dry Hg(II)-bearing substrates demonstrated that they have a similar amount of influence although O3 appeared to be slightly more dominant. Experiments using water-saturated substrates showed that the presence of high-substrate moisture content minimizes reactions between atmospheric O3 and substrate-bound Hg. Using conservative calculations developed in this paper, we conclude that because O3 concentrations have roughly doubled in the last 100 years, this could have increased Hgo emissions from terrestrial substrates by 65-72%. ?? 2005 Elsevier Ltd. All rights reserved.

Conference Paper

Bulk and intramolecular carbon isotopic compositions of hydrocarbon gases from laboratory pyrolysis of oil shale of the Green River Formation: Implications for isotope structures of kerogens

Evaluation of intramolecular isotope distributions within organic compounds can provide important insights into gas formation processes and structural properties of gas-generating precursors, such as kerogen, bitumen, and oil, in natural reservoirs. Until recently, little has been known about the intramolecular isotope distributions within kerogens. In this study, we conducted systematic pyrolysis experiments of gas generation from a lacustrine oil shale of the Eocene Green River Formation under hydrous and anhydrous conditions (equivalent maturity or Easy %R o : 0.76 to 3.27 at 310 to 480 °C for 3 to 50 days), measuring gas yields and compositions, as well as bulk and position-specific (PS) carbon isotope compositions. Gas generation processes were investigated in combination with kinetic Monte Carlo (kMC) simulations on a model Type I kerogen based on the chemical structures of oil shale of the Green River Formation. The comparison of our experimental results with kMC modelling indicates a series of β-scission, radical isomerization, and recombination reactions better represent the bulk isotope compositions of propane in the pyrolysis of the oil shale of the Green River Formation, but the ΔC c-t (= δ 13 C cen – δ 13 C ter ) values of propane at Easy %R o > 1.5 can be better simulated by a simple combination of propyl groups with H radicals. Combining our previous works on marine shale of the Woodford Formation and Springfield Coal Member of the Carbondale Formation, PS carbon isotopes of propane indicate that in the lacustrine shales of the Green River Formation and the marine Woodford Shale, propane is sourced from C C bond cleavage, while C O bond cracking generates propane from coal at the initial kerogen cracking stage. At high maturity, the differences of late-stage propane production among the source rocks lead to the different bulk and PS C kinetic isotope effects of propane. Our findings suggest that the δ 13 C at the terminal position of propane precursors is likely up to 3.6‰ higher than at the central position in the Green River kerogen, while they are similar in the marine shale of Woodford Formation. In addition, the δ 13 C at the central position of propyl groups attached to heteroatom compounds is relatively more positive in the Springfield Coal Member of the Carbondale Formation than in Green River kerogen. A comparison of intramolecular C isotopes of propyl groups in the kerogens with their bulk δ 13 C, based on the PS δ 13 C of early-generated propane, contributes to our understanding of heterogeneities of isotopic structures of sedimentary organic matter.

International Journal of Coal Geology

Decreased atmospheric nitrogen deposition in eastern North America: Predicted responses of forest ecosystems

Historical increases in emissions and atmospheric deposition of oxidized and reduced nitrogen (N) provided the impetus for extensive, global-scale research investigating the effects of excess N in terrestrial and aquatic ecosystems, with several regions within the Eastern Deciduous Forest of the United States found to be susceptible to negative effects of excess N. The Clean Air Act and associated rules have led to decreases in emissions and deposition of oxidized N, especially in eastern U.S., representing a research challenge and opportunity for ecosystem ecologists and biogeochemists. The purpose of this paper is to predict changes in the structure and function of North American forest ecosystems in a future of decreased N deposition. Hysteresis is a property of a system wherein output is not a strict function of corresponding input, incorporating lag, delay, or history dependence, particularly when the response to decreasing input is different from the response to increasing input. We suggest a conceptual hysteretic model predicting varying lag times in recovery of soil acidification, plant biodiversity, soil microbial communities, forest carbon (C) and N cycling, and surface water chemistry toward pre-N impact conditions. Nearly all of these can potentially respond strongly to reductions in N deposition. Most responses are expected to show some degree of hysteresis, with the greatest delays in response occurring in processes most tightly linked to “slow pools” of N in wood and soil organic matter. Because experimental studies of declines in N loads in forests of North America are lacking and because of the expected hysteresis, it is difficult to generalize from experimental results to patterns expected from declining N deposition. These will likely be long-term phenomena, difficult to distinguish from other, concurrent environmental changes, including elevated atmospheric CO 2 , climate change, reductions in acidity, invasions of new species, and long-term vegetation responses to past disturbance.

Environmental Pollution

Kinetics of elemental sulfur reduction by petroleum hydrocarbons and the implications for hydrocarbon thermal chemical alteration

Although sulfur-containing compounds are known to play a significant role in the diagenic and catagenic processes that generate oil and gas, relatively little is known about the kinetics of reactions between elemental S and petroleum hydrocarbons. To investigate this subject, a series of closed-system pyrolysis experiments using paraffin, a low-sulfur oil, and a high-sulfur oil with and without elemental S were conducted, and first-order chemical kinetics were fit to the experimental results. The average value for the activation energy required to reduce elemental S to H 2 S and to thermochemically alter higher molecular weight hydrocarbons to methane was calculated to be 193 kJ mol -1 (46 kcal mol -1 ). The results of this study demonstrate that under typical geologic conditions the rate of reduction of elemental S to H 2 S by petroleum hydrocarbons is quite rapid. The maximum time for substantial amounts of elemental S to persist in contact with petroleum hydrocarbons is estimated to be no more than a few million years in cool reservoirs (e.g., <80 °C), and in hotter reservoirs (e.g., >120 °C) the half-life of elemental S may be as short as hundreds of years. Additionally, the presence of elemental S substantially lowers the onset temperature of hydrocarbon thermal chemical alteration (TCA). The activation energy for TCA of a low-sulfur oil to generate methane is estimated to be lowered by 92 kJ mol -1 (22 kcal mol -1 ) due to the presence of elemental sulfur. Consequently, the presence of elemental S in petroleum reservoirs is expected to lower the thermal stability of oil and decrease the maximum depth at which oil occurs within a basin (thermal deadline). The observed acceleration of hydrocarbon TCA is possibly due to organic sulfur compounds (e.g., thiols and sulfides) that form through the reaction of H 2 S or polysulfides with hydrocarbons and subsequently thermally degrade leading to the formation of sulfur radicals that in turn enhance TCA reactions.

Geochimica et Cosmochimica Acta

Reactivation of a cryptobiotic stream ecosystem in the McMurdo Dry Valleys, Antarctica: A long-term geomorphological experiment

The McMurdo Dry Valleys of Antarctica contain many glacial meltwater streams that flow for 6 to 12??weeks during the austral summer and link the glaciers to the lakes on the valley floors. Dry valley streams gain solutes longitudinally through weathering reactions and microbial processes occurring in the hyporheic zone. Some streams have thriving cyanobacterial mats. In streams with regular summer flow, the mats are freeze-dried through the winter and begin photosynthesizing with the onset of flow. To evaluate the longer term persistence of cyanobacterial mats, we diverted flow to an abandoned channel, which had not received substantial flow for approximately two decades. Monitoring of specific conductance showed that for the first 3??years after the diversion, the solute concentrations were greater in the reactivated channel than in most other dry valley streams. We observed that cyanobacterial mats became abundant in the reactivated channel within a week, indicating that the mats had been preserved in a cryptobiotic state in the channel. Over the next several years, these mats had high rates of productivity and nitrogen fixation compared to mats from other streams. Experiments in which mats from the reactivated channel and another stream were incubated in water from both of the streams indicated that the greater solute concentrations in the reactivated channel stimulated net primary productivity of mats from both streams. These stream-scale experimental results indicate that the cryptobiotic preservation of cyanobacterial mats in abandoned channels in the dry valleys allows for rapid response of these stream ecosystems to climatic and geomorphological change, similar to other arid zone stream ecosystems. ?? 2006 Elsevier B.V. All rights reserved.

Geomorphology

The effect of wet-dry weathering on the rate of bedrock river channel erosion by saltating gravel

Previous work has shown that the bedrock erosion rate E because of collisions of saltating bedload can be expressed by E = βq b (1- P c ), where q b is the sediment transport rate, P c is the extent of alluvial cover, and β is the abrasion coefficient. However, the dependence of the abrasion coefficient on the physical characteristics of the bedrock material is poorly known, and in particular, the effects of wet-dry weathering on the saltation-abrasion bedrock incision has not been specifically characterized. Observation suggests that the typical wet-dry cycling of exposed bedrock in river beds gives rise to cracks and voids that are likely to alter the incision rate of the material when subjected to impacts of moving sediment. In this study, flume experiments are performed to develop an understanding of how wet-dry cycling affects the rock tensile strength and the bedrock erosion rate. To represent the physical effects of weathering, boring cores taken from natural bedrock channel are exposed to artificial wet-dry cycles. The experimental results suggest the following: (1) the abrasion coefficient for fresh bedrock is estimated by β = 1.0 × 10 − 4 σ T − 2 ( d / k sb ) 0.5 , where σ T is the tensile strength, d is the diameter of colliding gravel, and k sb is the hydraulic roughness height of bedrock; (2) the tensile strength of the bedrock decreases exponentially as a result of repeated wet-dry cycles, σ T /σ T 0 = exp (- C T NW a 0 /σ T 0 ), where σ T 0 is the initial tensile strength, W a 0 is the initial normalized rate of water absorption., N is the number of wet-dry cycles, and C T is a constant; (3) the erosion rate of fresh bedrock depends on the inverse of the square of tensile strength, but the erosion rate of weathered bedrock depends on the − 1.5 power of tensile strength.

Geomorphology

FFT-enhanced IHS transform method for fusing high-resolution satellite images

Existing image fusion techniques such as the intensity-hue-saturation (IHS) transform and principal components analysis (PCA) methods may not be optimal for fusing the new generation commercial high-resolution satellite images such as Ikonos and QuickBird. One problem is color distortion in the fused image, which causes visual changes as well as spectral differences between the original and fused images. In this paper, a fast Fourier transform (FFT)-enhanced IHS method is developed for fusing new generation high-resolution satellite images. This method combines a standard IHS transform with FFT filtering of both the panchromatic image and the intensity component of the original multispectral image. Ikonos and QuickBird data are used to assess the FFT-enhanced IHS transform method. Experimental results indicate that the FFT-enhanced IHS transform method may improve upon the standard IHS transform and the PCA methods in preserving spectral and spatial information. ?? 2006 International Society for Photogrammetry and Remote Sensing, Inc. (ISPRS).

ISPRS Journal of Photogrammetry and Remote Sensing

Degradation of 1,1,2,2-tetrachloroethane and accumulation of vinyl chloride in wetland sediment microcosms and in situ porewater: Biogeochemical controls and associations with microbial communities

The biodegradation pathways of 1,1,2,2-tetrachloroethane (TeCA) and 1,1,2-trichloroethane (112TCA) and the associated microbial communities in anaerobic wetland sediments were evaluated using concurrent geochemical and genetic analyses over time in laboratory microcosm experiments. Experimental results were compared to in situ porewater data in the wetland to better understand the factors controlling daughter product distributions in a chlorinated solvent plume discharging to a freshwater tidal wetland at Aberdeen Proving Ground, Maryland. Microcosms constructed with wetland sediment from two sites showed little difference in the initial degradation steps of TeCA, which included simultaneous hydrogenolysis to 112TCA and dichloroelimination to 1,2-dichloroethene (12DCE). The microcosms from the two sites showed a substantial difference, however, in the relative dominance of subsequent dichloroelimination of 112TCA. A greater dominance of 112TCA dichloroelimination in microcosms constructed with sediment that was initially iron-reducing and subsequently simultaneously iron-reducing and methanogenic caused approximately twice as much vinyl chloride (VC) production as microcosms constructed with sediment that was methanogenic only throughout the incubation. The microcosms with higher VC production also showed substantially more rapid VC degradation. Field measurements of redox-sensitive constituents, TeCA, and its anaerobic degradation products along flowpaths in the wetland porewater also showed greater production and degradation of VC with concurrent methanogenesis and iron reduction. Molecular fingerprinting indicated that bacterial species [represented by a peak at a fragment size of 198 base pairs (bp) by MnlI digest] are associated with VC production from 112TCA dichloroelimination, whereas methanogens (190 and 307 bp) from the Methanococcales or Methanobacteriales family are associated with VC production from 12DCE hydrogenolysis. Acetate-utilizing methanogens (acetotrophs) appear to be involved in the biodegradation of VC. The relative abundance of Methanosarcinaceae, the only methanogen group with acetotrophic members, doubled in microcosms in which degradation of VC was observed. In addition, molecular analyses using primers specific for known dehalorespiring bacteria in the Dehalococcoides and Desulfuromonas groups showed the presence of these bacteria in microcosm slurry from the site that showed the highest VC production and degradation. Determination of biogeochemical controls and microbial consortia involved in TeCA degradation is leading to a better understanding of the heterogeneity in biodegradation rates and daughter product distribution in the wetland, improving capabilities for developing remediation and monitoring plans.

Journal of Contaminant Hydrology

Effect of compost age and composition on the atrazine removal from solution

Compost samples from two composting facilities, the Urbana (Illinois) Landscape Recycling Center (ULRC) and Illinois State University (ISU), were selected to examine the effect of compost age on atrazine removal from solution. The ULRC samples were made from yard waste without an additional nitrogen source. The ISU samples were made from yard waste or sawdust with the addition of manure. The 6-month-old ULRC compost had the greater capacity to remove atrazine from solution, which we attributed to its greater organic carbon content. The addition of nitrate into ULRC compost could influence the extent of atrazine removal, but did not have a significant impact on atrazine removal when applied to ISU compost, probably because manure was added to the yard waste to produce the compost. For both ULRC and ISU samples, the presence of sodium azide inhibited atrazine removal, suggesting that microbial activity contributed to the atrazine removal. Metabolic analysis demonstrated that hydroxyatrazine was the major identified metabolite that accumulated in solution before significant ring mineralization could occur. When compared with the ISU compost, the ULRC compost sample had a greater capacity to remove atrazine from solution during the 120 days of study because of the larger humic acid content. The experimental results suggested that less-mature compost may be better suited for environmental applications such as removing atrazine from tile-drainage waters. ?? 2006 Elsevier B.V. All rights reserved.

Journal of Hazardous Materials

The feasibility of applying immature yard-waste compost to remove nitrate from agricultural drainage effluents: A preliminary assessment

Nitrate is a major agricultural pollutant found in drainage waters. Immature yard-waste compost was selected as a filter media to study its feasibility for removing nitrate from drainage water. Different operation parameters were tested to examine the denitrification efficiency, including the amounts of compost packed in columns, the flow rate, and the compost storage periods. The experimental results suggested that hydraulic retention time was the major factor to determine the extent of nitrate removal, although the amount of compost packed could also contribute to the nitrate removal efficiency. The effluent nitrate concentration increased as the flow rate decreased, and the compost column reduced nitrate concentrations from 20 mg/L to less than 5 mg/L within 1.5 h. The solution pH increased at the onset of experiment because of denitrification, but stabilized at a pH of about 7.8, suggesting that the compost had a buffering capacity to maintain a suitable pH for denitrification. Storing compost under air-dried conditions may diminish the extent nitrate removed initially, but the effects were not apparent after longer applications. It appeared that immature yard-waste compost may be a suitable material to remove nitrate from tile drainage water because of its relatively large organic carbon content, high microbial activity, and buffering capacity. ?? 2006 Elsevier B.V. All rights reserved.

Journal of Hazardous Materials

Compressibility and particle crushing of Krishna-Godavari Basin sediments from offshore India: Implications for gas production from deep-water gas hydrate deposits

Depressurizing a gas hydrate reservoir to extract methane induces high effective stresses that act to compress the reservoir. Predicting whether a gas hydrate reservoir is viable as an energy resource requires enhanced understanding of the reservoir’s compressibility and susceptibility to particle crushing in response to elevated effective stress because of their impact on the long-term permeability and geomechanical stability of the reservoir. This study investigates physical and geomechanical properties of natural sediments with and without tetrahydrofuran (THF) hydrate subjected to high effective stresses of up to 25 MPa. Experimental results show the stiffness of hydrate-free sediments is mainly governed by the stress state and history, while the stiffness of hydrate-bearing sediments reflects both the grain supporting nature of the interconnected hydrate phase and stress effects. The Poisson’s ratio of hydrate-bearing sediments at low stresses is dominated by the Poisson’s ratio of the interconnected pore-filling phases, and dominated at high stresses by elastic properties of both the skeleton and pore-filling phases. The stress-void ratio responses of hydrate-bearing sediments above the pre-consolidation stress yields a slightly convex-downward trend, suggesting compressibility is influenced by the stiffness of THF hydrate and sediment grains rather than only by void space reduction. The shape of the compression index (Cc) trend may be attributed to an increasing effective gas hydrate saturation as the total pore volume decreases under loading. The results also show that the presence of THF hydrate in sediments can mitigate particle crushing by suppressing particle rearrangement and supporting a portion of the load that would otherwise have to be carried by the sediment. Therefore, the loss of hydrate crystals during gas production may exacerbate sand crushing.

Marine and Petroleum Geology

Potential freshening impacts on fines migration and pore-throat clogging during gas hydrate production: 2-D micromodel study with Diatomaceous UBGH2 sediments

The methane gas hydrate stored in natural sediments is considered a potential gas resource. Countries such as China, India, Japan, and Korea are interested in commercializing this resource, and offshore field pilot tests for gas production have been conducted using depressurization methods to destabilize gas hydrate and facilitate the migration of methane to the production well. However, fine-grained sediments (fines), which are present even in coarse-grained, gas hydrate-bearing sediments, can be resuspended in the production fluid, subsequently clogging pore throats in the formation and reducing the overall production efficiency. We conducted laboratory tests to evaluate the suspension and clogging potential of fines collected from the Ulleung Basin, East Sea, Korea during the 2010 Ulleung Basin Gas Hydrate Expedition 2 (UBGH2). Experimental results reveal that diatoms are prevalent in the sediment and largely control the suspension and clogging behavior. Fluid flow experiments in 2D micromodels show clogging occurs even when injecting the minimum sediment concentration (0.1wt% in the fluid) through micromodels with pore-throat widths at the high end of the anticipated range for UBGH2 gas hydrate-bearing sands (100µm). Mobile gas/fluid interfaces forming during gas hydrate dissociation accentuate clogging by concentrating and mobilizing fines. Sedimentation tests show pore-water freshening during dissociation is not anticipated to change the potential for diatoms to become entrained in the pore water flow, even for the observed gas hydrate saturations of ~80%. Muscovite and illite are also significant components of the tested sediment, however, and pore-water freshening increases their potential for resuspension and clogging. Overall, the resuspension and clogging potential of these fine sediments should increase as gas hydrate dissociation progresses in the thin, gas hydrate-bearing sands investigated in the Ulleung Basin.

Marine and Petroleum Geology

Experimental investigation of the role of rock fabric in gas generation and expulsion during thermal maturation: Anhydrous closed-system pyrolysis of a bitumen-rich Eagle Ford Shale

Gold-tube pyrolysis experiments were conducted on miniature core plugs and powdered rock from a bitumen-rich sample of Eagle Ford Shale to investigate the role of rock fabric in gas generation and expulsion during thermal maturation. The samples were isothermally heated at 130, 300, 310, 333, 367, 400, and 425 °C for 72 h under a confining pressure of 68.0 MPa, corresponding to six levels of induced thermal maturity: pre-oil generation (130 °C/72 h), incipient oil/bitumen generation (300 and 310 °C/72 h), early oil generation (333 °C/72 h), peak oil generation (367 °C/72 h), early oil cracking (400 °C/72 h), and late oil cracking (425 °C/72 h). Experimental results show that gas retention coupled with compositional fractionation occurs in the core plug experiments and varies as a function of thermal maturity. During the incipient oil/bitumen generation stage, yields of methane through pentane (C 1 –C 5 ) from core plugs are significantly lower than those from rock powder, and gases from core plugs are enriched in methane. However, the differences in C 1 –C 5 gas yield and composition decrease throughout the oil generation stage, and by the oil cracking stage no obvious compositional difference in C 1 –C 5 gases exists. The decrease in the effect of rock fabric on gas yield and composition with increasing maturity is the result of an increase in gas expulsion efficiency. Pyrolysis of rock powder yields 4–16 times more CO 2 compared to miniature core plugs, with δ 13 C CO2 values ranging from −2.9‰ to −0.6‰, likely due to carbonate decomposition accelerated by reactions with organic acids. Furthermore, lower yields of gaseous alkenes and H 2 from core plug experiments sugge

Organic Geochemistry

Carrying capacity of spatially distributed metapopulations

Carrying capacity is a key concept in ecology. A body of theory, based on the logistic equation, has extended predictions of carrying capacity to spatially distributed, dispersing populations. However, this theory has only recently been tested empirically. The experimental results disagree with some theoretical predictions of when they are extended to a population dispersing randomly in a two-patch system. However, they are consistent with a mechanistic model of consumption on an exploitable resource (consumer–resource model). We argue that carrying capacity, defined as the total equilibrium population, is not a fundamental property of ecological systems, at least in the context of spatial heterogeneity. Instead, it is an emergent property that depends on the population’s intrinsic growth and dispersal rates.

Trends in Ecology and Evolution

Sediment resuspension characteristics in Baltimore Harbor, Maryland

Critical bed shear stress for sediment resuspension and sediment erosion rate were measured in-situ at sites from inner to outer Baltimore Harbor using the VIMS Sea Carousel. Clay mineral contents and biological conditions were almost the same at the four study sites. The experimental results indicated that the erosion rate increased from the outer harbor toward the inner harbor with a maximum difference of about 10 times at an excess bed shear stress of 0.1 Pa. The measured critical bed shear stress strongly depended on the existence of a fluff layer. It was approximately 0.05 Pa if a fluff layer existed, and increases to about 0.1 Pa in the absence of a fluff layer.

Marine Geology

Impact of sensor's point spread function on land cover characterization: Assessment and deconvolution

Measured and modeled point spread functions (PSF) of sensor systems indicate that a significant portion of the recorded signal of each pixel of a satellite image originates from outside the area represented by that pixel. This hinders the ability to derive surface information from satellite images on a per-pixel basis. In this study, the impact of the PSF of the Moderate Resolution Imaging Spectroradiometer (MODIS) 250 m bands was assessed using four images representing different landscapes. Experimental results showed that though differences between pixels derived with and without PSF effects were small on the average, the PSF generally brightened dark objects and darkened bright objects. This impact of the PSF lowered the performance of a support vector machine (SVM) classifier by 5.4% in overall accuracy and increased the overall root mean square error (RMSE) by 2.4% in estimating subpixel percent land cover. An inversion method based on the known PSF model reduced the signals originating from surrounding areas by as much as 53%. This method differs from traditional PSF inversion deconvolution methods in that the PSF was adjusted with lower weighting factors for signals originating from neighboring pixels than those specified by the PSF model. By using this deconvolution method, the lost classification accuracy due to residual impact of PSF effects was reduced to only 1.66% in overall accuracy. The increase in the RMSE of estimated subpixel land cover proportions due to the residual impact of PSF effects was reduced to 0.64%. Spatial aggregation also effectively reduced the errors in estimated land cover proportion images. About 50% of the estimation errors were removed after applying the deconvolution method and aggregating derived proportion images to twice their dimensional pixel size. ?? 2002 Elsevier Science Inc. All rights reserved.

Remote Sensing of Environment

Observations of quasistatic fault growth from acoustic emissions

The location of acoustic emission (AE) sources during deformation of rock has proven to be a useful non-destructive analytic technique. We present experimental results,based on AE observations, that show the nucleation and growth of macroscopic fault planes in granite and sandstone samples. By controlling axial stress to maintain constant AE rate rather than more conventional loading conditions such as constant strain rate or constant stress, we have been successful in retarding the failure process in triaxial experiments. As a result, the post-failure stress curve has been followed quasistatically, extending to minutes or hours the fault growth process that normally would occur violently in a fraction of a second. In addition to this novel control system, three-dimensional locations of AE events were determined by analyzing the relative arrival times of AE pulses recorded on a network of transducers attached to the sample. In this manner, as many as 40 000 AE events were located in the course of a single experiment. While the details of fault formation varied from experiment to experiment, a number of features were consistently observed. In all three granite experiments, the fault plane nucleated abruptly at a point on the sample surface soon after reaching peak stress. Prior to fault nucleation, microcrack growth was distributed evenly throughout the granite samples. From the nucleation site, the fault plane grew across the sample, accompanied by a gradual drop in axial stress. AE locations showed that the fault propagated as a fracture front (process zone) with in-plane dimension of 10-50 mm. As the fracture front passed, the AE from a given region would drop to a low level. If allowed to progress to completion, stress eventually dropped to the frictional sliding strength. Sandstone samples showed somewhat different response. In these experiments, a diffuse damage zone appeared prior to peak strength and gradually localized into an incipient fault plane. After passing through peak stress, this plane grew, as in the granite samples, to eventually bisect the sample.

International Geophysics