Hydraulic Effects of Shales in Fluvial-Deltaic Deposits: Ground-Penetrating Radar, Outcrop Observations, Geostatistics, and Three-Dimensional Flow Modeling for the Ferron Sandstone, Utah

Ground-penetrating radar (GPR) surveys, outcrop measurements, and cores provide a high-resolution 3D geologic model to investigate the hydraulic effects of shales in marine-influenced lower delta-plain distributary channel deposits within the Cretaceous-age Ferron Sandstone at Corbula Gulch in central Utah, USA. Shale statistics are computed from outcrop observations. Although slight anisotropy was observed in mean length and variogram ranges parallel and perpendicular to pale of low , the anisotropy is not statistically significant and the estimated mean length is 5.4 m. Truncated Gaussian simulation was used to create maps of shales that are placed on variably dipping stratigraphic surfaces interpreted from high-resolution 3D GPR surveys, outcrop interpretations, and boreholes. Sandstone permeability is estimated from radar responses calibrated to permeability measurements from core samples. Experimentally designed flow simulations examine the effects of variogram range, shale coverage fraction, and trends in shale coverage on predicted upscaled permeability, breakthrough time, and sweep efficiency. Approximately 1500 flow simulations examine three different geologic models, flow in the 3 coordinate directions, 16 geostatistical parameter combinations, and 10 realizations for each model. ANOVA and response models computed from the flow simulations demonstrate that shales decrease sweep, recovery, and permeability, especially in the vertical direction. The effect on horizontal flow is smaller. Flow predictions for ideal tracer displacements at Corbula Gulch are sensitive to shale-coverage fraction, but are relatively insensitive to twofold variations in variogram range or to vertical trends in shale coverage. Although the hydraulic effects of shale are statistically significant, the changes in flow responses rarely exceed 20%. As a result, it may be reasonable to use simple models when incorporating analogous shales into models of reservoirs or aquifers.     

Inflight Calibration of the NEAR Multispectral Imager: II. Results from Eros Approach and Orbit

During the Near-Earth Asteroid Rendezvous (NEAR) spacecraft's investigation of asteroid 433 Eros, inflight calibration measurements from the multispectral imager (MSI) have provided refined knowledge of the camera's radiometric performance, pointing, and light-scattering characteristics. Measurements while at Eros corroborate most earlier calibration results, although there appears to be a small, gradual change in instrument dark current and flat field due to effects of aging in the space environment. The most pronounced change in instrument behavior, however, is a dramatic increase in scattered light due to contaminants accumulated on the optics during unscheduled fuel usage in December 1998. Procedures to accurately quantify and to remediate the scattered light are described in a companion paper (Li et al. 2002, Icarus155, 00-00). Acquisition of Eros measurements has clarified the relative, filter-to-filter, radiometric performance of the MSI. Absolute radiometric calibration appears very well constrained from flight measurements, with an accuracy of ∼5%. Pointing relative to the spacecraft coordinate system can be determined from the temperature of the spacecraft deck with an accuracy of ∼1 pixel.     

Detection of Temperature-Dependent Spectral Variation on the Asteroid Eros and New Evidence for the Presence of an Olivine-Rich Silicate Assemblage

Data obtained by the near-infrared spectrometer carried by the NEAR-Shoemaker spacecraft show that the spectral properties of the asteroid Eros vary with temperature. The manner in which they vary demonstrates that the mineral olivine is a major constituent of the surface. The near-IR temperature-dependent spectral properties of Eros in the northern hemisphere, and for two individual regions on the surface, show clear evidence of the presence of the mineral olivine and are a close match to the temperature-spectral behavior of LL-type ordinary chondrite meteorites. While the presence of other olivine-rich meteorites cannot be excluded, H-type ordinary chondrites are clearly too pyroxene-rich to be permitted as a major surface component of Eros. The results of the thermal-spectral analysis are consistent with results from analysis of conventional reflectance spectra of the asteroid and contribute unambiguous detection of olivine to the understanding of the surface composition of Eros.     

A preliminary investigation of strong-motion data from the French Antilles

Strong-motion networks have been operating in the Caribbean region since the 1970s, however, until the mid-1990s only a few analogue stations were operational and the quantity of data recorded was very low. Since the mid-1990s, digital accelerometric networks have been established on islands within the region. At present there are thought to be about 160 stations operating in this region with a handful on Cuba, 65 on the French Antilles (mainly Guadeloupe and Martinique), eight on Jamaica, 78 on Puerto Rico (plus others on adjacent islands) and four on Trinidad.After briefly summarising the available data from the Caribbean islands, this article is mainly concerned with analysing the data that has been recorded by the networks operating on the French Antilles in terms of their distribution with respect to magnitude, source-to-site distance, focal depth and event type; site effects at certain stations; and also with respect to their predictability by ground motion estimation equations developed using data from different regions of the world. More than 300 good quality triaxial acceleration time-histories have been recorded on Guadeloupe and Martinique at a large number of stations from earthquakes with magnitudes larger than 4.8, however, most of the records are from considerable source-to-site distances. From the data available it is found that many of the commonly-used ground motion estimation equations for shallow crustal earthquakes poorly estimate the observed ground motions on the two islands; ground motions on Guadeloupe and Martinique have smaller amplitudes and are more variable than expected. This difference could be due to regional dependence of ground motions because of, for example, differing tectonics or crustal structures or because the ground motions so far recorded are, in general, from smaller earthquakes and greater distances than the range of applicability of the investigated equations.     

The Enso-Fire Dynamic in Insular Southeast Asia

We examined the spatiotemporal patterns of fire in insular Southeast Asia from July 1996 to December 2001 using a set of consistent, nighttime fire observations provided by the Along Track Scanning Radiometer (ATSR) sensor. Monthly ATSR fire counts were analyzed relative to georeferenced climatic and land-cover data from a variety of sources. We found that fires were strongly correlated with Southern Oscillation Index (SOI) (r = ?0.75) and Niño 3.4 index (r = 0.72) in forested land-cover types within the equatorial belt (5.5^°S–5.5^°N). Cross-correlation analysis revealed that detrended SOI was modestly correlated (r = 0.42) with detrended monthly fire count with a positive lag of four months. However, our analysis also revealed that fire counts reached their maximum 6 months before the absolute maximum of SOI. Annual sums of SOI (∑_SOI) and fire counts revealed linearity for ∑_SOI≤ 0. Overall, the results suggest that ENSO indices may have limited predictive utility at a monthly time scale, but that temporal aggregation and additional fire observations may enhance our capacity to forecast fires in different cover types based on ENSO data.     

Microbial reduction of chromium from the hexavalent to divalent state

We demonstrate that Shewanella oneidensis, a metal-reducing bacteria species with cytoplasmic-membrane-bound reductases and remarkably diverse respiratory capabilities, reduced Cr(VI) to Cr(II) in anaerobic cultures where chromate was the sole terminal electron acceptor. Individual cell microanalysis by transmission electron microscopy (TEM) using electron energy-loss spectroscopy (EELS) and energy dispersive X-ray spectroscopy (EDXS) demonstrates Cr(II) concentrated near the cytoplasmic membrane, suggesting the terminal reduction pathway is intracellularly localized. Further, estimated cellular Cr(II) concentrations are relatively high at upwards of 0.03-0.09 g Cr/g bacterium. Accumulation of Cr(II) is observed in S. oneidensis cells prior to the formation of submicron-sized precipitates of insoluble Cr(III) on their surfaces. Furthermore, under anaerobic conditions, Cr(III) precipitates that encrust cells are shown to contain Cr(II) that is likely bound in the net negatively charged extracellular biopolymers which can permeate the surfaces of the precipitates. In otherwise nearly identical incubations, Cr(III) precipitate formation was observed in cultures maintained anaerobic with bubbled nitrogen but not in three replicate cultures in an anaerobic chamber.     

Ferrihydrite dissolution by pyridine-2,6-bis(monothiocarboxylic acid) and hydrolysis products

Pyridine-2,6-bis(monothiocarboxylate) (pdtc), a metabolic product of microorganisms, including Pseudomonas putida and Pseudomonas stutzeri was investigated for its ability of dissolve Fe(III)(hydr)oxides at pH 7.5. Concentration dependent dissolution of ferrihydrite under anaerobic environment showed saturation of the dissolution rate at the higher concentration of pdtc. The surface controlled ferrihydrite dissolution rate was determined to be 1.2 × 10⁻⁶ mol m⁻² h⁻¹. Anaerobic dissolution of ferrihydrite by pyridine-2,6-dicarboxylic acid or dipicolinic acid (dpa), a hydrolysis product of pdtc, was investigated to study the mechanism(s) involved in the pdtc facilitated ferrihydrite dissolution. These studies suggest that pdtc dissolved ferrihydrite using a reduction step, where dpa chelates the Fe reduced by a second hydrolysis product, H₂S. Dpa facilitated dissolution of ferrihydrite showed very small increase in the Fe dissolution when the concentration of external reductant, ascorbate, was doubled, suggesting the surface dynamics being dominated by the interactions between dpa and ferrihydrite. Greater than stoichiometric amounts of Fe were mobilized during dpa dissolution of ferrihydrite assisted by ascorbate and cysteine. This is attributed to the catalytic dissolution of Fe(III)(hydr)oxides by the in situ generated Fe(II) in the presence of a complex former, dpa.     

Evaluation of Simultaneous Analyte Leaching/Vapour Phase Introduction for Direct Osmium Isotope Ratio Measurements in Solid Samples by Double-Focusing Sector Field ICP-MS

The analytical performance of a method for Os isotope ratio measurement by double‐focusing, sector field ICP‐MS (ICP‐SFMS) was evaluated. The method is based on several optimised, concurrent processes: Os extraction from samples in hot concentrated nitric acid; separation of Os from the digest solution by the formation of volatile osmium tetroxide accelerated by continuous hydrogen peroxide addition; transport of analyte vapour by an oxygen flow into the ICP; and isotopic determination by ICP‐SFMS. Due to the very efficient utilisation of analyte (approaching 0.5‰), Os isotope ratio measurement could be performed at low pg levels. Combined with an ability to process sample sizes up to 2 g (up to 50 g if the organic matrix of biological or botanical samples is eliminated by ashing), materials with Os concentrations in the low, or even sub pg g^?1 range could be determined by this method. Given that two complete digestion/distillation systems were available for interchangeable use, throughputs of up to fifteen samples per 8 hour shift could be achieved. The method precision, evaluated as the long‐term reproducibility of ¹⁸⁷ Os/¹⁸⁸Os ratio measurements in a commercial Os reference sample containing 0.5 ng Os, was 0.16% relative standard deviation (RSD, 1s). The method has been applied to perform replicate ¹⁸⁷ Os/¹⁸⁸ Os ratio measurements on a suite of fifty reference materials of various origins and matrix compositions, with Os concentrations varying from < 0.1 pg g^?1 to > 100 ng g^?1, yielding an average precision of 3% RSD. Though none of the materials tested are certified for Os content or Os isotope composition, comparison of the obtained data with published Os isotope information for similar sample types revealed close agreement between the two. The method can also be used for the simultaneous, semi‐quantitative determination of Os concentrations.     

Chemical ozone loss in the Arctic vortex in the winter 1995–96: HALOE measurements in conjunction with other observations

Severe chemical ozone loss has been detected in the Arctic in the winter and spring of 1995–96 by a variety of methods. Extreme reductions in column ozone due to halogen catalysed chemistry were derived from measurements of the Halogen Occultation Experiment (HALOE) on board the Upper Atmosphere Research Satellite in the Arctic vortex. Here, we discuss further aspects of the HALOE observations in the Arctic over this period. Potential problems, both in the data themselves and in the methodology of the data analysis are considered and the reason for the differences between the Arctic ozone losses deduced from HALOE data version 17 and 18 is analysed. Moreover, it is shown that HALOE measurements in the Arctic in winter and spring 1995–96 compare well with observations by other ground-based and satellite instruments.