Carbonaceous chondrites as analogs for the composition and alteration of Ceres

The mineralogy and geochemistry of Ceres, as constrained by Dawn's instruments, are broadly consistent with a carbonaceous chondrite (CM/CI) bulk composition. Differences explainable by Ceres’s more advanced alteration include the formation of Mg‐rich serpentine and ammoniated clay; a greater proportion of carbonate and lesser organic matter; amounts of magnetite, sulfide, and carbon that could act as spectral darkening agents; and partial fractionation of water ice and silicates in the interior and regolith. Ceres is not spectrally unique, but is similar to a few other C‐class asteroids, which may also have suffered extensive alteration. All these bodies are among the largest carbonaceous chondrite asteroids, and they orbit in the same part of the Main Belt. Thus, the degree of alteration is apparently related to the size of the body. Although the ammonia now incorporated into clay likely condensed in the outer nebula, we cannot presently determine whether Ceres itself formed in the outer solar system and migrated inward or was assembled within the Main Belt, along with other carbonaceous chondrite bodies.     

Inversion for Range-Dependent Sediment Compressional-Wave-Speed Profiles From Modal Dispersion Data

A perturbative inversion method for estimating sediment compressional-wave-speed profiles from modal travel-time data is extended to include range-dependent environments. The procedure entails dividing a region into range-independent sections and obtaining estimates of the sediment properties for each region. Inversion results obtained using synthetic data show that range-dependent properties can be obtained if an experiment is designed to include multiple source/receiver combinations. This approach is applied to field data collected during the 2006 Shallow Water Experiment (SW06). The sediment compressional-wave-speed profiles resulting from analysis of the field data are evaluated by comparing acoustic fields predicted based on the inversion to acoustic fields measured during a different experiment conducted in the same region. The model is also compared to seismic reflection survey data collected during SW06. Resolution and variance estimated for the inversion results are also presented.      

Analytic element modelling for strip aquifers

The Analytic Element Method (AEM) provides a convenient tool for groundwater flow analysis in unbounded continuous domains. The AEM is based on the superposition of analytic functions, known as elements, useful at both regional and local scales. In this study, analytic elements for strip aquifers are presented. Such aquifers occur in riverine or coastal deposits and in outcrop zones of confined aquifers. Local flow field is modelled indirectly, using a reference plane related to the aquifer domain through the Schwarz‐Christoffel transform. The regional flow is obtained as a solution of the one‐dimensional flow equation. The proposed methodology was tested by modelling two hypothetical situations, which were compared to exact solutions. It is shown that regional boundaries can be reproduced exactly while local fields are adequately reproduced with analytic elements. The developed elements are applied to simulate a real flow field in northeastern Brazil showing good agreement with measured water levels. Copyright © 2011 John Wiley & Sons, Ltd.     

Gas phase reactions of alkyl nitrates with hydroxyl radicals under tropospheric conditions in comparison with photolysis

Rate constants for the reaction of OH radicals with some branched alkyl nitrates have been measured applying a competitive technique. Methyl nitrite photolysis in synthetic air was used as OH radical source at 295±2 K and 1000 mbar total pressure. Using a rate constant of 2.53×10^-12 cm³ s^-1 for the reaction of OH radicals with n-butane as reference, the following rate constants were obtained (units: 10^-12 cm³ s^-1): isopropyl nitrate, 0.59±0.22; isobutyl nitrate, 1.63±0.20; 3-methyl-2-butyl nitrate, 1.95±0.15; 2-methyl-1-butyl nitrate, 2.50±0.15; 3-methyl-1-butyl nitrate, 2.55±0.35. These values have been combined with the literature data to recalculate the substituent factors F(X) for the different nitrate groups which can be used to predict OH rate constants for organic nitrates for which experimental data are not available.Preliminary measurements of the photolysis frequency of isopropyl nitrate have shown that for this nitrate as a model substance, OH reactions and direct photolysis are of equal importance under tropospheric conditions.     

Infrared spectroscopic investigation of hydroxyl in β-(Mg,Fe)2SiO4 and coexisting olivine: Implications for mantle evolution and dynamics

Wadsleyite (β-(Mg,Fe)₂SiO₄) is a major constituent of the Earth's transition zone and is known to accommodate OH. The portion of the transition zone between 400–550 km could be an important source or sink for hydroxyl in plumes and slabs intersecting this region. Micro-infrared spectroscopy has been carried out on the β-phase and coexisting metastable olivine synthesized in a multianvil apparatus at 14 GPa and 1550–1650 K under hydrous conditions. Single-crystal and polycrystal specimens of both phases were analyzed in the 1800–8500 cm^?1 frequency region to determine the speciation, abundances, and partitioning behavior of the hydrous components in coexisting β-phase and olivine. β-phase spectra consistently show three distinct OH bands at 3329, 3580, and 3615 cm^?1. OH concentrations range from 10000–65000 H/10⁶ Si. A strong positive correlation of grain size and extent of transformation with OH concentration in the β-phase indicates that grain-growth and transformation rates are enhanced in a hydrous environment. Olivine spectra are variable, but consistently show a prominent broad-band absorbance representing molecular H₂O, consistent with the infrared signature of the starting material. OH concentrations in olivine range from <300–1400 H/10⁶ Si. The highest OH concentrations measured for olivine and the β-phase may represent solubility limits, in which case the OH solubility ratio between these two phases is approximately 1∶40. Where both phases coexist and are undersaturated with OH, the partitioning ratio of OH between them is about 1∶100. The large solubility contrast between olivine and the β-phase suggests a mechanism for hydrating the transition zone via olivine carried down in subducting slabs. Plumes impinging on an OH-rich upper transition region could cause H₂ or H₂O to be released upon transformation of the β-phase to olivine, resulting in initiation of secondary upwellings. If dissolution of OH weakens the β-phase, and if OH is present in the mantle, the region between 400–550 km could be a zone of low viscosity.     

Significance of the remotely sensed thermal infrared measurements obtained over a citrus orchard

In this work we have developed a theoretical model that helps the interpretation of the remotely sensed thermal infrared measurements carried out over citrus orchards. A detailed analysis of the different factors which take part in the definition of the effective emissivity and temperature (observation height, viewing angle, type of soil, dimensions and separation between orange trees) is made. The model was validated under vertical observation in a citrus orchard during seven nights. In this situation we have determined that the model performs to an accuracy of about 1%.     

Geochemical Indicators of Intrinsic Bioremediation

A detailed field investigation has been completed at a gasoline-contaminated aquifer near Rocky Point, NC, to examine possible indicators of intrinsic bioremediation and identify factors that may significantly influence the rate and extent of bioremediation. The dissolved plume of benzene, toluene, ethylbenzene, and xylene (BTEX) in ground water is naturally degrading. Toluene and o-xylene are most rapidly degraded followed by m-, p-xylene, and benzene. Ethylbenzene appears to degrade very slowly under anaerobic conditions present in the center of the plume. The rate and extent of biodegradation appears to be strongly influenced by the type and quantity of electron acceptors present in the aquifer. At the upgradient edge of the plume, nitrate, ferric iron, and oxygen are used as terminal electron acceptors during hydrocarbon biodegradation. The equivalent of 40 to 50 mg/I of hydrocarbon is degraded based on the increase in dissolved CO₂ relative to background ground water. Immediately downgradient of the source area, sulfate and iron are the dominant electron acceptors. Toluene and o-xylene are rapidly removed in this region. Once the available oxygen, nitrate, and sulfate are consumed, biodegradation is limited and appears to be controlled by mixing and aerobic biodegradation at the plume fringes.     

Volcanic hazards from Bezymianny- and Bandai-type eruptions

Major slope failures are a significant degradational process at volcanoes. Slope failures and associated explosive eruptions have resulted in more than 20 000 fatalities in the past 400 years; the historic record provides evidence for at least six of these events in the past century. Several historic debris avalanches exceed 1 km³ in volume. Holocene avalanches an order of magnitude larger have traveled 50–100 km from the source volcano and affected areas of 500–1500 km². Historic eruptions associated with major slope failures include those with a magmatic component (Bezymianny type) and those solely phreatic (Bandai type). The associated gravitational failures remove major segments of the volcanoes, creating massive horseshoe-shaped depressions commonly of caldera size. The paroxysmal phase of a Bezymianny-type eruption may include powerful lateral explosions and pumiceous pyroclastic flows; it is often followed by construction of lava dome or pyroclastic cone in the new crater. Bandai-type eruptions begin and end with the paroxysmal phase, during which slope failure removes a portion of the edifice. Massive volcanic landslides can also occur without related explosive eruptions, as at the Unzen volcano in 1792.The main potential hazards from these events derive from lateral blasts, the debris avalanche itself, and avalanche-induced tsunamis. Lateral blasts produced by sudden decompression of hydrothermal and/or magmatic systems can devastate areas in excess of 500km² at velocities exceeding 100 m s^–1. The ratio of area covered to distance traveled for the Mount St. Helens and Bezymianny lateral blasts exceeds that of many pyroclastic flows or surges of comparable volume. The potential for large-scale lateral blasts is likely related to the location of magma at the time of slope failure and appears highest when magma has intruded into the upper edifice, as at Mount St. Helens and Bezymianny.Debris avalanches can move faster than 100 ms^–1 and travel tens of kilometers. When not confined by valley walls, avalanches can affect wide areas beyond the volcano's flanks. Tsunamis from debris avalanches at coastal volcanoes have caused more fatalities than have the landslides themselves or associated eruptions. The probable travel distance (L) of avalanches can be estimated by considering the potential vertical drop (H). Data from a catalog of around 200 debris avalanches indicates that the H/L rations for avalanches with volumes of 0.1–1 km³ average 0.13 and range 0.09–0.18; for avalanches exceeding 1 km³, H/L ratios average 0.09 and range 0.5–0.13.Large-scale deformation of the volcanic edefice and intense local seismicity precede many slope failures and can indicate the likely failure direction and orientation of potential lateral blasts. The nature and duration of precursory activity vary widely, and the timing of slope faliure greatly affects the type of associated eruption. Bandai-type eruptions are particularly difficult to anticipate because they typically climax suddenly without precursory eruptions and may be preceded by only short periods of seismicity.     

Carbon,hydrogen and nitrogen isotopes in solvent-extractable organic matter from carbonaceous chondrites

Solvent extractions were done on the carbonaceous chondrites Murray, Murchison, Orgueil and Renazzo, using CCl₄ and CH₃OH. Between 2 and 10% of the total carbon in these meteorites is extractable by ordinary techniques, most of it in CH₃OH. After demineralization with HF, perhaps as much as 30% of the total carbon in Murray may be extractable with CH₃OH. The extracts from Renazzo have isotopic ratios which suggest that they are mainly terrestrial organic matter, with lesser contributions from indigenous organics. The CH₃OH-soluble organic matter from Murchison and both untreated and HF-treated Murray has δ¹³C values of about +5 to + 10%. and δ¹⁵N values of about +90 to +100%., both of which are significantly higher than the bulk meteorite values. The Orgueil CH₃OH-extract also has a δ¹⁵N value well above the value in residual organic matter. Values for δD of +300 to +500%. are found for the CH₃OH-soluble organic matter. The combined data for C, H and N isotopes makes it highly unlikely that the CH₃OH-soluble components are derivable from, or simply related to, the insoluble organic polymer found in the same meteorites. A relationship is suggested between the event that formed hydrous minerals in CI1 and CM2 meteorites and the introduction of water-soluble (methanol-soluble) organic compounds. Organic matter soluble in CCl₄ has essentially no nitrogen, and δ³C and δD values are lower than for CH₃OH-soluble phases. Either there are large isotopic fractionations for carbon and hydrogen between different soluble organic phases, or the less polar components are partially of terrestrial origin.     

Petrogenesis of the Elephant Moraine A79001 meteorite: Multiple magma pulses on the shergottite parent body

The EETA 79001 achondrite consists of two distinct igneous lithologies joined along a planar, non-brecciated contact. Both are basaltic rocks composed primarily of pigeonite, augite, and maskelynite, but one contains zoned megacrysts of olivine, orthopyroxene, and chromite that represent disaggregated xenoliths of harzburzite. Both lithologies probably formed from successive volcanic flows or multiple injections of magma into a small, shallow chamber. Many similarities between the two virtually synchronous magmas suggest that they are related. Possible mechanisms to explain their differences involve varying degrees of assimilation, fractionation from similar parental magmas, or partial melting of a similar source peridotite; of these, assimilation of the observed megacryst assemblage seems most plausible. However, some isotopic contamination may be required in any of these petrogenetic models. The meteorite has suffered extensive shock metamorphism and localized melting during a large impact event that probably excavated and liberated it from its parent body. Both basaltic lithologies and the inferred ultramafic protolith of the megacryst assemblage are petrologically similar to other members of the shergottite group, and all may have been derived from a volcanic-plutonic complex on a planetary body.