Chemical abundances determined from meteor spectra: I. Ratios of the main chemical elements

Abstract— Relative chemical abundances of 13 meteoroids were determined by averaging the composition of the radiating gas along the fireball path that originated during their penetration into the Earth's atmosphere. Mg, Fe, Ni, Cr, Mn, and Co abundances, relative to Si, are similar to those reported for CI and CM carbonaceous chondrites and interplanetary dust particles. In contrast, relative abundances of Ca and Ti in meteor spectra indicate that these elements suffer incomplete evaporation processes. The chemical composition of all meteoroids studied in this work differs from that of 1P/Halley dust.     

Transient biouptake flux and accumulation by microorganisms: The case of two types of sites with Langmuir adsorption

The uptake of a chemical species by an aquatic microorganism is modelled considering two kinds of sites where Langmuirian adsorption is followed by first order internalisation kinetics. Simpler models, such as only one internalisation route (while most of the adsorption takes place on non-internalising sites) or a linear isotherm for adsorption on one or both sites, become limiting cases of this double-Langmuirian model. The model considers the sites located on the spherical (or semi-spherical) surface of the organism, and takes diffusion from the medium into explicit account. The numerical solution for the internalisation flux shows a maximum. We provide an estimate for the time needed to reach a certain proximity to steady state. The transient solution confirms that the analytical expressions for the steady-state flux are usually valid and that the accumulated amounts reflect the impact of the short-time uptake. The Instantaneous Steady-State Approximation (ISSA), where an intercept of the linear regression of accumulated amount as a function of time is interpreted as an adsorbed amount, can be critically assessed with the transient numerical code for two cases: (i) when the total burden of metal on the cell is the input data and (ii) when an extraction procedure provides further information on the adsorbed and internalised amount.     

Applicability of a Backprojection Algorithm to Reconstruct Images of Subsurface Horizontal Planes for Laboratory Experiments in Electrical Resistance Tomography

This paper describes the use of a backprojection algorithm to reconstruct subsurface images of the electrical resistivity in horizontal planes parallel to the surface. The algorithm can be applied to detect buried objects such as tanks or pipes and possible leakages from them. Two imaging strategies are compared: juxtaposition of vertical planes, and 3D reconstruction from the sensitivity matrix corresponding to the entire volume whose surface is explored. The electrode arrays used for voltage measurement are the dipole–dipole array and a modified Schlumberger array. A personal computer controls current injection, electrode switching, and voltage detection. The system injects 1 kHz, 20 V peak-to-peak square waveforms, thus avoiding electrode polarization effects. Experimental laboratory measurements show that the algorithm detects localized objects such as an insulating sphere and a conductive cylinder immersed in water. Furthermore, covering half of the cylinder by a rubber sleeve to simulate a nonconductive leak, yields a distinct image for the leak. The backprojection algorithm does not need any regularization parameter and it is very fast in inverting the sensitivity matrix because it approximates the inverse matrix by its transposed. The dipole–dipole array usually yields a lower overall pixel error than the modified Schlumberger array but both allow the detection of simulated underground leaks.     

A mass transfer model of bauxite formation

The formation of bauxite due to weathering of a granitic protolith has been simulated by means of a one-dimensional flow and reaction model based on the mass transfer principle. The model couples mineral dissolution and precipitation reactions, speciation in solution, and advective solute transport in a porous medium. A very important aspect of the modeling study is the use of mineral reaction rates determined experimentally in the laboratory. The important effects of solution saturation state and pH have been incorporated into the kinetic rate laws governing the heterogeneous reactions. The values of these parameters have been obtained from the scientific literature to guarantee that realistic reaction rates are used in the simulations. Albite and quartz are the minerals that make up the parent rock in the model. Gibbsite, kaolinite, and a Na-mica (as a surrogate for smectite) are the secondary minerals that have been taken into account. Long-term simulations (>1 Ma) have been run, and the formation of a bauxitic profile, with an upper gibbsite-rich and a lower kaolinite-rich zone, is predicted. In early stages of the process (up to a few hundreds of thousands of years), both gibbsite and kaolinite precipitate directly from solution as a consequence of albite dissolution. In later stages, the bulk of gibbsite precipitation derives from the incongruent dissolution of kaolinite, while kaolinite precipitation is still caused by the dissolution of albite. This is also reflected by the formation of two reaction fronts in the profile. These results are compared with weathering sequences from the Los Pijiguaos bauxite deposit, Venezuela. The overlap between the gibbsite and kaolinite zones and the replacement of kaolinite by gibbsite are consistent with model calculations. Mechanical denudation has to be called upon to explain the limited thicknesses of the weathering profiles in the field. The role of mechanical erosion is supported by the presence of microsedimentary structures in the bauxite and the balance between dissolved and suspended loads in the streams draining the area.     

Impact of anthropogenic CO 2 on the next glacial cycle

The model of Paillard and Parrenin (Earth Planet Sci Lett 227(3–4):263–271, 2004) has been recently optimized for the last eight glacial cycles, leading to two different relaxation models with model-data correlations between 0.8 and 0.9 (García-Olivares and Herrero (Clim Dyn 1–25, 2012b)). These two models are here used to predict the effect of an anthropogenic CO ₂ pulse on the evolution of atmospheric CO ₂, global ice volume and Antarctic ice cover during the next 300 kyr. The initial atmospheric CO ₂ condition is obtained after a critical data analysis that sets 1300 Gt as the most realistic carbon Ultimate Recoverable Resources (URR), with the help of a global compartmental model to determine the carbon transfer function to the atmosphere. The next 20 kyr will have an abnormally high greenhouse effect which, according to the CO ₂ values, will lengthen the present interglacial by some 25 to 33 kyr. This is because the perturbation of the current interglacial will lead to a delay in the future advance of the ice sheet on the Antarctic shelf, causing that the relative maximum of boreal insolation found 65 kyr after present (AP) will not affect the developing glaciation. Instead, it will be the following insolation peak, about 110 kyr AP, which will find an appropriate climatic state to trigger the next deglaciation.     

New observations on high‐pressure phases in a shock melt vein in the Villalbeto de la Peña meteorite: Insights into the shock behavior of diopside

The petrology and mineralogy of shock melt veins in the L6 ordinary chondrite host of Villalbeto de la Peña, a highly shocked, L chondrite polymict breccia, have been investigated in detail using scanning electron microscopy, transmission electron microscopy, Raman spectroscopy, and electron probe microanalysis. Entrained olivine, enstatite, diopside, and plagioclase are transformed into ringwoodite, low‐Ca majorite, high‐Ca majorite, and an assemblage of jadeite‐lingunite, respectively, in several shock melt veins and pockets. We have focused on the shock behavior of diopside in a particularly large shock melt vein (10 mm long and up to 4 mm wide) in order to provide additional insights into its high‐pressure polymorphic phase transformation mechanisms. We report the first evidence of diopside undergoing shock‐induced melting, and the occurrence of natural Ca‐majorite formed by solid‐state transformation from diopside. Magnesiowüstite has also been found as veins injected into diopside in the form of nanocrystalline grains that crystallized from a melt and also occurs interstitially between majorite‐pyrope grains in the melt‐vein matrix. In addition, we have observed compositional zoning in majorite‐pyrope grains in the matrix of the shock‐melt vein, which has not been described previously in any shocked meteorite. Collectively, all these different lines of evidence are suggestive of a major shock event with high cooling rates. The minimum peak shock conditions are difficult to constrain, because of the uncertainties in applying experimentally determined high‐pressure phase equilibria to complex natural systems. However, our results suggest that conditions between 16 and 28 GPa and 2000–2200 °C were reached.     

Salt tectonics in a double salt‐source layer setting (Eastern Persian Gulf,Iran): Insights from interpretation of seismic profiles and sequential cross‐section restoration

Salt tectonics in the Eastern Persian Gulf (Iran) is linked to a unique salt‐bearing system involving two overlapping ‘autochthonous’ mobile source layers, the Ediacaran–Early Cambrian Hormuz Salt and the Late Oligocene–Early Miocene Fars Salt. Interpretations of reflection seismic profiles and sequential cross‐section restorations are presented to decipher the evolution of salt structures from the two source layers and their kinematic interaction on the style of salt flow. Seismic interpretations illustrate that the Hormuz and Fars salts started flowing in the Early Palaeozoic (likely Cambrian) and Early Miocene, respectively, shortly after their deposition. Differential sedimentary loading (downbuilding) and subsalt basement faults initiated and localized the flow of the Hormuz Salt and the related salt structures. The resultant diapirs grew by passive diapirism until Late Cretaceous, whereas the pillows became inactive during the Mesozoic after a progressive decline of growth in the Late Palaeozoic. The diapirs and pillows were then subjected to a Palaeocene–Eocene contractional deformation event, which squeezed the diapirs. The consequence was significant salt extrusion, leading to the development of allochthonous salt sheets and wings. Subsequent rise of the Hormuz Salt occurred in wider salt stocks and secondary salt walls by coeval passive diapirism and tectonic shortening since Late Oligocene. Evacuation and diapirism of the Fars Salt was driven mainly by differential sedimentary loading in annular and elongate minibasins overlying the salt and locally by downslope gliding around pre‐existing stocks of the Hormuz Salt. At earlier stages, the Fars Salt flowed not only towards the pre‐existing Hormuz stocks but also away from them to initiate ring‐like salt walls and anticlines around some of the stocks. Subsequently, once primary welds developed around these stocks, the Fars Salt flowed outwards to source the peripheral salt walls. Our results reveal that evolving pre‐existing salt structures from an older source layer have triggered the flow of a younger salt layer and controlled the resulting salt structures. This interaction complicates the flow direction of the younger salt layer, the geometry and spatial distribution of its structures, as well as minibasin depocentre migration through time. Even though dealing with a unique case of two ‘autochthonous’ mobile salt layers, this work may also provide constraints on our understanding of the kinematics of salt flow and diapirism in other salt basins having significant ‘allochthonous’ salt that is coevally affected by deformation of the deeper autochthonous salt layer and related structures.     

A comparative study of the modelling of cement hydration and cement-rock laboratory experiments

The use of cement and concrete as fracture grouting or as tunnel seals in a geological disposal facility for radioactive wastes creates potential issues concerning chemical reactivity. From a long-term safety perspective, it is desirable to be able model these interactions and changes quantitatively. The ‘Long-term Cement Studies’ (LCS) project was formulated with an emphasis on in situ field experiments with more realistic boundary conditions and longer time scales compared with former experiments. As part of the project programme, a modelling inter-comparison has been conducted, involving the modelling of two experiments describing cement hydration on one hand and cement-rock reaction on the other, with teams representing the NDA (UK), Posiva (Finland), and JAEA (Japan).This modelling exercise showed that the dominant reaction pathways in the two experiments are fairly well understood and are consistent between the different modelling teams, although significant differences existed amongst the precise parameterisation (e.g. reactive surface areas, dependences of rate upon pH, types of secondary minerals), and in some instances, processes (e.g. partition of alkali elements between solids and liquid during cement hydration; kinetic models of cement hydration). It was not conclusive if certain processes such as surface complexation (preferred by some modellers, but not by others) played a role in the cement-rock experiment or not. These processes appear to be more relevant at early times in the experiment and the evolution at longer timescales was not affected. The observed permeability profile with time could not be matched. The fact that no secondary minerals could be observed and that the precipitated mass calculated during the simulations is minor might suggest that the permeability reduction does not have a chemical origin, although a small amount of precipitates at pore throats could have a large impact on permeability.The modelling exercises showed that there is an interest in keeping the numerical models as simple as possible and trying to obtain a reasonable fit with a minimum of processes, minerals and parameters. However, up-scaling processes and model parameterisation to the timescales appropriate to repository safety assessment are of considerable concern. Future modelling exercises of this type should focus on a suitable natural or industrial analogue that might aid assessing mineral-fluid reactions at these longer timescales.     

Occurrence and fate of polycyclic aromatic hydrocarbons in the coastal surface microlayer

Polycyclic aromatic hydrocarbons (PAHs) were measured in the coastal sea surface microlayer (SML), the sub-surface waters (SSW) and the overlying atmosphere in order to investigate the influence of the SML on contaminant enrichment and air-sea exchange. Samples were collected at two contrasting locations of the NW Mediterranean, one urban influenced (off Barcelona, Spain) and another comparatively clean (off Banyuls-sur-Mer, France). Statistical data analysis confirmed the accumulation of PAHs in the SML with respect to the SSW (20.3+/-9.1 vs. 13.1+/-10.0 ng L(-1) in the dissolved phase; 709+/-207 vs. 158+/-111 ng g(-1) in the particulate phase). This accumulation was higher at the contaminated location (Barcelona station) compared with the more pristine one, with PAH enrichments 1.5 and 4.5 times higher for the dissolved and particulate phases, respectively, indicating that the enrichment of PAHs in the SML is dominated by particle transport processes.