A Reflection on Mg, Cd, Ca, Li and Si Isotopic Measurements and Related Reference Materials

This contribution aims to report the reflections we had with the scientific community during two international workshops on reference materials for stable isotopes in Davos (2002) and Nice (2003). After evaluating the isotopic homogeneity of some existing reference materials, based on either certificates, literature data or specific inter-laboratory rounds, we confirm these as primary reference materials or propose new ones relative to which stable isotope compositions should be reported. We propose DSM-3 for Mg, NIST SRM 915a for Ca, L-SVEC for Li and NBS28 for Si. Cadmium does not yet have a well identified delta zero material, although three commercial mono-elemental Cd solutions have yielded the same isotopic composition relative to one another. In order to scale the linearity of any mass spectrometer, some secondary reference materials are also proposed: Cambridge-1 solution for Mg, the "Münster-Cd" and JEPPIM Cd solutions for Cd and the "Big Batch" silicate for Si. The team from Nancy propose to prepare a mixed spike solution for Li isotopes. Well-characterised natural samples such as ocean or continental waters, diatoms, sponges, rocks and minerals are needed to validate the entire analytical procedure, particularly to take into account the effect of sample mineralisation and of chemical manipulations for elemental separation prior to analysis.     

Eocene-Pliocene time scale and stratigraphy of the Upper Rhine Graben (URG) and the Swiss Molasse Basin (SMB)

We present a general stratigraphic synthesis for the Upper Rhine Graben (URG) and the Swiss Molasse Basin (SMB) from Eocene to Pliocene times. The stratigraphic data were compiled both from literature and from research carried out by the authors during the past 6 years ; an index of the stratigraphically most important localitites is provided. We distinguish 14 geographical areas from the Helvetic domain in the South to the Hanau Basin in the North. For each geographical area, we give a synthesis of the biostratigraphy, lithofacies, and chronostratigraphic ranges. The relationships between this stratigraphic record and the global sea-level changes are generally disturbed by the geodynamic (e.g., subsidence) evolution of the basins. However, global sea-level changes probably affected the dynamic of transgression–regression in the URG (e.g., Middle Pechelbronn Beds and Serie Grise corresponding with sea-level rise between Ru1/Ru2 and Ru2/Ru3 sequences, respectively) as well as in the Molasse basin (regression of the UMM corresponding with the sea-level drop at the Ch1 sequence). The URGENT-project (Upper Rhine Graben evolution and neotectonics) provided an unique opportunity to carry out and present this synthesis. Discussions with scientists addressing sedimentology, tectonics, geophysics and geochemistry permitted the comparison of the sedimentary history and stratigraphy of the basin with processes controlling its geodynamic evolution. Data presented here back up the palaeogeographic reconstructions presented in a companion paper by the same authors (see Berger et al. in Int J Earth Sci 2005).     

Performance results of HESP physical model

As a continuation to the published work on model based calibration technique with HESP(Hanle Echelle Spectrograph) as a case study, in this paper we present the performance results of the technique. We also describe how the open parameters were chosen in the model for optimization, the glass data accuracy and handling the discrepancies. It is observed through simulations that the discrepancies in glass data can be identified but not quantifiable. So having an accurate glass data is important which is possible to obtain from the glass manufacturers. The model’s performance in various aspects is presented using the ThAr calibration frames from HESP during its pre-shipment tests. Accuracy of model predictions and its wave length calibration comparison with conventional empirical fitting, the behaviour of open parameters in optimization, model’s ability to track instrumental drifts in the spectrum and the double fibres performance were discussed. It is observed that the optimized model is able to predict to a high accuracy the drifts in the spectrum from environmental fluctuations. It is also observed that the pattern in the spectral drifts across the 2D spectrum which vary from image to image is predictable with the optimized model. We will also discuss the possible science cases where the model can contribute.     

Microstructure modifications of silicates induced by the collection in aerogel: Experimental approach and comparison with Stardust results

Abstract– Particles from comet 81P/Wild 2 were captured with silica aerogel during the flyby Stardust mission. A significant part of the collection was damaged during the impact at hypervelocity in the aerogel. In this study, we conducted impact experiments into aerogel of olivine and pyroxene powder using a light‐gas gun in similar conditions as that of the comet Wild 2 particles collection. The shot samples were investigated using transmission electron microscopy to characterize their microstructure. Both olivine and pyroxene samples show evidence of thermal alteration due to friction with the aerogel. All the grains have rounded edges after collection, whereas their shape was angular in the initial shot powder set. This is probably associated with mass loss of particles. The rims of the grains are clearly melted and mixed with aerogel. The core of olivine grains is fairly well preserved, but some grains contain dislocations in glide configuration. We interpret these dislocations as generated by the thermal stresses that have emerged due to the high temperature gradients between the core and the rim of the grains. Most of the pyroxene grains have been fully melted. Their high silica concentration reflects a strong impregnation with melted aerogel. The preferential melting of pyroxene compared with olivine is due to a difference in melting temperatures of 300°. This melting point difference probably induces a bias in the measurements of the ratio olivine/pyroxene in the Wild 2 comet. The proportion of pyroxene was probably higher on Wild 2 than expected from the samples collected into aerogel.     

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.