ESR dating of fluvial quartz: Estimate of the minimal distance transport required for getting a maximum optical bleaching

An ESR experimental study of artificial optical bleaching of sedimentary quartz has shown that the aluminum center was maximally bleached after a 6-month illumination equivalent to natural light. This duration seems too long to apply in natural conditions. Nevertheless, the measurement of the ESR intensity of aluminum centers in quartz extracted from modern sediments and deposited in sandy bars shows that the maximum bleaching has effectively been reached.

In order to determine the relationship between the bleaching and the distance covered by a quartz grain in a river, samples were collected along the Creuse River (France) from its spring to about 170 km downstream, where maximum bleaching levels were observed in previous studies. The ESR intensities of the aluminum and titanium centers in quartz were measured, using X-band spectroscopy, before and after artificial bleaching. The difference measured between these sub-samples shows that the maximum bleaching level is obtained in the course of the first kilometer. Hence, the assumption that ESR dating of fluvial sediment is based on the optical bleaching was validated.     

Topographic effects on solitary Rossby waves

The model for baroclinic solitary waves previously described by Flierl is developed to include effects of bottom variations.Topographic disturbances are shown to act, through their first and second derivatives, on both the phase speed correction and the maximum horizontal amplitude.The combined effects of mean shear flow steepening and bottom variations are considered; an equation is derived, showing the relative importance of each effect.     

Oscillations in a simple air-water system driven by a stabilizing heat flux

An air-water system coupled by heat and stress is modelled by two interacting fluid loops. When heated from above and cooled from below the system can become unstable and self-sustained oscillations develop, whereas a single fluid system is stable in the same situation. The oscillations are explained by thermal lag between the loops. The water loop oscillates stably under its restoring buoyancy torque but the coresponding air oscillations, generated by heat conduction from the water loop, lag by roughly half a period, and the air stress therefore acts to amplify rather than damp oscillations in the water loop.     

The NdSr isotopic correlation in mantle materials and geodynamic consequences

The neodymium-strontium isotopic correlation observed in most of the Earth mantle materials is evaluated by means of direct modelling. Several geochemical models are quantitatively developed to explain the observations. The main results of this modelling are that such a correlation is not geochemically trivial and that it corresponds to specific conditions in chemical fractionation. These specific conditions seem to be satisfied by solid-liquid partitioning in magmatic conditions. The discussion of the experimental data supports a continuous convecting-magmatic fractionation model for a large proportion of the mantle.     

Neodymium and strontium isotope study of ophiolite and orogenic lherzolite petrogenesis

Neodymium isotopic analyses have been measured on nine ophiolites and four orogenic lherzolites. ε_Nd varies from +12 to +3 in the ophiolites and from +18 to +2 in the orogenic lherzolites. The majority of the analyses plot on a ε_Nd-ε_Sr correlation line as defined by Nd and Sr isotopic analyses of oceanic basalts. However, certain ophiolitic and lherzolitic samples exhibit high⁸⁷Sr/⁸⁶Sr ratios and as such lie to the right of the correlation line towards seawater compositions.From these data one can postulate several origins for ophiolites including that of mid-ocean ridges and ocean islands. If the orogenic lherzolites are interpreted as representative of the mantle occurring below active ridges a more complex model is required involving mantle heterogeneity and multi-episodic chemical fractionation starting prior to 2 Ga ago.     

Low-degree partial melting trends recorded in upper mantle minerals

The study of glass inclusions inside mantle minerals provides direct information about the chemistry of naturally occurring mantle-derived melts and the fine-scale complexity of the melting process responsible for their genesis. Minerals in a spinel lherzolite nodule from Grande Comore island contain glass inclusions which, after homogenization by heating, exhibit a continuous suite of chemical compositions clearly distinct from that of the host basanitic lava. The compositions range from silicic, with nepheline–olivine normative, 64 wt% SiO₂ and 11 wt% alkali oxides, to almost basaltic, with quartz normative, 50 wt% SiO₂ and 1–2 wt% alkali oxides. Within a single mineral phase, olivine, the inferred primary melt composition varies from 54 to 64 wt% SiO₂ for MgO content ranging from 8 to 0.8 wt%. An experimental study of the glass and fluid inclusions indicates that trapped melts represent liquids that are in equilibrium with their host phases at moderate temperature and pressure (T≈1230°C and P≈1.0 Gpa for melts trapped in olivine). Quantitative modelling of the compositional trends defined in the suite shows that all of the glasses are part of a cogenetic set of melts formed by fractional melting of spinel lherzolite, with F varying between 0.2 and 5%. The initial highly silicic, alkali-rich melts preserved in Mg-rich olivine become richer in FeO, MgO, CaO and Cr₂O₃ and poorer in SiO₂, K₂O, Na₂O, Al₂O₃ and Cl with increasing melt fractions, evolving toward the basaltic melts found in clinopyroxene. These results confirm the connection between glass inclusions inside mantle minerals and partial mantle melts, and indicate that primary melts with SiO₂ >60 wt%, alkali oxides >11%, FeO <1 wt% and MgO <1 wt% are generated during incipient melting of spinel peridotite. The composition of the primary melts is inferred to be dependent on pressure, and to reflect both the speciation of dissolved CO₂ and the effect of alkali oxides on the silica activity coefficient in the melt. At pressures around 1 GPa, low-degree melts are characterized by alkali and silica-rich compositions, with a limited effect of dissolved CO₂ and a decreased silica activity coefficient caused by the presence of alkali oxides, whereas at higher pressures alkali oxides form complexes with carbonates and, consequently, alkali-rich silica-poor melts will be generated.     

Perspectives on present-day sea level change: a tribute to Christian le Provost

In this paper, we first discuss the controversial result of the work by Cabanes et al. (Science 294:840–842, 2001), who suggested that the rate of past century sea level rise may have been overestimated, considering the limited and heterogeneous location of historical tide gauges and the high regional variability of thermal expansion which was supposed to dominate the observed sea level. If correct, this conclusion would have solved the problem raised by the IPCC third assessment report [Church et al, Cambridge University Press, Cambridge, pp 881, 2001], namely, the factor two difference between the 20th century observed sea level rise and the computed climatic contributions. However, recent investigations based on new ocean temperature data sets indicate that thermal expansion only explains part (about 0.4 mm/year) of the 1.8 mm/year observed sea level rise of the past few decades. In fact, the Cabanes et al.’s conclusion was incorrect due to a contamination of abnormally high ocean temperature data in the Gulf Stream area that led to an overestimate of thermal expansion in this region. In this paper, we also estimate thermal expansion over the last decade (1993–2003), using a new ocean temperature and salinity database. We compare our result with three other estimates, two being based on global gridded data sets, and one based on an approach similar to that developed here. It is found that the mean rate of thermosteric sea level rise over the past decade is 1.5±0.3 mm/year, i.e. 50% of the observed 3 mm/year by satellite altimetry. For both time spans, past few decades and last decade, a contribution of 1.4 mm/year is not explained by thermal expansion, thus needs to be of water mass origin. Direct estimates of land ice melt for the recent years account for about 1 mm/year sea level rise. Thus, at least for the last decade, we have moved closer to explaining the observed rate of sea level rise than the IPCC third assessment report.     

Relations entre déformation et métamorphisme alpin dans les schistes noirs helvétiques : l’apport de la fabrique magnétique

Résumé

La fabrique magnétique des schistes noirs du Jurassique helvétique au pourtour des massifs de l’Aar et du Gothard (Alpes suisses) reflète, en fonction du métamorphisme croissant, l’orientation préférentielle de minéraux magnétiques d’origines diverses : la magnétite primaire, les phyllosilicates et la pyrrhotite métamorphiques. La foliation magnétique est parallèle à la première schistosité pénétrative même si celle-ci est effacée par une seconde schistosité. La linéation magnétique indique retirement lié à la direction de transport des nappes. Dans la partie la plus métamorphique où apparaît la pyrrhotite au cours de la déformation, la fabrique magnétique permet de situer l’apparition de ce minéral dans la tectonique polyphasée. Les propriétés magnétiques anisotropes de la pyrrhotite s’avèrent plus complexes que le modèle usuel de marqueurs planaires et l’interprétation des linéations observées doit en tenir compte.     

Bioaccumulation et elimination du 65Zn par Gammarus aequicauda martimov

Uptake of ⁶⁵Zn by Gammarus aequicauda results in a concentration factor of approximately 50 and it is characterised by a maximal accumulation level attained as early as the third day of the experiment. After ingestion by the gammarids of twenty contaminated meals which are distributed over a 45-day period, a transfer of ⁶⁵Zn between the food and the consumer can be observed but there is no sign of the biomagnification phenomenon. The retention rate of the radionuclide is only about 1·5% and the ⁶⁵Zn concentration in the gammarids remains markedly inferior to that of the ingested food.The elimination of the ⁶⁵Zn fixed directly from water takes place according to an exponential model which corresponds to the existence of three biological half-lives of the radionuclide, $\text{Tb}{}_1\text{? 0·5 day, Tb}{}_2\text{? 3·5 days and Tb}{}_3\text{? days}$. The excretion of ⁶⁵Zn accumulated from food is a simple exponential phenomenon which corresponds to only one biological half-life of approximately 17 days.