Mineral compositions in Antarctic and Greenland micrometeorites

Abstract— The mineral compositions of 250 micrometeorites have been studied and olivines and low-calcium pyroxenes with crystals larger than 5 μm have been analyzed. While magnesium-rich grains dominate, the Fa content of olivine may reach 50% and the Fs content of pyroxene may reach 26%. The Ca and Mn of the olivine show no consistent trends with increasing Fe, but Cr shows a negative correlation. For low-Ca pyroxene, Al and Cr contents are generally higher than in pyroxenes of equilibrated chondrites but similar to those of highly unequilibrated chondrites. Calcium-bearing pyroxene, feldspar and chromite are rare in the micrometeorites which were selected because of their high Mg, Si, Fe and their low Ca and Al content. All these minerals are found as coarse-grained particles often with adhering iron-rich scoria or as clasts in fine-grained or scoriaceous micrometeorites. Apart from a few particles which could be the debris of ordinary chondrites, most micrometeorites probably come from a common source similar, but not identical to carbonaceous chondrites, as shown by their lower Ni and S content and their different oxygen isotopic composition assuming two measurements performed on olivine grains prove to be typical.     

Occurrence of noble metals in aluminum- and chromium- rich objects in ordinary chondrites and of baddeleyite (ZrO2) in a chromite inclusion

Abstract— Platinum group elements (PGE) enrichments are found in Fe-Ni blebs (<1 μm) in Al- and Cr-rich objects in the ordinary chondrites Ste. Marguerite, Forest Vale, Montferré. In Ste. Marguerite, high ZrO₂ concentrations (baddeleyite) are also present in a chromite inclusion. Iridium enrichment in this material compared to its metal content is confirmed by INAA. The widespread occurrence of PGE in Al- and Cr-rich objects, mostly present in H-group chondrites of nearly equilibrated types, must be taken into account to understand their conditions of formation.     

Dahmani,a highly oxidised LL6 chondrite bearing Ni-rich taenite

Abstract Dahmani is a shocked LL6 fragmental breccia. According to the composition of the silicates (olivine Fa_30,32.6, orthopyroxene Fs_24.5–26.3) and of the metal (a 60% Ni taenite) it is one of the most oxidised known.     

Geochemical and hydrodynamic constraints on the distribution of trace metal concentrations in the lagoon of Nouméa, New Caledonia

Seawater samples were collected in the lagoon of Nouméa (southwest New Caledonia) along two transects from eutrophic coastal bays to the oligotrophic barrier reef. Land-based emissions to the lagoon were measured with dissolved and particulate concentrations of chromium (Cr) and nickel (Ni), used as tracers of both terrigenous and industrial (Ni ore treatment) activities, as well as dissolved and particulate concentrations of zinc (Zn), used as a tracer of urban effluents. The spatial variability of metal concentrations was related to geochemical and hydrodynamic conditions, i.e., respectively: (1) natural and anthropogenic emission sources, and chemical processes occurring in the water column; and (2) water residence times. The parameter used to describe the residence time of water masses was the local e-flushing time, i.e. the time required for a tracer mass contained within a given station to be reduced by a factor 1/e. High metal concentrations were found in coastal areas (up to 9000 ng dissolved Ni L⁻¹), and steeply decreased with distance from the coast (down to 101 ng dissolved Ni L⁻¹ near the barrier reef) to reach levels similar to those found in remote Pacific waters, suggesting a rapid renewal of waters close to the barrier. Distributions of metals in the lagoon are controlled upstream by land-based emission sources and later chemical processes. Then hydrodynamics constrain metal distributions, as shown by the observed relationship between local e-flushing times and the spatial variability of metal concentrations. In addition, a change in the direction of prevailing winds yielded a decrease of dissolved metal concentrations at the same site by a factor of 2.5 (Cr and Ni) and 2.9 (Zn). It is suggested that the residence time is a key parameter in the control of elemental concentrations in the lagoon waters, as much as land-based emission sources.     

Mid-Holocene emergence of southern Tunisian coasts

We present new sea-level data from the coasts of southern Tunisia, between the Gulf of Gabès and the Libyan border. The work tests, previously, published evidence on Holocene shorelines, and confirmed that a distinct emergence has occurred in this area during this time. The emergence peak lies at least 186 ± 11 cm above present and is inferred from: (1) AMS radiocarbon dates of subtidal vermetids and boring shells collected in growth position, and (2) careful assessment of tidal heights. Maximum emergence took place between about 6000 and 5000 ¹⁴C years BP; it cannot be ascribed to tectonics and is probably related to post-glacial hydro-isostatic effects. It challenges the inference of a 3-m global sea-level rise since 6000 years BP due to residual Antarctic melting.     

Hazard appraisal and hazard-zone mapping of flooding and debris flowage in the Rio Combeima valley and Ibague city,Tolima Department,Colombia

Since a state law issued in 1989, every big town in Colombia has to promote its own preparedness programme for disaster relief in the framework of the Oficina Nacional para la Atencion de Desastres (1987). Such a programme includes a very detailed hazard-zone map for flooding and debris flows in the densely inhabited suburbs of Ibagué city (capital of Tolima Department), as well as enquiries about risk knowledge and consciousness among people who live at high risk. We stress the fact that both detailed hazard-zone maps and enquiries should be closely undertaken at the same time, and that distinguishing previous knowledge, existing consciousness and risk perception to forecast the behaviour of people and of the community in case of disaster, are criteria for a better risk assessment.     

On the role of heat flow, lithosphere thickness and lithosphere density on gravitational potential stresses

Gravitational potential stresses (GPSt) are known to play a first-order role in the state of stress of the Earth's lithosphere. Previous studies focussed mainly on crust elevation and structure and little attention has been paid to modelling GPSt using realistic lithospheric structures. The aim of the present contribution is to quantify gravitational potential energies and stresses associated with stable lithospheric domains. In order to model realistic lithosphere structures, a wide variety of data are considered: surface heat flow, chemical depletion of mantle lithosphere, crustal thickness and elevation. A numerical method is presented which involves classical steady-state heat equations to derive lithosphere thickness, geotherm and density distribution, but additionally requires the studied lithosphere to be isostatically compensated at its base. The impact of varying surface and crustal heat flow, topography, Moho depth and crust density on the signs and magnitudes of predicted GPSt is systematically explored. In clear contrast with what is assumed in most previous studies, modelling results show that the density structure of the mantle lithosphere has a significant impact on the value of the predicted GPSt, in particular in the case of thick lithospheres. Using independent information from the literature, the method was applied to get insights in the state of stress of continental domains with contrasting tectono-thermal ages. The modelling results suggest that in the absence of tectonic stresses Phanerozoic and Proterozoic lithospheres are spontaneously submitted to compression whereas Archean lithospheres are in a neutral to slightly tensile stress state. These findings are in general in good agreement with global stress measurements and observed geoid undulations.     

L'archivage des activités humaines par les neiges et glaces polaires : le cas du plomb

The investigation of the occurrence of lead in dated snow and ice from Greenland and Antarctica has played a major role in our understanding of the history of the pollution of the atmosphere of our planet by this metal. Such studies have however proved to be very demanding, mainly because of the extreme purity of polar snow and ice. Reliable measurements can be obtained only if ultra-clean and highly sensitive procedures are used, as pioneered by Clair Patterson. The Greenland data show evidence of large-scale pollution of the atmosphere of the Northern Hemisphere for lead as early as two millennia ago during Greco–Roman times, especially because of mining and smelting activities in southern Spain. It peaked at the end of the 1960s, with lead concentrations in snow about 200 times higher than natural values, before declining during recent times because of the fall in the use of leaded gasoline. Lead pollution in Antarctica was already significant at the end of the 19th century as a consequence of whaling activities, the traffic of coal-powered ships crossing the Cape Horn, and mining activities in South America, South Africa and Australia. After declining because of the opening of the Panama Canal, the great economic depression and World War II, it reached a maximum during the 1980s, with lead concentrations 20 times higher than natural values. Other studies focus on past natural variations of lead in ancient ice dated from the last climatic cycles. To cite this article: C. Boutron et al., C. R. Geoscience 336 (2004).     

A Compilation of Silicon,Rare Earth Element and Twenty‐One other Trace Element Concentrations in the Natural River Water Reference Material SLRS‐5 (NRC‐CNRC)

The natural river water certified reference material SLRS‐5 (NRC‐CNRC) was routinely analysed in this study for major and trace elements by ten French laboratories. Most of the measurements were made using ICP‐MS. Because no certified values are assigned by NRC‐CNRC for silicon and 35 trace element concentrations (rare earth elements, Ag, B, Bi, Cs, Ga, Ge, Li, Nb, P, Rb, Rh, Re, S, Sc, Sn, Th, Ti, Tl, W, Y and Zr), or for isotopic ratios, we provide a compilation of the concentrations and related uncertainties obtained by the participating laboratories. Strontium isotopic ratios are also given.