Éditeur(s) : HAL CCSD Elsevier
Résumé : Carbon emission at volcanic centers requires a constant balance between output (mostly by volcanism, either at plate boundaries or intraplate) and input (mostly at trench settings) of carbon from and to the Earth's mantle. The form of carbon that resides in the mantle is controlled by depth (pressure) and oxygen fugacity, the latter in turn depending on the depth and the concentration of iron in the mantle. In the shallow, lithospheric mantle, carbon is likely to be present in the oxidized form of CO2 (except under cratons where carbon is reduced to graphite or diamond). Below approximately 90 km, in the asthenosphere, the oxidized form of carbon is carbonate, either mineral or melt, depending on the thermal regime. At depths greater than approximately 150 km, the asthenospheric mantle is too reducing for carbon to stay in its oxidized form and only diamond is present, unless there is sufficient hydrogen to form reduced C–H fluids. Hence, the region located in the depth range of 90 to 150 km deep is where carbonatitic melts can most likely be produced and impregnate the surrounding mantle through metasomatism. The upper bound of this region is called the carbonate ledge. This limit prevents carbonate (either solid or molten) from ascending because of degassing and CO2 liberation. The lower bound is a redox front where redox melting (that is, melting caused by oxidation) may take place in an ascending portion of carbon-containing mantle. Carbonatite eruptions and presence of carbonate mineral inclusions in deep-seated diamonds provide evidence that these boundaries can be trespassed in some cases.An analysis of the experimental data that has bearing on silicate melting in the presence of carbon further shows that the carbonate ledge is a melting curve with a negative or flat Clapeyron (dP/dT) slope. In the carbonated ultrabasic (peridotite) systems, the carbonate ledge is located between ~ 2–3 GPa. The ledge divides the pressure–temperature space into a region of low-pressure silicate melt production, and a high-pressure region where carbonatites can be produced. Carbonatitic melts in equilibrium with mantle peridotite have compositions close to dolomitic (approximately equal amounts of Ca and Mg) with a general trend of becoming markedly more magnesian with increasing pressure. Calcic carbonatites may be stable at pressures < 2 GPa if clinopyroxene is absent. At mantle transition zone pressure range, there seems to be a melting temperature decrease (negative fusion slope), which may be caused by the stabilization of majoritic garnet.The carbonated basic (broadly eclogitic) system is more complex than the peridotitic one, because of the strong control of bulk silicate composition on melting temperatures, and hence, on melt composition. In carbonated eclogite systems, we propose that the effect of bulk composition upon all observed features can perhaps be related to silica super-saturation, or lack thereof. In some cases, high calcium (> 80 mol% CaCO3) melts can be produced, making the melting of carbonated eclogites an appealing scenario for the genesis of calcio-carbonatites in the Earth's mantle. Comparison with modeled pressure–temperature paths of subducted oceanic lithosphere shows that fusion of carbonated eclogite at depths shallower than 200 km should be expected for hot (Cascadian-type) subduction thermal regimes. On the other hand, in the case of cooler thermal regimes (Honshu-type, for instance), subducted carbonates may be stable to greater depths in Earth at trench settings, depending on the bulk composition of the system.Furthermore, high-pressure experiments show evidence of a continuum among carbonatitic, kimberlitic, melilititic, and basaltic liquids, for increasing melting degree of carbonated peridotite. This continuum has not been documented in the case of fusion of carbonated eclogite. It may be present, however, when certain sediments are fused, although the silicate melts are granitic to rhyodacitic instead of being kimberlitic in composition. Additional high-pressure work on phase relations in the simple binary system CaCO3–MgCO3 and specific focus on oxide solubility in the vapor phase have the potential to further clarify phase relations on complex silicate–carbonate systems at mantle conditions.
ISSN: 0009-2541

hal-01277770
https://hal.archives-ouvertes.fr/hal-01277770
DOI : 10.1016/j.chemgeo.2015.05.018

Résumé : Favorisées par les gouvernants en quête d’un nouveau modèle post-industriel, les économies basées sur la connaissance vont devenir en quelques décennies le référentiel à atteindre pour le développement de territoires soumis aux pressions de la globalisation.Longtemps considérés comme des éléments indispensables à la production et à la transmission du savoir, les établissements d’enseignement supérieur et de recherche, comme les universités, ont été de plus en plus intégrés dans les analyses sur le développement territorial à mesure que s’imposait le paradigme américain de la valorisation des activités de la recherche publique. Cette nouvelle mission imposée aux établissements de recherche, suppose qu’ils sont des facteurs d’un développement localisé. Mais le rôle qui leur est assigné est-il justifié ? À travers l’impact singulier de la recherche publique, on peut analyser la place de ces établissements sur leur territoire d’accueil. Apres avoir fait un état de l’art en matière d’analyse d’impact nous utilisons le cadre méthodologique de l’étude d’un cas illustrant cette problématique. L’agglomération de Brest mise sur la forte concentration d’établissements de recherche à vocation maritime pour développer le cluster local. Bien que non généralisable, ce cas éclaire les recherches dans ce domaine. Au-delà, la thèse apporte une autre vision sur les réformes de type top down des systèmes d’enseignement supérieur et de recherche considérant le savoir comme n’importe quel bien économique. Or la connaissance n’est pas un bien comme les autres. Et c’est cette singularité qui explique les difficultés d’analyse dans le champ de l’économie de la connaissance.
Promoted by governments seeking for a new post-industrial model, the knowledge-based economies will become in a few decades the repository to reach for the development of territories subject to the pressures of globalization. Regarded as essential to the production and transmission of knowledge, higher education and research institutions, such as universities, have been increasingly integrated into the analysis of territorial development while was emerging the american paradigm for valorisation of public research activities. This new mission imposed on research institutions, assume they are factors of localized development. Is this assigned role justified? Through the singular impact of public research, we can analyze the role of these institutions on their home territory. After a state of the art on the impact assessments, we developed a methodological framework for case study illustrating this problem. In the agglomeration of Brest, there is a high concentration of research institutions with maritime vocation on which rely the local cluster. Although not generalizable, this case enlightens the research in this domain. In addition, the thesis sheds new light on the top-down reforms of higher education and research systems considering knowledge as any economic good. But knowledge is not a commodity like others. And that would explain the difficulties of analysis in the field of the knowledge economy.

http://www.theses.fr/2014AGUY0807/document

Éditeur(s) : HAL CCSD Elsevier
Résumé : International audience
Quartz is a common crustal mineral that deforms plastically in a wide range of temperatures and pressures, leading to the development of different types of crystallographic preferred orientation (CPO) patterns. In this contribution we present the results of an extensive modeling of quartz fabric transitions via a viscoplastic self-consistent (VPSC) approach. For that, we have performed systematic simulations using different sets of relative critical resolved shear stress of the main quartz slip systems. We have performed these simulations in axial compression and simple shear regimes under constant Von Mises equivalent strain of 100% (γ = 1.73), assuming that the aggregates deformed exclusively by dislocation glide. Some of the predicted CPOs patterns are similar to those observed in naturally and experimentally deformed quartz. Nevertheless, some classical CPO patterns usually interpreted as result from dislocation glide (e.g. Y-maxima due to prism < a > slip) are clearly not developed in the simulated conditions. In addition we reported new potential preferred orientation patterns that might happen in high temperature conditions, both in axial compression and simple shear. We have demonstrated that CPOs generated under axial compression are usually stronger that those predicted under simple shear, due to the continuous rotation observed in the later simulations. The fabric strength depends essentially on the dominant active slip system, and normally the stronger CPOs result from dominant basal slip in < a >, followed by rhomb < a > and prism [c] slip, whereas prism < a > slip does not produce strong fabrics. The opening angle of quartz [0001] fabric used as a proxy of temperature seems to be reliable for deformation temperatures of ~ 400 °C, when the main slip systems have similar behaviors.
ISSN: 0040-1951

hal-01115674
https://hal.archives-ouvertes.fr/hal-01115674
DOI : 10.1016/j.tecto.2014.08.011

Éditeur(s) : Elsevier
Résumé : The combined use of Lu-Hf and Sm-Nd isotope systems potentially offers a unique perspective for investigating continental erosion, but little is known about whether, and to what extent, the Hf-Nd isotope composition of sediments is related to silicate weathering intensity. In this study, Hf and Nd elemental and isotope data are reported for marine muds, leached Fe-oxide fractions and zircon-rich turbidite sands collected off the Congo River mouth, and from other parts of the SE Atlantic Ocean. All studied samples from the Congo fan (muds, Fe-hydroxides, sands) exhibit indistinguishable Nd isotopic composition (epsilon(Nd)similar to - 16), indicating that Fe-hydroxides leached from these sediments correspond to continental oxides precipitated within the Congo basin. In marked contrast, Hf isotope compositions for the same samples exhibit significant variations. Leached Fe-hydroxide fractions are characterized by epsilon(Hf) values (from -1.1 to +13) far more radiogenic than associated sediments (from -7.1 to -12.0) and turbidite sands (from -27.2 to -31.6). epsilon(Hf) values for Congo fan sediments correlate very well with Al/K (i.e. a well-known index for the intensity of chemical weathering in Central Africa). Taken together, these results indicate that (1) silicate weathering on continents leads to erosion products having very distinctive Hf isotope signatures, and (2) a direct relationship exists between epsilon(Hf) of secondary clay minerals and chemical weathering intensity. These results combined with data from the literature have global implications for understanding the Hf-Nd isotope variability in marine precipitates and sediments. Leached Fe-hydroxides from Congo fan sediments plot remarkably well on an extension of the 'seawater array' (i.e. the correlation defined by deep-sea Fe-Mn precipitates), providing additional support to the suggestion that the ocean Hf budget is dominated by continental inputs. Fine-grained sediments define a diffuse trend, between that for igneous rocks and the,seawater array', which we refer to as the 'zircon-free sediment array' (epsilon(Hf)=0-91 epsilon(Nd)+3.10). Finally, we show that the Hf-Nd arrays for seawater, unweathered igneous rocks, zircon-free and zircon-bearing sediments (epsilon(Hf)= 1.80 epsilon(Nd)+2.35) can all be reconciled, using Monte Carlo simulations, with a simple weathering model of the continental crust. (C) 2008 Elsevier B.V. All rights reserved.
Earth and Planetary Science Letters (0012-821X) (Elsevier), 2009 , Vol. 277 , N. 3-4 , P. 318-326

Droits : 2009 Elsevier B.V. All rights reserved.
http://archimer.ifremer.fr/doc/2009/publication-6451.pdf
DOI:10.1016/j.epsl.2008.10.028
http://archimer.ifremer.fr/doc/00000/6451/