Éditeur(s) : Pergamon-elsevier Science Ltd
Résumé : We report rare earth element (REE) and neodymium (Nd) isotope data for the organic fraction of sediments collected from various depositional environments, i.e. rivers (n=25), estuaries (n=18), open-ocean settings (n=15), and cold seeps (n=12). Sedimentary Organic Matter (SOM) was extracted using a mixed hydrogen peroxide/nitric acid solution (20%-H2O2 – 0.02M-HNO3), after removal of carbonate and oxy-hydroxide phases with dilute hydrochloric acid (0.25M-HCl). A series of experimental tests indicate that extraction of sedimentary organic compounds using H202 may be complicated occasionally by partial dissolution of sulphide minerals and residual carbonates. However, this contamination is expected to be minor for REE because measured concentrations in H2O2 leachates are about two-orders of magnitude higher than in the above mentioned phases. The mean REE concentrations determined in the H2O2 leachates for samples from rivers, estuaries, coastal seas and open-ocean settings yield relatively similar levels, with ΣREE = 109 ± 86 ppm (mean ± s; n=58). The organic fractions leached from cold seep sediments display even higher concentration levels (285 ± 150 ppm; mean ± s; n=12). The H2O2 leachates for most sediments exhibit remarkably similar shale-normalized REE patterns, all characterized by a mid-REE enrichment compared to the other REE. This suggests that the distribution of REE in leached sedimentary organic phases is controlled primarily by biogeochemical processes, rather than by the composition of the source from which they derive (e.g. pore, river or sea- water). The Nd isotopic compositions for organic phases leached from river sediments are very similar to those for the corresponding detrital fractions. In contrast, the SOM extracted from marine sediments display εNd values that typically range between the εNd signatures for terrestrial organic matter (inferred from the analysis of the sedimentary detrital fractions) and marine organic matter (inferred from the analysis of local surface seawater). A notable exception is the case of organic matter (OM) fractions leached from cold seep sediment samples, which sometimes exhibit εNd values markedly different from both terrigenous and surface seawater signatures. This suggests that a significant fraction of organic compounds in these sediments may be derived from chemosynthetic processes, recycling pore water REE characterized by a distinct isotopic composition. Overall, our results confirm that organic matter probably plays an important role in the oceanic REE budget, through direct scavenging and remineralization within the water column. Both the high REE abundances and the shape of shale-normalized patterns for leached SOM also suggest that OM degradation in sub-surface marine sediments during early diagenesis could control, to a large extent, the distribution of REE in pore waters. Benthic fluxes of organic-bound REE could hence substantially contribute to the exchange processes between particulates and seawater that take place at ocean margins. Neodymium isotopes could provide useful information for tracing the origin (terrestrial versus marine) and geographical provenance of organic matter, with potential applications in paleoceanography. In particular, future studies should further investigate the potential of Nd isotopes in organic compounds preserved in sedimentary records for reconstructing past variations of surface ocean circulation.
Geochimica Et Cosmochimica Acta (0016-7037) (Pergamon-elsevier Science Ltd), 2014-09 , Vol. 140 , P. 177-198

Droits : 2014 Elsevier Ltd. All rights reserved.
http://archimer.ifremer.fr/doc/00191/30250/28682.pdf
DOI:10.1016/j.gca.2014.05.016
http://archimer.ifremer.fr/doc/00191/30250/

Éditeur(s) : HAL CCSD Elsevier
Résumé : International audience
Tsavorite, the vanadian variety of green grossular, is a high value economic gemstone. It is hosted exclusively in the metasedimentary formations from the Neoproterozoic Metamorphic Mozambique Belt. The deposits are mined in Kenya, Tanzania and Madagascar and other occurrences are located in Pakistan and East Antarctica. They are located within metasomatized graphitic rocks such as graphitic gneiss and calc-silicates, intercalated with meta-evaporites. Tsavorite is found as primary deposits either in nodule (type I) or in quartz vein (type II), and in placers (type III). The primary mineralizations (types I and II) are controlled by lithostratigraphy and/or structure. For the African occurrences, the protoliths of the host-rocks were deposited at the beginning of the Neoproterozoic within a marine coastal sabkha environment, located at the margin of the Congo-Kalahari cratons in the Mozambique Ocean. During the East African-Antarctican Orogeny, the rocks underwent high amphibolite to granulite facies metamorphism and the formation of tsavorite deposits occurred between 650 and 550 Ma. The nodules of tsavorite were formed during prograde metamorphism, calcium coming from sulphates and carbonates, whereas alumina, silicates, vanadium and chromium probably came from clays and chlorite. The veins were formed during the deformation of the metasedimentary platform units which experienced shearing, leading to the formation of fault-filled veins. Metasomatism developed during retrograde metamorphism. The metasedimentary sequences are characterized by the presence of evaporitic minerals such as gypsum and anhydrite, and scapolite. Evaporites are essential as they provide calcium and permit the mobilization of all the chemical elements for tsavorite formation. The H2S-S8 metamorphic fluids characterized in primary fluid inclusions of tsavorites and the δ11B values of coeval dravite confirm the evaporitic origin of the fluids. The V2O3 and Cr2O3 contents of tsavorite range respectively from 0.05 to 7.5 wt.%, while their δ18O values are in the range of 9.5-21.1‰. The genetic model proposed for tsavorite is metamorphic, based on chemical reactions developed between an initial assemblage composed of gypsum and anhydrite, carbonates and organic matter deposited in a sabkha-like sedimentary basin.
ISSN: 0169-1368

hal-00853279
https://hal.archives-ouvertes.fr/hal-00853279
DOI : 10.1016/j.oregeorev.2013.01.016

Éditeur(s) : HAL CCSD
Résumé : International audience
Tin mineralization in Achmmach deposit (NE of Moroccan Central Massif) is associated with tourmaline-rich alteration halos and faults, within N70 shear zones, hosted in sandstones and metapelites of the Upper Visean-Namurian. Such deposits were reported as late-Variscan in age and related to the emplacement of late orogenic granite not outcropping in the studied area.From field constraints, it appears that the late Variscan phase is marked by a transition from transpression to extension with conditions of deformation evolving from ductile to brittle environments. During the transpressive phase (horizontal shortening direction roughly trending E-W), pervasive tourmaline is deposited under the form of metasomatic halos around fractures in the upper levels relative to the deep batholith. This hydrothermal activity is coeval with ductile shear zones within a large corridors trending N70. Tourmaline-rich alteration appears as a hardening stage contributing to the modification of the tectonic style of rocks. Thereafter, a strong brecciation occurs in response of re-using and re-opening of the strike-slip structure. The result is (1) the formation of dextral (N070, N020) and sinistral (N120) shears, and (2) the circulation of fluids within early tourmalinites and formation of tourmaline-rich breccia. Subsequently, during the late orogenic extensional phase, tourmalinite breccias reopened as normal faults acting as overpressure fluid pathways for developing other breccias and veins. Such event is marked by deposition of tin mineralization i.e., cassiterite followed by sulphides, and then fluorite and carbonates at the end.From analysis of the shear-zone structure and superimposition of tourmalines and tin mineralization in the same structures, it is possible to suggest a structural control continuum. Such control is well expressed during metasomatism and deposition of hydrothermal tourmaline under the transpressive phase. Thereafter, under the extensive phase allowing open-space, tin-mineralization were trapped.This study has been supported by AI MA/09/210
24ème RST
Pau, France

insu-01546927
https://hal-insu.archives-ouvertes.fr/insu-01546927

Éditeur(s) : Elsevier
Résumé : A previously unknown pattern of multiple bottom-simulating reflections (BSRs) occurs on high-resolution reflection seismic data in the Danube deep-sea fan, associated with acoustic features indicating free gas. Our study provides evidence that this pattern is developed in relation with the architecture of distinct channel-levee systems of the Danube fan. Channel-levee systems hosting multiple BSRs act as relatively sealed gas-bearing systems whose top is situated above the base of the gas hydrate stability zone (BGHSZ). Inside these systems, free gas accumulates below the BGHSZ under a combined lithological, structural and stratigraphical control. The uppermost BSR marks the current equilibrium BGHSZ, for a gas composition of more than 99% methane. Model-derived depths of the BGHSZ for different gas compositions and pressure-temperature conditions show that multiple BSRs would correspond to the BGHSZ either for (1) layers of gas hydrates with high contents of heavy hydrocarbons or hydrogen sulphide, or (2) stable climatic episodes with temperatures between glacial values and the present-day conditions. As the gas hydrate compositions required by hypothesis (I) are in sharp contradiction with the general background of the gas composition in the study area, we suggest that multiple BSRs are most probably relics of former positions of the BGHSZ, corresponding to successive steps of climate warming. In this case, they can provide sea-bottom paleotemperature values for these episodes, and hence they are potential new proxies for deciphering past climate conditions.
Marine Geology (0025-3227) (Elsevier), 2006-03 , Vol. 227 , N. 3-4 , P. 163-176

Droits : 2006 Elsevier B.V. All rights reserved
http://archimer.ifremer.fr/doc/2006/publication-1210.pdf
DOI:10.1016/j.margeo.2005.12.006
http://archimer.ifremer.fr/doc/00000/1210/

Éditeur(s) : HAL CCSD Elsevier
Résumé : International audience
Type I and Type II eclogite xenoliths from the Roberts Victor kimberlite (South Africa) show marked differences in terms of microstructures, mineralogy, major-and trace-element compositions and oxygen-isotope compositions. The unequilibrated microstructures of Type I eclogites, their typical accessory assemblages (phologopite, diamond, sulphides, fluid inclusions) and the ubiquitous presence of "melt pockets" in garnets provide strong evidence of metasomatism. Type II eclogites systematically lack such features and are microstructurally more equilibrated. Type I eclogites are more magnesium-rich than most Type II (mean Mg# = 0.56 vs. 0.46), while Type II eclogites are generally more Ca-rich (mean CaO = 9 vs. 12 wt%) and Fe-rich (mean FeO = 10 vs. 12 wt%). Type I eclogites are systematically enriched in LREE, Sr, Ba, alkali elements, HFSE, Th and U compared to the more depleted Type II eclogites. Calculated trace-element patterns of fluids in equilibrium with Type I eclogites are closely similar to those of volatile-rich small-volume mantle melts in the carbonatite-kimberlite spectrum commonly inferred to be responsible for mantle metasomatism. Although oxygen isotopes are often used to argue for a subduction origin of mantle eclogites, correlations between delta O-18 of garnet and typical metasomatic tracers suggest that the metasomatic process also has shifted the oxygen-isotope compositions of the Type I eclogites toward heavier values. Roberts Victor Type I eclogites thus carry the imprint of a metasomatic process that strongly modified their major-element, trace-element and isotopic compositions, while the more pristine Type II eclogites escaped this modification. Therefore, attempts to constrain the origin of Roberts Victor eclogites should not be based on the much more abundant Type I eclogites, which retain little geochemical memory of their protoliths. The most suitable materials for such investigations may be the less metasomatised, but more rare, Type II eclogites.
ISSN: 0016-7037

hal-00669867
https://hal.archives-ouvertes.fr/hal-00669867
DOI : 10.1016/j.gca.2011.08.035

Résumé : L’incorporation de sous-produits agricoles ou de matériaux naturels dans la matrice cimentaire confère des propriétés intéressantes aux composites élaborés. L’objectif de cette thèse est d’élaborer un matériau pouvant répondre aux exigences mécaniques, thermiques et de durabilité des matériaux de construction en zone tropicale humide. Dans un premier temps, l’activité pouzzolanique d’une pouzzolane naturelle, de cendres de tronc de bambou et de cendres de bagasse de canne à sucre ont été évaluées. L’influence de leur incorporation a été ensuite étudiée sur les propriétés mécaniques et la durabilité des mortiers exposés à des ions chlorures et sulfates. Dans un second temps, l’influence de l’ajout de fibres de bagasse sur les propriétés thermiques et mécaniques des composites a été étudiée en fonction de différents paramètres (teneur en fibres, environnement de vieillissement, type de matrice cimentaire).Les résultats obtenus ont permis de montrer que les matériaux étudiés possèdent une activité pouzzolanique et qu’il est possible de les incorporer au ciment afin de lutter contre la corrosion. De plus, les composites élaborés avec des fibres de bagasse sont plus isolants que ceux élaborés sans fibres. Cependant, du point de vue des propriétés mécaniques, l’incorporation de fibres de bagasse diminue les contraintes à la flexion des composites.
The incorporation of crop wastes or natural materials in the cement matrix confers interesting properties to composites prepared. The aim of this thesis is to develop a material that can reach the mechanical, thermal and durability requirements for building materials in the humid tropical zone. Firstly, pozzolanic activity of a natural pozzolan, bamboo stem and sugar cane bagasse ashes has been determined. Influence of their incorporation on mechanical properties and durability of mortars exposed to chloride and sulphate ions was studied. Secondly, influence of addition of bagasse fibers on thermal and mechanical properties of composites was studied as a function of various parameters (fibers content, curing, type of cement matrix).These results has shown that the materials studied have pozzolanic activity and it is possible to incorporate them into the cement to fight against corrosion. Moreover, composites elaborated with bagasse fibers are more insulating than those elaborated without fibers. However, from the viewpoint of mechanical properties, incorporation of bagasse fibers decreases flexural strength of composites in the present work and under the conditions producing procedures that were adopted.

http://www.theses.fr/2014AGUY0804/document