Éditeur(s) : HAL CCSD Elsevier
Résumé : International audience
Most peridotite massifs and mantle xenoliths show a wide range of isotopic variations, often involving significant decoupling between Hf, Nd and Sr isotopes. These variations are generally ascribed either to mingling of individual components of contrasted isotopic compositions or to time integration of parent-element enrichment by percolating melts/fluids, superimposed onto previous depletion event(s). However, strong isotopic decoupling may also arise during porous flow as a result of daughter-elements fractionation during solid-liquid interaction. Although porous flow is recognized as an important process in mantle rocks, its effects on mantle isotopic variability have been barely investigated so far. The peridotites of the Lherz massif (French Pyrenees) display a frozen melt percolation front separating highly refractory harzburgites from refertilized lherzolites. Isotopic signatures observed at the melt percolation front show a strong decoupling of Hf from Nd and Sr isotopes that cannot be accounted for by simple mixing involving the harzburgite protolith and the percolating melt. Using one dimensional percolation-diffusion and percolation-reaction modeling, we show that these signatures represent transient isotopic compositions generated by porous flow. These signatures are governed by a few critical parameters such as daughter element concentrations in melt and peridotite, element diffusivity, and efficiency of isotopic homogenization rather than by the chromatographic effect of melt transport and the refertilization reaction. Subtle variations in these parameters may generate significant inter-isotopic decoupling and wide isotopic variations in mantle rocks. (C) 2009 Elsevier B.V. All rights reserved.
ISSN: 0012-821X

hal-00413135
https://hal.archives-ouvertes.fr/hal-00413135
DOI : 10.1016/j.epsl.2008.12.033

Éditeur(s) : HAL CCSD Oxford University Press (OUP)
Résumé : International audience
Two types of olivine occur in kimberlites from Greenland, Canada and southern Africa. The first, xenocrystic olivine, displays several different forms. Most distinctive are 'nodules', a term we use to describe the large (1-5 mm), rounded, single crystals or polycrystalline aggregates that are a common constituent of many kimberlites. Olivine compositions are uniform within single nodules but vary widely from nodule to nodule, from Fo81 to 93. Within many nodules, sub- to euhedral asymmetric tablets have grown within larger anhedral olivine grains. Dislocation structures, particularly in the anhedral grains, demonstrate that this olivine was deformed before being incorporated into the kimberlite magma. Olivine grains in the kimberlite matrix between the nodules have morphologies similar to those of the tablets, suggesting that most matrix olivine grains are parts of disaggregated nodules. We propose that a sub- to euhedral form is not sufficient to identify phenocrysts in kimberlites and provide some criteria, based on morphology, internal deformation and composition, that distinguish phenocrysts from xenocrysts. The second type of olivine is restricted to rims surrounding xenocrystic grains. Only this olivine crystallized from the kimberlite magma. Major and trace element data for the rim olivine are used to calculate the composition of the parental kimberlite liquid, which is found to contain between about 20 and 30% MgO. The bulk compositions of many kimberlites contain higher MgO contents as a result of the presence of xenocrystic olivine. The monomineralic, dunitic, character of the nodules, and the wide range from Fo-rich to Fo-poor olivine compositions, provide major constraints on the origin of the nodules. Dunite is a relatively rare rock in the mantle and where present its olivine is persistently Fo-rich. The dunitic source of the nodules in kimberlites lacked minerals such as pyroxene and an aluminous phase, which make up about half of most mantle-derived rocks. It appears that these minerals were removed from the mantle peridotite that was to become the source of the nodules, and the Fo content of the retained olivine was modified during interaction with CO2-rich fluids whose arrival at the base of the lithosphere immediately preceded the passage of the kimberlite magmas. Fragments of the resultant dunite were entrained into the kimberlite, where they were retained both as intact nodules and as disaggregated grains in the matrix.
ISSN: 0022-3530

insu-00543321
https://hal-insu.archives-ouvertes.fr/insu-00543321
BIBCODE : 10.1093/petrology/egp080
DOI : 10.1093/petrology/egp080

Éditeur(s) : HAL CCSD
Résumé : International audience
At the time of the collision with India (55Ma), the southern margin of Asia was a composite continental domainresulting from an already long history of successive accretions of different terranes having different rheologies.Knowledge about the structure, composition and thermal state of the Tibetan lithosphere through time is thusfundamental to understand the respective contributions of pre-Cenozoïc and Cenozoïc tectonics in the building ofthe Plateau to its present-day elevations.We focused on the boundary between the Qiangtang terrane to the south, and the Songpan-Ganze terrane to thenorth.We jointly studied deep crustal xenoliths and associated (ultra-)potassic magmatism from the Eocene basinsof Nangqian and Xialaxiu (Qinghai Province, China), north of the Qiangtang terrane. The aims were to retrievethe composition and the thermal state of the lower crust during Eocene times, to study the behavior of the lowercrust and lithospheric mantle of the Eastern Qiangtang terrane and the adjacent Songpan-Ganze terrane at the timeof the collision, and the link with the magmatic activity.Crustal xenoliths are of two types: biotite-rich, amphibole bearing metasediments; and garnet-bearing quartzofeldspathicgneisses. Such assemblages are typical of very high-grade amphibolite and granulite faciesmetamorphism; further study should allow us to quantify the pressures and temperatures those rocks experienceduntil the time they were sampled by their host lavas.Major element geochemistry places the c.a. 51-49 Ma (Spurlin et al., 2005) Xialaxiu volcanic field in a fairlydifferentiated (SiO265-70 wt%) high-K field of the calc-alcaline series. Trace element analysis suggests a strongcrustal contamination of the primary mantellic melts. C.a. 38-37 Ma (Spurlin et al., 2005) Nangqian magmaticbodies span across the alkaline series, with high to extreme (K2O6wt%) values. Complex major and traceelement patterns, coupled with high-resolution microprobe data on pyroxene xenocrysts, suggest that enrichmentoccurred at the source by metasomatism of the lithospheric mantle.Further work will precise which mechanisms could have accounted for such a metasomatism of the mantle beneaththe Northern Qiangtang terrane during Eocene, and whether the lower crust had an autochtonous or allochtonousnature.
Geophysical Research Abstracts
Vienne, Austria

insu-01308919
https://hal-insu.archives-ouvertes.fr/insu-01308919

Éditeur(s) : HAL CCSD Elsevier
Résumé : International audience
We report chlorine (Cl) and fluorine (F) abundances in minerals, interstitial glasses, and melt inclusions in 12 andesite-hosted, spinel harzburgite xenoliths and crosscutting pyroxenite veins exhumed from the sub-arc lithospheric mantle beneath Avacha volcano in the Kamchatka Arc (NE Russia). The data are used to calculate equilibrium mineral-melt partition coefficients (Dmineral/meltDmineral/melt) for Cl and F relevant to subduction-zone processes and unravel the history of volatile depletion and enrichment mechanisms in an arc setting.Chlorine is ∼100 times more incompatible in pyroxenes (View the MathML sourceDClmineral/melt = 0.005–0.008 [±0.002–0.003]) than F (View the MathML sourceDFmineral/melt = 0.50–0.57 [±0.21–0.24]), which indicates that partial melting of mantle sources leads to strong depletions in Cl relative to F in the residues. The data set in this study suggests a strong control of melt composition on View the MathML sourceDCl,Fpyroxene/melt, in particular H2O contents and Al/(Al + Si), which is in line with recent experiments. Fluorine is compatible in Ca-amphibole in the ‘wet’ sub-arc mantle (View the MathML sourceDFamphibole/melt = 3.5–3.7 [±1.5]) but not Cl (View the MathML sourceDClamphibole/melt = 0.03–0.05 [±0.01–0.03]), indicating that amphibole may fractionate F from Cl in the mantle wedge. The inter-mineral partition coefficients for Cl and F in this study are consistent amongst different harzburgite samples, whether they contain glass or not. In particular, disseminated amphibole hosts much of the Cl and F bulk rock budgets of spinel harzburgites (View the MathML sourceDClamphibole/pyroxene up to 14 and View the MathML sourceDFamphibole/pyroxene up to 40). Chlorine and fluorine are variably enriched (up to 1500 ppm Cl and 750 ppm F) in the parental arc picrite and boninite melts of primitive pyroxenite veins (and related melt inclusions) crosscutting spinel harzburgites.Based on the data in this study, the main inferences on the behaviour of Cl and F during melting and metasomatic processes in the sub-arc mantle are as follow:(i) Melting models show that most depleted mantle protoliths of intra-oceanic arc sources can have extremely low Cl/F (0.002–0.007) before being overprinted by subduction-derived components.(ii) Chlorine has a higher percolation distance in the mantle than F. Even for small fluid or melt volumes, Cl and F signatures of partial melting are overprinted by those of pervasive percolation, which increases Cl/F in percolating agents and bulk peridotites during chromatographic interaction and/or amphibole-forming metasomatic reactions. These processes ultimately control the bulk Cl and F compositions of the residual mantle lithosphere beneath arcs, and likely in other tectonic settings.(iii) Fluxed melting models suggest that Cl enrichment in arc picrite and boninite melts in this study, and in many arc melt inclusions reported in the literature, could be related to the infiltration of high Cl/F fluids derived from subducted serpentinite or altered crust in mantle wedge sources. However, these high Cl/F signatures should be re-evaluated with new models in light of the possible overprint of pervasive percolation effects in the mantle. The breakdown of amphibole (and/or mica) in the deep metasomatised mantle at higher pressure and temperature conditions than in the slab may explain, at least in part, the positive correlations between F abundances and Cl/F in primitive arc melt inclusions and slab depth.
ISSN: 0016-7037

hal-01553610
https://hal.archives-ouvertes.fr/hal-01553610
DOI : 10.1016/j.gca.2016.10.035

Éditeur(s) : HAL CCSD Mineralogical Society of America
Résumé : International audience
Hydrogen distribution between nominally anhydrous minerals (NAMs) of a garnet-lherzolite under subsolidus conditions has been investigated. Separated NAMs from a garnet-peridotite from Patagonia (Chile) are annealed together (olivine, orthopyroxene, clinopyroxene, and garnet) using a piston-cylinder at 3 GPa and 1100 °C using talc-pyrex cell assembly for 10, 25, and 100 h. The talc-pyrex assembly provides enough hydrogen in the system to re-equilibrate the hydrogen concentrations at high pressure. The three coexisting nominally anhydrous minerals (NAMs, i.e., olivine, orthopyroxene, and clinopyroxene) were successfully analyzed using FTIR. The resulting hydrogen concentrations exceed significantly the initial hydrogen concentration by a factor of 13 for olivine and a factor of 3 for both pyroxenes. Once mineral-specific infrared calibrations are applied, the average concentrations in NAMs are 115 ± 12 ppm wt H2O for olivine, 635 ± 75 ppm wt H2O for orthopyroxene, and 1214 ± 137 ppm wt H2O for clinopyroxene, garnet grains are dry. Since local equilibrium seems achieved over time (for 100 h), the calculated concentration ratios are interpreted as mineral-to-mineral hydrogen partition coefficients (i.e., Nernst’s law) for a garnet-peridotite assemblage. It yields, based on mineral-specific infrared calibrations, DOpx/Ol = 5 ± 1, DCpx/Ol = 10 ± 2, and DCpx/Opx = 1.9 ± 0.4. While DCpx/Opx is in agreement (within error) with previous results from experimental studies and concentration ratios observed in mantle-derived peridotites, the DPx/Ol from this study are significantly lower than the values reported from mantle-derived xenoliths and also at odd with several previous experimental studies where melt and/or hydrous minerals co-exists with NAMs. The results confirm the sensitivity of hydrogen incorporation in olivine regarding the amount of water-derived species (H) in the system and/or the amount of water in the coexisting silicate melt. The results are in agreement with an important but incomplete dehydration of mantle-derived olivine occurring at depth, during transport by the host magma or during slow lava flow cooling at the surface. The rapid concentration modification in mantle pyroxenes also points out that pyroxenes might not be a hydrogen recorder as reliable as previously thought.
ISSN: 0003-004X

hal-01622132
https://hal.archives-ouvertes.fr/hal-01622132
DOI : 10.2138/am-2017-6089

Éditeur(s) : HAL CCSD Elsevier
Résumé : International audience
To constrain the relations between deformation and metasomatism in the subcratonic lithospheric mantle, we have analyzed the microstructures and crystal preferred orientations in 50 mantle xenoliths from the Kaapvaal craton. Water contents in olivine and pyroxenes were measured in 14 samples equilibrated at different depths. Coarse-granular microstructures recording deformation by dislocation creep followed by annealing predominate. Mylonitic (sheared) peridotites with partially or totally recrystallized microstructures are however common below 140 km. Refractory compositions predominate, but multiple metasomatic events resulted in orthopyroxene enrichment or secondary crystallization of clinopyroxene and phlogopite. Coherent orthopyroxene and olivine CPO in most coarse-grained peridotites implies in pre- to syn-kinematic orthopyroxene enrichment or epitaxial growth on primary orthopyroxene. Undeformed, interstitial orthopyroxene, clinopyroxene, and phlogopite with random orientations in coarse-grained peridotites record post-kinematic modal metasomatic events. Deformation of these phases in the sheared peridotites implies that mylonitization results from a later event, which affected locally the deep cratonic lithosphere. Olivine CPO recording dominant [100] glide predominate at all depths. Only two samples, equilibrated at ~ 3.3 GPa show olivine [001] and orthopyroxene [001] axes subparallel, suggesting dominant [001] glide. Water contents in olivine are maximum (150 wt. ppm H2O) in peridotites equilibrated at ~ 160 km depth. Peridotites equilibrated below 180 km depth are, in contrast, almost dry. Lack of correlation between olivine mg# and water content indicates that the high water contents in olivine record re-hydration after the extensive partial melting, which produced the cratonic root. The vertical variation in water contents in olivine observed in the Kaapvaal peridotites may result from hydrogen addition or loss during extraction by the kimberlites. Comparison with magnetotelluric electrical conductivity data suggests, however, that the observed vertical variation of water contents in olivine may be representative of the present-day state of the Kaapvaal mantle, implying that extensive metasomatism resulted in hydration of the cratonic mantle at intermediate depths. The annealed microstructures of Kaapvaal peridotites indicate however that this metasomatism was not followed by remobilization of the cratonic root.
ISSN: 0024-4937

hal-00750328
https://hal.archives-ouvertes.fr/hal-00750328
DOI : 10.1016/j.lithos.2012.05.001

Éditeur(s) : HAL CCSD Elsevier
Résumé : International audience
Geodetic data support a short-term continental deformation localized in faults bounding lithospheric blocks. Whether major "faults" observed at the surface affect the lithospheric mantle and, if so, how strain is distributed are major issues for understanding the mechanical behavior of lithospheric plates. A variety of evidence, from direct observations of deformed peridotites in orogenic massifs, ophiolites, and mantle xenoliths to seismic reflectors and seismic anisotropy beneath major fault zones, consistently supports prolongation of major faults into the lithospheric mantle. This review highlights that many aspects of the lithospheric mantle deformation remain however poorly understood. Coupling between deformation in frictional faults in the uppermost crust and localized shearing in the ductile crust and mantle is required to explain the post-seismic deformation, but mantle viscosities deduced from geodetic data and extrapolated from laboratory experiments are only reconciled if temperatures in the shallow lithospheric mantle are high (> 800 °C at the Moho). Seismic anisotropy, especially shear wave splitting, provides strong evidence for coherent deformation over domains several tens of km wide in the lithospheric mantle beneath major transcurrent faults. Yet it cannot detect narrow strain localization zones or shallowly dipping faults. Seismic profiling images shallow-dipping seismic reflectors in the lithospheric mantle interpreted as the continuation of normal or, less frequently, inverse faults in the mantle. However the nature of these reflectors is poorly understood. There is a large discrepancy between the scale at which deformation processes are studied (a few kilometers, at most, due to the limited size of continuous mantle exposures at the Earth's surface) and the scale inferred for strain localization in the mantle from geophysical observations (tens of kilometers). Combining data on deformation microstructures and crystal preferred orientations in naturally deformed peridotites and seismologic observations allows nevertheless discussing strain localization processes that may play a role on the development of mantle shear zones.
ISSN: 0040-1951

hal-00750314
https://hal.archives-ouvertes.fr/hal-00750314
DOI : 10.1016/j.tecto.2012.06.006

Éditeur(s) : HAL CCSD Elsevier
Résumé : International audience
We report concentrations of hydrogen (H) in upper mantle minerals of peridotites (olivine and pyroxenes) transported by alnöitic lavas, which erupted on the southwestern border of the Ontong Java Plateau (Malaita, Solomon Islands, West Pacific). Unpolarized FTIR analyses show that olivine, orthopyroxene, and diopside contain 2–32 ppm, 162–362 ppm and 159–459 ppm wt H2O, respectively. In the studied lherzolites, garnets are anhydrous. The concentration of hydrogen within individual olivine and pyroxene grains is almost homogeneous, indicating no evidence of dehydration or hydration by ionic diffusion. In the lherzolite, the concentration of hydrogen in olivine tends to increase weakly with depth (based on geothermobarometry), consistent with the increase of water solubility with increasing water fugacity as a function of pressure, but concentrations remain well below water-saturation values determined experimentally. The highest concentration of H in olivine (32 ppm wt H2O) is, however, found in refractory spinel harzburgites, which equilibrated at depths of 85 km., while deeper specimens as the high-temperature spinel harzburgites, and some of the garnet lherzolites, contain less hydrogen in olivine. Olivines from pyroxene- or pargasite-rich peridotites have also lower hydrogen concentrations. We interpret the high hydrogen concentrations in olivine from the refractory spinel harzburgites as due to (1) simultaneous hydration and metasomatism of the lithospheric mantle by a water-rich silicate melt/fluid, during which hydrogen follows MREE and where spinel harzburgite have experienced ‘stealth’ metasomatism, and/or (2) to a late ‘fleeting’ hydrogen metasomatism, which would hydrate the rock after this first ‘stealth’ metasomatism event. In the second case, the composition of the ‘fleeting’ percolating fluid (small volume fraction of very evolved fluids, with high volatiles concentration and transient properties) is likely to be linked to the decrease of the plume activity and resulting in the downwelling of the lithosphere asthenosphere boundary. The difference in hydrogen concentration between harzburgites and lherzolites could be linked to variation in trace elements in olivine induced by the first ‘stealth’ metasomatism alone or associated to the late ‘fleeting’ hydrogen metasomatism, triggered by the lack of secondary crystallization of clinopyroxenes in the harzburgite. To conclude, H concentrations in upper mantle minerals may thus be correlated to metasomatic events, with the later yielding variation of the mineral assemblage and trace element composition that constitute the peridotites.
ISSN: 0024-4937

hal-01143385
https://hal.archives-ouvertes.fr/hal-01143385
DOI : 10.1016/j.lithos.2014.11.005

Éditeur(s) : HAL CCSD Mineralogical Society of America
Résumé : International audience
To test if hydrogen incorporation by ionic diffusion can occur between a volatile-rich kimberlitic liquid and forsterite, results of high-pressure and high-temperature experiments using a piston-cylinder apparatus at 1200–1300 °C and 1 GPa for durations of 1 min, 5 h, and 23 h, are reported here. Kimberlitic liquid in the system CaO-MgO-Al2O3-SiO2-CO2-H2O and synthetic forsterite single crystals were chosen as a first simplification of the complex natural kimberlite composition. Unpolarized Fourier transform infrared spectroscopy was used to quantify the concentrations of OH in the crystallographically oriented forsterite. Scanning electron microscopy, electron backscattered diffraction, electron microprobe analyses, and transmission electron microscopy were performed to identify the run products. After 5 and 23 h, a forsterite overgrowth crystallized with the same orientation as the initial forsterite single crystal. The kimberlitic liquid has crystallized as micrometer-scale euhedral forsterite neocrystals with random crystallographic orientations, as well as a nanoscale aluminous phase and a calcic phase. Despite theoretical water-saturation of the system and long duration, none of the initial forsterite single crystals display signs of hydration such as hydrogen diffusion profile from the border toward the center of the crystal. Most likely, the presence of CO2 in the system has lowered the H2O fugacity to such an extent that there is no significant hydration of the starting forsterite single crystal or its overgrowth. Also, the presence of CO2 enhances rapid forsterite crystal growth. Forsterite growth rate is around 2 × 108 μm3/h at 1250 °C. These experimental results suggest a deep mantle origin of the high OH content found in natural mantle-derived xenoliths transported in kimberlites, as reported from the Kaapvaal craton. In agreement with previous studies, it also points out to the fact that significant hydration must take place in a CO2-poor environment.
ISSN: 0003-004X

hal-01217157
https://hal.archives-ouvertes.fr/hal-01217157
DOI : 10.2138/am-2015-5200

Éditeur(s) : HAL CCSD Springer
Résumé : International audience
In the Dent Blanche Tectonic System, the Mont Morion biotite-bearing granite is a km-scale intrusion preserved in a low-strain volume. Zircon saturation thermometry suggests that it crystallised from a melt that reached about 800 °C. U–Pb zircon and allanite geochronology indicates crystallization of the magma in the Permian (290 ± 3 Ma; 280 ± 8 Ma, respectively). Migmatitic biotite-gneiss and amphibolite are found as xenoliths within the Mont Morion granite and constitute its country-rocks. In two samples of migmatitic biotite-gneiss zircon has metamorphic overgrowths that yield U–Pb ages of 285 ± 3 Ma and 281 ± 4 Ma, and are thus contemporaneous with the intrusion of the granite. The Mont Morion granite with its country-rocks of migmatitic biotite-bearing gneiss and amphibolite was thus emplaced at middle crustal levels while amphibolite facies metamorphism affected its country rocks. The magmatic and metamorphic record in the Mont Morion area reflects the high-temperature regime and lithospheric thinning of the Adriatic continental margin during Permian.
ISSN: 1661-8726

insu-01622179
https://hal-insu.archives-ouvertes.fr/insu-01622179
DOI : 10.1007/s00015-017-0284-1