Éditeur(s) : HAL CCSD Elsevier
Résumé : International audience
Seismic tomography and high surface heat flow models indicate an anomalously thin and hot lithospheric mantle beneath the Canadian Cordillera. To understand the thermal and deformational history of the lithospheric mantle under these conditions, we performed a study of the microstructures, crystal preferred orientations (CPO), and seismic anisotropy of mantle xenoliths collected in the Summit Lake volcano in the southern Canadian Cordillera. The xenoliths vary in composition between spinel lherzolites, cpx-rich lherzolites, and wehrlites. All samples are coarse-grained and show clear evidence for annealing, but deformation microstructures are well-preserved in the spinel lherzolites. Olivine CPO is characterized by a strong point-maximum of [100] and by a girdle distribution of [010[ and [001] axes normal to it; CPO strength is variable, spinel-lherzolites have the strongest CPO. Some samples show a weak orthopyroxene CPO consistent with the olivine one. However most pyroxenes have random CPO, interstitial shapes and undeformed appearance, which suggest a secondary origin by reactive melt percolation under static conditions, leading to crystallization of cpx + sp +/- opx at the expenses of olivine, followed by crystallization of cpx + sp +/- ol at the expenses of opx to produce the wehrlites. The studied xenoliths have typical upper mantle seismic properties patterns with fastest propagation of P-waves and polarization of S-waves parallel to the olivine [100] maxima. Maximum P- and S-waves anisotropy for lherzolites are 8 and 5% respectively. Dispersion of the olivine CPO due to neocrystallization of olivine results in weaker anisotropies (6.5 and 3.5%) in wehrlites. Seismic velocities calculated using a geotherm consistent with the equilibrium temperatures of the Summit Lake xenoliths are 3-4% lower than those expected in a normal, 100 km-thick lithosphere, consistent with seismic tomography models for the region. This high geothermal gradient may be partially explained by considering the anisotropy of thermal conductivity of olivine and subhorizontal foliations in the lithospheric mantle, which result in a decrease by up to 15% of the thermal conductivity in the vertical direction.
ISSN: 0040-1951

hal-00618332
https://hal.archives-ouvertes.fr/hal-00618332
DOI : 10.1016/j.tecto.2011.04.014

Éditeur(s) : HAL CCSD Elsevier
Résumé : International audience
A subject of continuing debate is how the Earth's lithospheric portion of the upper mantle has remained the thickest (> 200 km) and oldest (> 3 Gy) beneath cratons and is yet surrounded by a vigorously convecting asthenosphere. It is generally admitted that water is a key parameter in the strength and longevity of cratonic roots, because olivine, the main phase of the lithospheric mantle, becomes stronger if its water content decreases. Expanding upon the work presented in Novella et al. (2015) and Taylor et al. (2016), we report new water contents for additional olivine inclusions in diamonds together with the trace-element composition for all olivine inclusions, as well as for mantle xenoliths from various kimberlite pipes located on the Siberian craton. The olivine diamond inclusions from this study have systematically low-water contents (< 50 ppmw H2O), moderate to high forsterite (e.g., Fo91–94) contents and low Ni, Co, and Zn ppm contents (e.g., < 2848, < 108, and < 47 ppm, respectively). In contrast, olivines from Siberian craton mantle xenoliths have a wide range of water contents (6–323 ppmw H2O) and extend to lower-Fo (91–92), Ni, Co, and Zn-rich compositions, compared to the diamond inclusions. Depleted incompatible trace-element concentrations in olivine (0.1–0.001 × Primitive Mantle) advance our hypothesis for the protogenetic origins for the majority of Siberian diamond inclusions. These observations are consistent with the peridotite xenoliths as representing a part of the cratonic lithosphere that has experienced melt re-fertilization, which has also transported water. The olivine diamond inclusions, on the other hand, preserve “micro-samples” of an initial, dry cratonic lithosphere, mostly resulting from melting events. These inclusions are likely sourced from the initial cratonic mantle lithosphere, which thereby, resisted delamination over time, due to its buoyancy and strength, imparted from melt and water depletion, respectively. And thus, our data provides a major argument that the kimberlite-hosted mantle xenoliths may be more metasomatized than common rocks at the base of the Siberian and other cratonic roots away from kimberlite fields.
ISSN: 0024-4937

hal-01467731
https://hal.archives-ouvertes.fr/hal-01467731
DOI : 10.1016/j.lithos.2016.07.023

Éditeur(s) : HAL CCSD Elsevier
Résumé : "Tectonically emplaced" mantle rocks include subcontinental, suboceanic, and subarc mantle rocks that were tectonically exhumed from the upper mantle and occur:(i) as dispersed ultramafic bodies, a few meters to kilometers in size, in suture zones and mountain belts (i.e., the "alpine," or "orogenic" peridotite massifs - De Roever (1957), Thayer (1960), Den Tex (1969));(ii) as the lower ultramafic section of large (tens of kilometers) ophiolite or island arc complexes, obducted on continental margins (e.g., the Oman Ophiolite and the Kohistan Arc Complex - Coleman (1971), Boudier and Coleman (1981), Burg et al. (1998));(iii) exhumed above the sea level in ocean basins (e.g., Zabargad Island in the Red Sea, St. Paul's islets in the Atlantic and Macquarie Island in the southwestern Pacific - Tilley (1947), Melson et al. (1967), Varne and Rubenach (1972), Bonatti et al. (1981)).The "abyssal peridotites" are samples from the oceanic mantle that were dredged on the ocean floor, or recovered from drill cores (e.g., Bonatti et al., 1974; Prinz et al., 1976; Hamlyn and Bonatti, 1980).Altogether, tectonically emplaced and abyssal mantle rocks provide insights into upper mantle compositions and processes that are complementary to the information conveyed by mantle xenoliths (See Chapter 2.05). They provide coverage to vast regions of the Earth's upper mantle that are sparsely sampled by mantle xenoliths, particularly in the ocean basins and beneath passive continental margins, back-arc basins, and oceanic island arcs.Compared with mantle xenoliths, a disadvantage of some tectonically emplaced mantle rocks for representing mantle compositions is that their original geodynamic setting is not exactly known and their significance is sometimes a subject of speculation. For instance, the provenance of orogenic lherzolite massifs (subcontinental lithosphere versus upwelling asthenosphere) is still debated (Menzies and Dupuy, 1991, and references herein), as is the original setting of ophiolites (mid-ocean ridges versus supra-subduction settings - e.g., Nicolas, 1989). In addition, the mantle structures and mineralogical compositions of tectonically emplaced mantle rocks may be obscured by deformation and metamorphic recrystallization during shallow upwelling, exhumation, and tectonic emplacement. Metamorphic processes range from high-temperature recrystallization in the stability field of plagioclase peridotites ( Rampone et al., 1993) to complete serpentinization (e.g., Burkhard and O'Neill, 1988). Some garnet peridotites record even more complex evolutions. They were first buried to, at least, the stability field of garnet peridotites, and, in some cases to greater than 150 km depths ( Dobrzhinetskaya et al., 1996; Green et al., 1997; Liou, 1999). Then, they were exhumed to the surface, dragged by buoyant crustal rocks ( Brueckner and Medaris, 2000).Alternatively, several peridotite massifs are sufficiently well preserved to allow the observation of structural relationships between mantle lithologies that are larger than the sampling scale of mantle xenoliths. It is possible in these massifs to evaluate the scale of mantle heterogeneities and the relative timing of mantle processes such as vein injection, melt-rock reaction, deformation, etc... Detailed studies of orogenic and ophiolitic peridotites on centimeter- to kilometer-scale provide invaluable insights into melt transfer mechanisms, such as melt flow in lithospheric vein conduits and wall-rock reactions (Bodinier et al., 1990), melt extraction from mantle sources via channeled porous flow ( Kelemen et al., 1995) or propagation of kilometer-scale melting fronts associated with thermalerosion of lithospheric mantle ( Lenoir et al., 2001). In contrast, mantle xenoliths may be used to infer either much smaller- or much larger-scale mantle heterogeneities, such as micro-inclusions in minerals ( Schiano and Clocchiatti, 1994) or lateral variations between lithospheric provinces ( O'Reilly et al., 2001).The abyssal peridotites are generally strongly affected by oceanic hydrothermal alteration. Most often, their whole-rock compositions are strongly modified and cannot be used straightforwardly to assess mantle compositions (e.g., Baker and Beckett, 1999). However, even in the worst cases the samples generally contain fresh, relic minerals (mainly clinopyroxene) that represent the only available direct information on the oceanic upper mantle in large ocean basins, away from hot-spot volcanic centers. In situ trace-element data on clinopyroxenes from abyssal peridotites provide constraints on melting processes at mid-ocean ridges (Johnson et al., 1990).In this chapter, we review the main inferences on upper mantle composition and heterogeneity that may be drawn from geochemical analyses of the major elements, lithophile trace elements, and Nd-Sr isotopes in tectonically emplaced and abyssal mantle rocks. In addition we emphasize important insights into the mechanisms of melt/fluid transfer that can be deduced from detailed studies of these mantle materials.
Treatise on Geochemistry Update12.04

hal-00407944
https://hal.archives-ouvertes.fr/hal-00407944
DOI : 10.1016/B0-08-043751-6/02004-1

Éditeur(s) : HAL CCSD Elsevier
Résumé : International audience
We carried out detailed petrographic, major and trace element geochemical, microstructural and FTIR analyses on eight characteristic ultramafic xenoliths from Nyos and Barombi Mbo Lakes in the continental sector of the Cameroon Volcanic Line (CVL). The studied xenoliths are spinel lherzolites showing lithologies similar to the other xenoliths reported previously along the CVL. They have protogranular and porphyroclastic textures. One of the Barombi xenolith contains amphibole, which had not been previously reported in this locality. Amphibole is common in the Nyos xenoliths suite. Peridotite xenoliths from both localities show some chemical heterogeneity, but Barombi xenoliths generally are less depleted in basaltic elements with respect to Nyos xenoliths. Trace element compositions of Nyos spinel lherzolites show a moderately depleted initial (premetasomatic) composition and variable enrichment in REE. Evidence for both modal and cryptic metasomatism is present in Nyos xenoliths. Rare earth element patterns of clinopyroxene suggest that interaction between mafic melts and the upper mantle occurred beneath the Nyos locality. Barombi Mbo xenoliths, on the other hand, record a small degree of partial melting. The Barombi Mbo xenoliths have weak, dominantly orthorhombic olivine crystal preferred orientations, whereas Nyos ones have strong axial-[010] patterns, which may have formed in response to transpression. Nominally anhydrous mantle minerals (NAMs) of the Barombi Mbo xenoliths show generally higher bulk concentrations of ‘water’ (70–127 ppm) than Nyos xenoliths (32–81 ppm). The Barombi Mbo xenoliths could originate from a juvenile segment of the lithospheric mantle, which had been originally part of the asthenosphere. It became a part of the lithosphere in response to thermal relaxation following the extension, forming a weakly deformed lower lithospheric mantle region along the CVL. The Nyos xenoliths, however, represent a shallow lithospheric mantle bearing imprints of several depletion and enrichment events probably prior or following the extension (at ∼30 Ma).
ISSN: 0899-5362

hal-01236039
https://hal.archives-ouvertes.fr/hal-01236039
DOI : 10.1016/j.jafrearsci.2015.07.006

Éditeur(s) : HAL CCSD
Résumé : This thesis compiles two distinct studies that both document the control of microstructures on rock seismic properties. The first part deals with the development of crystallographic preferred orientations (CPO) in the uppermost mantle associated with melt/fluid-rock interactions, recorded in peridotites xenoliths from the Japan sea back-arc basin. The microstructural and geochemical characteristics of the studied samples reveal that active spreading is associated to uppermost mantle deformation similar to that observed in the Oman ophiolite. At the onset of back-arc spreading, there are no strong interactions between melt percolation and deformation in comparison to continental rift zones, probably due to the relatively small size and short duration of the spreading event. The second part presents a unique database of plagioclase CPO from variously deformed mafic rocks. CPO are grouped in three main types; their characteristics as a function of deformation regime (magmatic or crystal-plastic) are outlined and discussed. Calculated seismic properties of gabbroic rocks show that anisotropy tends to increase as a function of fabric strength, although it is generally weak, due to the competing effect of olivine/clinopyroxene and plagioclase.
Cette thèse regroupe deux études distinctes, qui documentent le contrôle des microstructures sur les propriétés sismiques des roches. La première partie traite du développement des orientations préférentielles cristallographiques (OPC) dans le manteau supérieur, associé aux interactions liquide/magma-roche, enregistré dans des xénolites de péridotites du bassin d'arrière-arc de la mer du Japon. Les caractéristiques microstucturales et géochimiques des échantillons étudiés montrent que l'ouverture arrière-arc active est associée à une déformation du manteau supérieure similaire à celle observée dans l'ophiolite d'Oman. L'initiation de l'extension d'arrière-arc n'est pas associée à de fortes interactions entre percolation magmatique et déformation, en comparaison avec les zones de rifting continentales, probablement en raison des taille et durée relativement petites de l'épisode d'ouverture. La seconde partie présente une base de données unique d'OPC de plagioclase de roches mafiques plus ou moins déformées. Les OPC sont classées en 3 types principaux; leurs caractéristiques en fonction du régime de déformation (magmatique ou plastique) sont présentées et discutées. Les propriétés sismiques calculées des roches gabbroiques montrent que l'anisotropie tend à croitre avec l'intensité des fabriques, bien qu'elle soit généralement faible, en raison des effets opposés des olivines/clinopyroxènes et du plagioclase.
https://tel.archives-ouvertes.fr/tel-00795505

tel-00795505
https://tel.archives-ouvertes.fr/tel-00795505
https://tel.archives-ouvertes.fr/tel-00795505/document
https://tel.archives-ouvertes.fr/tel-00795505/file/Satsukawa_thesis_UM2.pdf

Éditeur(s) : HAL CCSD Elsevier
Résumé : International audience
To understand the deep cycle of water, upper mantle water content and distribution between nominally anhydrous minerals (NAMs) and hydrous minerals (e.g., amphibole) must be constrained. We need then to understand H behaviour during mantle melting and metasomatism. Major, minor and trace element compositions including water contents were obtained on ten xenoliths of spinel-bearing peridotites from the Ray Pic locality, in the Southern part of the Massif Central (France). The sample suite investigated here is composed of rather fertile lherzolites (89.4 ≤ Fo ≤ 90.8%; 11.3 ≤ cr# in spinel ≤ 21.1%; 0.942 ≤ [Yb]cpx ≤ 1.90 ppm; cpx: clinopyroxene), which can be best explained by batch melting, with degree of melting between 3 and 10%. These xenoliths contain up to 8% modal amphibole. Three groups are defined as a function of the amphibole modal abundance (above or below 1%) and equilibrium temperature (above or below 1000 °C). Results show no clear positive correlation between modal metasomatism (amphibole) and incompatible element enrichment in cpx. Trace element compositions in cpx show strong enrichments of the most incompatible elements (e.g., (La/Sm)PM as high as 15.7; PM: normalised to primitive mantle values), but strong negative anomalies of the high field strength elements (e.g., (Th/Nb)PM as high as ~ 680). Such trace element fractionations are usually ascribed to the so-called carbonatitic metasomatism involving the percolation of small volume melts which are enriched in volatiles. The hydrogen concentrations in cpx range from 203 to 330 ppm wt. H2O, in orthopyroxene from 66 to 160 ppm wt. H2O and in olivine from 2 to 6 ppm wt. H2O. These values are within the common concentration range of other spinel-bearing peridotites. Amphiboles contain 1.9 ± 0.5 wt.% of H2O.The effect of metasomatism on water abundances in NAMs is not straightforward. Hydrous metasomatism (i.e., leading to the crystallisation of OH-bearing amphibole) has no effect on the water content of the co-existing NAMs. This suggests thus that the occurrence of hydrous minerals, such as amphibole, does not systematically imply that the coexisting NAMs are water-rich (saturated). Further, the percolation of volatile-rich small volume melts, which is fingerprinted by the strong enrichment of the incompatible elements, has also no clear effect on the water content of the NAMs. These data are thus difficult to reconcile with the admitted highly incompatible behaviour of H in upper mantle minerals.
ISSN: 0024-4937

hal-01278062
https://hal.archives-ouvertes.fr/hal-01278062
DOI : 10.1016/j.lithos.2015.08.013

Éditeur(s) : HAL CCSD Elsevier
Résumé : International audience
Cratons represent the oldest preserved lithospheric domains. Their lithosphere (lithospheric mantle welded to overlying Precambrian crystalline basement) is considered to be particularly robust and long-lived due to the protecting presence of buoyant and rigid “keels” made up of residual harzburgites. Although the cratons are mostly assumed to form in the Archaean, the timing of their formation remains poorly constrained. In particular, there are very few datasets describing concurrently the age of both the crustal and mantle portions of the lithosphere. In this study, we report new U–Pb ages and Hf isotope compositions for zircons in crustal xenoliths from the Udachnaya kimberlite in the central Siberian craton; this dataset includes samples from both the upper and lower portions of the crust. The zircon ages agree well with model melt-extraction Re–Os ages on refractory peridotite xenoliths from the same pipe; taken together they allow an integrated view of lithosphere formation. Our data reveal that the present day upper crust is Archaean, whereas both the lower crust and the lithospheric mantle yield Paleoproterozoic ages. We infer that the deep lithosphere beneath the Siberian craton was not formed in a single Archaean event, but grew in at least two distinct events, one in the late Archaean and the other in the Paleoproterozoic. Importantly, a complete or large-scale delamination and rejuvenation of the Archaean lower lithosphere (lower crust and lithospheric mantle) took place in the Paleoproterozoic. This further demonstrates that craton formation can be a protracted, multi-stage process, and that the present day crust and mantle may not represent complementary reservoirs formed through the same tectono-magmatic event. Further, deep cratonic lithosphere may be less robust and long living than often assumed, with rejuvenation and replacement events throughout its history.
ISSN: 0012-821X

hal-01467648
https://hal.archives-ouvertes.fr/hal-01467648
DOI : 10.1016/j.epsl.2016.09.046

Éditeur(s) : HAL CCSD Elsevier
Résumé : International audience
The minerals constituting the Earth's upper mantle are nominally anhydrous silicates (NAMs). However they do contain hydrogen as a trace element, decorating point defects in their crystalline structure. Experimental petrology and mineralogy have quantified the maximum concentration under several compositional and thermodynamic conditions, but systematic studies on the hydrogen concentration in minerals from mantle-derived rocks have only recently been carried out. Here, we have compiled the distribution of hydrogen in upper mantle peridotite xenoliths, from which several conclusions can be drawn. NAMs from peridotite xenoliths contain a few ppm wt. H2O in their structure. From the current database, the hydrogen concentrations in olivine regularly increase with increasing depth. The amount of hydrogen in NAMs from peridotite xenoliths from subduction contexts is not higher than in other geological context for similar temperature and pressure conditions. The highest hydrogen concentrations is found in peridotitic olivines from cratonic mantle, and are likely due to the depth of origin. The increasing hydrogen concentration in olivine with increasing depth is likely controlled by the increase of H partitioning into olivine at the expense of orthopyroxene as imposed by a decrease in Al content in opx with depth. However, the sparse data could also indicate that the bulk hydrogen concentration slightly increases with depth > 150 km. In this case, it would suggest, locally (Udachnaya for example), a possible increase in water fugacity due to fluid saturation. Even if the most abundant mineral in mantle rocks is olivine, the bulk hydrogen concentration in peridotites is controlled by the amount of hydrogen stored in pyroxenes. However, hydrogen concentration in olivine remains crucial for consequences on physical properties such as rheology and electrical conductivity. Kinetics of hydrogen transport is reviewed and hydrous melt/fluid percolation appears necessary to homogenize the hydrogen distribution at km-scale. Sampling of natural rock specimens is currently biased (e.g., in favor of optically attractive samples) and needs improvement, which will be achieved by increasing sample diversity (all type of grain sizes, lithologies, geological settings) and size of rock samples, as well as advances in analytical techniques. Acquisition of high quality data will be achieved by studying the co-existing minerals in mantle specimens, exploring each sample by linear and mapping measurements, and using appropriate FTIR calibrations for polarized and unpolarized radiation.
ISSN: 0024-4937

hal-01306676
https://hal.archives-ouvertes.fr/hal-01306676
DOI : 10.1016/j.lithos.2015.11.012

Éditeur(s) : HAL CCSD Elsevier
Résumé : International audience
The subcontinental lithospheric mantle evolves through time due to tectonic events and processes as static recrystallization and melt percolation. To constrain the extent of these processes in the South Patagonian subcontinental mantle lithosphere we performed a microstructural and Electron Backscattered Diffraction (EBSD) study of a suite of 35 peridotite xenoliths brought to the surface by Plio-Pleistocene alkaline volcanic rocks from Gobernador Gregores and Pali Aike. All samples show a well-developed olivine and pyroxene crystallographic preferred orientation (CPO), consistent with deformation by dislocation creep with dominant activation of [100]{0kl} in olivine. The coarse granular or tabular textures and the low density of intracrystalline deformation features indicate that deformation was followed by annealing under static conditions. The xenoliths also show microstructural evidence of multiple episodes of reactive melt percolation. Neither annealing nor melt percolation erased the olivine CPO, which has [010]-fiber, [100]-fiber and orthorhombic patterns in Pali Aike xenoliths and essentially [010]-fiber and orthorhombic patterns in Gobernador Gregores xenoliths. Seismic properties calculated based on the CPO and modal compositions are, however, rather homogeneous, with fast S-wave polarization and P-wave propagation parallel to the [100] olivine axis. The variation in the olivine CPO solely changes the minimum S-wave birefringence direction, which is normal to the foliation for axial-[010] olivine CPO. Average samples for the two localities, obtained by adding up the individual samples CPO data in a common reference frame, show, however, a 'normal' upper mantle anisotropy with a maximum S-wave birrenfringence of ca. 5% at high angle to the both the maximum [010] and [100] axes concentrations, that is in the foliation, but normal to the lineation, and a minimum birefringence at low angle to the [100] maximum, that is parallel to the lineation.
ISSN: 0040-1951

hal-01053500
https://hal.archives-ouvertes.fr/hal-01053500
DOI : 10.1016/j.tecto.2014.02.017

Éditeur(s) : HAL CCSD Oxford University Press (OUP)
Résumé : International audience
Despite a relatively 'uniform' fertile composition (Al2O3 = 2 center dot 19-4 center dot 47 wt %; Fo% = 89 center dot 2 +/- 0 center dot 3%; Cr#(Spl) = 8 center dot 9 +/- 1 center dot 5%), the Montferrier peridotite xenoliths show a wide range of S contents (22-590 ppm). Most sulphides are interstitial and show peculiar pyrrhotite-pentlandite intergrowths and low abundances of Cu-rich phases. Sulphide-rich samples are characterized by strong enrichment in the light rare earth elements and large ion lithophile elements without concomitant enrichment of the high field strength elements. Such trace-element fractionation is commonly ascribed to metasomatism by volatile-rich melts and/or carbonatitic melts. S and Se (11-67 ppb), as well as S/Se (up to approximate to 12 000), are correlated with La/Sm. Cu, however, remains broadly constant (30 +/- 5 ppm). These features strongly suggest that the percolation-reaction of such volatile-rich fluids has led to sulphide enrichment with an atypical signature marked by strong fractionation of the chalcophile elements (i.e. S vs Se and Cu). S-rich xenoliths are also characterized by high (Pd/Ir)(N) (1 center dot 2-1 center dot 9; where subscript N indicates normalized to chondrite), (Pd/Pt)(N) between 1 center dot 5 and 2 center dot 2, and (Os/Ir)(N) up to 1 center dot 85. Despite the relative uniform fertile composition of the xenoliths, Re/Os ranges between 0 center dot 02 and 0 center dot 18. Os-187/Os-188 is extremely variable even within a single sample and can be as high as 0 center dot 1756 for the most S-rich samples. Sulphides show highly fractionated and variable abundances of the highly siderophile elements (HSE) [0 center dot 03 (Pd/Ir)(N) < 1283] and Re-Os isotopic composition (0 center dot 115 < Os-187/Os-188 < 0 center dot 172). Such variation can be observed at the thin-section scale. Whole-rock and in situ sulphide data demonstrate that chalcophile and HSE systematics and the Os isotopic composition of the upper mantle could be significantly modified through metasomatism, even with volatile-rich fluids. These features highlight the complex behaviour of the HSE in fluid-rock percolation-reaction models and suggest a complex interplay between sulphide addition (crystallization or sulphidation) and partial equilibration of pre-existing sulphide. The specific fractionations observed in chemical proxies such as S and Se, Os and Ir, and Pd and Pt, as well as the low abundance of Cu-rich sulphides, suggest that sulphide addition may not have occurred via sulphide melts. Rather, we infer that S was present as a dissolved species in a (supercritical) oxidizing, volatile-rich fluid (C-O-H-S +/- Cl) along with other chalcophile and siderophile elements such as Os, Pd, Re and Au. The highly radiogenic Os composition of this fluid ( Os-187/ Os-188 > 0 center dot 17) would imply that such fluids are derived from an uncommon type of mantle source possibly related to carbonatite melts.
ISSN: 0022-3530

hal-00644524
https://hal.archives-ouvertes.fr/hal-00644524
DOI : 10.1093/petrology/egr038

Éditeur(s) : HAL CCSD Elsevier
Résumé : International audience
Whole-rock concentrations of Se and Te were determined in 53 peridotite samples collected in orogenic bodies from the Eastern Pyrenees, including the Lherz massif (33 samples), the type-locality of Iherzolite. Orogenic Iherzolites tectonically emplaced into the continental crust escaped devolatilisation that may strongly alter concentrations of those volatile trace elements in basalt-hosted peridotite xenoliths. The Se and Te concentration ranges (<3.5-100.7 ppb; <1-11 ppb) are consistent with the few analyses of mantle samples yet available, yet extending to higher Se concentrations. In-situ analyses performed by LAM-ICPMS on base metal sulfides indicate that the Se budget is controlled by sulfides whereas a large fraction of Te (50 +/- 30%) does not reside in sulfides. The missing fraction is accounted for by fractional crystallization of Pt-Pd tellurides from Cu-Ni sulfide melts. A maximum of one third of the S budget of Eastern Pyrenean peridotites was added by assimilation of crustal sulfides, which crystallized as pyrite. Disregarding those contaminated samples, some features of the Se and Te systematics (e.g. bivariate plots vs. fertility index) cannot be explained by partial melting processes. The best fit for 33 peridotites (mostly from Lherz) yields higher than chondritic S/Se (3.1213 +/- 500; r(2) = 0.96) for near chondritic Se/Te (8.6 +/- 2; r(2) = 0.9). Our study suggest that such superchondritic S/Se ratios are better explained by petrogenetic processes involving refertilization of harzburgitic lithosphere by metal (Cu,Ni)-rich sulfide melts precipitated along with clinopyroxene and Al-spinel from silicate melts en-route to the surface.
ISSN: 0009-2541

hal-00544577
https://hal.archives-ouvertes.fr/hal-00544577
DOI : 10.1016/j.chemgeo.2010.09.007

Éditeur(s) : HAL CCSD Springer Verlag (Germany) Springer Verlag
Résumé : International audience
We have investigated the partitioning of Fe3+ between orthopyroxene (Opx) and garnet (Grt) in well-equilibrated mantle xenoliths using Mössbauer spectroscopy. The samples cover a wide range of P–T conditions (2.1–6.6 GPa, 690–1,412 °C) and geothermal gradients, and are thus representative for Earth’s upper mantle in both on-craton and off-craton continental settings. Garnet has Fe3+/Fetot ratios of 0.03–0.13 and Fe2O3 contents of 0.24–1.00 wt%. Orthopyroxene has, on average, lower Fe3+/Fetot ratios (0.01–0.09) and Fe2O3 contents (0.05–0.63 wt%). In low-pressure, high-temperature samples, however, Opx is systematically richer in Fe2O3 than the coexisting Grt. The Fe3+ Opx/Grt partition coefficient (DOpx/GrtFe3+) shows no obvious relationship with temperature, but increases with decreasing pressure and with increasing NaOpx. The observed Opx/Grt Fe3+ systematics imply that the Opx–Grt Fe–Mg exchange thermometer is not robust against redox changes if total Fe is treated as Fe2+. An approximate evaluation of errors on T estimates due to redox effects predicts negligible deviations for strongly reduced conditions (<65 °C), but potentially large deviations (> to ≫100 °C) for strongly oxidized conditions, especially at very high pressure and when both P and T are calculated by iteration.
ISSN: 0010-7999

hal-01121606
https://hal.archives-ouvertes.fr/hal-01121606
DOI : 10.1007/s00410-014-1101-8

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
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