Éditeur(s) : HAL CCSD Elsevier
Résumé : International audience
Wasilewski et al. (1979) concluded that no magnetic remanence existed in the uppermost mantle and that even if present, such sources would be at temperatures too high to contribute to long wavelength magnetic anomalies (LWMA). However, new collections of unaltered mantle xenoliths indicate that the uppermost mantle could contain ferromagnetic minerals. 1. The analysis of some LWMA over cratons and forearcs suggest magnetic sources in the uppermost mantle. 2. The most common ferromagnetic phase in the uppermost mantle is stoichiometric magnetite. Assuming a 30 km-thick crust, and crustal and mantle geotherms of 15 °C/km and 5 °C/km, respectively, the 600 °C Curie temperature implies a 30 km-thick layer of mantle. 3. The uppermost mantle is cooler than 600 °C in Archean and Proterozoic shields (> 350 °C), subduction zones (> 300 °C) and old oceanic basins (> 250 °C). 4. Recently investigated sets of unaltered mantle xenoliths contain pure magnetite inclusions in olivine and pyroxene formed in equilibrium with the host silicate. 5. The ascent of mantle xenoliths occurs in less than a day. Diffusion rates in olivine suggest that the growth of magnetite possible within this time frame cannot account for the size and distribution of magnetite particles in our samples. 6. Demagnetization of natural remanent magnetization (NRM) of unaltered mantle xenoliths unambiguously indicates only a single component acquired upon cooling at the Earth's surface. This is most easily explained as a thermoremanent magnetization acquired by pre-existing ferromagnetic minerals as xenoliths cool rapidly at the Earth's surface from magmatic temperatures, acquired during ascent. 7. Modern experimental data suggest that the wüstite-magnetite oxygen buffer and the fayalite-magnetite-quartz oxygen buffer extend several tens of km within the uppermost mantle. 8. The magnetic properties of mantle xenoliths vary consistently across tectonic settings. In conclusion, the model of a uniformly non-magnetic mantle should be revisited. Keywords
ISSN: 0040-1951

hal-01053923
https://hal.archives-ouvertes.fr/hal-01053923
DOI : 10.1016/j.tecto.2014.01.004

Éditeur(s) : HAL CCSD Springer Verlag (Germany) Springer Verlag
Résumé : International audience
The Cerro del Almirez massif (Spain) represents a unique fragment of serpentinized oceanic lithosphere that has been first equilibrated in the antigorite stability field (Atg-serpentinites) and then dehydrated into chlorite–olivine–orthopyroxene (Chl-harzburgites) at eclogite facies conditions during subduction. The massif preserves a dehydration front between Atg-serpentinites and Chl-harzburgites. It constitutes a suitable place to study redox changes in serpentinites and the nature of the released fluids during their dehydration. Relative to abyssal serpentinites, Atg-serpentinites display a low Fe3+/FeTotal(BR) (=0.55) and magnetite modal content (=2.8–4.3 wt%). Micro-X-ray absorption near-edge structure (μ-XANES) spectroscopy measurements of serpentines at the Fe–K edge show that antigorite has a lower Fe3+/FeTotal ratio (=0.48) than oceanic lizardite/chrysotile assemblages. The onset of Atg-serpentinites dehydration is marked by the crystallization of a Fe3+-rich antigorite (Fe3+/FeTotal = 0.6–0.75) in equilibrium with secondary olivine and by a decrease in magnetite amount (=1.6–2.2 wt%). This suggests a preferential partitioning of Fe3+ into serpentine rather than into olivine. The Atg-breakdown is marked by a decrease in Fe3+/FeTotal(BR) (=0.34–0.41), the crystallization of Fe2+-rich phases and the quasi-disappearance of magnetite (=0.6–1.4 wt.%). The observation of Fe3+-rich hematite and ilmenite intergrowths suggests that the O2 released by the crystallization of Fe2+-rich phases could promote hematite crystallization and a subsequent increase in fo2 inside the portion of the subducted mantle. Serpentinite dehydration could thus produce highly oxidized fluids in subduction zones and contribute to the oxidization of the sub-arc mantle wedge.
ISSN: 0010-7999

hal-01172310
https://hal.archives-ouvertes.fr/hal-01172310
DOI : 10.1007/s00410-015-1130-y