HR: 0800h
AN: V41E-1503 [Abstracts]
TI: Nitrogen isotopic composition of ultramafic xenoliths
AU: * Marty, B
EM: bmarty@crpg.cnrs-nancy.fr
AF: Centre de Recherches P‚trographiques et G‚ochimiques, 15 rue Notre Dame des Pauvres, Vandoeuvre, 54501
France
AU: * Marty, B
EM: bmarty@crpg.cnrs-nancy.fr
AF: Ecole Nationale Sup‚rieure de G‚ologie, rue du Doyen Marcel Roubault, BP 40, Vandoeuvre, 54501
France
AU: Yokochi, R
EM: yokochi@crpg.cnrs-nancy.fr
AF: Centre de Recherches P‚trographiques et G‚ochimiques, 15 rue Notre Dame des Pauvres, Vandoeuvre, 54501
France
AU: Yokochi, R
EM: yokochi@crpg.cnrs-nancy.fr
AF: Dpt. of Earth and Environmental Sciences, University of Illinois at Chicago, SES2456, 845 W. Taylor St.,
Chicago, IL 60607-7059
United States
AU: Pik, R
EM: rpik@crpg.cnrs-nancy.fr
AF: Centre de Recherches P‚trographiques et G‚ochimiques, 15 rue Notre Dame des Pauvres, Vandoeuvre, 54501
France
AU: Chazot, G
EM: G.Chazot@opgc.univ-bpclermont.fr
AF: Laboratoire Magmas et Volcans, Universit‚ Blaise Pascal et OPGC, 5 rue Kessler, Clermont-Ferrand,
63038
France
AB:
The nitrogen isotopic composition of mantle-derived samples provides important information on the origin of the terrestrial
volatile and on the evolution of the mantle through time. Two decades of studies have revealed that there is an isotopic
disequilibrium between the atmosphere (δ15N≡ 0 ‰) and the mantle source of MORB (δ15N = -3
to -5 ‰). The N isotopic composition of other mantle-derived materials, however, scatters significantly from -15.3 up
to +30 ‰ in mantle xenoliths (by melting extraction) and diamonds (Cartigny et al., 1997: Mohapatra and Murty,
2000). Whether this variation reflects real mantle heterogeneity or is due to isotopic fractionation during e.g. magmatic
processes is crucial to our understanding of the volatile element evolution of the Earth. N isotope ratios can be sensitive
to (i) contamination by surface nitrogen , (ii) kinetic isotope fractionation during gas extraction, and (iii) isotopic
fractionation during crystal growth, as documented in the case of diamonds. Peridotitic xenoliths provide a unique
opportunity to study the lithospheric mantle. In order to explore the potential role of the above mentioned processes, we
have analyzed nine peridotite xenoliths by step-wise heating combustion with a high resolution. Samples were from Yemen
(three spinel lherzolites), Eifel, Germany (two wehrlites, two harzburgites and a dunite) and Massif Central, France (one
harzburgite).
The extraction of N from refractory minerals was characterized by two release peaks, showing successful discrimination of
trapped components from contaminants. We also observed Kinetic isotope fractionation during thermal extraction. Nitrogen in
seven peridotite xenoliths is characterized by 15N enrichments compared to the atmosphere, probably representing
metasomatised subcontinental lithospheric mantle. In contrast, the bulk N isotope composition of a mica-bearing wehrlite from
Eifel, related to Cenozoic magmatism, is MORB-like (depleted in 15N by 5 ‰ relative to ATM) . However, an
extreme isotopic disequilibrium of Δ15N = 25 ‰ is observed between olivine and phlogopite in this wehrlite.
Nitrogen isotopic disequilibrium within a single ultramafic xenoltih suggests that significant isotopic fractionation may
occur during magmatic processes.
Compared to the component trapped in fluid inclusions, bulk mantle xenoliths as well as mineral separates display high
N_2/40Ar ratios. We suggest that the N2 enrichment relative to Ar is due either to high nitrogen solubility in
refractory minerals, or to chemical speciation of nitrogen in magmas.
DE: 1000 GEOCHEMISTRY
DE: 1030 Geochemical cycles (0330)
DE: 1036 Magma chamber processes (3618)
DE: 1041 Stable isotope geochemistry (0454, 4870)
SC: Volcanology, Geochemistry, Petrology [V]
MN: Fall Meeting 2005