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Géochimie isotopique du lithium dans les basaltes-Géochimie des ...

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tel-00344949, version 1 - 7 Dec 2008<br />

3. Article soumis à GCA en révision<br />

However, high mobility and large isotopic fractionations of Li, may also be viewed as<br />

severe potential limitations to the use of its isotopes as a reliable tracer in mantle<br />

petrology. One obvious indication of these limitations is the fact that, at the micrometer<br />

scale, the Li isotopic variations are often larger by at least one order of magnitude than<br />

they are in bulk for a given rock �Fig. 3.5�. In the case of meteoritic components such as<br />

refractory inclusions and chondru<strong>les</strong> �not shown in Fig. 3.5�, a great deal of complexity is<br />

added to the Li isotopic variations by the fact that early solar system irradiation processes<br />

or recent exposure to galactic cosmic rays may have pro<strong>du</strong>ced �i� Li with a 7 Li/ 6 Li ratio of<br />

�2 �instead of �12.1 for chondrites� and �ii� short‐lived 7 Be which decays to 7 Li<br />

�Chaussidon and Robert, 1998; Chaussidon and Gounelle, 2006; Chaussidon et al., 2006�.<br />

Despite these processes which cannot affect terrestrial rocks, theoretical considerations<br />

indicate that the fast diffusivity of Li in melts and minerals �Jambon and Semet, 1978;<br />

Lowry et al., 1981; Giletti and Shanahan, 1997; Richter et al., 2003� may in<strong>du</strong>ce strong Li<br />

isotopic variations at the micrometer scale because 6 Li is diffusing faster than 7 Li �Jambon,<br />

1980; Richter et al., 2003�. These transient Li isotopic variations may be quenched in<br />

minerals at the micrometer scale in the case of specific cooling paths and may obscure<br />

isotopic<br />

variations resulting from earlier geological events.<br />

The search for such isotopic effects in minerals was originally carried out in<br />

differentiated meteorites because it was anticipated that they would have favorable �i.e.<br />

fast� cooling histories and, in the case of lunar rocks, would not have been subjected to any<br />

secondary alteration by fluids. Large δ 7 Li variations �� 30‰ over 500 μm� were initially<br />

found in pyroxene grains from the shergottite NWA 480 and were first interpreted as<br />

resulting from Li isotopic fractionations taking place <strong>du</strong>ring the degassing of martian melts<br />

�Beck et al., 2004�. However subsequent studies on the lunar meteorite NWA 479 showed<br />

similar Li isotopic variations which, because of the dry character of lunar melts, can only be<br />

<strong>du</strong>e to a Li redistribution �and to the associated Li isotopic fractionation� by diffusion<br />

between Li‐poor pyroxene phenocrysts and Li‐rich matrix upon cooling after emplacement<br />

�Barrat et al., 2005�. A detailed investigation of the Li isotopic composition of pyroxene and<br />

olivine phenocrysts in several nakhlites demonstrated that microscale variations of Li<br />

abundances and isotopic compositions in martian rocks were <strong>du</strong>e to Li diffusion �Beck et<br />

al., 2006; Treiman et al., 2006�. Similar effects were recently found in terrestrial minerals<br />

from a peridotite �Jeffcoate et al., 2006� and from primitive arc lavas from Solomon Islands<br />

93

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