Géochimie isotopique du lithium dans les basaltes-Géochimie des ...
Géochimie isotopique du lithium dans les basaltes-Géochimie des ...
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 />
study: The first one is within the glassy quenched part of the pillow, and the second one is<br />
an internal fragment located 5 cm below the pillow natural surface �i.e., 5 cm below the<br />
interface sea water/lava�. Three olivine crystals were chosen for the detailed chemical and<br />
isotopic study: in the first section, an euhedral crystal, 5 mm in size, located in the glassy<br />
rim of the pillow �crystal Ol4‐11, see Fig. 3.7� and, in the second section, two joined olivine<br />
crystals embedded in the microcrystalline groundmass �3 mm in size for the larger one:<br />
crystal Ol5‐20, see Fig. 3.8�. Major elements, Li concentrations and Li isotopic compositions<br />
were measured by electron and ion microprobes. Electron microprobe analyses for major<br />
elements were carried out at Ifremer �Centre de Brest� with a Cameca SX50. The analyses<br />
were obtained at 15 kV accelerating voltage with a sample current of �12 nA using a set of<br />
oxide<br />
and silicate standards.<br />
2.1. Li concentrations measurements<br />
The <strong>lithium</strong> concentrations and isotopic compositions were measured by ion<br />
microprobe at CRPG‐CNRS �Nancy� using the analytical proce<strong>du</strong>res which were developed<br />
on the small radius �Cameca ims 3f� and the large radius �Cameca ims 1270� instruments,<br />
as previously <strong>des</strong>cribed �Chaussidon and Robert, 1998; Beck et al., 2004, 2006; Barrat et<br />
al., 2005�. On both instruments, carbon‐coated polished samp<strong>les</strong> were sputtered with an O ‐<br />
beam of approximately 25 μm size. The secondary 6 Li � and 7 Li � ions were accelerated at<br />
4.5 kV for the ims 3f and at 10kV for the ims 1270 and were counted in mono‐collection<br />
mode on an electron multiplier using magnetic peak switching. The background on the two<br />
multipliers was monitored <strong>du</strong>ring the different sessions: it was below 0.05 cps �count per<br />
second� for the ims 3f and below 0.02 cps for the ims 1270. The count rates, which were in<br />
the range from ≈ 50 000 cps to ≈ 250 000 cps on 7 Li � , were corrected for a dead time of 44<br />
ns.<br />
The Li concentration were measured with the ims 3f �the greater transmission of the<br />
ims 1270 is not required in this case� by classical energy filtering �‐60V�10V�. The ion<br />
yield of Li relative to Si was determined on a silicate glass standard �UTR 2 having 63.4<br />
μg/g Li and 74.12 wt% SiO2, courtesy of John Stix�. Eight analyses of this standard gave an<br />
ion yield of Li �yield Li � �Li � /Si � �/�Li/Si�� of 1.48 � 0.03. The repro<strong>du</strong>cibility of this yield<br />
on one of our olivine standards �Ol BZ 29� having a much lower content �3.1 μg/g� was of<br />
4% relative. The Li concentrations are thus given in Table 3.2 with an error of � 5%<br />
95