Oxygen-isotope heterogeneity in the Northwest Africa 3358 (H3.1) refractory inclusions − Fluid-assisted isotopic exchange on the H-chondrite parent body

2020 ◽  
Vol 282 ◽  
pp. 98-112
Author(s):  
Samuel Ebert ◽  
Kazuhide Nagashima ◽  
Alexander N. Krot ◽  
Addi Bischoff
2020 ◽  
Author(s):  
Hideyuki Hayashi ◽  
Nak Kyu Kim ◽  
Hwayoung Kim ◽  
Changkun Park ◽  
Takashi Mikouchi

2003 ◽  
Vol 67 (20) ◽  
pp. 3959-3970 ◽  
Author(s):  
J.A. Barrat ◽  
A. Jambon ◽  
M. Bohn ◽  
J. Blichert-Toft ◽  
V. Sautter ◽  
...  

2014 ◽  
Vol 390 ◽  
pp. 165-174 ◽  
Author(s):  
Richard C. Greenwood ◽  
Jean-Alix Barrat ◽  
Akira Yamaguchi ◽  
Ian A. Franchi ◽  
Edward R.D. Scott ◽  
...  

2020 ◽  
Author(s):  
Martine Couapel ◽  
Corinne Sonzogni ◽  
Anne Alexandre ◽  
Florence Sylvestre

<p>Recent studies showed that the <sup>17</sup>O-excess of plant leaf biogenic silicates (phytoliths) can be used to quantify the atmospheric relative humidity occurring during leaf water transpiration. The <sup>17</sup>O-excess vs ∂<sup>18</sup>O signature of phytoliths can also be used to trace back to the signature of leaf water. In a similar way, the signature of lacustrine diatoms is expected to record the signature of the lake water in which they formed. Therefore, the triple oxygen isotope composition of biogenic silicates extracted from well-dated sedimentary cores may bring new insights for past climate and hydrological reconstructions. However, for high time-resolution reconstructions, we need to be able to measure microsamples (300 to 800 µg) of biogenic silica. In another context, the triple oxygen isotope composition of micro-meteorites constitutes an efficient tool to determine their parent-body. In this case too, micro-samples need to be handled.</p><p>Here we report the results of new ∂<sup>18</sup>O and ∂<sup>17</sup>O measurements of macro- and micro-samples of international and laboratory silicate standards (e.g. NBS28 quartz, San Carlos Olivine, Boulangé quartz, MSG phytoliths and PS diatoms). Molecular O<sub>2</sub> is extracted from silica and purified in a laser-fluorination line, passed through a 114°C slush to condense potential interfering gasses and sent to the dual-inlet Isotope Ratio Mass Spectrometer (IRMS) Thermo-Scientific Delta V. In order to get sufficient 34/32 and 33/32 signals for microsamples the O<sub>2</sub> gas is concentrated within the IRMS in an additional auto-cooled 800 ml microvolume tube filled with silica gel. Accuracy and reproducibility of the ∂<sup>18</sup>O, ∂<sup>17</sup>O and <sup>17</sup>O excess measurements are assessed. Attention is payed to determine the concentration from which O<sub>2</sub> gas yields offsets in ∂<sup>18</sup>O, ∂<sup>17</sup>O and <sup>17</sup>O-excess are measured and whether these offsets are reproducible and can be corrected for.</p>


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