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Title: The isotope effect for Mg-Fe interdiffusion in olivine and its dependence on crystal orientation, composition and temperature

Journal Article · · Geochimica et Cosmochimica Acta
 [1];  [2];  [3];  [4];  [5];  [4]
  1. Carnegie Inst. of Washington, Washington, DC (United States). Geophysical Lab.; Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States)
  2. Sorbonne Univ., Paris (France). Muséum National d'Histoire Naturelle, Inst. de Minéralogie, de Physique des Matériaux et de Cosmochimie
  3. Univ. of Chicago, IL (United States). Origins Lab., Dept. of the Geophysical Sciences and Enrico Fermi Inst
  4. Carnegie Inst. of Washington, Washington, DC (United States). Geophysical Lab.
  5. Carnegie Inst. of Washington, Washington, DC (United States). Dept. of Terrestrial Magnetism

Isotopic fractionation associated with diffusion in crystals is the most reliable means of understanding the origin of mineral zoning in igneous and metamorphic rocks. We have experimentally determined the relative diffusivities of iron isotopes in olivine as a function of crystallographic orientation, composition, and temperature. For two isotopes i and j of an element, the isotope effect for diffusion is parameterized as Di/Dj = (mj/mi)β, where β is a dimensionless parameter, and D and m stand for diffusivity and mass, respectively. A series of single crystal diffusion couple experiments were conducted at an oxygen fugacity of QFM – 1.5 at temperatures of 1200, 1300, and 1400 °C. Here, for the Fo83.4-Fo88.8 composition pair, βFe is isotropic and a value of 0.16 ± 0.09 can be used to describe diffusion along all major crystallographic axes in olivine. Based on our experiments and previously reported coupled Mg-Fe isotopic data, we also estimate βMg = 0.09 ± 0.05 for this range of olivine composition. For the Fo88.8-Fo100 composition pair, βFe becomes anisotropic with βFe [100] = 0.11 ± 0.03, βFe [010] = 0.14 ± 0.03 (both within error of the value measured for the Fo83.4-Fo88.8 pair), and βFe [001] = 0.03 ± 0.03. For Fo# between 83.4 and 100, βFe [100] and βFe [010] are thus independent of composition. The reason why βFe [001] transitions from ~0.16 to ~0.03 close to the Mg-endmember is unclear. Over the temperature range studied, a dependence of βFe on temperature was not resolved. General analytical expressions are introduced to calculate isotopic fractionation as a function of distance, time, β, and the concentration contrast between the diffusing media for spherical, cylindrical, and planar geometries.

Research Organization:
Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States)
Sponsoring Organization:
USDOE National Nuclear Security Administration (NNSA)
Grant/Contract Number:
AC52-07NA27344; EAR1444951; EAR1502591; LLNL-JRNL-736676; NNX15AJ25G; NNX17AE87G; NNX17AE86G; 2011JS56 004 01
OSTI ID:
1479057
Alternate ID(s):
OSTI ID: 1775794
Report Number(s):
LLNL-JRNL-736676; 889349
Journal Information:
Geochimica et Cosmochimica Acta, Vol. 239, Issue C; ISSN 0016-7037
Publisher:
The Geochemical Society; The Meteoritical SocietyCopyright Statement
Country of Publication:
United States
Language:
English
Citation Metrics:
Cited by: 11 works
Citation information provided by
Web of Science

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