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Diffusion in a multi-component system. (1) Diffusion without interaction. (2) Diffusion with electrostatic (chemical) interaction. Which D? Which species (Mg,, Si or O)? 2. Diffusion through grains or diffusion along grain-boundaries? (m=2 or 3). diffusion in olivine (volume diffusion).
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Diffusion in a multi-component system (1) Diffusion without interaction (2) Diffusion with electrostatic (chemical) interaction
Which D? Which species (Mg,, Si or O)? 2. Diffusion through grains or diffusion along grain-boundaries? (m=2 or 3)
dislocation (slip direction, slip plane: slip system)
Stress-strain field and energy of a dislocation Stress field Energy of a dislocation (J/m)
Dislocation creep The Orowan equation (m~2) v=v(s) for low stress Non-linear rheology (strain-rate~s, n~3) Anisotropic rheology: depends on the slip system n
Grain-size dependence of strength: grain-size reduction can result in significant weakening
Slip systems: deformation by dislocation motion is anisotropic
Plastic anisotropy (olivine) • Rate of deformation depends on the orientation of crystal (slip system). Durham et al. (1977) Bai et al. (1991)
Slip systems and deformation • The strength of a polycrystalline material is controlled largely by the strength of the hardest (strongest) slip system. • The deformation microstructure (lattice preferred orientation) is large controlled by the softest slip system.
Slip Systems and LPO Seismic anisotropy is likely due to lattice preferred orientation (LPO). Deformation of a crystal occurs by crystallographic slip on certain planes along certain directions (slip systems). During deformation, a crystal rotates to direction in which microscopic shear coincides with imposed macroscopic shear to form LPO. Therefore, if the dominant slip system changes, LPO will change (fabric transition), then the nature of seismic anisotropy will change. olivine
Deformation along the [001] orientation is more enhanced by water than deformation along the [100] orientation.
Water-induced fabric transitions in olivine Distribution of orientation of crystallographic axes is non-uniform after deformation (lattice preferred orientation). The pattern of orientation distribution changes with water content (and stress,----). Type A: “dry” low stress Type B: “wet” high stress Type C: “wet” low stress Jung and Karato (2001)
A lattice preferred orientation diagram for olivine (at high temperatures) Dominant LPO depends on the physical conditions of deformation. This diagram was constructed based on high-T data. What modifications could one need to apply this to lower-T? (Jung and Karato, 2001)
Thermal activation under stress jump probability At low stress At high stress
The Peierls mechanism At high stresses, the activation enthalpy becomes stress dependent.-> highly non-linear creep H*: enthalpy of formation of a kink pair p: Peierls stress slip system dependent (anisotropic) Effective activation enthalpy decreases with stress. Highly non-linear rheology (important at high stress, low temperature)
Pressure effects Pressure effects are large. In a simple model, pressure either enhances or suppresses deformation.
Reliable quantitative rheological data from currently available apparatus are limited to P<0.5 GPa (15 km depth: Rheology of more than 95% of the mantle is unconstrained!).
30-100% for P2-P1<0.5 GPa 3-10% for P2-P1<15 GPa Although uncertainties in each measurements are larger at higher-P experiments, the pressure effects (V*) can be much better constrained by higher-P experiments.
Various methods of deformation experiments under high-pressures Rotational Drickamer Apparatus (RDA) Multianvil apparatus stress-relaxation tests DAC D-DIA Very high-P Mostly at room T Unknown strain rate (results are not relevant to most regions of Earth’s interior.) Stress changes with time in one experiment. Complications in interpretation Constant shear strain-rate deformation experiments Large strain possible High-pressure can be achieved. Stress (strain) is heterogeneous. (complications in stress measurements) Constant displacement rate deformation experiments Easy X-ray stress (strain) measurements Strain is limited. Pressure may be limited.
Effect of pressure at the presence of water (water-saturated conditions) • Increased water fugacity enhances deformation at high P. • Pressure suppresses mobility of defects (V* effect). • non-monotonic dependence on P log viscosity pressure, GPa (Karato, 1989)
How could water be dissolved in nominally anhydrous minerals? • Water (hydrogen) is dissolved in nominally anhydrous minerals as “point defects” (impurities). • [Similar to impurities in Si (Ge).] (Karato, 1989; Bai and Kohlstedt, 1993)
Pressure effects under“wet” conditions can be more complicated. • Fugacity of water affects rheological properties. • Fugacity of water increases significantly with pressure.
Solubility of water in olivine • Given a plausible atomistic model, we can quantify the relation between solubility of water and thermodynamic conditions (pressure, temperature). • Solubility of water in olivine (mineral) increases with pressure. Kohlstedt et al. (1996)
Pressure effects on creep strength of olivine (“dry” conditions) • Strength increases monotonically with P under “dry” conditions. Strength, GPa Pressure, GPa
Pressure effects on creep strength of olivine (“wet” conditions) • Variation in the strength of olivine under “wet” conditions is different from that under “dry” conditions. • The strength changes with P in a non-monotonic way. • High-P data show much higher strength than low-P data would predict. strength, GPa pressure, GPa
nornalized strength water fugacity, GPa A two-parameter (r, V*) equation fits nicely to the data. nornalized strength pressure, GPa
The effects of water to reduce the viscosity are very large. (COH: water content) (Karato and Jung, 2003)
Stress measurement from X-ray diffraction d-spacing becomes orientation-dependent under nonhydrostatic stress. Strain (rate) can also be measured from X-ray imaging.