guide to thin section microscopy - Mineralogical Society of America
guide to thin section microscopy - Mineralogical Society of America
guide to thin section microscopy - Mineralogical Society of America
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Guide <strong>to</strong> Thin Section Microscopy<br />
Double refraction<br />
4.2.3.1 Observation without analyzer (plane-polarized light mode)<br />
In plane-polarized light, anisotropic minerals can only be distinguished from isotropic<br />
minerals if characteristic grain shapes are observed (e.g., elongate or platy habit), if the grains<br />
display relief changes such as chagrin contrast as the stage is turned (only in minerals with<br />
large differences in n z ' and n x '), or if the absorption colour changes with changing orientation<br />
(pleochroism).<br />
The birefringence (∆n) <strong>of</strong> minerals is commonly not large enough <strong>to</strong> create distinct chagrin<br />
effects, with the exception <strong>of</strong> carbonates. Fig. 4-22 shows the striking change <strong>of</strong> chagrin in<br />
calcite and dolomite due <strong>to</strong> their extreme birefringence (∆n = 0.172 Cal resp. 0.177 Dol ).<br />
Figure 4-22. Change <strong>of</strong> chagrin in calcite and dolomite during a 360˚ rotation <strong>of</strong> the stage.<br />
Crystal <strong>section</strong>s are oriented parallel <strong>to</strong> the c axis. Shown are the four positions where the vibration<br />
directions <strong>of</strong> the two waves in the crystal coincide exactly with the polarizer directions. In these<br />
positions, only the E-W vibrating wave is passing through the crystal. The large difference between the<br />
refractive indices <strong>of</strong> the O- and E-waves causes the change in chagrin (∆n = 0.172 Cal resp. 0.177 Dol ).<br />
The majority <strong>of</strong> minerals show no or very little pleochroism. Exceptions include <strong>to</strong>urmaline,<br />
members <strong>of</strong> the amphibole group, Fe-Ti-rich biotites as well as less common minerals such as<br />
piemontite, sapphirine, dumortierite, yoderite and lazulite (Fig. 4-10).<br />
Raith, Raase & Reinhardt – February 2012<br />
Pleochroic minerals <strong>of</strong> tetragonal, hexagonal and trigonal symmetry show two characteristic<br />
absorption colours parallel <strong>to</strong> the vibration directions <strong>of</strong> the E- and O-waves (dichroism).<br />
Crystal <strong>section</strong>s normal <strong>to</strong> the crystallographic c-axis (= optic axis) only show the absorption<br />
colour <strong>of</strong> the O-wave as the stage is rotated. Crystal <strong>section</strong>s parallel <strong>to</strong> the c-axis show an<br />
alternation between the absorption colour <strong>of</strong> the E-wave (E-W orientation <strong>of</strong> c) and the O-<br />
wave (N-S orientation <strong>of</strong> c) every 90˚ during stage rotation (Ch. 4.2.1, Figs. 4-11,12).<br />
Pleochroic minerals <strong>of</strong> orthorhombic, monoclinic and triclinic symmetry show three<br />
characteristic absorption colours parallel <strong>to</strong> the principal indicatrix axes X, Y and Z<br />
(trichroism). Crystal <strong>section</strong>s normal <strong>to</strong> one <strong>of</strong> the two optic axes show the absorption colour<br />
<strong>of</strong> the Y vibration direction as the stage is rotated. An identification <strong>of</strong> the absorption colours<br />
in the X, Y and Z directions requires specific crystal <strong>section</strong>s (Ch. 4.2.1, Figs. 4-14−17).<br />
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