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 />
Conoscopy<br />
4.2.5 Conoscopic methods<br />
4.2.5.1 Some basic principles<br />
In "normal" orthoscopic view light enters the <strong>thin</strong> <strong>section</strong> orthogonally as a set <strong>of</strong> parallel,<br />
E-W vibrating light waves. The objective creates an enlarged, real, inverted image <strong>of</strong> the <strong>thin</strong><br />
<strong>section</strong>, which is then further enlarged and viewed through the ocular. The light rays entering<br />
the <strong>thin</strong> <strong>section</strong> travel through the mineral grains in defined crystallographic directions that<br />
depend on the respective orientation <strong>of</strong> the crystals. In order <strong>to</strong> record the optical behaviour<br />
<strong>of</strong> an anisotropic mineral species, crystal <strong>section</strong>s <strong>of</strong> different orientations must be studied, as<br />
outlined in previous chapters (e.g., crystal <strong>section</strong>s with maximum interference colour are<br />
needed <strong>to</strong> determine birefringence).<br />
Optic axial angle and optic sign cannot be determined directly in the orthoscopic mode <strong>of</strong><br />
operation, except in specific circumstances where the crystal symmetry is known <strong>to</strong> be high<br />
(hexagonal, trigonal, tetragonal) and where the crystal shape allows <strong>to</strong> identify the c-axis<br />
direction (cf. Ch. 4.2.4).<br />
As opposed <strong>to</strong> orthoscopy, the conoscopic view involves a convergent set <strong>of</strong> light rays, which<br />
means that a wide-angle cone <strong>of</strong> differently inclined light rays transmits the <strong>thin</strong> <strong>section</strong> (Fig.<br />
4-47). To achieve this, the illumination aperture is enlarged <strong>to</strong> a maximum by putting the<br />
auxiliary condenser lens in<strong>to</strong> the light path and opening the substage iris diaphragm.<br />
Raith, Raase & Reinhardt – February 2012<br />
Dependent on their propagation direction, the rays <strong>of</strong> this light cone will form an image in the<br />
focal plane above the objective, whereby the maximum opening angle <strong>of</strong> the cone <strong>of</strong> rays<br />
forming that image depends on the aperture <strong>of</strong> the objective used (Fig. 4-48). Since two<br />
orthogonally vibrating waves propagate generally in all directions wi<strong>thin</strong> optically anisotropic<br />
minerals, these wave couplets are brought in<strong>to</strong> interference in the analyzer, generating an<br />
interference figure. This interference figure can be viewed, either as an enlarged image by<br />
putting an auxiliary lens (Amici-Bertrand lens) in<strong>to</strong> the light path, or with the naked eye by<br />
removing an ocular and looking down the ocular tube. Light waves that travel in the direction<br />
<strong>of</strong> the microscope axis, and are thus oriented orthogonal <strong>to</strong> the <strong>thin</strong> <strong>section</strong> plane, form the<br />
centre <strong>of</strong> the interference figure. The larger the angle <strong>of</strong> the ray propagation direction <strong>to</strong> the<br />
microscope axis, the larger the distance <strong>of</strong> the image point from the centre <strong>of</strong> the interference<br />
figure. Thus, the conoscopic interference figure allows <strong>to</strong> study the propagation behaviour <strong>of</strong><br />
light in an anisotropic crystal quasi-simultaneously for a multitude <strong>of</strong> crystallographic<br />
directions wi<strong>thin</strong> that crystal.<br />
From the geometry <strong>of</strong> the interference figure and its modification through the use <strong>of</strong><br />
compensa<strong>to</strong>rs, the number <strong>of</strong> optic axes (uniaxial vs. biaxial), the optic axial angle (2V) and<br />
the optic sign (positive vs. negative) can be determined.<br />
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