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
You also want an ePaper? Increase the reach of your titles
YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.
Guide <strong>to</strong> Thin Section Microscopy<br />
Double refraction<br />
Interference colours:<br />
In contrast <strong>to</strong> monochromatic light, the use <strong>of</strong> white light provides a full spectrum <strong>of</strong> wavelengths<br />
(spectral colours) which, for a given retardation, is modified in the analyzer through<br />
interference such that certain wavelengths are transmitted at full intensity; others are reduced<br />
<strong>to</strong> a variable degree or are obliterated entirely. White light exiting a colourless anisotropic<br />
crystal comprises an infinite number <strong>of</strong> wave couples corresponding <strong>to</strong> all spectral colours,<br />
each wavelength represented by a wave couple with mutually orthogonal vibration directions<br />
that are fixed by the crystal's orientation (cf. Figs. 4-25A and B which show such single wave<br />
couples). Interference in the analyzer between the two waves <strong>of</strong> each couple across the light<br />
spectrum is a way <strong>of</strong> making retardation visible and also quantifiable. Any specific<br />
retardation modifies the full white-light spectrum, generating a characteristic wavelength<br />
spectrum and wave amplitude pattern, which in combination produce a unique interference<br />
colour. Evidently, interference colours can only be generated from polychromatic light. They<br />
correlate directly with retardation. The sequence <strong>of</strong> interference colours in relation <strong>to</strong><br />
increasing retardation is explained graphically in Figs. 4-27 and 4-28.<br />
Raith, Raase & Reinhardt – February 2012<br />
Figure 4-27. Constructive and destructive interference as a function <strong>of</strong> wavelength λ and<br />
retardation Γ in the spectral range <strong>of</strong> visible light (see also Fig. 4-28). The variation <strong>of</strong> the<br />
intensity <strong>of</strong> the light being transmitted by the analyzer is described by the equation I =<br />
100[sin 2 (Γ/λ)180°].<br />
To give a few examples: In the lower range <strong>of</strong> retardation (Γ = 0 ↔ 200 nm) black and grey<br />
colour <strong>to</strong>nes dominate as the complete colour spectrum <strong>of</strong> white light is affected by a<br />
reduction <strong>of</strong> intensities. At around Γ = 250 nm only wavelengths from both ends <strong>of</strong> the<br />
spectrum are slightly diminished which is perceived as close <strong>to</strong> white ("first-order white").<br />
The range Γ = 400 ↔ 500 nm shows characteristic orange <strong>to</strong> light red interference colours, as<br />
blue and green wavelengths are suppressed, while longer wavelengths dominate the spectrum.<br />
This situation is reverse in the range Γ = 600 ↔ 650 nm. Here, the shorter wavelengths<br />
dominate, which results in a blue interference colour. The distinctive purple colour at Γ = 551<br />
nm ("first-order red") lies in a position where the intermediate wavelengths (green <strong>to</strong> orange)<br />
89