Study of Ore Minerals in Reflected Light
Study of Ore Minerals in Reflected Light
TO OBSERVE COLOR
IFD (Illuminator Field Diaphragm) and IAD (Illuminator Aperture
Diaphragm) opened wide
Low power objective
High voltage for light of good intensity
Polarizer inserted, Analyzer withdrawn
Reflectivity: is the ratio of the intensity of light reflected by a mineral to the intensity of light
incident upon it, expressed in per cent (R or R%). Reflectance of minerals varies as a
function of the following:
a) Crystallographic orientation of the polished surface relative to the vibration directions
of linearly polarized incident light.
b) Wavelength of light.
c) Angle of incidence.
d) Degree of polish.
Quantitative reflectance measurements are done with various types of photometers, but rough
visual estimates may be made and minerals in a section may be arranged in an order of
increasing or decreasing reflectance. Eg. Quartz (5%), magnetite (20%), galena (43%), pyrite
(55%).
Bireflectance: Most minerals of the non isometric groups show changes in reflectance or
color (or tint) or both, when sections of certain orientations are rotated under plane polarized
light. These properties are collectively termed bireflectance. In some literature, bireflectance
refers only to change in reflectivity and reflection pleochroism is the term used to describe a
change in color. All sections of the cubic minerals and basal sections of the hexagonal and
tetragonal crystals do not exhibit these properties. In addition to noting this property it is
TO OBSERVE BIREFLECTANCE
IFD and IAD opened wide
Polarizer inserted, analyzer withdrawn
Low power objective
High voltage
Anisotropism: Polished sections of non-isotropic minerals, when rotated through 360o under
„crossed‟ nicols, will show either a) complete darkness, or b) faint illumination with no
change in intensity or color of illumination. Such minerals are termed isotropic. Minerals
crystallizing in the non-isometric systems will show a change in the intensity of illumination
or color of illumination (or both) in white light. Such minerals are termed anisotropic.
Sections of certain special orientations of anisotropic minerals (e.g. the basal sections of
hexagonal and tetragonal crystals) may be isotropic. As with pleochroism, the anisotropy can
range from a maximum to zero depending upon the orientation of the section, and therefore
the terms very weak, weak, moderate, strong and very strong are used to describe it.
Anisotropy is best observed under intense illumination using a plane glass reflector and a low
power occular. In cases of weak anisotropy, the effects may be detectable only when a
number of adjacent grains of a mineral are minutely examined while rotating the stage.
Observation of anisotropy may be more easily accomplished by either a) throwing the
analyzer slightly off from the precise crossed position, or b) leaving the stage stationary and
slowly rotating the analyzer 5-10o back and forth through its crossed position.
NOTE: Fine parallel scratches of improper polishing or careless buffing
can produce effects similar to pleochroism and anisotropy
Polarization colors: The change in color of a mineral during rotation under crossed nicols
produces a beautiful effect. These are the polarization colors. The polarization colors of
certain minerals are highly characteristic and extremely useful in identification. However
they are used less than they deserve to be for several reasons:
a) The colors are constant only if the nicols are precisely crossed, which is rarely the case.
b) Polarization colors appear different to different observers, hence the difficulty in applying
precise color terms.
c) The intensity and hue of polarization colors varies from microscope to microscope.
d) Constant illumination is necessary for consistent results.
Internal Reflections: Translucent minerals, when observed under reflected light, allow light
to penetrate beneath the surface and be reflected back to the observer from cracks, crystal
boundaries, cleavages and other flaws within the crystal. Such light will appear as diffuse
areas or patches known as internal reflections. Although visible in plane polarized light,
internal reflections are best seen under crossed nicols and intense illumination using oil
immersion and high power magnification. They are best seen at the edges of grains or in fine
grains. It is important to note that many grains of a mineral that could show internal
reflections may not exhibit them. Both the occurrence and colors of internal reflections are of
diagnostic value. The following are some examples:
Sphalerite Yellow to brown (sometimes red to green)
Cinnabar Blood red
Proustite-pyrargyrite Ruby red
Rutile Clear yellow to deep red-brown
Anatase Blue
Azurite Blue
Malachite Green
Cassiterite Yellow brown to yellow
Hematite Blood red
Wolframite Deep brown
Chromite Very deep brown
Crystal Form and Habit: Some ore minerals, particularly the harder ones viz., pyrite,
hematite, wolframite, arsenopyrite, cobaltite and magnetite have a remarkable power of
crystallization and develop well formed crystals even under adverse conditions. The softer
minerals, e.g. chalcopyrite, galena, tetrahedrite and pyrargyrite have somewhat lower powers
of crystallization and form crystals only in open spaces. Since a polished surface shows two
dimensional sections rather than whole crystals, the shape as seen in a polished section
depends upon the manner the crystal is intersected by the polished surface. Thus cubes
appear rectangular or triangular of various shapes; hexagonal prisms appear hexagonal or
rectangular, etc., so that the crystal form must be mentally reconstructed from observations of
a number of crystals of a particular mineral.
Terms used in mineralogy e.g. cubic, octahedral, acicular, radiating, columnar, bladed,
tabular, foliate, micaceous, concentric, colloform, prismatic, fibrous, etc. are appropriate for
describing crystal form and habit as seen in polished sections.
Zoning: Many ore minerals exhibit zonal growth in the form of concentrically shelled
structure indicating deposition in successive layers around a nucleus. The shells may be few
or many and thin or thick. Zoning is sometimes visible in ordinary light due to color
contrasts, physical discontinuities or zonally arranged inclusions. In other cases zoning is
visible only in crossed nicols or after etching with an appropriate chemical. Zoning in
minerals is due to either of the following reasons:
a) Pauses in deposition
b) changes in the rate of growth
c) Simultaneous crystallization of more than one mineral at certain stage / stages.
d) Variation in the composition of successively deposited layers.
Galena, sphalerite, pyrite, stibnite, cobaltite, safflorite and arsenopyrite are some of the many
minerals that show zonal structure.
Cleavage and Parting: In polished surfaces the cleavages of minerals are not as well
developed as in thin sections. Cleavage or parting is evident in the form of one or more sets
of parallel, distinct or indistinct cracks. Minerals may exhibit one to three sets of cleavages
depending upon the number of sets present and the orientation of the polished surface with
respect to these. The presence of three or more sets of cleavages may give rise to triangular
pits usually arranged in rows parallel to one set. Such pits are characteristic of galena, and
may also be present in magnetite, pentlandite, gersdorffite, etc. A prismatic cleavage gives
rise to diamond-shaped, triangular or rectangular patterns; a pinacoidal cleavage gives rise to
a set of parallel cracks.
Cleavage of a mineral may not be evident in a well polished surface, or in minerals occurring
in fine grained aggregates. It is likely to be more evident in slightly weathered ores, during
the earlier stages of polishing, at the margins of grains, or after etching.
Twinning: Three major types of twinning may be observed in ore minerals seen in polished
sections - growth, inversion and deformation. Twinning is best seen in anisotropic minerals
Study of Ore Minerals in Reflected Light 7
S. Farooq, Dept of Geology AMU
under crossed polars. In isotropic minerals it is generally not visible unless the surface is
etched. It is sometimes evident from abrupt changes in the orientation of cleavages or of
rows of inclusions. The crystallographic planes involved in twinning are usually not
determinable in polished sections.
Nevertheless, the twin patterns in some minerals are quite characteristic e.g. “arrowhead”
twins (growth) in marcasite, lamellar twins (deformation) in hematite and chalcopyrite and
“oleander leaf” twins (inversion) in chalcopyrite, stannite and acanthite.
Hardness: The term hardness as used in ore microscopy refers to a number of phenomenon.
Three types of hardnesses are particularly important – polishing, scratch and
microindentation. It is important to note that these three forms are not entirely equivalent,
being the response to different kinds of deformation or abrasion. Only the polishing hardness
shall be discussed here.
Polishing hardness is the resistance of a particular mineral to abrasion during the polishing
process. The fact that hard minerals are worn away more slowly than soft minerals means
that they may stand slightly above the surface of softer grains giving rise to an effect called
"polishing relief".
Polishing hardness can be examined under a standard ore microscope by comparing the
relative hardness (i.e. relief) of adjacent phases and can be very helpful in mineral
identification. The determination involves a simple test using the Kalb light line, a
phenomenon analogus to the Becke line used in transmitted light (see figure 2).