There are about 4000 different mineral species known, and classifying
them can range from simple (for a couple of hundred) to very difficult.
A mineral can be identified by several physical properties, some
of them being sufficient for full identification without equivocation.
In other cases, minerals can only be classified by more complex
analyses including some modern techniques such as chemical analysis
and X-ray diffraction, which
however, can be costly, time-consuming, and even risk damaging
the sample.
Physical properties of minerals:
Cleavage describe
the way a mineral may come apart or cleave in different ways.
In thin sections, cleavage is visible as thin lines across
a mineral.
Color indicates
the appearance of the mineral in reflected light (i.e. what
it looks like to the naked eye).
Diaphaneity refers
to the degree to which a material transmits light.
Fracture describes
how a mineral breaks other than along natural cleavage planes.
Hardness: the physical hardness of a mineral is usually measured
according to the Mohs scale of mineral hardness.
Luster indicates the way a mineral's surface interacts with
light and can range from dull to glassy (vitreous).
Specific
Gravity: (or density) relates the mineral weight to the
weight of an equal volume of water.
Streak is
the color of a crushed mineral's powder.
Other properties: fluorescence (response to ultraviolet light),
magnetism, radioactivity, tenacity (response to mechanical induced
changes of shape or form.)
Chemical properties of minerals:
Minerals may be classified according to their chemical makeup
and are listed below in approximate order of their abundance
in the
Earth's crust.
The largest groups of minerals by far are the silicate. Some
important rock-forming silicates include the feldspars,
quartz, olivines,
pyroxenes, garnets and micas.
The carbonates consist of those minerals containing the
anion (CO3)2- and include calcite and aragonite (both
calcium carbonate),
dolomite
(magnesium/calcium carbonate) and siderite (iron carbonate).
Carbonates are commonly deposited in marine settings
when the shells of dead
planktonic life settle and accumulate on the sea floor.
Carbonates are also found in evaporitic settings (e.g.
the Great Salt
Lake, Utah) and also in karst regions, where the dissolution
and reprecipitation
of carbonates leads to the formation of caves, stalactites
and stalagmites.
Sulfates all contain the sulfate cation, in the form
SO4. Sulfates commonly form in evaporitic settings
where highly
saline waters
slowly evaporate, allowing the formation of both
sulfates and halides (q.v.) at the water-sediment interface.
Common sulfates
include
anhydrite (calcium sulfate) and gypsum (hydrated
calcium
sulfate).
The halides are the group of minerals forming the
natural salts and include fluoride, common
salt (known as halite)
and sal
ammoniac (ammonium chloride). Halides, like
sulfates, are commonly found
in evaporitic settings such as playa lakes
and landlocked seas (e.g. the Red Sea).
Oxides are extremely important in mining as
they form the ores from which valuable
metals can
be extracted. They
thus commonly
occur as precipitates close to the Earth's
surface. Common oxides include hematite
(hydrated iron
oxide = rust),
spinel (magnesium
aluminium oxide - a common component of
the mantle) and ice (hydrogen oxide!).
The phosphate group actually includes
any mineral with a tetrahedral
unit AO4 where
A can be
phosphorus, antimony,
arsenic or vanadium.
By far the most common phosphate
is apatite which is an important
biological mineral found in teeth
and bones of many animals.