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Rocks
Sedimentary rocks only make up 5% of the Earth's crust, but cover about 75% of the surface
of the earth. The raw material for sedimentary rocks comes from weathering. Two basic
:sources of sedimentary material are
1. Mineral and rock fragments or clasts produced by mechanical weathering or erosion
of rock. Resulting sediment deposits are called detrital, and rocks formed from the
sediment are called detrital sedimentary rocks.
2. Dissolved material that precipitates from solution. Rocks formed from this nondetrital
or chemical sediment are called chemical sedimentary rocks, and can be derived from
either inorganic or biochemical processes.
Depositional Environments
:Sediment can be deposited in many different environments
1. Continental
.a) Fluvial - Sediment was deposited by a stream
.b) Eolian - Sediment deposited by wind (deserts)
.c) Lacustrine - Lake sedimentary deposits
.d) Glacial - Sediment deposited by ice and meltwater
2. Marine - Sediment accumulates on the ocean floor in shallow (continental shelf and
reef) to deep (abyssal plain) environments.
3. Transitional - between land (terrestrial) and marine environments.
Lithification
:Lithification is the conversion of sediment into rock, and results from a number of processes
1. Compaction involves packing together of sediment grains through burial, leading to a
sediment particles together. Most common cements are calcite (CaCO3) and quartz
(SiO2), but dolomite [(CaMg)CO3], iron oxides (Fe2O3), and iron hydroxides
[FeO(OH)] may also serve as cements.
4. Crystallization characterizes chemical sediments, and primarily involves formation of
interlocking crystals.
B. Inorganic chemical sedimentary rocks originate from dissolved material that is precipitated
:inorganically. These rocks include
Limestone made up of calcite. Oolltic, travertine, and tufa forms of limestone are
precipitated inorganically; travertine, a freshwater limestone, differs from the other
types which are precipitated from seawater.
Dolostone made up of dolomite. Dolostone has been thought to form by the
replacement of limestone, although recent evidence indicates that some dolomite may
be biochemical in origin. Very little primary dolomite has been found.
Silica can precipitate as quartz, opal, or chert (cryptocrystalline silica including jasper,
agate, and flint), and can occur as irregular masses or nodules in other rocks,
especially limestone.
Bedded chert (silica) forms from accumulations of microscopic marine organisms that
secrete silica shells around their bodies.
that reflects changing conditions during deposition. Texture and composition are fairly
uniform within a bed. Layering is usually horizontal or sub-horizontal. Original
bedding can be obscured or destroyed through sediment flow or the action of
burrowing animals. Kinds of bedding include:
o
2. Ripple marks, small waves on the surface of sediment caused by water or wind
currents, can in some cases be used as a top of bed indicator. Two forms of ripples are
recognized:
o
Wave-formed ripple marks are symmetric ripple marks formed in a surf zone.
Current ripple marks, asymmetric ripple marks formed by water or air currents
moving generally in one direction, can be used as a current direction indicator.
Sedimentary Facies
Sedimentary rocks tend to change in composition and nature laterally due to changes in
depositional environment. Sediment can be deposited in different places at the same time, yet
look very different because of a different depositional environment. Sedimentary facies
reflect the characteristics of a particular depositional environment. These deposits each have a
distinctive set of physical, chemical and biological attributes. Sea level fluctuations can result
:in a particular facies being deposited over wide areas
MINERAL PROPERTIES
and identification procedures
Minerals represent just another complex structure in this greatly varied earth. There are endless
amounts of studies that can be covered when dealing with the topic of minerals. Minerals embody
numerous physical properties, which make them much more interesting and complex than commonly
perceived. Several of these properties are essential in mineral identification. With enough experience,
a mineral can often be accurately identified by simply viewing it. However, by conducting a few simple
tests, the identification procedure is exact and unmistakable.
Scientists identify elemental makeup by conducting complex test with expensive equipment, such as
x-rays and high powered electron microscopes. They use these techniques to identify minerals. For
the most part, though, minerals can be identified by conducting a few simple, costless tests. Once a
person becomes experienced in this field, he can usually identify a mineral by observing it and taking
into account its specific features, such as color and crystal formation.
Below is a list of all of these properties. Select a property to learn about it, and how it is used as an
identification procedure.
Color
Streak
hardness
Crystals
transparency
Specific Gravity
Luster
Cleavage
Parting
Fracture
Tenacity
Additional Properties
X-ray analysis
Blowpipe Test
Bead Test
Flame Test
Tube Test
Acid Test
color
is one of the most eye-catching feature of many minerals. Some minerals always have the same
color, such as gold, whereas some minerals, such as quartz and calcite, come in all colors. The
presence and intensity of certain elements determines a specimens color. Minerals with an
inherent color (i.e. all specimens of the mineral are the same color) have essential elements in
them which cause their color. Good examples are azurite and malachite, which have their strong
blue and green color due to their copper in their atomic structure. But there are many minerals
which have slight additions of color-causing elements in some specimens that cause it to be a
different color. For example, pure quartz (SiO2), is colorless, whereas amethyst, a purple variety of
quartz, has its purple color caused by traces of iron. The amount of iron present determines the
intensity of the color.
Certain minerals exhibit a color change when exposed to light, heat, or radiation. Realgar
transforms into orpiment, and orpiment crumbles into a light-yellow powder if exposed to light.
Some minerals, such as proustite and vivianite, darken upon prolonged exposure to light,
whereas other minerals, such as kunzite fade. Some minerals undergo color changes when
put under intense heat. This method is sometimes used to artificially enhance the color of
some gemstones. Some varieties of topaz, beryl, and corundum are heat treated to produce
deep colored gemstones from rather dull ones. Radioactivity can also have an effect, as is the
cause of smoky quartz.
Most secondary copper minerals show a bright blue (and sometimes green) color. Iron usually
causes a mineral to exhibit a dark red or brown color, and manganese is responsible for the
coloring of many pink minerals. Some minerals, such as cassiterite and zincite, have chemical
structures that would cause them to be colorless, but due to impurities they are never found
colorless. Most secondary uranium minerals exhibit either a bright neon yellow or green color.
Often, a mineral is coated or "pseudomorphed", causing it to exhibit the color of the replaced
or coated mineral. Two common examples are: hematite coating quartz, and limonite
pseudomorph after pyrite.
Minerals containing the elements aluminum, sodium, and potassium are usually colorless or
very lightly colored. In some cases, the color of a mineral may depend on its atomic bonding
rather than composition, such as by diamond and graphite. Both these minerals have the
same are formed from the same material (carbon), yet one is almost always white or very
lightly colored, while the other is dark gray to black.
Many times, minute traces of a mineral in or over another mineral can cause a color change.
Two fine examples are:
1) Malachite on quartz, causing the quartz appear to be green.
2) Rutile inclusions in quartz, giving the quartz a golden hue.
Several minerals tarnish, thereby affecting their color. The best examples are:
1) Silver, which tarnishes black, yellow, or brown
2) Copper, which tarnishes green
3) Bornite and chalcopyrite, which tarnish an iridescent play of colors
Some minerals, such as opal, display a multicolored effect when viewed from different angles.
This is called opalescence. A few minerals appear to change color when viewed in different
light. Alexandrite, a variety of chrysoberyl, is dark green in natural light, but takes on a
purplish hue in artificial light. Other minerals will change color when viewed at different
angles. This is called dichroism or pleochroism. Cordierite, the most famous dichroic mineral
is bluish-purple but turns gray when rotated or viewed at a different angle. The properties of
Streak
is the color of a crushed mineral's powder. The color of a mineral's powder may differ from the actual
color of the mineral. This property is useful for mineral identification.
Almost every mineral has an inherent streak color, no matter what color the actual mineral is. For
example, calcite occurs in many different colors, shapes, and varieties. But every single variety of
calcite has a white streak. Streak is very useful in distinguishing two minerals with the same color but
different streak. A fine example where streak is very useful is gold (yellow streak), and chalcopyrite
(black streak).
Most light colored, nonmetallic minerals have a white or colorless streak, as do most silicates,
carbonates, and most transparent minerals. The streak test is most useful for identifying dark colored
minerals, especially metals.
Most mineral references dont make a distinction between a white and colorless streak, since the
difference is minimal. A mineral with a white or colorless streak will not leave a visible streak on a
streak plate.
Hardness plays a major role in identifying a mineral. It can make the identification process much
simpler by considerably narrowing a search.
Hardness is defined by how well a substance will resist scratching by another substance. For
example, if mineral A scratches mineral B, and mineral B does not scratch mineral A, then mineral A is
harder than mineral B. If mineral A and B both scratch each other, then their hardness is equal or very
similar. A scale to measure hardness was devised by Austrian mineralogist Frederick (Friedrich) Mohs
in 1822, and is currently the standard scale for measuring hardness. The scale consists of numbers
one through ten; 1 being the softest and 10 being the hardest. Each number represents a different
mineral - each harder than the previous. The 10 minerals are:
1. Talc
2. Gypsum
3. Calcite
4. Fluorite
5. Apatite
6. Feldspar
7. Quartz
8. Topaz
9. Corundum
10. Diamond
All conceivable minerals fit in this scale, since talc is the softest known mineral and diamond the
hardest. To demonstrate how to use the scale, understand the following example: Suppose a mineral
scratches fluorite, but not apatite, then it has a hardness between 4 and 5.
Several common household items have a fixed hardness, and can be used to test for hardness:
fingernail
copper penny
knife blade
glass
steel file
Action
Conclusion
Two minerals with equal hardness will scratch each other. This gives an advantage to the hardness
testing kit that includes real minerals over rods. One can scratch the mineral from the kit instead of
scratching a nice specimen. In addition, one can also get more exact results by seeing if both
minerals scratch each other. We can add another step to the chart above for those that have
hardness testing kits composed of minerals rather than rods:
Mineral strikes testing kit mineral number 3 (Calcite). Testing kit mineral gets
scratched.
Mineral hardness is 3.
If the mineral strikes testing kit mineral 2 and 3 and scratches neither, the mineral has a hardness of 2.
Minerals can be damaged and lose value if not scratched properly. If a mineral testing kit is composed
of minerals (as opposed to rods), it is preferable for the testing kit mineral to be scratched over the
specimen. If this cannot be done, than the specimen has to be scratched. This should be done in an
area where a scratch will not make a noticeable mark.
Hardness can be easily detected without a "kit". All one needs to know is the hardness of certain
items (including the ones mentioned above) and minerals in his collection. These can be used instead
of purchasing a kit, which is an inessential investment.
Hardness testing is done by "swiping" one mineral with the other. The swipe should be strong enough
to make a scratch, but not so much as to damage the specimen. To get the most accurate results, a
sharp edge should be swiped against a smooth surface, on a small an area as possible. The scratch
should not be conducted on a surface that is coated, chipped, or weathered, for it will give inaccurate
results. Neither should it be conducted on a visible surface; a bad scratch on the face of a mineral can
diminish its value.
When a mineral is scratched, a permanent indentation is created. Powder of the softer mineral will
come off, and it will cover the scratch area. This powder must be brushed away to see if the mineral
really got scratched, or if the powder of the softer mineral that was swiped across the specimen being
tested created a scratch-like marking. When minerals of similar hardness are scratched together, it is
difficult to tell which mineral (if not both of them) is really getting scratched because of this.
All minerals are anisotropic, meaning their hardness varies in different directions. Kyanite is famous
for this habit. When scratched in one direction, it exhibits a hardness of 4 to 5. When struck from the
perpendicular direction, it exhibits a hardness of 6 to 7. Kyanite is the only mineral exhibiting such
strong anisotropism. In virtually all minerals, the anisotropism is so weak that it cannot be determined.
Micromounts and small embedded crystals are very hard to determine in terms of hardness. One may
not be able to test for hardness because of the small size.
Transparency
The amount of light passed through a mineral determines its transparency. Most light passes through
transparent minerals, translucent minerals partially let light pass through, and opaque minerals do not
let any light through. A mineral type can exhibit more than one level of transparency, and, in fact, most
transparent minerals also occur in translucent forms. Flaws, inclusions, and impurities degrade the
transparency of a mineral. Many minerals exhibit some forms that are completely transparent and
other forms that are completely opaque. Such minerals are labeled in the transparency section of this
guide as transparent to opaque. A number of minerals may seem opaque, but when held to a light
source seem to be letting a small amount of light pass through at its corners. A specimen with such
characteristics is said to be transparent in thin splinters or transparent in thin sections. All minerals
with a metallic luster are opaque. Most minerals with a submetallic luster are translucent in thin
splinters.
Specific Gravity, also known as SG, is a measurement that determines the density of minerals.
Two minerals may be the same size, but their weight may be very different. The specific gravity of a
mineral determines how heavy it is by its relative weight to water. The specific gravity value is
expressed upon how much greater the weight of the mineral is to an equal amount of water. Water
has a specific gravity of 1. If a mineral has a specific gravity of 2.7, it is 2.7 times heavier than water.
Minerals with a specific gravity under 2 are considered light, between 2 and 4.5 average, and greater
than 4.5 heavy. Most minerals with a metallic luster are heavy. The specific gravity may slightly vary
within a mineral because of impurities present in the minerals structure.
Luster describes how a mineral appears to reflects light, particularly how brilliant or dull the mineral
is. The terms applied to luster are:
Silky
Metallic - Minerals with a metallic luster are opaque and reflective, like metal. Metal elements, most
sulfides, and some oxides belong in this category.
Submetallic - For a mineral to fall in this category, it must be opaque to nearly opaque and reflect
well. Thin splinters or sections of submetallic minerals are translucent.
Vitreous - This luster accounts for roughly 70 percent of all minerals. Minerals with a vitreous luster
have reflective properties similar to glass. Most of the silicates, carbonates, phosphates, sulfates,
halides, and hydroxides have a vitreous luster.
Adamantine - Transparent to translucent minerals with a high refractive index yield an adamantine
luster, meaning they display extraordinary brilliance and shine.
Resinous - This is the luster of many yellow, dark orange, or brown minerals with moderately high
refractive indices -- honey like, but not necessarily the same color.
Silky - A silky luster is the result of a mineral having a fine fibrous structure. Minerals with a silky
luster have optical properties similar to silk cloth.
Pearly - Describes a luster similar to the inside of a mollusk shell or shirt button. Many mica's have
a pearly luster, and many minerals with a pearly luster have an iridescent hue. Some minerals may
exhibit a pearly luster on cleaved crystal surfaces parallel and below the reflecting surface of a
mineral.
Waxy - A waxy luster indicates a mineral that appears as if it were coated with a layer wax.
Dull - This luster defines minerals with poor reflective qualities, much like unglazed porcelain. Most
minerals with a dull luster have a rough or porous surface.
Every mineral has a characteristic luster, but some minerals may have a different luster on different
specimens. There is no scientific method to determine luster. Often, determining the luster of a
particular specimen is personal; to some it may appear as one type of luster, and to others as a
different type.
Cleavage, fracture, and parting all have to do with the positioning of atoms in a mineral and how it
breaks when put under stress. These three properties are listed on the same page due to their
comparability, but are each individually discussed.
Cleavage
Parting
Fracture
CLEAVAGE:
In mineral terms, cleavage describes how a crystal breaks when subject to stress on a particular
plane. If part of a crystal breaks due to stress and the broken piece retains a smooth plane or crystal
shape, the mineral has cleavage. A mineral that never produces any crystallized fragments when
broken off due to stress has no cleavage.
Cleavage is measured by two factors: quality and number of sides exhibiting cleavage. Quality of
cleavage can be categorized into four qualities:
Perfect
Good
Poor
None
Minerals with perfect cleavage cleave without leaving any rough surfaces; a full, smooth plane is
formed where the crystal broke. Minerals with good cleavage also leave smooth surfaces, but often
leave over some rough surfaces. In minerals with poor cleavage, the smooth crystal edge is barely
visible, since the rough surface is dominant. Minerals with no cleavage (none) never exhibit any
cleavage, thus broken surfaces are jagged and rough. If a mineral exhibits cleavage, but it so poor
that it is hardly noticeable, it has "indistinct" cleavage.
Categorization of cleavage qualities is not scientifically affirmed. The above categorization is used by
most mineral references, but some references categorize cleavage in three or five different groups,
and may give them different names, such as "excellent" and "distinct".
Many minerals exhibit cleavage only on one side, and some may exhibit different quality cleavage on
different sides. We may expect to find the following criteria when analyzing the cleavage of any
particular mineral:
One Direction
Two Directions
Three Directions
All Directions
These tell us how many crystal "directions" or planes of a mineral exhibit cleavage. Each direction
means two opposite sides of a three-dimensional figure, (since opposite sides exhibit the same
cleavage properties). If a mineral has cleavage in three directions, then every side of the mineral has
cleavage. If a mineral often occurs in modified crystals with more than six sides (i.e. octahedron) and
exhibits cleavage on all the sides, than we call that cleavage "all directions".
When we combine the cleavage level together with the number of sides, we have measured cleavage.
For example: A book states that the cleavage of a particular minerals is: Good, Two Directions. This
informs us that the mineral has good cleavage on four out of six sides (while the other sides exhibit no
cleavage). If the book tells us a different minerals cleavage is: Perfect, One Direction; Poor, Two
Directions, it means that the mineral has perfect cleavage on two sides, and poor cleavage on the
other four.
In this guide, cleavage is measured in numbers, first the quality, then the number of sides, separated
by a comma. If the cleavage of a mineral is written as 1,2 , the mineral has perfect cleavage. If the
word Indiscernible is written in the cleavage field of a mineral, then the cleavage of the mineral is so
poor it is hardly recognizable. If all sides of mineral have the same cleavage, and the mineral often
occurs in modified crystals with more than six sides, than All Sides is written instead of a number. If a
mineral exhibits different cleavage on different crystal planes, there will be two cleavage indicators
separated by a semi-colon (;). For example, if the cleavage of a mineral is written as 1,2-;- 3,1, than it
has perfect cleavage in one direction, and poor cleavage on two other directions. If a mineral exhibits
no cleavage, None is written in the field.
Different forms of cleavage exist on different minerals, depending on the mode of a minerals
crystallization. These forms of cleavage are:
Basal cleavage
Cleavage exhibited on a horizontal plane of the mineral by way of its base. Minerals with basal
cleavage can sometimes be "peeled".
Example = minerals of mica group.
Cubic cleavage
Cleavage exhibited on minerals of the isometric crystal system crystallized as cubes. In this method of
cleavage, small cubes evenly break off of an existing cube.
Example = galena.
Octahedral cleavage
Cleavage exhibited on minerals of the isometric crystal system crystallized as octahedrons. In this
method of cleavage, flat, triangular "wedges" peel off of an existing octahedron.
Example = fluorite.
Prismatic cleavage
Cleavage exhibited on some prismatic minerals in which a crystal cleaves by breaking off thin,
vertical, prismatic crystals off of the original prism.
Example = aegirine.
Pinicoidal cleavage
Cleavage exhibited on some prismatic and tabular minerals in which a crystal cleaves on the
pinicoidal plane, which is the third dimension aside from the basal and prismatic sides.
Example = barite.
Rhombohedral cleavage
Cleavage exhibited on minerals crystallizing in the hexagonal crystal system as rhombohedrons, in
which small rhombohedrons break off of the existing rhombohedron.
Example = calcite.
PARTING:
Parting is characteristically similar to cleavage. It is easily confused with cleavage, and is often
present on minerals that do not exhibit any cleavage. There are two causes of parting:
1. Two separate pressures pushed toward the center of a crystal after its formation, causing the
crystal interior to evenly dislodge on a flat, smooth plane.
2. Twin crystals that separated from one another, leaving a flat, smooth plane.
With enough perception, a distinction can be made between parting and cleavage. If fracture marks
are present on a crystal in addition to a cleaved plane, the "cleaved" surface is usually the result of
parting, not cleavage. An outline of a crystal etched in a mineral is also the result of parting, in the
form of twinned crystals that separated.
In general, one need not worry about confusing parting with cleavage. Parting is uncommon, and it
can usually be determined by the distinguishing characteristics mentioned above.
FRACTURE:
Fracture is the characteristic mark left when a mineral chips or breaks. Cleavage and fracture differ in
that cleavage is the break of a crystal face where a new face (resulting in a smooth plane) is formed,
whereas fracture is the "chipping" of a mineral. All minerals exhibit a fracture, even those that exhibit
cleavage. If a mineral with cleavage is chipped a certain way, it will fracture rather than cleave.
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