3.2 Formation of Minerals

Minerals form when atoms bond together in a crystalline arrangement. Three main ways this occurs in nature are: 1) precipitation directly from an aqueous (water) solution with a temperature change, 2) crystallization from a magma with a temperature change, and 3) biological precipitation by the action of organisms.

3.2.1 Precipitation from aqueous solution

Solutions consist of ions or molecules, known as solutes, dissolved in a medium or solvent. In nature this solvent is usually water. Many minerals can be dissolved in water, such as halite or table salt, which has the composition sodium chloride, NaCl. The Na+1 and Cl-1 ions separate and disperse into the solution.

Precipitation is the reverse process, in which ions in solution come together to form solid minerals. Precipitation is dependent on the concentration of ions in solution and other factors such as temperature and pressure. The point at which a solvent cannot hold any more solute is called saturation. Precipitation can occur when the temperature of the solution falls, when the solute evaporates, or with changing chemical conditions in the solution. An example of precipitation in our homes is when water evaporates and leaves behind a rind of minerals on faucets, shower heads, and drinking glasses.

In nature, changes in environmental conditions may cause the minerals dissolved in water to form bonds and grow into crystals or cement grains of sediment together. In Utah, deposits of tufa formed from mineral-rich springs that emerged into the ice age Lake Bonneville. Now exposed in dry valleys, this porous tufa was a natural insulation used by pioneers to build their homes with a natural protection against summer heat and winter cold. The travertine terraces at Mammoth Hot Springs in Yellowstone Park are another example formed by calcite precipitation at the edges of the shallow spring-fed ponds.

Another example of precipitation occurs in the Great Salt Lake, Utah, where the concentration of sodium chloride and other salts is nearly eight times greater than in the world’s oceans [zotpressInText item=”{DU5CMSHJ}” format=”%num%” brackets=”yes”]. Streams carry salt ions into the lake from the surrounding mountains. With no other outlet, the water in the lake evaporates and the concentration of salt increases until saturation is reached and the minerals precipitate out as sediments. Similar salt deposits include halite and other precipitates, and occur in other lakes like Mono Lake in California and the Dead Sea.

3.2.2 Crystallization from Magma

Heat is energy that causes atoms in substances to vibrate. Temperature is a measure of the intensity of the vibration. If the vibrations are violent enough, chemical bonds are broken and the crystals melt releasing the ions into the melt. Magma is molten rock with freely moving ions. When magma is emplaced at depth or extruded onto the surface (then called lava), it starts to cool and mineral crystals can form.

3.2.3 Precipitation by Organisms

Many organisms build bones, shells, and body coverings by extracting ions from water and precipitating minerals biologically. The most common mineral precipitated by organisms is calcite, or calcium carbonate (CaCO3). Calcite is often precipitated by organisms as a polymorph called aragonite. Polymorphs are crystals with the same chemical formula but different crystal structures. Marine invertebrates such as corals and clams precipitate aragonite or calcite for their shells and structures. Upon death, their hard parts accumulate on the ocean floor as sediments, and eventually may become the sedimentary rock limestone. Though limestone can form inorganically, the vast majority is formed by this biological process. Another example is marine organisms called radiolaria, which are zooplankton that precipitate silica for their microscopic external shells. When the organisms die, the shells accumulate on the ocean floor and can form the sedimentary rock chert. An example of biologic precipitation from the vertebrate world is bone, which is composed mostly of a type of apatite, a mineral in the phosphate group. The apatite found in bones contains calcium and water in its structure and is called hydroxycarbonate apatite, Ca5(PO4)3(OH). As mentioned above, such substances are not technically minerals until the organism dies and these hard parts become fossils.

3.3 Silicate Minerals

Minerals are categorized based on their composition and structure. Silicate minerals are built around a molecular ion called the silicon-oxygen tetrahedron. A tetrahedron has a pyramid-like shape with four sides and four corners. Silicate minerals form the largest group of minerals on Earth, comprising the vast majority of the Earth’s mantle and crust. Of the nearly four thousand known minerals on Earth, most are rare. There are only a few that make up most of the rocks likely to be encountered by surface dwelling creatures like us. These are generally called the rock-forming minerals.

The silicon-oxygen tetrahedron (SiO4) consists of a single silicon atom at the center and four oxygen atoms located at the four corners of the tetrahedron. Each oxygen ion has a -2 charge and the silicon ion has a +4 charge. The silicon ion shares one of its four valence electrons with each of the four oxygen ions in a covalent bond to create a symmetrical geometric four-sided pyramid figure. Only half of the oxygen’s valence electrons are shared, giving the silicon-oxygen tetrahedron an ionic charge of -4. This silicon-oxygen tetrahedron forms bonds with many other combinations of ions to form the large group of silicate minerals.

The silicon ion is much smaller than the oxygen ions (see the figures) and fits into a small space in the center of the four large oxygen ions, seen if the top ball is removed (as shown in the figure to the right). Because only one of the valence electrons of the corner oxygens is shared, the silicon-oxygen tetrahedron has chemically active corners available to form bonds with other silica tetrahedra or other positively charged ions such as Al+3, Fe+2,+3, Mg+2, K+1, Na+1, and Ca+2. Depending on many factors, such as the original magma chemistry, silica-oxygen tetrahedra can combine with other tetrahedra in several different configurations. For example, tetrahedra can be isolated, attached in chains, sheets, or three dimensional structures. These combinations and others create the chemical structure in which positively charged ions can be inserted for unique chemical compositions forming silicate mineral groups.

3.3.1 The dark ferromagnesian silicates

The Olivine Family

Olivine is the primary mineral component in mantle rock such as peridotite and basalt. It is characteristically green when not weathered. The chemical formula is (Fe,Mg)2SiO4. As previously described, the comma between iron (Fe) and magnesium (Mg) indicates these two elements occur in a solid solution. Not to be confused with a liquid solution, a solid solution occurs when two or more elements have similar properties and can freely substitute for each other in the same location in the crystal structure.

Olivine is referred to as a mineral family because of the ability of iron and magnesium to substitute for each other. Iron and magnesium in the olivine family indicates a solid solution forming a compositional series within the mineral group which can form crystals of all iron as one end member and all mixtures of iron and magnesium in between to all magnesium at the other end member. Different mineral names are applied to compositions between these end members. In the olivine series of minerals, the iron and magnesium ions in the solid solution are about the same size and charge, so either atom can fit into the same location in the growing crystals. Within the cooling magma, the mineral crystals continue to grow until they solidify into igneous rock. The relative amounts of iron and magnesium in the parent magma determine which minerals in the series form. Other rarer elements with similar properties to iron or magnesium, like manganese (Mn), can substitute into the olivine crystalline structure in small amounts. Such ionic substitutions in mineral crystals give rise to the great variety of minerals and are often responsible for differences in color and other properties within a group or family of minerals. Olivine has a pure iron end-member (called fayalite) and a pure magnesium end-member (called forsterite). Chemically, olivine is mostly silica, iron, and magnesium and therefore is grouped among the dark-colored ferromagnesian (iron=ferro, magnesium=magnesian) or mafic minerals, a contraction of their chemical symbols Ma and Fe. Mafic minerals are also referred to as dark-colored ferromagnesian minerals. Ferro means iron and magnesian refers to magnesium. Ferromagnesian silicates tend to be more dense than non-ferromagnesian silicates. This difference in density ends up being important in controlling the behavior of the igneous rocks that are built from these minerals: whether a tectonic plate subducts or not is largely governed by the density of its rocks, which are in turn controlled by the density of the minerals that comprise them.

The crystal structure of olivine is built from independent silica tetrahedra. Minerals with independent tetrahedral structures are called neosilicates (or orthosilicates). In addition to olivine, other common neosilicate minerals include garnet, topaz, kyanite, and zircon.

Two other similar arrangements of tetrahedra are close in structure to the neosilicates and grade toward the next group of minerals, the pyroxenes. In a variation on independent tetrahedra called sorosilicates, there are minerals that share one oxygen between two tetrahedra, and include minerals like pistachio-green epidote, a gemstone. Another variation are the cyclosilicates, which as the name suggests, consist of tetrahedral rings, and include gemstones such as beryl, emerald, aquamarine, and tourmaline

3.3.2 Pyroxene Family

Pyroxene is another family of dark ferromagnesian minerals, typically black or dark green in color. Members of the pyroxene family have a complex chemical composition that includes iron, magnesium, aluminum, and other elements bonded to polymerized silica tetrahedra. Polymers are chains, sheets, or three-dimensional structures, and are formed by multiple tetrahedra covalently bonded via their corner oxygen atoms. Pyroxenes are commonly found in mafic igneous rocks such as peridotite, basalt, and gabbro, as well as metamorphic rocks like eclogite and blue schist.

Pyroxenes are built from long, single chains of polymerized silica tetrahedra in which tetrahedra share two corner oxygens. The silica chains are bonded together into the crystal structures by metal cations. A common member of the pyroxene family is augite, itself containing several solid solution series with a complex chemical formula (Ca,Na)(Mg,Fe,Al,Ti)(Si,Al)2O6 that gives rise to a number of individual mineral names.

This single-chain crystalline structure bonds with many elements, which can also freely substitute for each other. The generalized chemical composition for pyroxene is XZ(Al,Si)2O6. X represents the ions Na, Ca, Mg, or Fe, and Z represents Mg, Fe, or Al. These ions have similar ionic sizes, which allows many possible substitutions among them. Although the cations may freely substitute for each other in the crystal, they carry different ionic charges that must be balanced out in the final crystalline structure. For example Na has a charge of +1, but Ca has charge of +2. If a Na+ ion substitutes for a Ca+2 ion, it creates an unequal charge that must be balanced by other ionic substitutions elsewhere in the crystal. Note that ionic size is more important than ionic charge for substitutions to occur in solid solution series in crystals.

3.3.3 Amphibole Family

Amphibole minerals are built from polymerized double silica chains and they are also referred to as inosilicates. Imagine two pyroxene chains that connect together by sharing a third oxygen on each tetrahedra. Amphiboles are usually found in igneous and metamorphic rocks and typically have a long-bladed crystal habit. The most common amphibole, hornblende, is usually black; however, they come in a variety of colors depending on their chemical composition. The metamorphic rock, amphibolite, is primarily composed of amphibole minerals.

Amphiboles are composed of iron, magnesium, aluminum, and other cations bonded with silica tetrahedra. These dark ferromagnesian minerals are commonly found in gabbro, baslt, diorite, and often form the black specks in granite. Their chemical formula is very complex and generally written as (RSi4O11)2, where R represents many different cations. For example, it can also be written more exactly as AX2Z5((Si,Al,Ti)8O22)(OH,F,Cl,O)2. In this formula A may be Ca, Na, K, Pb, or blank; X equals Li, Na, Mg, Fe, Mn, or Ca; and Z is Li, Na, Mg, Fe, Mn, Zn, Co, Ni, Al, Cr, Mn, V, Ti, or Zr. The substitutions create a wide variety of colors such as green, black, colorless, white, yellow, blue, or brown. Amphibole crystals can also include hydroxide ions (OH–), which occurs from an interaction between the growing minerals and water dissolved in magma.

3.3.4 Sheet Silicates

Sheet silicates are built from tetrahedra which share all three of their bottom corner oxygens thus forming sheets of tetrahedra with their top corners available for bonding with other atoms. Micas and clays are common types of sheet silicates, also known as phyllosilicates. Mica minerals are usually found in igneous and metamorphic rocks, while clay minerals are more often found in sedimentary rocks. Two frequently found micas are dark-colored biotite, frequently found in granite, and light-colored muscovite, found in the metamorphic rock called schist.

Chemically, sheet silicates usually contain silicon and oxygen in a 2:5 ratio (Si4O10). Micas contain mostly silica, aluminum, and potassium. Biotite mica has more iron and magnesium and is considered a ferromagnesian silicate mineral. Muscovite micas belong to the felsic silicate minerals. Felsic is a contraction formed from feldspar, the dominant mineral in felsic rocks.

The illustration of the crystalline structure of mica shows the corner O atoms bonded with K, Al, Mg, Fe, and Si atoms, forming polymerized sheets of linked tetrahedra, with an octahedral layer of Fe, Mg, or Al, between them. The yellow potassium ions form Van der Waals bonds (attraction and repulsion between atoms, molecules, and surfaces) and hold the sheets together. Van der Waals bonds differ from covalent and ionic bonds, and exist here between the sandwiches, holding them together into a stack of sandwiches. The Van der Waals bonds are weak compared to the bonds within the sheets, allowing the sandwiches to be separated along the potassium layers. This gives mica its characteristic property of easily cleaving into sheets.

Clays minerals occur in sediments formed by the weathering of rocks and are another family of silicate minerals with a tetrahedral sheet structure. Clay minerals form a complex family, and are an important component of many sedimentary rocks. Other sheet silicates include serpentine and chlorite, found in metamorphic rocks.

Clay minerals are composed of hydrous aluminum silicates. One type of clay, kaolinite, has a structure like an open-faced sandwich, with the bread being a single layer of silicon-oxygen tetrahedra and a layer of aluminum as the spread in an octahedral configuration with the top oxygens of the sheets.

3.3.5 Framework Silicates

Quartz and feldspar are the two most abundant minerals in the continental crust. In fact, feldspar itself is the single most abundant mineral in the Earth’s crust. There are two types of feldspar, one containing potassium and abundant in felsic rocks of the continental crust, and the other with sodium and calcium abundant in the mafic rocks of oceanic crust. Together with quartz, these minerals are classified as framework silicates. They are built with a three-dimensional framework of silica tetrahedra in which all four corner oxygens are shared with adjacent tetrahedra. Within these frameworks in feldspar are holes and spaces into which other ions like aluminum, potassium, sodium, and calcium can fit giving rise to a variety of mineral compositions and mineral names.

Feldspars are usually found in igneous rocks, such as granite, rhyolite, and basalt as well as metamorphic rocks and detrital sedimentary rocks. Detrital sedimentary rocks are composed of mechanically weathered rock particles, like sand and gravel. Quartz is especially abundant in detrital sedimentary rocks because it is very resistant to disintegration by weathering. While quartz is the most abundant mineral on the Earth’s surface, due to its durability, the feldspar minerals are the most abundant minerals in the Earth’s crust, comprising roughly 50% of the total minerals that make up the crust.

Quartz is composed of pure silica, SiO2, with the tetrahedra arranged in a three dimensional framework. Impurities consisting of atoms within this framework give rise to many varieties of quartz among which are gemstones like amethyst, rose quartz, and citrine. Feldspars are mostly silica with aluminum, potassium, sodium, and calcium. Orthoclase feldspar (KAlSi3O8), also called potassium feldspar or K-spar, is made of silica, aluminum, and potassium. Quartz and orthoclase feldspar are felsic minerals. Felsic is the compositional term applied to continental igneous minerals and rocks that contain an abundance of silica. Another feldspar is plagioclase with the formula (Ca,Na)AlSi3O8, the solid solution (Ca,Na) indicating a series of minerals, one end of the series with calcium CaAl2Si2O8, called anorthite, and the other end with sodium NaAlSi3O8, called albite. Note how the mineral accommodates the substitution of Ca++ and Na+. Minerals in this solid solution series have different mineral names.

Note that aluminum, which has a similar ionic size to silicon, can substitute for silicon inside the tetrahedra (see figure). Because potassium ions are so much larger than sodium and calcium ions, which are very similar in size, the inability of the crystal lattice to accommodate both potassium and sodium/calcium gives rise to the two families of feldspar, orthoclase and plagioclase respectively. Framework silicates are called tectosilicates and include the alkali metal-rich feldspathoids and zeolites.

3.4 Non-Silicate Minerals

The crystal structure of non-silicate minerals (see table) does not contain silica-oxygen tetrahedra. Many non-silicate minerals are economically important and provide metallic resources such as copper, lead, and iron. They also include valuable non-metallic products such as salt, construction materials, and fertilizer.

Mineral Group Examples Formula Uses

Native elements gold, silver, copper Au, Ag, Cu Jewelry, coins, industry

Carbonates calcite, dolomite CaCO3, CaMg(CO3)2 Lime, Portland cement

Oxides hematite, magnetite, bauxite Fe2O3, Fe3O4, a mixture of aluminum oxides

Ores of iron & aluminum, pigments

Halides halite, sylvite NaCl, KCl Table salt, fertilizer

Sulfides galena, chalcopyrite, cinnabar PbS, CuFeS2, HgS Ores of lead, copper, mercury

Sulphates gypsum, epsom salts CaSo4·2H2O, MgSO4·7H2O Sheetrock, therapeutic soak

Phosphates apatite Ca5(PO4)3(F,Cl,OH) Fertilizer, teeth, bones

3.4.1 Carbonates

Calcite (CaCO3) and dolomite (CaMg(CO3)2) are the two most frequently occurring carbonate minerals, and usually occur in sedimentary rocks, such as limestone and dolostone rocks, respectively. Some carbonate rocks, such calcite and dolomite, are formed via evaporation and precipitation. However, most carbonate-rich rocks, such as limestone, are created by the lithification of fossilized marine organisms. These organisms, including those we can see and many microscopic organisms, have shells or exoskeletons consisting of calcium carbonate (CaCO3). When these organisms die, their remains accumulate on the floor of the water body in which they live and the soft body parts decompose and dissolve away. The calcium carbonate hard parts become included in the sediments, eventually becoming the sedimentary rock called limestone. While limestone may contain large, easy to see fossils, most limestones contain the remains of microscopic creatures and thus originate from biological processes.

Calcite crystals show an interesting property called birefringence, meaning they polarize light into two wave components vibrating at right angles to each other. As the two light waves pass through the crystal, they travel at different velocities and are separated by refraction into two different travel paths. In other words, the crystal produces a double image of objects viewed through it. Because they polarize light, calcite crystals are used in special petrographic microscopes for studying minerals and rocks.

Many non-silicate minerals are referred to as salts. The term salts used here refers to compounds made by replacing the hydrogen in natural acids. The most abundant natural acid is carbonic acid that forms by the solution of carbon dioxide in water. Carbonate minerals are salts built around the carbonate ion (CO3-2) where calcium and/or magnesium replace the hydrogen in carbonic acid (H2CO3). Calcite and a closely related polymorph aragonite are secreted by organisms to form shells and physical structures like corals. Many such creatures draw both calcium and carbonate from dissolved bicarbonate ions (HCO3–) in ocean water. As seen in the mineral identification section below, calcite is easily dissolved in acid and thus effervesces in dilute hydrochloric acid (HCl). Small dropper bottles of dilute hydrochloric acid are often carried by geologists in the field as well as used in mineral identification labs.

Other salts include halite (NaCl) in which sodium replaces the hydrogen in hydrochloric acid and gypsum (Ca[SO4] • 2 H2O) in which calcium replaces the hydrogen in sulfuric acid. Note that some water molecules are also included in the gypsum crystal. Salts are often formed by evaporation and are called evaporite minerals.

The figure shows the crystal structure of calcite (CaCO3). Like silicon, carbon has four valence electrons. The carbonate unit consists of carbon atoms (tiny white dots) covalently bonded to three oxygen atoms (red), one oxygen sharing two valence electrons with the carbon and the other two sharing one valence electron each with the carbon, thus creating triangular units with a charge of -2. The negatively charged carbonate unit forms an ionic bond with the Ca ion (blue), which as a charge of +2.

3.4.2 Oxides, Halides, and Sulfides

After carbonates, the next most common non-silicate minerals are the oxides, halides, and sulfides.

Oxides consist of metal ions covalently bonded with oxygen. The most familiar oxide is rust, which is a combination of iron oxides (Fe2O3) and hydrated oxides. Hydrated oxides form when iron is exposed to oxygen and water. Iron oxides are important for producing metallic iron. When iron oxide or ore is smelted, it produces carbon dioxide (CO2) and metallic iron.

The red color in rocks is usually due to the presence of iron oxides. For example, the red sandstone cliffs in Zion National Park and throughout Southern Utah consist of white or colorless grains of quartz coated with iron oxide which serve as cementing agents holding the grains together.

Other iron oxides include limonite, magnetite, and hematite. Hematite occurs in many different crystal forms. The massive form shows no external structure. Botryoidal hematite shows large concentric blobs. Specular hematite looks like a mass of shiny metallic crystals. Oolitic hematite looks like a mass of dull red fish eggs. These different forms of hematite are polymorphs and all have the same formula, Fe2O3.

Other common oxide minerals include:

ice (H2O), an oxide of hydrogen

bauxite (Al2H2O4), hydrated oxides of aluminum, an ore for producing metallic aluminum

corundum (Al2O3), which includes ruby and sapphire gemstones.

The halides consist of halogens in column VII, usually fluorine or chlorine, ionically bonded with sodium or other cations. These include halite or sodium chloride (NaCl), common table salt; sylvite or potassium chloride (KCl); and fluorite or calcium fluoride (CaF2).

Halide minerals usually form from the evaporation of sea water or other isolated bodies of water. A well-known example of halide mineral deposits created by evaporation is the Bonneville Salt Flats, located west of the Great Salt Lake in Utah.

Many important metal ores are sulfides, in which metals are bonded to sulfur. Significant examples include: galena (lead sulfide), sphalerite (zinc sulfide), pyrite (iron sulfide, sometimes called “fool’s gold”), and chalcopyrite (iron-copper sulfide). Sulfides are well known for being important ore minerals. For example, galena is the main source of lead, sphalerite is the main source of zinc, and chalcopyrite is the main copper ore mineral mined in porphyry deposits like the Bingham mine (see chapter 16). The largest sources of nickel, antimony, molybdenum, arsenic, and mercury are also sulfides.

3.4.3 Sulfates

Sulfate minerals contain a metal ion, such as calcium, bonded to a sulfate ion. The sulfate ion is a combination of sulfur and oxygen (SO4–2). The sulfate mineral gypsum (CaSO4ᐧ2H2O) is used in construction materials such as plaster and drywall. Gypsum is often formed from evaporating water and usually contains water molecules in its crystalline structure. The ᐧ2H2O in the formula indicates the water molecules are whole H2O. This is different from minerals like amphibole, which contain a hydroxide ion (OH–) that is derived from water, but is missing a hydrogen ion (H+). The calcium sulfate without water is a different mineral than gypsum called anhydrite (CaSO4).

3.4.4 Phosphates

Phosphate minerals have a tetrahedral phosphate unit (PO4-3) combined with various anions and cations. In some cases arsenic or vanadium can substitute for phosphorus. Phosphates are an important ingredient of fertilizers as well as detergents, paint, and other products. The best known phosphate mineral is apatite, Ca5(PO4)3(F,Cl,OH), variations of which are found in teeth and bones. The gemstone turquoise [CuAl6(PO4)4(OH)8·4H2O ] is a copper-rich phosphate mineral that, like gypsum, contains water molecules.

3.4.5 Native Element Minerals

Native element minerals, usually metals, occur in nature in a pure or nearly pure state. Gold is an example of a native element mineral; it is not very reactive and rarely bonds with other elements so it is usually found in an isolated or pure state. The non-metallic and poorly-reactive mineral carbon is often found as a native element, such as graphite and diamonds. Mildly reactive metals like silver, copper, platinum, mercury, and sulfur sometimes occur as native element minerals. Reactive metals such as iron, lead, and aluminum almost always bond to other elements and are rarely found in a native state.

3.5 Identifying Minerals

Geologists identify minerals by their physical properties. In the field, where geologists may have limited access to advanced technology and powerful machines, they can still identify minerals by testing several physical properties: luster and color, streak, hardness, crystal habit, cleavage and fracture, and some special properties. Only a few common minerals make up the majority of Earth’s rocks and are usually seen as small grains in rocks. Of the several properties used for identifying minerals, it is good to consider which will be most useful for identifying them in small grains surrounded by other minerals.

Ways to identify minerals is by: Luster and color, streak, hardness, chrystal habit, and cleavage

3.5.1 Luster and Color

The first thing to notice about a mineral is its surface appearance, specifically luster and color. Luster describes how the mineral looks. Metallic luster looks like a shiny metal such as chrome, steel, silver, or gold. Submetallic luster has a duller appearance. Pewter, for example, shows submetallic luster. Nonmetallic luster doesn’t look like a metal and may be described as vitreous (glassy), earthy, silky, pearly, and other surface qualities. Nonmetallic minerals may be shiny, although their vitreous shine is different from metallic luster. See the table for descriptions and examples of nonmetallic luster.

Surface color may be helpful in identifying minerals, although it can be quite variable within the same mineral family. Mineral colors are affected by the main elements as well as impurities in the crystals. These impurities may be rare elements—like manganese, titanium, chromium, or lithium—even other molecules that are not normally part of the mineral formula. For example, the incorporation of water molecules gives quartz, which is normally clear, a milky color.

Some minerals predominantly show a single color. Malachite and azurite are green and blue, respectively, because of their copper content. Other minerals have a predictable range of colors due to elemental substitutions, usually via a solid solution. Feldspars, the most abundant minerals in the earth’s crust, are complex, have solid solution series, and present several colors including pink, white, green, gray and others. Other minerals also come in several colors, influenced by trace amounts of several elements. The same element may show up as different colors, in different minerals. With notable exceptions, color is usually not a definitive property of minerals. For identifying many minerals. a more reliable indicator is streak, which is the color of the powdered mineral.

3.5.2 Streak

Streak examines the color of a powdered mineral, and can be seen when a mineral sample is scratched or scraped on an unglazed porcelain streak plate. A paper page in a field notebook may also be used for the streak of some minerals. Minerals that are harder than the streak plate will not show streak, but will scratch the porcelain. For these minerals, a streak test can be obtained by powdering the mineral with a hammer and smearing the powder across a streak plate or notebook paper.

While mineral surface colors and appearances may vary, their streak colors can be diagnostically useful. An example of this property is seen in the iron-oxide mineral hematite. Hematite occurs in a variety of forms, colors and lusters, from shiny metallic silver to earthy red-brown, and different physical appearances. A hematite streak is consistently reddish brown, no matter what the original specimen looks like. Iron sulfide or pyrite, is a brassy metallic yellow. Commonly named fool’s gold, pyrite has a characteristic black to greenish-black streak.

3.5.3 Hardness

Hardness measures the ability of a mineral to scratch other substances. The Mohs Hardness Scale gives a number showing the relative scratch-resistance of minerals when compared to a standardized set of minerals of increasing hardness. The Mohs scale was developed by German geologist Fredrick Mohs in the early 20th century, although the idea of identifying minerals by hardness goes back thousands of years. Mohs hardness values are determined by the strength of a mineral’s atomic bonds.

The figure shows the minerals associated with specific hardness values, together with some common items readily available for use in field testing and mineral identification. The hardness values run from 1 to 10, with 10 being the hardest; however, the scale is not linear. Diamond defines a hardness of 10 and is actually about four times harder than corundum, which is 9. A steel pocketknife blade, which has a hardness value of 5.5, separates between hard and soft minerals on many mineral identification keys.

3.5.4 Crystal Habit

Minerals can be identified by crystal habit, how their crystals grow and appear in rocks. Crystal shapes are determined by the arrangement of the atoms within the crystal structure. For example, a cubic arrangement of atoms gives rise to a cubic-shaped mineral crystal. Crystal habit refers to typically observed shapes and characteristics; however, they can be affected by other minerals crystallizing in the same rock. When minerals are constrained so they do not develop their typical crystal habit, they are called anhedral. Subhedral crystals are partially formed shapes. For some minerals characteristic crystal habit is to grow crystal faces even when surrounded by other crystals in rock. An example is garnet. Minerals grown freely where the crystals are unconstrained and can take characteristic shapes often form crystal faces. A euhedral crystal has a perfectly formed, unconstrained shape. Some minerals crystallize in such tiny crystals, they do not show a specific crystal habit to the naked eye. Other minerals, like pyrite, can have an array of different crystal habits, including cubic, dodecahedral, octahedral, and massive. The table lists typical crystal habits of various minerals.

Another crystal habit that may be used to identify minerals is striations, which are dark and light parallel lines on a crystal face. Twinning is another, which occurs when the crystal structure replicates in mirror images along certain directions in the crystal.

Striations and twinning are related properties in some minerals including plagioclase feldspar. Striations are optical lines on a cleavage surface. Because of twinning in the crystal, striations show up on one of the two cleavage faces of the plagioclase crystal.

3.5.5 Cleavage and Fracture

Minerals often show characteristic patterns of breaking along specific cleavage planes or show characteristic fracture patterns. Cleavage planes are smooth, flat, parallel planes within the crystal. The cleavage planes may show as reflective surfaces on the crystal, as parallel cracks that penetrate into the crystal, or show on the edge or side of the crystal as a series of steps like rice terraces. Cleavage arises in crystals where the atomic bonds between atomic layers are weaker along some directions than others, meaning they will break preferentially along these planes. Because they develop on atomic surfaces in the crystal, cleavage planes are optically smooth and reflect light, although the actual break on the crystal may appear jagged or uneven. In such cleavages, the cleavage surface may appear like rice terraces on a mountainside that all reflect sunlight from a particular sun angle. Some minerals have a strong cleavage, some minerals only have weak cleavage or do not typically demonstrate cleavage.

Graphite has its carbon atoms arranged into layers with relatively strong bonds within the layer and very weak bonds between the layers. Thus graphite cleaves readily between the layers and the layers slide easily over one another giving graphite its lubricating quality.

Mineral fracture surfaces may be rough and uneven or they may be show conchoidal fracture. Uneven fracture patterns are described as irregular, splintery, fibrous. A conchoidal fracture has a smooth, curved surface like a shallow bowl or conch shell, often with curved ridges. Natural volcanic glass, called obsidian, breaks with this characteristic conchoidal pattern

To work with cleavage, it is important to remember that cleavage is a result of bonds separating along planes of atoms in the crystal structure. On some minerals, cleavage planes may be confused with crystal faces. This will usually not be an issue for crystals of minerals that grew together within rocks. The act of breaking the rock to expose a fresh face will most likely break the crystals along cleavage planes. Some cleavage planes are parallel with crystal faces but many are not. Cleavage planes are smooth, flat, parallel planes within the crystal. The cleavage planes may show as parallel cracks that penetrate into the crystal (see amphibole below), or show on the edge or side of the crystal as a series of steps like rice terraces. For some minerals characteristic crystal habit is to grow crystal faces even when surrounded by other crystals in rock. An example is garnet. Minerals grown freely where the crystals are unconstrained and can take characteristic shapes often form crystal faces (see quartz below).

In some minerals, distinguishing cleavage planes from crystal faces may be challenging for the student. Understanding the nature of cleavage and referring to the number of cleavage planes and cleavage angles on identification keys should provide the student with enough information to distinguish cleavages from crystal faces. Cleavage planes may show as multiple parallel cracks or flat surfaces on the crystal. Cleavage planes may be expressed as a series of steps like terraced rice paddies. See the cleavage surfaces on galena above or plagioclase below. Cleavage planes arise from the tendency of mineral crystals to break along specific planes of weakness within the crystal favored by atomic arrangements. The number of cleavage planes, the quality of the cleavage surfaces, and the angles between them are diagnostic for many minerals and cleavage is one of the most useful properties for identifying minerals. Learning to recognize cleavage is an especially important and useful skill in studying minerals.

As an identification property of minerals, cleavage is usually given in terms of the quality of the cleavage (perfect, imperfect, or none), the number of cleavage surfaces, and the angles between the surfaces. The most common number of cleavage plane directions in the common rock-forming minerals are: one perfect cleavage (as in mica), two cleavage planes (as in feldspar, pyroxene, and amphibole), and three cleavage planes (as in halite, calcite, and galena). One perfect cleavage (as in mica) develops on the top and bottom of the mineral specimen with many parallel cracks showing on the sides but no angle of intersection. Two cleavage planes intersect at an angle. Common cleavage angles are 60°, 75°, 90°, and 120°. Amphibole has two cleavage planes at 60° and 120°. Galena and halite have three cleavage planes at 90° (cubic cleavage). Calcite cleaves readily in three directions producing a cleavage figure called a rhomb that looks like a cube squashed over toward one corner giving rise to the approximately 75° cleavage angles. Pyroxene has an imperfect cleavage with two planes at 90°.

Cleavages on common rock-forming minerals

Quartz—none (conchoidal fracture)

Olivine—none (conchoidal fracture)

Mica—1 perfect

Feldspar—2 perfect at 90°

Pyroxene—2 imperfect at 90°

Amphibole—2 perfect at 60°/120°

Calcite—3 perfect at approximately 75°

Halite, galena, pyrite—3 perfect at 90°