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Mineral Classes
Learn how minerals are organized into classes based on their chemical composition.
Overview
Minerals are classified into groups based on their chemical composition and crystal structure. The Dana and Strunz classification systems organize thousands of minerals into manageable groups. Understanding mineral classes helps identify minerals, predict their properties, and understand their formation. This systematic approach is fundamental to mineralogy.
Silicates: The Most Abundant Class
Silicates make up about 90% of Earth's crust:
Basic Structure: Silicates contain silicon and oxygen, forming the fundamental building block - the SiO₄ tetrahedron. Four oxygen atoms surround one silicon atom in a tetrahedral arrangement.
Subclasses:
- Nesosilicates: Isolated tetrahedra (olivine, garnet, zircon)
- Sorosilicates: Double tetrahedra (epidote, vesuvianite)
- Cyclosilicates: Ring structures (beryl, tourmaline)
- Inosilicates: Chain structures - single chains (pyroxenes) or double chains (amphiboles)
- Phyllosilicates: Sheet structures (micas, clays, talc)
- Tectosilicates: Framework structures (quartz, feldspars, zeolites)
Common Silicates: Quartz, feldspars, micas, pyroxenes, amphiboles, olivine, and garnet are all silicates. These are the rock-forming minerals.
Properties: Silicates vary widely in properties. Framework silicates (quartz, feldspars) are hard and common. Sheet silicates (micas) have perfect cleavage. Chain silicates (pyroxenes, amphiboles) form prismatic crystals.
Formation: Form in igneous, metamorphic, and some sedimentary environments. Most common minerals in all rock types.
Carbonates
Minerals containing the carbonate ion (CO₃²⁻):
Common Carbonates:
- Calcite (CaCO₃): Most common carbonate. Forms limestone and marble. Reacts with acid (effervesces).
- Dolomite (CaMg(CO₃)₂): Similar to calcite but with magnesium. Forms dolomite rock.
- Aragonite (CaCO₃): Different crystal structure than calcite. Less stable, converts to calcite over time.
- Siderite (FeCO₃): Iron carbonate, often brown.
- Rhodochrosite (MnCO₃): Manganese carbonate, often pink to red.
Properties: Generally soft (3-4 on Mohs scale), react with acid, often have rhombohedral cleavage. Many are colorful.
Formation: Form in sedimentary environments (limestone, dolomite), metamorphic environments (marble), and some hydrothermal environments.
Economic Importance: Limestone is used for cement, construction, and many industrial applications. Marble is valued for sculpture and building stone.
Identification: Acid test (dilute HCl) causes effervescence. This is a key identifying feature.
Oxides
Minerals where oxygen is combined with metals:
Important Oxides:
- Quartz (SiO₂): Technically an oxide, but usually classified separately. Most common mineral.
- Hematite (Fe₂O₃): Iron oxide, red to black. Important iron ore.
- Magnetite (Fe₃O₄): Magnetic iron oxide. Black, strongly magnetic.
- Corundum (Al₂O₃): Very hard (9). Ruby and sapphire are corundum.
- Rutile (TiO₂): Titanium oxide. Often forms needle-like crystals in quartz.
- Ilmenite (FeTiO₃): Iron-titanium oxide. Important titanium ore.
Properties: Wide range of properties. Some are very hard (corundum), others soft. Many are important ores.
Formation: Form in various environments - igneous, metamorphic, sedimentary, and through weathering. Many form through oxidation.
Economic Importance: Many oxides are important ores (iron, aluminum, titanium). Gem varieties (ruby, sapphire) are highly valued.
Special Properties: Some oxides have special properties - magnetite is magnetic, some are fluorescent, others have interesting colors.
Sulfides
Minerals containing sulfur combined with metals:
Common Sulfides:
- Pyrite (FeS₂): "Fool's gold." Metallic luster, brassy yellow. Cubic crystals common.
- Galena (PbS): Lead sulfide. Very dense, perfect cubic cleavage. Important lead ore.
- Sphalerite (ZnS): Zinc sulfide. Variable color, resinous luster. Important zinc ore.
- Chalcopyrite (CuFeS₂): Copper-iron sulfide. Brassy yellow, tarnishes to iridescent colors. Important copper ore.
- Arsenopyrite (FeAsS): Iron-arsenic sulfide. Silvery, often forms distinctive crystals.
Properties: Generally have metallic luster, are opaque, and many are important ores. Often form in cubic or other geometric shapes.
Formation: Primarily form in hydrothermal environments. Often associated with igneous activity and ore deposits.
Economic Importance: Many sulfides are important ores. Galena (lead), sphalerite (zinc), chalcopyrite (copper) are major sources of these metals.
Identification: Metallic luster, often brassy or silvery colors, and association with ore deposits are key characteristics. Some have distinctive crystal habits.
Caution: Some sulfides can be toxic or produce acid when exposed to air and water. Handle with care, especially in collections.
Sulfates, Halides, and Other Classes
Additional important mineral classes:
Sulfates: Contain the sulfate ion (SO₄²⁻)
- Gypsum (CaSO₄·2H₂O): Soft (2), forms crystals and massive forms (alabaster, selenite)
- Barite (BaSO₄): Very dense, often forms tabular crystals
- Anhydrite (CaSO₄): Gypsum without water. Harder than gypsum
Halides: Contain halogen elements (F, Cl, Br, I)
- Halite (NaCl): Table salt. Cubic crystals, perfect cubic cleavage, salty taste
- Fluorite (CaF₂): Often colorful, cubic crystals, fluorescent. Important industrial mineral
- Sylvite (KCl): Potassium chloride, similar to halite
Phosphates: Contain the phosphate ion (PO₄³⁻)
- Apatite (Ca₅(PO₄)₃(F,Cl,OH)): Common in igneous rocks, source of phosphorus
- Turquoise (CuAl₆(PO₄)₄(OH)₈·4H₂O): Valued gemstone, blue to green
Native Elements: Elements found in pure form
- Gold (Au): Precious metal, often in nuggets or flakes
- Silver (Ag): Precious metal, often tarnishes black
- Copper (Cu): Native copper, often in distinctive shapes
- Diamond (C): Pure carbon, hardest mineral
- Graphite (C): Also pure carbon, but very soft
Other Classes: Nitrates, borates, tungstates, molybdates, and others. Less common but include interesting and valuable minerals.
Classification Systems
How minerals are organized:
Dana Classification: Developed by James Dana in the 1800s. Organizes minerals by chemical composition and crystal structure. Still widely used, especially in the United States.
Strunz Classification: Developed by Hugo Strunz. Also based on chemical composition. More commonly used in Europe. Organizes minerals into 10 classes.
Chemical Classification: Groups minerals by their dominant anion (negative ion) or anionic group. This is the basis for most classification systems.
Crystal System: Minerals are also classified by their crystal system (cubic, tetragonal, etc.). This is a secondary classification.
Practical Use: Classification helps organize knowledge, predict properties, and identify minerals. Understanding classes helps narrow down identification possibilities.
Evolution: Classification systems evolve as new minerals are discovered and our understanding improves. New minerals are added to appropriate classes.
For Rockhounds: Understanding mineral classes helps you identify finds, understand where to look for specific minerals, and appreciate the diversity of the mineral world.