Endmember in the context of "Anorthite"

Plagioclase (/ˈplædʒ(i)əˌkleɪs, ˈpleɪdʒ-, -ˌkleɪz/ PLAJ-(ee)-ə-klayss, PLAYJ-, -⁠klayz) is a series of tectosilicate (framework silicate) minerals within the feldspar group. Rather than referring to a particular mineral with a specific chemical composition, plagioclase is a continuous solid solution series, more properly known as the plagioclase feldspar series. This was first shown by the German mineralogist Johann Friedrich Christian Hessel (1796–1872) in 1826. The series ranges from albite to anorthite endmembers (with respective compositions NaAlSi₃O₈ to CaAl₂Si₂O₈), where sodium and calcium atoms can substitute for each other in the mineral's crystal lattice structure. Plagioclase in hand samples is often identified by its polysynthetic crystal twinning or "record-groove" effect.

Plagioclase is a major constituent mineral in Earth's crust and is consequently an important diagnostic tool in petrology for identifying the composition, origin and evolution of igneous rocks. Plagioclase is also a major constituent of rock in the highlands of the Moon. Analysis of thermal emission spectra from the surface of Mars suggests that plagioclase is the most abundant mineral in the crust of Mars.

Orthoclase, or orthoclase feldspar (endmember formula KAlSi₃O₈), is an important tectosilicate mineral which forms igneous rock. The name is from the Ancient Greek for "straight fracture", because its two cleavage planes are at right angles to each other. It is a type of alkali feldspar, also known as potassium feldspar or K-spar. The gem known as moonstone (see below) is largely composed of orthoclase.

Biotite is a common group of phyllosilicate minerals within the mica group, with the approximate chemical formula K(Mg,Fe)₃AlSi₃O₁₀(F,OH)₂. It is primarily a solid-solution series between the iron-endmember annite, and the magnesium-endmember phlogopite; more aluminous end-members include siderophyllite and eastonite. Biotite was regarded as a mineral species by the International Mineralogical Association until 1998, when its status was changed to a mineral group. The term biotite is still used to describe unanalysed dark micas in the field. Biotite was named by J.F.L. Hausmann in 1847 in honor of the French physicist Jean-Baptiste Biot, who performed early research into the many optical properties of mica.

Members of the biotite group are sheet silicates. Iron, magnesium, aluminium, silicon, oxygen, and hydrogen form sheets that are weakly bound together by potassium ions. The term "iron mica" is sometimes used for iron-rich biotite, but the term also refers to a flaky micaceous form of haematite, and the field term Lepidomelane for unanalysed iron-rich Biotite avoids this ambiguity. Biotite is also sometimes called "black mica" as opposed to "white mica" (muscovite) – both may form in the same rocks, and in some instances side by side.

Hydroxyapatite (IMA name: hydroxylapatite) (Hap, HAp, or HA) is a naturally occurring mineral form of apatite with the formula Ca₅(PO₄)₃(OH), often written Ca₁₀(PO₄)₆(OH)₂ to denote that the crystal unit cell comprises two entities. It is the hydroxyl endmember of the complex apatite group. The OH ion can be replaced by fluoride or chloride, producing fluorapatite or chlorapatite. It crystallizes in the hexagonal crystal system. Pure hydroxyapatite powder is white. Naturally occurring apatites can, however, also have brown, yellow, or green colorations, comparable to the discolorations of dental fluorosis.

Up to 50% by volume and 70% by weight of human bone is a modified form of hydroxyapatite, known as bone mineral. Carbonated calcium-deficient hydroxyapatite is the main mineral of which dental enamel and dentin are composed. Hydroxyapatite crystals are also found in pathological calcifications such as those found in breast tumors, as well as calcifications within the pineal gland (and other structures of the brain) known as corpora arenacea or "brain sand".

Lizardite is a mineral from the serpentine subgroup with formula Mg₃(Si₂O₅)(OH)₄, and the most common type of mineral in the subgroup. It is also a member of the kaolinite-serpentine group.

Lizardite may form a solid-solution series with the nickel-bearing népouite (pure end-member: Ni₃(Si₂O₅)(OH)₄). Intermediate compositions (Mg,Ni)₃(Si₂O₅)(OH)₄ are possible, with varying proportions of magnesium and nickel. However, the lizardite end-member is much more common than pure népouite, a relatively rare mineral most often formed by the alteration of ultramafic rocks.