Mineralogy is an active science in which
minerals are discovered or recognised on a regular basis. Use of old mineral names is also discontinued, for example when a name is no longer considered valid. Therefore, a list of recognised mineral species is never complete.
Minerals are distinguished by various chemical and physical properties. Differences in chemical composition and crystal structure distinguish the various species. Within a mineral species there may be variation in physical properties or minor amounts of impurities that are recognized by mineralogists or wider society as a mineral variety.
The
International Mineralogical Association (IMA) is the international scientific group that recognises new minerals and new mineral names. However, minerals discovered before 1959 did not go through the official naming procedure. Some minerals published previously have been either confirmed or discredited since that date. This list contains a mixture of mineral names that have been approved since 1959 and those mineral names believed to still refer to valid mineral species (these are called "grandfathered" species). Presently, each year about 90–110 new mineral species (the sum of all mutations c. 120 per year) are officially approved by the Commission on New Minerals, Nomenclature and Classification (CNMNC) of the International Mineralogical Association.[1]
As of July 2023[update], the IMA - CNMNC Master List of Minerals lists 5,955 valid minerals, including 1,153 pre-IMA minerals (grandfathered), and 97 questionable minerals.[2] Also as of July 2023[update], the Handbook of Mineralogy lists 5,663 species,[3] and the IMA Database of Mineral Properties/Rruff Project lists 5,956 valid species (IMA/CNMNC) of a total of 6,189 minerals.[4] The IMA/Rruff database includes 1,164 pre-IMA minerals.[4]
Due to the length of this list, it is divided into alphabetical groups. The minerals are sorted by name.
Q or "?" – questionable/doubtful (IMA/CNMNC, mindat.org or mineralienatlas.de status).
N – published without approval of the IMA/CNMNC, or just not an IMA approved mineral but with some acceptance in the scientific community nowadays. The 'IMA database of mineral properties' (rruff.info/ima) has 173 species with 'not an IMA approved mineral' tag, some are an intermediate member of a
solid solution series, others are "recently" discredited minerals.[4]
I – intermediate member of a solid-solution series.
H – hypothetical mineral (synthetic, anthropogenic, etc.)
ch – incomplete description, hypothetical solid solution end member. Published without approval and formally discredited or not approved, yet.
group – a name used to designate a group of species, sometimes only a mineral group name.
Working practices
The name of a new mineral is kept confidential by the IMA until it is approved or until its full description is published, its authors' option (approved decision: 'IMA2009-D').[5] The IMA uses a code for its own procedures for the supposed new mineral (and so it is a synonym). Ferri-ottoliniite's proposal was assigned code 'IMA2001-067', it was redefined and approved as 'IMA2001-067a' in 2003, for instance (the ottoliniite root name is discredited since 2012).[6]
Current IMA regulations do not allow substances of anthropogenic origin (burning coal mine dumps, coal mine fires, slag, etc.) to be validated as a mineral species. Since 1998, the majority of
polymorphs (especially polytypes and polytypoids) are not regarded as separate mineral species anymore.[7]
IMA/CNMNC identifiers are usually written without space, as years don't get meaningful hits on Google search.
"The System of Mineralogy of James Dwight Dana and Edward Salisbury Dana" (8 ed.) was the reference of CNMNC/CNMMN's (IMA) initial work. At the
Kobe 2006 general meeting, the IMA council endorsed the creation of an Internet site on minerals ('rruff.info/ima'). So a Master List was needed and the older minerals were reviewed in a document of 130 pages. The final GQN List was published (grandfathered, questionable and published without approval) after a final review of Burke E A J and Nickel E H (approved decision: 'IMA2006-C'). Not only the well established minerals before 1959 was grandfathered (G), but the minerals that could not be discredited as well. The merging of the 'ARD List' (approved, revalidated and discredited) with the 'GQN List' resulted in the first 'IMA/CNMNC List of Mineral Names'. The 2007 draft of the 'IMA/CNMNC List of Mineral Names' was a courtesy of the Materials Data, Inc. (MDI), its 2009 review had important modifications.[8][9] The RRUFF database was built with the help of the MDI's 2007 draft, the IMA Master List is an update of the MDI's 2009 review.[10][11][12] Some grandfathered minerals had their status changed to approved afterwards, based on IMA approved reports. Note: the list of approved minerals was revised with 'The New IMA List of Minerals (September 2012)'.[13]
The IMA was founded in a meeting in Madrid (1958). The CNMMN (now CNMNC) was one of the original eight commissions, it was founded in 1959. Not all grandfathered mineral were first described prior to 1959.
Hatrurite, a phase in cement clinker (
alite, C3S), was first described in 1977, for instance.[14]
Some IMA/CNMNC (1959–2000) approved minerals had their complete description published only 2012: 'IMA1998-018' (
fluornatromicrolite, published 2011), 'IMA1987-046a' (
ferrolaueite, published 2012), 'IMA1978-064' (approval probably based on fake data), 'IMA1977-006' (
whelanite, published 2012) and 'IMA1968-003' (discredited, 'IMA2008-B'). 'IMA1995-025' was listed as well, a mistake (
natroglaucocerinite, published 1995).[1]
The paper of Armbruster et al. (2006) misunderstood the naming rules and renamed a well established mineral name (
hancockite).[23] Hatert et al. (2013) modified the naming rules.[24] and proposal IMA2015 s.p. was accepted, reverting the renaming.[25]
Sample:
bergenite was discredited as a barium bearing mineral variety of
phosphuranylite (IMA1962 s.p., special procedure). So phosphuranylite was already a valid mineral, and it is listed in the
Michael Fleischer's mineral list (1966).[26] Both are listed as grandfathered minerals as they are not listed in the 'ARD List' (approved, revalidated and discredited minerals; 2004).[27][28]
The review and approval of new mineral is straight forward most of the time, but there are exceptions. Proposal IMA2009-096 was not accepted, proposal IMA2009-096a was approved as
fontarnauite (6.DA.60) in 2014. Proposal IMA1995-020 was not accepted, proposal IMA1995-020c was approved as
jarandolite (6.CB.25).[27]
Every year some valid names get discredited (in the broader sense).
Tohdite (hydrous alumina) was conditionally approved as 'IMA2004-051'. But the re-examination of the holotype material of
akdalaite ((Al2O3)5·H2O, 'IMA1969-002') from the
Fersman Mineralogical Museum in Moscow showed that both minerals were identical (
space group was corrected).[29]
Tellurocanfieldite was conditionally approved as 'IMA2012-013'. Its approval was withdrawn as further studies showed it to be a Te-rich variety of
canfieldite (Y: 1894, 2.BA.70).[30]
Some old minerals were known before their 20th century names were first published.
Ramdohr (1936) discovered that the
type material of
schapbachite (Ag0.4Pb0.2Bi0.4S) was a mixture of
galena (PbS) and
matildite (AgBiS2).[32] It was discredited (1982) as it was found unstable at 'standard temperature and pressure' (STP).[33] It was revalidated (2004) as Pb-bearing schabachite is stable at STP.[34] The
type locality is not Schapbach now, but Silberbrünnle mine, Gengenbach; both
Black Forest localities.
Epsilon iron,
hexagonal close-packed (HCP) phase of iron is stable only at extremely high pressure. It can be found as a mineral (chemical formula: (Fe,Os,Ru,Ir)).
It is not only schapbachite that had a longer controversy. Other minerals have a complicated history, as well.
Imogolite, 9.ED.20, was first published 1962.[35][36] Its formal discreditation by the IMA was published 1967, as its description was incomplete.[37] The IMA referred it to the AIPEA (Association Internationale Pour l'Étude des Argiles) for advice and it was approved by the AIPEA (Nomenclature Committee) at its Tokyo meeting (1970).[38][39] Fleischer (1983) described it as a variety of
allophane and it was finally redefined and approved by the IMA/CNMNC 1986.[40][41]
Amorphous allophane,
nanotube-like imogolite (Al 2SiO 3(OH) 4),
halloysite-10Å (Al 2Si 2O 5(OH) 4·2H 2O), halloysite-7Å (Al 2Si 2O 5(OH) 4) and
gibbsite (Al(OH) 3) are thought to be products of
tuffweathering.
Betalommosovite was described by Gerasimovskiy and Kazakova (1962) and discredited by the IMA-CNMMN (IMA1967 s.p.). It was published without approval and listed as discredited on the 'IMA/CNMNC List of Mineral Names' (2009). Later, betalomonosovite was revalidated (IMA2014-J).[42][43]
Jichengite as xinghuaite (IMA1984-047) was rejected by the IMA-CNMMN. Jichengite (IMA1994-039) was rejected by the IMA-CNMMN, as well. Unfortunately, it was published without approval in 2011.[44][45]
UM1991-//-COF:BaCaCe (IMA1989-012), a calcium analogue of
cordylite-(Ce) from Bayan Obo mine, had the approval procedure suspended by
Joseph A. Mandarino, because of the cerium dominant cordylite (IMA2000-C).[46]
Other curiosities:
Niggliite (former 1.AG.60, year: 1938),
sorosite (former 1.AC.15, IMA1994-047),
yuanjiangite (former 1.AC.15, IMA1993-028) are not classified as tin alloys (PGE-metal alloys and indium-tin family) in Fleischer's Glossary. But, they are stannide minerals (nickeline mineral group), sulfide mineral class there.[47][48]
Tiragalloite (9.BJ.25, IMA1969-061, Mn2+4(HAsSi3O13)), is an arsenosilicate and
grenmarite (9.BE.25, IMA2003-024, (Na,Ca)4(Mn,Na)(Zr,Mn)2(Zr,Ti)(Si2O7)2(O,F)4) is a zirconium silicate (analogous to the more common
aluminosilicates, borosilicates and titanium silicates).[49][50]
Studtite (4.GA.15, year: 1947) is the first peroxide mineral, the
facies radioactivity generate peroxide.
Ianthinite (4.GA.10, year: 1926),
U(IV) is one of the constituents of the mineral), it gets a layer of
schoepite/
metaschoepite in the presence of oxygen.
Attention with the
amphiboles: some mineral names have been redefined (IMA2012 s.p. was the last revision), some even more than once; i.e. their chemical formula range changed.[6] For example, aluminotaramite ('IMA2006-023', 9.DE.20) is a synonym of
ferro-taramite, sodic-ferri-ferropedrizite (IMA2003 s.p., 9.DE.25) was renamed to
ferro-ferri-pedrizite, ehimeite is a synonym of
chromio-pargasite ('IMA2011-023', 9.DE.15), kôzulite is a synonym of
mangano-arfvedsonite ('IMA1968-028', 9.DE.25) and kornite is a synonym of
potassic-mangani-leakeite ('IMA1992-032', 9.DE.25).
Some IMA-CNMNC approved minerals have a questionable status on mineralienatlas.de, but their unit cell parameters are given on mindat.org (or vice versa). Their status here doesn't change, it remains 'approved mineral'.
The mineral systematic given on Nickel-Strunz (9 and 10 ed) is not controversial.
Dmisteinbergite (
feldspar, 9.EG.15), uranyl sorovanadates (4.HD. ids) and silica family (4.DA. ids) are some exceptions, for instance.
Great care must be taken with definitions and their redefinitions. There is a difference between rocks, natural minerals and chemical compounds. Some examples: rocksalt (a redirect),
halite and sodium chloride; kaolin earth (a redirect) and
kaolinite; apatite, strict sense (
chlorapatite,
fluorapatite and
hydroxylapatite), apatite group and apatite supergroup; kaolinite-serpentine group (alias serpentine),
serpentine subgroup, serpentinization and
serpentinite; olivine structural group (after rruff.nfo/ima); olivine group and
olivine (a
fosterite var.);
spessartine (a
garnet) and spessartite (a
lamprophyre);
iron (element),
telluric iron (alias native iron) and
meteoric iron;
phyllosilicate minerals (alias sheet silicates) and
clays;
pyrochlore (invalid mineral name since 2010), pyrochlore group and pyrochlore supergroup;
antimony and
stibnite (alias antimonite); etc.
The data of a mineral on the databases is similar but not equal. For instance:
Opal is a valid IMA/CNMNC name but it is a mineraloid (a mixture of
cristobalite and/or
tridymite and amorphous silica), it has a page on Mindat.org and Webmineral.com but not on the Handbook of Mineralogy.
Ice,
mercury (low melting point); allophane,
delvauxite,
hisingerite (amorphous/ poorly cristalline);
actinolite,
augite,
omphacite,
sanidine (intermediate member of a
solid solution series) are IMA/CNMNC valid names too. The reasons can be inherited pre-IMA status, practical reasons or entrenchment in the literature, including medical and legal usage.
OligoclaseI is an albite variety on Mindat.org and it has pages on the Handbook of Minerals and Webmineral.com, see 'List of minerals (synonyms)' (
plagioclase/
albite-
anorthite series). It is not the only intermediate member of a solid solution series with a page on the Handbook of Mineralogy (
mineral varieties).
Mindat.org uses to give the chemical formula of some minerals as a range (between parentheses, if tin dominant then
herzenbergite: (Sn,Pb)SnS2; otherwise
teallite: (Pb,Sn)SnS2), on the other side the IMA Database of Mineral Properties/ Rruff Project uses to give the ideal chemical formula of the solid solution end member (herzenbergite: SnS).
The given chemical names are a compromise for information purposes, being based on the Nickel-Strunz code too. Most of the time the chemical formula on rruff.info was used, sometimes the simpler one on mindat.org. To illustrate it:
bartonite, K3Fe10S14 (mindat.org), K6Fe20S26S (rruff.info);
bayleyite, Mg2(UO2)(CO3)3·18H2O (mindat.org), Mg2(UO2)(CO3)3(H2O)12·6H2O (rruff.info) and
bredigite, Ca7Mg(SiO4)4 (mindat.org), CaCa13Mg2(SiO4)8 (rruff.info).
Caution with the chemical formula units of silicates and their "formula masses". Some molecules have a repeating unit, these might be chains, networks,
polymers, and so the true molecule might be a multiple of the smallest repeating unit (the
unit cell of a crystal is formed by repeating 'Z' times the chemical formula). Examples:
wadsleyite (Mg2SiO4) a sorosilicate and high pressure polymorph of
forsterite and
ringwoodite;
leucophanite (NaCaBeSi2O6F), but it has Nickel-Strunz identifier 9.DH.05 (inosilicates with 4-periodic single chains, Si4O12);
clinoenstatite (MgSiO3), but it has Nickel-Strunz identifier 9.DA.10 (inosilicates with 2-periodic single chains, Si2O6);
scolecite (CaAl2Si3O10·3H2O), but it has Nickel-Strunz identifier 9.GA.05 (zeolites with T5O10 units – the fibrous zeolites);
mogánite (SiO2), but it has Nickel-Strunz identifier 4.DA.20 (oxides with small cations: silica family).
The existence in nature of some questionable/ doubtful minerals is very unlikely at all or at the
type locality. For example,
chloromagnesiteQ (Y: 1872, MgCl2) 3.AB.20 and
zinkositeQ (Y: 1852, ZnSO4) 7.AB.10.[52][53]
Some names are not names of minerals anymore, but names of a group of minerals:
The IMA/CNMMN, Subcommittee on Nomenclature of the Micas (1998, 1999) has recommended that the name biotite be used for a series including
phlogopite,
siderophyllite,
annite and
eastonite.[56]
Clark, A. (1993). Hey's Mineral Index (3 ed.). London: Chapman & Hall. p. 852.
Gaines, R.V.; Skinner, H.C.; Foord, E.E.; Mason, B.; Rosenzweig, A. (1997). Dana's New Mineralogy: The System of Mineralogy of James Dwight Dana and Edward Salisbury (8 ed.). New York: Wiley & Sons. p. 1819.
ISBN978-0-471-19310-4.
de Fourestier, Jeffrey (1999). Glossary of Mineral Synonyms. Canadian Mineralogist Special Publication 2 (2 ed.). Ottawa: Mineralogical Association of Canada. p. 445.
ISBN978-0-921294-44-3.
Strunz, Hugo; Nickel, Ernest H. (2001). Strunz Mineralogical Tables (9 ed.). Stuttgart: Schweizerbart. p. 869.
ISBN978-3-510-65188-7.
Ferraiolo, J.A. (2003). A Systematic Classification of Minerals. Bowie, US-MD. p. 441.{{
cite book}}: CS1 maint: location missing publisher (
link)
Back, Malcolm E. (2014). Fleischer's Glossary of Mineral Species (11 ed.). Tucson AZ: Mineralogical Record Inc. p. 434.
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^Nickel, E H; Mandarino, J A (1987). "Procedures involving the IMA Commission on New Minerals and Mineral Names and guidelines on mineral nomenclature". American Mineralogist. 72: 1031–1042.
^Bindi, L; Evain M; Spry P G; Menchetti S (2007). "The pearceite-polybasite group of minerals: crystal chemistry and new nomenclature rules". American Mineralogist. 92 (5–6): 918–925.
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^Wada, Koji; Yoshinaga, Naganori (January–February 1969).
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^Sokolova, E.; Hawthorne, F. C.; Abdu, Y.A.; Genovese, A.; Cámara, F. (2015). "Reapproval of betalomonosovite as a valid mineral species: single-crystal X-ray diffraction, HRTEM, Raman and IR". Periodico di Mineralogia. ECMS2015: 157–158.
^Whitney, D.L. (2002). "Coexisting andalusite, kyanite, and sillimanite: Sequential formation of three Al2SiO5 polymorphs during progressive metamorphism near the triple point, Sivrihisar, Turkey". American Mineralogist. 87 (4): 405–416.
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