Miyawakiite-(Y)

Microscopic photo (a) and back-scattered electron image (b) of Miyawakiite-(Y)
(Reprinted from a publication of the Japanese Association of Mineralogical Sciences)

For 2024 the “Mineral of the Year” award has been assigned to miyawakiite-(Y). The mineral was discovered in an abandoned pegmatite mine located at Suishoyama, Iizaka village, Kawamata, Date District, Fukushima Prefecture, Japan, and was fully characterized by a Japanese research team lead by Daisuke Nishio-Hamane (Institute for Solid State Physics, University of Tokyo, Japan).
The pegmatite at the Suishoyama mine is rich in REE-bearing minerals, such as allanite-(Y) and britholite-(Y), plus carbonates such as caysichite-(Y) and tengerite-(Y). Miyawakiite-(Y) and the other carbonates occur as the secondary minerals formed by supergene alteration of allanite-(Y) and britholite-(Y). Miyawakiite-(Y) is the third mineral having the Suishoyama pegmatite as the type locality, besides britholite-(Y) (1938) and iwashiroite-(Y) (2003). The approximate GPS coordinates are 37°40’ N, 140°37′ E.
At the type locality miyawakiite-(Y) occurs as thin plates or columnar crystal with a pale yellow colour, transparent with a vitreous lustre, with dimensions typically ranging from 0.2 to 0.5 mm. The.
The ideal chemical formula of miyawakiite-(Y) is □Y4Fe2+2(Si8O20)(CO3)4(H2O)3. In the empirical formula K partially substitutes for vacancy, other REEs and Ca partially substitute for Y, Mg and Mn2+ partially substitute for Fe2+. Miyawakiite-(Y) is chemically related to caysichite-(Y), both being silicate minerals including REEs and carbonate groups. However the two minerals have different crystal structures.

Crystal structure of Miyawakiite-(Y)
(Reprinted from a publication of the Japanese Association of Mineralogical Sciences)
Zeolite–like channels of tetrahedra (a) and guest sites (b) in Miyawakiite-(Y)
(Reprinted from a publication of the Japanese Association of Mineralogical Sciences)

Mineral of the Year

Lazaraskeite

Lazaraskeite, Mineral of the Year, 2022

Fig. 1. Greenish-blue prismatic crystals of lazaraskeite (polytype M2), associated with chrysocolla, muscovite, orthoclase, calcite, and quartz. Photo: Warren G. Lazar.

For 2022 the “Mineral of the Year” award has been assigned to lazaraskeite. The mineral was discovered in the area of Oro Valley, north of Tucson, Pima County, Arizona, USA. It was found and fully characterized by a research team lead by Hexiong Yang, from the Department of Geosciences, University of Arizona, Tucson, AZ 85721-0077, USA.

More precisely lazaraskeite was found on the western end of Pusch Ridge, in the high elevation (975 m) of the Santa Catalina Mountains. where it occurs as individual crystals up to 0.2×0.2×0.8 mm or as aggregates. Crystals have a greenish-blue color, and are transparent (Fig. 1). Associated minerals are chrysocolla, malachite, wulfenite, mimetite, hydroxylpyromorphite, hematite, microcline, muscovite, and quartz.

The ideal chemical formula of lazaraskeite is Cu(C2H3O3)2. Therefore, it represents the first known example of an organic mineral containing glycolate. Shortly thereafter, three other glycolate minerals were discovered and described from the same locality: stanvevansite, jimkriegite, and lianbinite.

Fig. 2. Greenish-blue prismatic crystals of lazaraskeite (polytype M1). Field of view: 3 mm. Photo: Ron Gibbs.

Lazaraskeite is monoclinic. Actually, two distinct polytypes occur, which have the same space group, P21/n, but different yet related structures. The unit cell parameters of lazaraskeite-M1 are a = 5.1049(2), b = 8.6742(4), c= 7.7566(3) Å, β = 106.834(2)°, whereas those of lazaraskeite-M2 are a = 5.1977(3), b = 7.4338(4), c = 8.8091(4) Å, β = 101.418(2)°. The crystal structures of both polytypes have been refined by single-crystal X-ray diffraction data to R = 2.6% (M1) and 2.4% (M2). The structure of lazaraskeite in both its variants is new among minerals, whereas synthetic Cu(C2H3O3)2 is known to have the same structure of polytype M1.

The mineral name is a composite after the names of the two mineral collectors who found it, Warren G. Lazar and Beverly Raskin. 

The state of Arizona is confirmed as the seat of beautiful and interesting crystals, since another mineral from Arizona got the “Mineral of the Year” award in 2017: rowleyite, after the Rowley mine, Maricopa County.

The full description of the new mineral has been published in the American Mineralogist [Yang, H., Gu, X., Gibbs, R., Evans, S., Downs, R.T., Jibrin, Z. (2022): Lazaraskeite, Cu(C2H3O3)2, the first organic mineral containing glycolate, from the Santa Catalina Mountains, Tucson, Arizona, U.S.A. American Mineralogist107, 509-516].

Ophirite

Ophirite, Mineral of the Year 2014

We are pleased to announce that for 2014 the “Mineral of the Year” award has been assigned to ophirite.

Ophirite, Ca2Mg4[Zn2Mn23+(H2O)2(Fe3+W9O34)2]·46H2O, is a new mineral species from the Ophir Hill Consolidated mine, Ophir district, Oquirrh Mountains, Tooele County, Utah, USA, and was described by Anthony R. Kampf of the Natural History Museum of Los Angeles County and co-authors: John M. Hughes (University of Vermont), Barbara P. Nash (University of Utah), Stephen E. Wright (Miami University), George R. Rossman (Caltech), and Joe Marty (Utah) (Kampf et al., 2014). Ophirite forms beautiful, orange-brown tablet-shaped crystals up to 1 mm in length and is the first known mineral to contain a lacunary defect derivative of the Keggin anion, i.e. a heteropolyanion missing some of its octahedral segments (Keggin, 1934). Phases with the Keggin anion are important in solid state chemistry as a catalyst (e.g. Sun et al., 2009).  

Kampf AR, Hughes JM, Nash BP, Wright SE, Rossman GR, Marty J (2014) Ophirite, Ca2Mg4[Zn2Mn23+(H2O)2(Fe3+WO34)2]·46H2O, a new mineral with a heteropolytungstate tri-lacunary Keggin anion. American Mineralogist 99: 1045-1051

Keggin JF (1934) The structure and formula of 12-phosphotungstic acid. Proceedings of the Royal Society A 144: 75-100 

Sun CY, Liu SX, Liang DD, Shao K9Z, Ren YH, Su ZM (2009) Highly stable crystalline catalysts based on a microporous metal−organic framework and polyoxometalates. Journal of the American Chemical Society 131: 1883-1888

Chanabayaite

Chanabayaite, Mineral of the Year 2015

We are pleased to announce that for 2015 the “Mineral of the Year” award has been assigned to  chanabayaite.

This mineral was discovered and studied by Nikita V. Chukanov of the Russian Academy of Sciences (Chernogolovka, Moscow Region) in collaboration with Natalia V. Zubkova (Moscow State University, MSU), Gerhard Möhn (Niedernhausen, Germany), Igor V. Pekov (MSU), Dmitry Yu. Pushcharovsky (MSU), and Aleksandr E. Zadov (NPP Teplokhim, Moscow). 

Chanabayaite, Cu2(N3C2H2)Cl(NH3,Cl,H2O,[])4, is a new mineral species from Mt. Pabellón de Pica near the village of Chanabaya in the Tarapacá region of Chile (Chukanov et al. 2015). This unusual organometallic mineral does not only have a unique crystal structure that features the 1,2,4-triazolate anion (N3C2H2)-, but also acts as a “bridge” between the geosphere and the biosphere because its deep-blue crystals formed where guano deposits (the source of the C and N) came into contact with a chalcopyrite-bearing gabbro (which supplied the Cu). Chanabayaite formed by Na and Cl leaching from, and by the dehydration of, another triazolate-bearing natural compound – and potentially another new mineral – NaCu2Cl3[N3C2H2]2[NH3]2·4H2O (Zubkova et al. 2016).


Chukanov NV (2014) Infrared Spectra of Mineral Species: Extended Library. Springer-Verlag GmbH, Dordrecht–Heidelberg–New York–London, 1, 716 pp
Chukanov NV, Chervonnyi AD (2016) Infrared Spectroscopy of Minerals and Related Compounds. Springer, Cham–Heidelberg– Dordrecht–New York–London, 1,109 pp
Chukanov NV and 5 coauthors (2015) Chanabayaite, Cu2(N3C2H2)Cl(NH3,Cl,H2O,[])4, a new mineral containing triazolate anion. Geology of Ore Deposits 57: 712-720
Zubkova NV and 7 coauthors (2016) The crystal structure of the natural 1,2,4-triazolate compound NaCu2Cl3[N3C2H2]2[NH3]2·4H2O. Zeitschrift für Kristallographie 231: 47-54

Merelaniite

Merelaniite, Mineral of the year 2016

We are pleased to announce that for 2016 the “Mineral of the Year” award has been assigned to  merelaniite. This mineral was discovered in collector specimens from the Merelani region in northeastern Tanzania, and investigated by John A. Jaszczak (Michigan Technological University, Houghton, USA), Michael S. Rumsey (Natural History Museum, London, UK), Luca Bindi (Università di Firenze, Florence, Italy), Stephen A. Hackney (MTU), Michael A. Wise (National Museum of Natural History, Washington, USA), Chris J. Stanley (NHM), and John Spratt (NHM). Merelaniite (Mo4Pb4VSbS15), whose unusual whisker-like crystals were initially mistaken for molybdenite, is actually a new member of the cylindrite group (Jaszczak et al. 2016). The new species is remarkable not only for its morphology, which is reminiscent of slender, partially unwound microscopic “scrolls”, or the structure composed of alternating pseudo-tetragonal (PbS-type) and pseudo-hexagonal (MoS2-type) layers, but also for the fact that it comes from the famous mining area that has produced the gemstone tanzanite (vanadium-bearing blue zoisite) for 50 years. Other unusual minerals found in association with merelaniite are well-crystallized wurtzite and alabandite, which represent just one evolutionary stage in the complex metamorphic history of the Merelani deposits. We would like to congratulate John Jaszczak and his co-authors on this award and encourage the readers to learn more about merelaniite from theiropen-access article in Minerals(www.mdpi.com/2075-163X/6/4/115).

Jaszczak JA, Rumsey MS, Bindi L, Hackney SA, Wise MA, Stanley CJ, Spratt J (2016) Merelaniite, Mo4Pb4VSbS15, a new molybdenum-essential member of the cylindrite group, from the Merelani tanzanite deposit, Lelatema Mountains, Manyara Region, Tanzania. Minerals 6:115.

Rowleyite

Rowleyite, Mineral of the year 2017

We are pleased to announce that for 2017 the “Mineral of the Year” award has been assigned to rowleyite.

The prestigious title went to black cuboctahedral crystals peppering green mottramite in an underground tunnel at the abandoned Rowley mine in Arizona, and named for the type locality rowleyite. The chemical formula of this new species is as complex as its crystal structure, and both are a testament to the capabilities of modern science and to the uniqueness of geological conditions that led to rowleyite crystallization. Although structurally related compounds are known in materials science as “salt-templated mesoporous solids” and “polyoxometalates”, it is difficult to succinctly identify something that has the formula [Na(NH4,K)9Cl4][V25+,4+(P,As)O8]6·n[H2O, Na,NH4,K,Cl]. Rowleyite can be described as a phosphovanadate with a zeolite-like, porous framework, in which small cages host the [(NH4,K)9Cl4]5+ clusters forming a “salt net” and large cages accommodate H2O, NH4, Na, K and Cl. This paragon of mineralogical complexity was discovered and published in American Mineralogist (volume 102, pages 1037-1044) by Anthony R. Kampf (Natural History Museum of Los Angeles County, USA), Mark A. Cooper (University of Manitoba, Canada), Barbara P. Nash and Thure E. Cerling (University of Utah, USA), Joe Marty (Salt Lake City, Utah), Daniel R. Hummer (Southern Illinois University, USA), Aaron J. Celestian (Natural History Museum of Los Angeles County), Timothy P. Rose (Lawrence Livermore National Laboratory, USA), and Thomas J. Trebisky (University of Arizona, USA). Congratulations to the winning team on this exciting discovery!

The two closest runners-up were kegginite (another polyoxovanadate from the Packrat mine in Colorado, described by Anthony R. Kampf and colleagues (2017) in American Mineralogist and the Ti3+-dominant garnet rubinite discovered in the Vigarano, Allende and Efremovka carbonaceous chondrites by Chi Ma et al. (2017).

How does it looks like, check it out, here.


Kampf AR, Cooper MA, Nash BP, Cerling TE, Marty J, Hummer DR, Celestian AJ, Rose TP, Trebisky TJ (2017) Rowleyite, [Na(NH4,K)9Cl4][V5+,4+2(P,As)O8]6·n[H2O,Na,NH4,K, Cl][Na(NH4,K)9Cl4][V25+,4+(P,As)O8]·n[H2O,Na,NH4,K,Cl]⁠, a new mineral with a microporous framework structure. American Mineralogist 102: 1037-1044

Kampf AR, Hughes JM, Nash BP, Marty J (2017) Kegginite, Pb3Ca3[AsV12O40(VO)]·20H2O, a new mineral with a novel ε-isomer of the Keggin anion. American Mineralogist 102: 461-465
Ma C, Yoshizaki T, Krot AN, Beckett JR, Nakamura T, Nagashima K, Muto J, Ivanova MA (2017) Discovery of rubinite, Ca3Ti3+2Si3O12, a new garnet mineral in refractory inclusions from carbonaceous chondrites. 80th Annual Meeting of the Meteoritical Society 2017 (LPI Contrib. No. 1987), 6023.pdf

Carmeltazite

Carmeltazite, Mineral of the year 2018

We are pleased to announce that for 2018 the “Mineral of the Year” award has been assigned to Carmeltazite.

The new complex oxide carmeltazite (ZrAl2Ti4O11) forms black inclusions in blue corundum crystals (“Carmel SapphireTM”) from Cretaceous pyroclastic rocks and associated alluvial deposits at Kishon Mid-Reach in northern Israel. Its name alludes to the type locality at Mt. Carmel and the three principal metals in its formula (Ti, Al and Zr). Carmeltazite was discovered by William L. Griffin (Macquarie University, Australia), Sarah E.M. Gain (University of Western Australia), Luca Bindi (Università degli Studi di Firenze, Italy), Vered Toledo (Shefa Gems Ltd., Israel), Fernando Cámara (Università degli Studi di Milano, Italy), Martin Saunders (University of Western Australia), and Suzanne Y. O’Reilly (Macquarie University). Since its description was published in Minerals (Griffin et al., 2018), the mineral has gained much publicity online as “the world’s newest gemstone” (EraGem, 2019), and even an “extraterrestrial mineral harder than diamonds” (Flatley, 2019). Although perfectly terrestrial in origin and not particularly gemmy, the Mineral of the Year 2018 does contain Ti3+, altogether rare in the geological environment, and possesses a peculiar crystal structure, which is remotely related to the close-packed arrangement of spinel. As can be seen from its formula, the structure of carmeltazite is cation- and anion-deficient relative to spinels, while its symmetry is reduced to orthorhombic. Perhaps even more remarkable than its public image or structure is the association of carmeltazite with other Ti3+ and carbide minerals, which indicates very unusual geological conditions in their volcanic cradle and promises new exciting discoveries in the future (Griffin et al., 2018).

We would also like to acknowledge here the close runners-up, which included the modular carbonato-phosphato-silicate aravaite from pyrometamorphic rocks of the Hatrurim Complex in Israel (Krüger et al., 2018) and the first-ever tin sulfate genplesite from the Oktyabr’skoe Cu-Ni-Pd-Pt deposit in Siberia, Russia (Pekov et al., 2018). Once again, we congratulate Bill Griffin and his co-authors on their interesting discovery.

Check out its structure, and its amazing color.

EraGem (2019) Carmeltazite the world’s newest gemstone (https://eragem.com/news/)
Griffin WL, Gain SEM, Bindi L, Toledo V, Cámara F, Saunders M, O’Reilly SY (2018) Carmeltazite, ZrAl2Ti4O11, a new mineral trapped in corundum from volcanic rocks of Mt Carmel, northern Israel. Minerals 8:601 (https://www.mdpi.com/2075-163X/8/12/601)

Seaborgite

Seaborgite, Mineral of the Year 2021

We are pleased to announce that for 2021 the “Mineral of the Year” award has been assigned to seaborgite. The mineral was found and fully characterized by a research team led by Anthony R. Kampf, from the Mineral Sciences Department of the Natural History Museum of Los Angeles County, Los Angeles, CA 90007, USA.

Seaborgite was found underground in the Blue Lizard mine, Red Canyon, White Canyon District, San Juan Co., Utah, USA, where it occurs on a thick crust of gypsum overlaying a matrix comprised mostly of quartz crystals. Associated minerals are copiapite, ferrinatrite, ivsite, metavoltine, römerite, and other currently unknown minerals.

Seaborgite occurs as long flattened prisms (or blades), light-yellow in color and up to 0.2 mm in length. Crystals typically occur in radiating sprays, and looks very nice (first figure).

The ideal chemical formula of seaborgite is LiNa6K2(UO2)(SO4)5(SO3OH)(H2O), hence is an uranyl sulfate mineral. Seaborgite is the only known mineral species containing both lithium and uranium as species-forming elements, and it is also one of the few minerals containing three distinct alkali metals.

Seaborgite is triclinic, with space group: P-1, and unit cell parameters = 5.4511(4), = 14.4870(12), = 15.8735(15) Å,  and alpha=76.295(5), beta = 81.439(6), gamma =85.511(6)° . Its crystal structure has been refined by single-crystal X-ray diffraction data to = 3.77%. The structure of seaborgite (second figure) is new and unprecedented, although it is based on the same uranyl sulfate cluster that is topologically identical to the one occurring in the crystal structure of bluelizardite.

The mineral was named after Glenn Seaborg (1912-1999), an American chemist who was involved in the synthesis, discovery and investigation of 10 transuranium elements, including seaborgium. These studies led him to win the 1951 Nobel Prize in Chemistry.

Seaborgite is the third “Mineral of the Year” winner having its type locality in the USA. The previous winners were ophirite (2014, after the Ophir mine, Tooele Co., Utah) and rowleyite (2017, after the Rowley mine, Maricopa Co., Arizona).

The Blue Lizard mine was a prolific mineralogical site, being the type locality for 22 other new mineral species besides seaborgite.

The full description of the new mineral has been published in the American Mineralogist [Kampf, A.R., Olds, T.A., Plášil, J., Marty, J., Perry, S.N., Corcoran, L., Burns, P.C. (2021): Seaborgite, LiNa6K2(UO2)(SO4)5(SO3OH)(H2O), the first uranyl mineral containing lithium. American Mineralogist, 106, 105-111].