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Manaevite-(Ce)
A valid IMA mineral species
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About Manaevite-(Ce)
Formula:
(Ca13Ce4[H2O]2)Mg(Al3Mg)(Mg3Ti3Fe3+2)(◻4)◻[Si2O7]4[(SiO4)8(H4O4)2]O(OH)9
The formula is a partial simplification of the full structural formula. The large (VII-IX)-coordinated (X4)2(X3)8(X2)8(X1) sites are here combined (e.g. Ca19) and are typically filled with Ca, although other large cations such as the REE may be present. The square-pyramidal Y1 site can host a variety of M2+ and M3+ ions and is the basis for the distinction of several species. The VI-coordinated Y2 site typically is filled with Al, whereas the also VI-coordinated Y3 site may contain Al, Mg, and other cations of similar charge and size. The tetrahedral T1 site is typically vacant but may contain B (less commonly Al); the trigonal T2 site is also typically vacant but may also contain B. Some of the (SiO4) may be replaced by (H4O4), akin to the Si4+ ↔︎ 4H+ hydrogarnet substitution. Among the oxygen that are not part of the silica tetrahedra, there are eight "O11" that typically occur as OH, two "O10" that are typically O & OH or OH & OH (the latter arrangement notably when Y1 is an M2+ cation). There may also be up to three "O12" that in most vesuvianite-group minerals are absent (and are not included here), but may be present particularly when T1 is occupied.
Note that in lieu of published structural data, the Y2 and Y3 site occupancies denoted here are distributed as per other members of the other vesuvianite group minerals (i.e. Y2 = Al-dominant; Ti & Fe3+ assigned to Y3). These occupancies may be re-assigned with updated data. Justification for the -(REE) suffix is that REE (in this case predominately Ce) is the dominant cation in the X3 site.
Note that in lieu of published structural data, the Y2 and Y3 site occupancies denoted here are distributed as per other members of the other vesuvianite group minerals (i.e. Y2 = Al-dominant; Ti & Fe3+ assigned to Y3). These occupancies may be re-assigned with updated data. Justification for the -(REE) suffix is that REE (in this case predominately Ce) is the dominant cation in the X3 site.
Colour:
dark orange
Lustre:
Vitreous, Greasy
Hardness:
4½
Specific Gravity:
3.80
Crystal System:
Tetragonal
Member of:
Name:
The new mineral is named in honor of Nikolay Mikhailovich Manaev (27.02.1936–02.03.2012), a former chief geologist of the Kovdorslyuda Mining and Dressing Company and a prominent mineral collector, for his contribution to the geology, mineralogy and exploitation of the world-largest Kovdor phlogopite deposit, Kola Peninsula, Russia.
Type Locality:
First group member with essential REE (rare earth elements) and hydrogarnet-like H4O4 substitution of the orthosilicate group.
Chemically related to dissakisite-(Ce), dollaseite-(Ce), gatelite-(Ce), västmanlandite-(Ce), and somewhat to khristovite-(Ce) and some unnamed species.
Chemically related to dissakisite-(Ce), dollaseite-(Ce), gatelite-(Ce), västmanlandite-(Ce), and somewhat to khristovite-(Ce) and some unnamed species.
Unique Identifiers
Mindat ID:
53139
Long-form identifier:
mindat:1:1:53139:3
Similar Names
| Mineevite-(Y) | A valid IMA mineral species | Na25Ba(Y,Gd,Dy)2(CO3)11(HCO3)4(SO4)2F2Cl |
IMA Classification of Manaevite-(Ce)
Approved
IMA Formula:
Ca11(Ce3+,H2O,Ca)8Mg(Al,Fe3+)4(Mg,Ti4+,Fe3+)8[Si2O7]4[(SiO4)8(H4O4)2](OH)9
Approval year:
2018
Classification of Manaevite-(Ce)
9.BG.35
9 : SILICATES (Germanates)
B : Sorosilicates
G : Sorosilicates with mixed SiO4 and Si2O7 groups; cations in octahedral [6] and greater coordination
9 : SILICATES (Germanates)
B : Sorosilicates
G : Sorosilicates with mixed SiO4 and Si2O7 groups; cations in octahedral [6] and greater coordination
Mineral Symbols
As of 2021 there are now IMA–CNMNC approved mineral symbols (abbreviations) for each mineral species, useful for tables and diagrams.
| Symbol | Source | Reference for Standard |
|---|---|---|
| Mv-Ce | IMA–CNMNC | Warr, L.N. (2021). IMA–CNMNC approved mineral symbols. Mineralogical Magazine, 85(3), 291-320. doi:10.1180/mgm.2021.43 |
Physical Properties of Manaevite-(Ce)
Vitreous, Greasy
Colour:
dark orange
Streak:
Brownish orange
Hardness:
4½ on Mohs scale
Tenacity:
Brittle
Cleavage:
None Observed
Parting:
none
Fracture:
Irregular/Uneven, Conchoidal
Density:
3.80(3) g/cm3 (Measured) 3.72 g/cm3 (Calculated)
Optical Data of Manaevite-(Ce)
Type:
Uniaxial (-)
RI values:
nω = 1.760(5) nε = 1.750(5)
Max. Birefringence:
δ = 0.010
Based on recorded range of RI values above.
Based on recorded range of RI values above.
Interference Colours:
The colours simulate birefringence patterns seen in thin section under crossed polars. They do not take into account mineral colouration or opacity.
Michel-Levy Bar The default colours simulate the birefringence range for a 30 µm thin-section thickness. Adjust the slider to simulate a different thickness.
Grain Simulation You can rotate the grain simulation to show how this range might look as you rotated a sample under crossed polars. Each grain retains its interference colour (retardation) while its brightness falls to black at extinction and reaches a maximum between extinction positions.
The colours simulate birefringence patterns seen in thin section under crossed polars. They do not take into account mineral colouration or opacity.
Michel-Levy Bar The default colours simulate the birefringence range for a 30 µm thin-section thickness. Adjust the slider to simulate a different thickness.
Grain Simulation You can rotate the grain simulation to show how this range might look as you rotated a sample under crossed polars. Each grain retains its interference colour (retardation) while its brightness falls to black at extinction and reaches a maximum between extinction positions.
Surface Relief:
Very High (positive)
Relative to Canada balsam mounting medium (n ≈ 1.537).
Relative to Canada balsam mounting medium (n ≈ 1.537).
This shows the grain boundary and Becke line effect under plane-polarised
light, based on the contrast between this mineral's average refractive
index and the mounting medium. It does not take into account mineral
colouration.
In focus
Interference Figure:
This shows the idealized uniaxial interference figure - the conoscopic
(convergent-light, Bertrand-lens-in) view, for a grain cut with the optic axis
centred and vertical. The coloured rings are isochromatics, computed with the
same physics as the Michel-Lévy bar above; the dark cross is the isogyre.
For a genuinely uniaxial mineral viewed this way, that cross stays perfectly stationary if you rotate the stage - unlike a biaxial mineral, where it splits apart on rotation. That invariance is itself the standard diagnostic test for telling uniaxial and biaxial minerals apart at the microscope.
For a genuinely uniaxial mineral viewed this way, that cross stays perfectly stationary if you rotate the stage - unlike a biaxial mineral, where it splits apart on rotation. That invariance is itself the standard diagnostic test for telling uniaxial and biaxial minerals apart at the microscope.
Dispersion:
strong dispersion
Pleochroism:
Weak
Comments:
[O (light yellowish-brown) < E (brown)]
Comments:
Sometimes slightly biaxial(2 V = 0°–5°)
Chemistry of Manaevite-(Ce)
Mindat Formula:
(Ca13Ce4[H2O]2)Mg(Al3Mg)(Mg3Ti3Fe3+2)(◻4)◻[Si2O7]4[(SiO4)8(H4O4)2]O(OH)9
The formula is a partial simplification of the full structural formula. The large (VII-IX)-coordinated (X4)2(X3)8(X2)8(X1) sites are here combined (e.g. Ca19) and are typically filled with Ca, although other large cations such as the REE may be present. The square-pyramidal Y1 site can host a variety of M2+ and M3+ ions and is the basis for the distinction of several species. The VI-coordinated Y2 site typically is filled with Al, whereas the also VI-coordinated Y3 site may contain Al, Mg, and other cations of similar charge and size. The tetrahedral T1 site is typically vacant but may contain B (less commonly Al); the trigonal T2 site is also typically vacant but may also contain B. Some of the (SiO4) may be replaced by (H4O4), akin to the Si4+ ↔︎ 4H+ hydrogarnet substitution. Among the oxygen that are not part of the silica tetrahedra, there are eight "O11" that typically occur as OH, two "O10" that are typically O & OH or OH & OH (the latter arrangement notably when Y1 is an M2+ cation). There may also be up to three "O12" that in most vesuvianite-group minerals are absent (and are not included here), but may be present particularly when T1 is occupied.
Note that in lieu of published structural data, the Y2 and Y3 site occupancies denoted here are distributed as per other members of the other vesuvianite group minerals (i.e. Y2 = Al-dominant; Ti & Fe3+ assigned to Y3). These occupancies may be re-assigned with updated data. Justification for the -(REE) suffix is that REE (in this case predominately Ce) is the dominant cation in the X3 site.
The formula is a partial simplification of the full structural formula. The large (VII-IX)-coordinated (X4)2(X3)8(X2)8(X1) sites are here combined (e.g. Ca19) and are typically filled with Ca, although other large cations such as the REE may be present. The square-pyramidal Y1 site can host a variety of M2+ and M3+ ions and is the basis for the distinction of several species. The VI-coordinated Y2 site typically is filled with Al, whereas the also VI-coordinated Y3 site may contain Al, Mg, and other cations of similar charge and size. The tetrahedral T1 site is typically vacant but may contain B (less commonly Al); the trigonal T2 site is also typically vacant but may also contain B. Some of the (SiO4) may be replaced by (H4O4), akin to the Si4+ ↔︎ 4H+ hydrogarnet substitution. Among the oxygen that are not part of the silica tetrahedra, there are eight "O11" that typically occur as OH, two "O10" that are typically O & OH or OH & OH (the latter arrangement notably when Y1 is an M2+ cation). There may also be up to three "O12" that in most vesuvianite-group minerals are absent (and are not included here), but may be present particularly when T1 is occupied.
Note that in lieu of published structural data, the Y2 and Y3 site occupancies denoted here are distributed as per other members of the other vesuvianite group minerals (i.e. Y2 = Al-dominant; Ti & Fe3+ assigned to Y3). These occupancies may be re-assigned with updated data. Justification for the -(REE) suffix is that REE (in this case predominately Ce) is the dominant cation in the X3 site.
Element Weights:
Crystallography of Manaevite-(Ce)
Crystal System:
Tetragonal
Class (H-M):
4/mmm(4/m2/m2/m) - Ditetragonal Dipyramidal
Space Group:
P4/nnc
Setting:
P4/nnc
Cell Parameters:
a = 15.9247(13) Å, c = 11.9661(10) Å
Ratio:
a:c = 1 : 0.751
Unit Cell V:
3,034.56 ų (Calculated from Unit Cell)
Z:
2
X-Ray Powder Diffraction
Powder Diffraction Data:
| d-spacing | Intensity |
|---|---|
| 5.98 Å | (27) |
| 4.61 Å | (30) |
| 3.289 Å | (31) |
| 2.991 Å | (100) |
| 2.787 Å | (95) |
| 2.636 Å | (81) |
| 2.503 Å | (47) |
| 1.659 Å | (25) |
Geological Environment
Paragenetic Mode(s):
| Paragenetic Mode | Earliest Age (Ga) |
|---|---|
| Stage 3a: Earth’s earliest Hadean crust | >4.50 |
| 7 : Ultramafic igneous rocks | |
| Stage 4b: Highly evolved igneous rocks | >3.0 |
| 35 : Ultra-alkali and agpaitic igneous rocks |
Type Occurrence of Manaevite-(Ce)
Place of Conservation of Type Material:
Collections of the (1) Fersman Mineralogical Museum, Russian Academy of Sciences, Leninskiy Prospekt 18-2, Moscow 119071, Russia, registration number 5075/1; (2) the Mineralogical Museum of St. Petersburg State University, St. Petersburg, Russia, registra
Geological Setting of Type Material:
skarn-like metasomatic rock
Synonyms of Manaevite-(Ce)
Other Language Names for Manaevite-(Ce)
Dutch:Manaeviet-(Ce)
German:Manaevit-(Ce)
Relationship of Manaevite-(Ce) to other Species
Member of:
Other Members of Vesuvianite Group:
| Alumovesuvianite | Ca19AlAl4(Al6Mg2)(◻4)◻[Si2O7]4[(SiO4)10]O(OH)9 | Tet. 4/m : P4/n |
| Cyprine | Ca19Cu2+Al4(Al6Mg2)(◻4)◻[Si2O7]4[(SiO4)10](OH)(OH)9 | Tet. 4/m : P4/n |
| Fluorvesuvianite | Ca19Fe3+Al4(Al6Mg2)(◻4)◻[Si2O7]4[(SiO4)10]O(F,OH)9 | Tet. 4/mmm(4/m2/m2/m) : P4/nnc |
| Hongheite | Ca19Fe2+Al4(Fe3+,Mg)8(◻4)B[Si2O7]4[(SiO4)10]O(OH,O)9 | Tet. 4/mmm(4/m2/m2/m) : P4/nnc |
| Magnesiovesuvianite | Ca19MgAl4(Al6Mg2)(◻4)◻[Si2O7]4[(SiO4)10](OH)(OH)9 | Tet. 4/m : P4/n |
| Manganvesuvianite | Ca19Mn3+Al4(Al6Mg2)(◻4)◻[Si2O7]4[(SiO4)10]O(OH)9 | Tet. 4/m : P4/n |
| Milanriederite | (Ca18[REE])Fe3+Al4(Mg4Al4)(◻4)◻[Si2O7]4[(SiO4)10](OH)(OH)9 | Tet. 4/mmm(4/m2/m2/m) : P4/nnc |
| Modraite | Ca19Fe2+Al4(Al6Fe2+2)(◻4)◻[Si2O7]4[(SiO4)10](OH)(OH)9 | Tet. 4/mmm(4/m2/m2/m) : P4/nnc |
| Vesuvianite | Ca19Fe3+Al4(Al6Mg2)(◻4)◻[Si2O7]4[(SiO4)10]O(OH)9 | Tet. 4/mmm(4/m2/m2/m) : P4/nnc |
| Wiluite | Ca19MgAl4(Al,Mg)8(B,◻)4◻[Si2O7]4[(SiO4)10]O(O,OH)9 | Tet. 4/mmm(4/m2/m2/m) : P4/nnc |
Related Minerals - Strunz-mindat Grouping
| 9.BG. | Alumovesuvianite | Ca19AlAl4(Al6Mg2)(◻4)◻[Si2O7]4[(SiO4)10]O(OH)9 |
| 9.BG. | Alnaperbøeite-(Ce) | Ca(Ce2.5Na0.5)(AlAl2Al)[Si2O7][SiO4]3O(OH)2 |
| 9.BG. | Zilbermintsite-(La) | (CaLa5)(Fe3+Al3Fe2+)[Si2O7][SiO4]5O(OH)3 |
| 9.BG. | Heflikite | (CaCa)(AlAlSc)O[Si2O7][SiO4](OH) |
| 9.BG. | Magnesiovesuvianite | Ca19MgAl4(Al6Mg2)(◻4)◻[Si2O7]4[(SiO4)10](OH)(OH)9 |
| 9.BG. | Zoisite-(Pb) | (CaPb)(AlAlAl)O[Si2O7][SiO4](OH) |
| 9.BG. | Shuiskite-(Cr) | Ca2Cr3+Cr3+2[Si2O6OH][SiO4](OH)2O |
| 9.BG. | Radekškodaite Group | |
| 9.BG.05 | Dissakisite-(La) | (CaLa)(AlAlMg)O[Si2O7][SiO4](OH) |
| 9.BG.05 | Manganiandrosite-(Ce) | (Mn2+Ce)(Mn3+AlMn2+)O[Si2O7][SiO4](OH) |
| 9.BG.05b | Dissakisite-(Ce) | (CaCe)(AlAlMg)O[Si2O7][SiO4](OH) |
| 9.BG.05b | Allanite-(Sm) | (CaSm)(AlAlFe2+)O[Si2O7][SiO4](OH) |
| 9.BG.05a | Hancockite | (CaPb)(AlAlFe3+)O[Si2O7][SiO4](OH) |
| 9.BG.05 | Dollaseite-(Ce) | (CaCe)(MgAlMg)F[Si2O7][SiO4](OH) |
| 9.BG.05a v | 'Unnamed (Ga-analogue of Epidote)' | (CaCa)(AlAlGa3+)O[Si2O7][SiO4](OH) |
| 9.BG.05a | Clinozoisite | (CaCa)(AlAlAl)O[Si2O7][SiO4](OH) |
| 9.BG.05a | Epidote-(Sr) | (CaSr)(AlAlFe3+)O[Si2O7][SiO4](OH) |
| 9.BG.05 | Vanadoandrosite-(Ce) | (Mn2+Ce)(V3+AlMn2+)O[Si2O7][SiO4](OH) |
| 9.BG.05b | Vanadoallanite-(La) | (CaLa)(V3+AlFe2+)O[Si2O7][SiO4](OH) |
| 9.BG.05b | 'Unnamed (Mg-analogue of Ferriallanite-(Ce))' | (CaCe)(Fe3+AlMg)O[Si2O7][SiO4](OH) |
| 9.BG.05b | Ferriallanite-(La) | (CaLa)(Fe3+AlFe2+)O[Si2O7][SiO4](OH) |
| 9.BG.05 | Uedaite-(Ce) | (Mn2+Ce)(AlAlFe2+)O[Si2O7][SiO4](OH) |
| 9.BG.05a | Epidote | (CaCa)(AlAlFe3+)O[Si2O7][SiO4](OH) |
| 9.BG.05 | Tweddillite | (CaSr)(Mn3+AlMn3+)O[Si2O7][SiO4](OH) |
| 9.BG.05b | Åskagenite-(Nd) | (Mn2+Nd)(AlAlFe3+)O[Si2O7][SiO4]O |
| 9.BG.05 | Piemontite-(Pb) | (CaPb)(AlAlMn3+)O[Si2O7][SiO4](OH) |
| 9.BG.05b | Allanite-(Ce) | (CaCe)(AlAlFe2+)O[Si2O7][SiO4](OH) |
| 9.BG.05b | Allanite-(La) | (CaLa)(AlAlFe2+)O[Si2O7][SiO4](OH) |
| 9.BG.05b | Allanite-(Y) | (CaY)(AlAlFe2+)O[Si2O7][SiO4](OH) |
| 9.BG.05a | Piemontite | (CaCa)(AlAlMn3+)O[Si2O7][SiO4](OH) |
| 9.BG.05b | Akasakaite-(Ce) | (CaCe)(AlAlMn2+)O[Si2O7][SiO4](OH) |
| 9.BG.05b | Manganiandrosite-(La) | (Mn2+La)(Mn3+AlMn2+)O[Si2O7][SiO4](OH) |
| 9.BG.05b | Akasakaite-(La) | (CaLa)(AlAlMn2+)O[Si2O7][SiO4](OH) |
| 9.BG.05b | Vanadoakasakaite-(La) | (CaLa)(V3+AlMn2+)O[Si2O7][SiO4](OH) |
| 9.BG.05 | Khristovite-(Ce) | (CaCe)(MgAlMn2+)F[Si2O7][SiO4](OH) |
| 9.BG.05b | Ferriakasakaite-(La) | (CaLa)(Fe3+AlMn2+)O[Si2O7][SiO4](OH) |
| 9.BG.05 | Ferriandrosite-(La) | (Mn2+La)(Fe3+AlMn2+)O[Si2O7][SiO4](OH) |
| 9.BG.05 | 'Androsite-(Ce)' | (Mn2+Ce)(AlAlMn2+)O[Si2O7][SiO4](OH) |
| 9.BG.05 | Vielleaureite-(Ce) | Mn2+Ce(MgAlMn2+)(Si2O7)(SiO4)F(OH) |
| 9.BG.05 | Ferriandrosite-(Ce) | (Mn2+Ce)(Fe3+AlMn2+)O[Si2O7][SiO4](OH) |
| 9.BG.05b | Ferriallanite-(Ce) | (CaCe)(Fe3+AlFe2+)O[Si2O7][SiO4](OH) |
| 9.BG.05b | 'Unnamed (Mn3+-analogue of Ferriakasakaite-(Ce))' | (CaCe)(Mn3+AlMn2+)O[Si2O7][SiO4](OH) |
| 9.BG.05b | Vanadoakasakaite-(Ce) | (CaCe)(V3+AlMn2+)O[Si2O7][SiO4](OH) |
| 9.BG.05 | Piemontite-(Sr) | (CaSr)(AlAlMn3+)O[Si2O7][SiO4](OH) |
| 9.BG.05 | Niigataite | (CaSr)(AlAlAl)O[Si2O7][SiO4](OH) |
| 9.BG.05b | Ferriakasakaite-(Ce) | (CaCe)(Fe3+AlMn2+)O[Si2O7][SiO4](OH) |
| 9.BG.05b | Vanadoandrosite-(La) | Mn2+La(V3+AlMn2+)(Si2O7)(SiO4)O(OH) |
| 9.BG.05b | Allanite-(Nd) | (CaNd)(AlAlFe2+)O[Si2O7][SiO4](OH) |
| 9.BG.05b | 'UM1989-32-SiO:AlCaFeHREE' | (Ca0.5◻0.5REE)(AlAlFe3+)O[Si2O7][SiO4](OH) |
| 9.BG.05a | Mukhinite | (CaCa)(AlAlV3+)O[Si2O7][SiO4](OH) |
| 9.BG.05b | Manganiakasakaite-(La) | (CaLa)(Mn3+AlMn2+)O[Si2O7][SiO4](OH) |
| 9.BG.10 | Zoisite | (CaCa)(AlAlAl)O[Si2O7][SiO4](OH) |
| 9.BG.15 | Macfallite | Ca2Mn3+3(SiO4)(Si2O7)(OH)3 |
| 9.BG.15 | Sursassite | Mn2+2Al3(SiO4)(Si2O7)(OH)3 |
| 9.BG.20 | Pumpellyite-(Al) | Ca2AlAl2[Si2O6OH][SiO4](OH)2O |
| 9.BG.20 | Shuiskite-(Mg) | Ca2MgCr3+2[Si2O6OH][SiO4](OH)2(OH) |
| 9.BG.20 | Julgoldite-(Fe2+) | Ca2Fe2+Fe3+2[Si2O6OH][SiO4](OH)2(OH) |
| 9.BG.20 | Okhotskite | Ca2Mn2+Mn3+2[Si2O6OH][SiO4](OH)2(OH) |
| 9.BG.20 | Julgoldite-(Mg) | Ca2MgFe3+2[Si2O6OH][SiO4](OH)2(OH) |
| 9.BG.20 | Poppiite | Ca2V3+V3+2[Si2O6OH][SiO4](OH)2O |
| 9.BG.20 | Julgoldite-(Fe3+) | Ca2Fe3+Fe3+2[Si2O6OH][SiO4](OH)2O |
| 9.BG.20 | Pumpellyite-(Fe2+) | Ca2Fe2+Al2[Si2O6OH][SiO4](OH)2(OH) |
| 9.BG.20 | Pumpellyite-(Fe3+) | Ca2Fe3+Al2[Si2O6OH][SiO4](OH)2O |
| 9.BG.20 | Pumpellyite-(Mg) | Ca2MgAl2[Si2O6OH][SiO4](OH)2(OH) |
| 9.BG.20 | Pumpellyite-(Mn2+) | Ca2Mn2+Al2[Si2O6OH][SiO4](OH)2(OH) |
| 9.BG.25 | Ganomalite | Pb9Ca5Mn(Si2O7)4(SiO4)O |
| 9.BG.25 | Wayneburnhamite | Pb9Ca6(Si2O7)3(SiO4)3 |
| 9.BG.30 | Rustumite | Ca10(Si2O7)2(SiO4)(OH)2Cl2 |
| 9.BG.35 | Modraite | Ca19Fe2+Al4(Al6Fe2+2)(◻4)◻[Si2O7]4[(SiO4)10](OH)(OH)9 |
| 9.BG.35 | Fluorvesuvianite | Ca19Fe3+Al4(Al6Mg2)(◻4)◻[Si2O7]4[(SiO4)10]O(F,OH)9 |
| 9.BG.35 | Vesuvianite | Ca19Fe3+Al4(Al6Mg2)(◻4)◻[Si2O7]4[(SiO4)10]O(OH)9 |
| 9.BG.35 | Milanriederite | (Ca18[REE])Fe3+Al4(Mg4Al4)(◻4)◻[Si2O7]4[(SiO4)10](OH)(OH)9 |
| 9.BG.35 | Hongheite | Ca19Fe2+Al4(Fe3+,Mg)8(◻4)B[Si2O7]4[(SiO4)10]O(OH,O)9 |
| 9.BG.35 | Wiluite | Ca19MgAl4(Al,Mg)8(B,◻)4◻[Si2O7]4[(SiO4)10]O(O,OH)9 |
| 9.BG.35 | Cyprine | Ca19Cu2+Al4(Al6Mg2)(◻4)◻[Si2O7]4[(SiO4)10](OH)(OH)9 |
| 9.BG.35 | Manganvesuvianite | Ca19Mn3+Al4(Al6Mg2)(◻4)◻[Si2O7]4[(SiO4)10]O(OH)9 |
| 9.BG.40 | Vyuntspakhkite-(Y) | (Y,Yb)4Al2.5-1.5(Si,Al)1.5-2.5(SiO4)4O(OH)7 |
| 9.BG.45 | Dellaite | Ca6Si3O11(OH)2 |
| 9.BG.50 | Ferriperbøeite-(Ce) | CaCe3(Fe3+Al2Fe2+)[Si2O7][SiO4]3O(OH)2 |
| 9.BG.50 | Perbøeite-(La) | CaLa3(AlAl2Fe2+)[Si2O7][SiO4]3O(OH)2 |
| 9.BG.50 | Perbøeite-(Ce) | CaCe3(AlAl2Fe2+)[Si2O7][SiO4]3O(OH)2 |
| 9.BG.50 | Gatelite-(Ce) | CaCe3(AlAl2Mg)[Si2O7][SiO4]3O(OH)2 |
| 9.BG.50 | Ferriperbøeite-(La) | CaLa3(Fe3+Al2Fe2+)[Si2O7][SiO4]3O(OH)2 |
| 9.BG.55 | Västmanlandite-(Ce) | CaCe3(MgAl2Mg)[Si2O7][SiO4]3F(OH)2 |
| 9.BG.60 | Radekškodaite-(La) | (CaLa5)(Al4Fe2+)[Si2O7][SiO4]5O(OH)3 |
| 9.BG.60 | Radekškodaite-(Ce) | (CaCe5)(Al4Fe2+)[Si2O7][SiO4]5O(OH)3 |
Fluorescence of Manaevite-(Ce)
none
Other Information
Health Risks:
No information on health risks for this material has been entered into the database. You should always treat mineral specimens with care.
Internet Links for Manaevite-(Ce)
mindat.org URL:
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References for Manaevite-(Ce)
Reference List:
Hålenius, U., Hatert, F., Pasero, M., Mills, S. J. (2018) CNMNC Newsletter 45, New minerals and nomenclature modifications approved in 2018. Mineralogical Magazine, 82 (5) 1225-1232 doi:10.1180/mgm.2018.160
Moiseev, Mikhail M., Panikorovskii, Taras L., Aksenov, Sergey M., Mazur, Anton S., Mikhailova, Julia A., Yakovenchuk, Victor N., Bazai, Ayya V., Ivanyuk, Gregory Yu., Agakhanov, Atali A., Shilovskikh, Vladimir V., Pekov, Igor V., Kasatkin, Anatoly V., Rusakov, Vyacheslav S., Yapaskurt, Vasiliy O., Karpenko, Vladimir Yu., Krivovichev, Sergey V. (2020) Insights into crystal chemistry of the vesuvianite-group: manaevite-(Ce), a new mineral with complex mechanisms of its hydration. Physics and Chemistry of Minerals, 47 (3) doi:10.1007/s00269-020-01086-7
Localities for Manaevite-(Ce)
Showing 2 localities.
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The Locality List
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- This locality has estimated coordinates.
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? - Indicates mineral may be doubtful at this locality.
- Good crystals or important locality for species.
- World class for species or very significant.
(TL) - Type Locality for a valid mineral species.
(FRL) - First Recorded Locality for everything else (eg varieties).
All localities listed without proper references should be considered as questionable.
Russia (TL) | |
| Hålenius et al. (2018) |
| In Press +1 other reference |
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Kovdor Phlogopite mine, Kovdor Massif, Kovdorsky District, Murmansk Oblast, Russia