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Sodium Amphibole Subgroup

A group of related mineral species
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About Sodium Amphibole SubgroupHide

Formula:
A0-1Na2(C2+2-4C3+1-2Li0-1)Σ5(Si8-mAlmO22)(OH,F,Cl)2
The sodium amphibole subgroup is one of the subgroups belonging to the W(OH,F,Cl) amphibole group. It is defined with Na as the dominant element in the B position.
(The IMA-CNMNC definition is B(Na + Li)/ΣB ≥ 0.75, BNa/ΣB ≥ BLi/ΣB)

The sodium amphibole subgroup are further divided into root-name groups that are defined by the charge balance and dominant elements in the A and C positions in the generic formula above. The various positions in the formula can have the following content:

A position: n=0 or 1, when 1, it contains Na or K as the dominant elements.

C position : For all root name groups except the Nybøite and Leakeite groups, the content in the C position is C2+3+nC3+2-n, and with Si8 in the T position.

The Nybøite group has n=1 and C2+3+n C3+2, balancing the formula with m=1 in the T position.

The leakeite group contains Li in the C position and it's C position is defined with C2+2 C3+2Li.

Mg, Fe2+, Al and Fe3+ are normally the dominant elements in the C2+ and C3+ positions for all root name groups.

(OH), F or Cl dominance define mineral species within a root name group.
Name:
This amphibole subgroup was named "Alkali-amphiboles" in Leake's "Nomenclature of amphiboles"(1978) and renamed as "Sodic amphiboles" in the 1997 amphibole nomenclature. The group was again renamed in the 2012 amphibole nomenclature to "sodium amphibole subgroup".
This page provides mineralogical data about Sodium Amphibole Subgroup.


Unique IdentifiersHide

Mindat ID:
29366
Long-form identifier:
mindat:1:1:29366:0

IMA Classification of Sodium Amphibole SubgroupHide

IMA status notes:
IMA Approved Group Name

Chemistry of Sodium Amphibole SubgroupHide

Mindat Formula:
A0-1Na2(C2+2-4C3+1-2Li0-1)Σ5(Si8-mAlmO22)(OH,F,Cl)2

The sodium amphibole subgroup is one of the subgroups belonging to the W(OH,F,Cl) amphibole group. It is defined with Na as the dominant element in the B position.
(The IMA-CNMNC definition is B(Na + Li)/ΣB ≥ 0.75, BNa/ΣB ≥ BLi/ΣB)

The sodium amphibole subgroup are further divided into root-name groups that are defined by the charge balance and dominant elements in the A and C positions in the generic formula above. The various positions in the formula can have the following content:

A position: n=0 or 1, when 1, it contains Na or K as the dominant elements.

C position : For all root name groups except the Nybøite and Leakeite groups, the content in the C position is C2+3+nC3+2-n, and with Si8 in the T position.

The Nybøite group has n=1 and C2+3+n C3+2, balancing the formula with m=1 in the T position.

The leakeite group contains Li in the C position and it's C position is defined with C2+2 C3+2Li.

Mg, Fe2+, Al and Fe3+ are normally the dominant elements in the C2+ and C3+ positions for all root name groups.

(OH), F or Cl dominance define mineral species within a root name group.

Age distributionHide

Recorded ages:
Mesoproterozoic to Paleogene : 1456 Ma to 31.7 ± 0.7 Ma - based on 52 recorded ages.
Sample ages:
Sample IDRecorded ageGeologic TimeDating method
131.7 ± 0.7 MaOligoceneK-Ar
241 MaEoceneK-Ar
351 MaEoceneK-Ar
480.1 ± 3.1 MaLate/Upper CretaceousK-Ar
5212 MaLate/Upper TriassicK-Ar
6226 ± 1.1 MaLate/Upper TriassicK-Ar
7226 ± 1.1 MaLate/Upper TriassicK-Ar
8239.2 ± 0.4 MaMiddle TriassicSHRIMP zircon U-Pb dating of riebeckite granite
9319 ± 8 MaPennsylvanianAr-Ar
10377 ± 7 MaLate/Upper DevonianK-Ar
11394 ± 15 MaEarly/Lower DevonianK-Ar
12430 ± 12 MaWenlockK-Ar
13551 MaEdiacaranK-Ar
141456 to 1359 MaMesoproterozoicK-Ar
Sample references:
IDTypeLocalityReferenceNotes
1Maoniuping carbonatite complex, Liangshan Yi, Sichuan, China
2Warsak Intrusions, Mohmand District, Khyber Pakhtunkhwa Province, PakistanRiebeckite from granite
3Gigye-Gyeongju granite, Gyeongju City, North Gyeongsang Province, South Korea
4Bardkish syenite, Urmia County, West Azerbaijan Province, Iran
5Longwangzhuang pluton, Luanchuan County, Luoyang, Henan, China
6Sams Creek, Cobb Valley, Tasman Region, New Zealand
7  "  "
8Hongge V-Ti-Fe deposit, Yanbian County, Panzhihua, Sichuan, China
9Sams Creek, Cobb Valley, Tasman Region, New Zealandmixture of arfvedsonite-riebeckite
10Victoria River Granite Complex, Southern Grampians Shire, Victoria, Australia
11Learnie Quarry, Black Isle, Highland, Scotland, UKUndue reliance should not be placed on this because it derives from a single specimen, the. amphibole of which contained only 0.081% K.
12Mount Bayliss, Prince Charles Mountains, Mac Robertson Land, East Antarctica, Antarctica
13Gem Park Complex Prospect, Custer County, Colorado, USA
14Norra Kärr, Gränna, Jönköping, Jönköping County, Sweden

Chemical AnalysisHide

Oxide wt%:
Showing 12 of 37 analyses on this page.
 123456789101112
SiO249.33 %56.48 %57.80 %57.50 %53.85 %53.84 %49.74 %50.15 %52.82 %54.25 %50.31 %49.03 %
TiO20.40 %0.08 %0.06 %0.12 %0.16 %0.63 %0.13 %0.77 %1.08 %0.57 %0.73 %
Al2O30.72 %9.53 %13.91 %9.69 %0.80 %12.92 %2.04 %0.51 %0.03 %0.63 %0.87 %
Fe2O31.55 %0.0 %2.94 %8.50 %8.07 %12.00 %14.51 %
FeO30.95 %16.04 %0.89 %10.77 %5.03 %33.36 %7.47 %13.82 %6.69 %22.14 %13.70 %
MnO2.15 %0.05 %0.05 %0.10 %0.02 %1.36 %0.09 %3.26 %0.32 %0.77 %5.46 %
MgO0.74 %7.90 %17.32 %10.86 %9.49 %14.21 %0.99 %12.07 %4.8 %13.99 %0.61 %
CaO1.01 %0.70 %0.60 %1.37 %1.40 %2.33 %0.80 %3.03 %0.09 %1.16 %0.05 %
Na2O7.07 %7.02 %5.89 %6.73 %6.39 %9.26 %6.56 %8.4 %7.65 %6.33 %8.82 %8.95 %
K2O1.81 %0.02 %0.07 %0.33 %0.14 %1.50 %0.32 %3.76 %5.20 %1.58 %1.29 %
ZrO20.20 %0.0 %
Cl0.01 %0.01 %
F0.18 %2.58 %1.21 %2.20 %2.31 %2.85 %
Cr2O30.07 %0.02 %
H2O2.12 %1.38 %(0.82) %
FeO223.42 %
Li2O0.73 %0.76 %0.6 %
O=F-0.51 %-0.97 %-1.20 %
NiO0.11 %
ZnO0.05 %0.11 %0.05 %0.49 %0.90 %
?O=F
Nb2O5
SnO2
Fe2O3*
FeO*
SrO
PbO
Li2O (by stoichiometry)
H2O (by stoichiometry)
-O=F
Äl2O312.35 %
O1.09 %
Ga2O3
V2O3
Total:95.93 %100.01 %96.59 %96.92 %96.09 %98.03 %96.98 %100.69 %98.9 %99.37 %99.41 %98.35 %
Empirical formulas:
Sample IDEmpirical Formula
13(Na0.62K0.47) 1.09 (Na1.93Ca0.07) 2.00 (Fe2+3.43Mg0.04Fe3+0.97Mn0.12Ti0.06Al0.15Zr0.01) 4.78(Si7.92 Al0.08) 8.00 O22[ (OH) 1.97 F0.03] 2.00
14(Na0,71K0,301) 1,011 (Na1,618Ca0,382) 2 (Fe2+3,869Fe3+0,664Ti0,27Mn0,115Al0,072) 4,99 (Si7,891Al0,109) 8O22 ((OH) 1,458O0,542) 2
4Na0.01 (Na1.80Ca0.20)Σ2.00 ( Mg2.24Fe2+0.92Fe3+0.33Al1.52)Σ5.01(Al0.06Si7.94)Σ8.00O22OH2
15(Na0.569K0.369)0.938 (Na1.603Ca0.397)2(Mg3.025Feii1.273FeIII0.411Ti0.202Al0.036Mnii0.031Li0.029)5.007Si8.002O22 ((OH)1,168F0,655O0.168)2
6(Na0.72K0.02)(Na1.67Ca0.33)(Mg1.82Fe2+0.18)(Mg0.32Fe3+0.24Ti0.02Al1.43)(Mg0.8Fe2+0.2) (Si7.24Al0.76)022(OH)2
16A(Na0.22K0.0,05)0.27 B( (Na1.90Ca0.10) 2.00 C( (Mg3.16Fe2+0.05Mn2+0.12Fe3+1.06Al0.61) 5.00 T( (Si7.96Al0.04) 8.00O22 W( (OH) 1.83 F0.17) 2.00
17(Na0.66K0.27)?0.93(Na1.83Ca0.17)?2.00(Mg0.06Fe2+3.15Mn0.31Zn0.01Fe3+1.38Ti0.06Al0.03)?5.00(Si7.35Al0.65)?8.00O22(OH1.58F0.42)?2.00
18(Na0.52K0.48)(Na1.90Li0.07Ca0.02)[(Fe2+0.63Mn2+0.56Mg0.47Zn0.23Ti0.12)(Fe3+1.93Al0.06)Li1.00][Si7.98Al0.02O22]([OH]0.90F0.87O0.23)
19(Na0.62K0.38)(Na1.89Ca0.11)[(Mn2+0.60Mg0.50Zn0.34Fe2+0.32Ti0.19Na0.05)(Fe3+1.96Al0.04)Li1.00][Si7.92Al0.08O22](F0.84[OH]0.77O0.39)
9(K0.73Na0.27) 1.00 (Na2.00Ca0.01) 2.01 (Fe2+ 1.77 Mg1.10Fe3+ 0.98Li0.45Mn0.42Ti0.09Zn0.01 Al0.09) 4.91Si8.09O22[(OH) 1.41F0.59] 2.00
20(K0.67Na0.33) 1.00 (Na1.74Ca0.27) 2.01 (Fe2+ 2.26 Mg1.79Fe3+ 0.55Mn0.25Ti0.09Zn0.01 Al0.05) 5.00(Si7.94 Al0.06) 8.00O22[(OH) 1.23F0.77] 2.00
21(K0.63 Na0.15) 0.78 (Na1.62Ca0.36Mn0.02) 2.00 (Mg3.72 Fe2+ 0.31 Fe3+ 0.95Mn0.00Ti0.02Al0.00) 5.00(Si7.85Al0.03 Fe3+ 0.11Cr0.01) 8.00O22[F1.06(OH) 0.94]2.00
10K0.98 (Na1.81Ca0.18) 1.99 (Mg3.07 Fe2+ 0.83 Fe3+ 0.90Mn0.04Ti0.12Zn0.01 Al0.01) 4.98Si8.00)O22[F1.03(OH) 0.73O 0.24] 2.00
22(K0.67Na0.22) 0.89(Na1.95Ca0.05) 2.00 (Fe2+ 3.29Fe3+ 1.26Li0.29Mn0.19Ti0.05Zn0.02Mg0.01) 5.11(Si7.76Fe3+ 0.13Al0.11) 8.00 O22[(OH) 1.81F0.18] 1.99
23(Na0.56K0.44)(Na1.90Li0.06Ca0.04)[(Mg0.78Mn2+0.45Fe2+0.40Zn0.26Ti0.14)(Fe3+1.90Al0.07)Li1.00][Si7.98Al0.02O22](F1.05[OH]0.66O0.29)
24A(Na0.68K0.32)S=1.00 BNa2.00 C(Mg1.69Mn2+ 0.25Fe2+ 0.24Zn0.29Al0.23Fe3+ 1.50Ti0.02Li0.78)S=5.00 TSi8O22 W(F1.59(OH)0.41)S=2.00
11(K0.32Na0.68)Na2(Li0.48Fe2.83Mn0.1Zn0.06Fe1.46Ti0.07)(Si7.88Al0.12)O22(F1.15OH0.85)
25(K0.25Na0.75)Na2(Li0.48Fe2.84Mn0.11Zn0.05Fe1.45Ti0.07)(Si7.89Al0.11)O22(F1.35OH0.65)
26A(Na0.526K0.207)B0.733( (Na1.514Ca0.485Mn0.072) C2.00( (Mg2.057Li0.160Fe2+0.631Mn2+0.544Zn0.015Fe3+1.552Ti0.042) 5.001 T( (Si7.652Al0.261) 7.913OW22( (F1.143(OH) 0.857) 2.00
12A(Na0.767K0.261)B1.028( (Na1.990Ca0.010)C2.00( (Mg0.144Li0.383Fe2+1.818Mn2+0.734Fe3+1.733Ti0.087) 5.004 T( (Si7.780Al0.163) 7.943OW22( (F1.448(OH) 0.552) 2.00
27A(Na0.74K0.24◻0.02)BΣ1.00(Na1.52Ca0.24Mn2+0.24)CΣ2.00(Mg2.54Mn2+1.45Mn3+0.71Fe3+0.26Ti0.04)Σ5.00T(Si7.97Al0.03)Σ8.00OW22[(OH)1.52O0.48]Σ2.00
Sample references:
IDTypeLocalityReferenceNotes
1Motzfeldt Centre, Igaliku Complex, Kujalleq, GreenlandSample from an alkali-rich syenite.
2Akeyazhi River valley, Ili Kazakh Autonomous Prefecture, Xinjiang, ChinaSample from blueschist
315632cCase Parigi, Martiniana Po, Cuneo Province, Piedmont, ItalyAnalyzed sample is a minute inclusion in pyrope from a coesite, phengite, pyrope whiteschist. Mineral analyses were performed by means of the Cameca electron microprobe (CAMEBAX) , using a wavelength-dispersive technique with PAP correction acceleration voltage 15 kV, beam current 15 nA, measuring time 20 s).
452iKovalo eclogites, Kechros, Arriana, Rhodope, Eastern Macedonia and Thrace, GreeceEMPA analysis of an amphibole inclusion in garnet from an eclogite
5Mud Tank Vermiculite Mine, Alcoota Station, Central Desert Region, Northern Territory, AustraliaAverage of 6 analyses. Sample from an alkali-syenite.
6Type SpecimenNybø eclogite pod, Sørpollen, Vågsøy, Kinn, Vestland, Norway
7Motzfeldt Centre, Igaliku Complex, Kujalleq, GreenlandSample from an alkali-rich syenite
8Jianchang, Donghai Co., Lianyungang, Jiangsu, ChinaType specimen analysis.58
9Palitra pegmatite, Karnasurt mine, Karnasurt Mountain, Lovozersky District, Murmansk Oblast, RussiaThe chemical composition of potassicarfvedsonite was obtained (fluorine and cations except Li) by a Camebax SX50 electron microprobe. Li was determined by atom emission using a Carl Zeiss AAS30 spectrophotometer. The water content calculated The Fe2+/ Fe3+ ratio was calculated.
10AS04-36Monte Metocha, Xixano, Montepuez District, Cabo Delgado Province, MozambiqueThe sample was analyzed by electron microprobe using a Cameca SX-100 operating in wavelength-dispersive mode. The powder-diffraction pattern was recorded from a small fragment on a 114.6 mm Debye-Scherrer powder camera with a Gandolfi attachment and Ni-filtered Cu-Ka X-radiation The Fe2+-Fe3+ ratio and the H2O content were derived from the results of crystal-structure refinement. The oxo component (O2 at the O(3) site) was estimated based on the Ti content.
11H1Hurricane Mountain localities, North Conway, Conway, Carroll County, New Hampshire, USA