Ashcroftine-(Y)
About Ashcroftine-(Y)
Named as kalithomsonite in 1932 by S. G. Gordon, for its resemblance to thomsonite and its potassium content. Later Hey & Bannister (1933) showed that the mineral has no close relationship to thomsonite and gave it the name ashcroftine. The suffix was added in 1987 by the IMA to denote the dominant REE.
Unique Identifiers
Similar Names
| Ashcroftine-(Ce) | Valid as an unnamed mineral | K5Na5(Ce,Ca)12Si28O70(OH)2(CO3)8 · 8H2O |
IMA Classification of Ashcroftine-(Y)
Classification of Ashcroftine-(Y)
9 : SILICATES (Germanates)
D : Inosilicates
N : Inosilicates with 6-periodic double chains
70 : INOSILICATES Column or Tube Structures
3 : Column or Tube Structures with balo-silicates
14 : Silicates not Containing Aluminum
8 : Silicates of Group III metals other than Al
Mineral Symbols
| Symbol | Source | Reference for Standard |
|---|---|---|
| Acf-Y | 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 Ashcroftine-(Y)
{100}, also {001} good
Optical Data of Ashcroftine-(Y)
Based on recorded range of RI values above.
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.
Relative to Canada balsam mounting medium (n ≈ 1.537).
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.
Chemistry of Ashcroftine-(Y)
Crystallography of Ashcroftine-(Y)
Crystal Structure
Unit Cell | Unit Cell Packed
2x2x2 | 3x3x3 | 4x4x4
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| ID | Species | Reference | Link | Year | Locality | Pressure (GPa) | Temp (K) |
|---|---|---|---|---|---|---|---|
| 0001130 | Ashcroftine-(Y) | Moore P B, Sen Gupta P K, Schlemper E O, Merlino S (1987) Ashcroftine, ca. K10Na10(Y,Ca)24(OH)4(CO3)16(Si56O140).16H2O, a structure with enormous polyanions American Mineralogist 72 1176-1189 | ![]() | 1987 | 0 | 293 | |
| 0001129 | Ashcroftine-(Y) | Moore P B, Sen Gupta P K, Schlemper E O, Merlino S (1987) Ashcroftine, ca. K10Na10(Y,Ca)24(OH)4(CO3)16(Si56O140).16H2O, a structure with enormous polyanions American Mineralogist 72 1176-1189 | ![]() | 1987 | 0 | 293 |
X-Ray Powder Diffraction
| d-spacing | Intensity |
|---|---|
| 17.00 Å | (100) |
| 12.0 Å | (90) |
| 7.62 Å | (60) |
| 7.10 Å | (20) |
| 6.01 Å | (30) |
| 5.38 Å | (30) |
| 3.11 Å | (50) |
| 2.69 Å | (50) |
Geological Environment
| Paragenetic Mode | Earliest Age (Ga) |
|---|---|
| Stage 4b: Highly evolved igneous rocks | >3.0 |
| 35 : Ultra-alkali and agpaitic igneous rocks |
Type Occurrence of Ashcroftine-(Y)
University of Copenhagen, Copenhagen, Denmark.
Harvard University, Cambridge, Massachusetts, USA, 110266.
National Museum of Natural History, Washington, D.C., USA, 95320, R4333.
Synonyms of Ashcroftine-(Y)
Other Language Names for Ashcroftine-(Y)
Common Associates
| 8 photos of Ashcroftine-(Y) associated with Calcite | CaCO3 |
| 3 photos of Ashcroftine-(Y) associated with Fluorite | CaF2 |
| 3 photos of Ashcroftine-(Y) associated with Aegirine | NaFe3+Si2O6 |
| 3 photos of Ashcroftine-(Y) associated with Elpidite | Na2ZrSi6O15 · 3H2O |
| 2 photos of Ashcroftine-(Y) associated with Polylithionite | KLi2Al(Si4O10)(F,OH)2 |
| 1 photo of Ashcroftine-(Y) associated with Graphite | C |
Related Minerals - Strunz-mindat Grouping
| 9.DN. | Letnikovite-(Ce) | (Na◻)Ca2Ce2[Si7O17(OH)]F4(H2O)4 |
| 9.DN.05 | Zektzerite | LiNaZrSi6O15 |
| 9.DN.05 | Emeleusite | Li2Na4Fe2Si12O30 |
| 9.DN.05 | Tuhualite | NaFe2+Fe3+Si6O15 |
| 9.DN.10 | Semenovite-(Ce) | Na8Ca2FeBe6Ce2Si14O40(OH)4F4 |
| 9.DN.15 | 'Ashcroftine-(Ce)' | K5Na5(Ce,Ca)12Si28O70(OH)2(CO3)8 · 8H2O |
Radioactivity
| Element | % Content | Activity (Bq/kg) | Radiation Type |
|---|---|---|---|
| Uranium (U) | 0.0000% | 0 | α, β, γ |
| Thorium (Th) | 0.0000% | 0 | α, β, γ |
| Potassium (K) | 4.9594% | 1,537 | β, γ |
For comparison:
- Banana: ~15 Bq per fruit
- Granite: 1,000–3,000 Bq/kg
- EU exemption limit: 10,000 Bq/kg
Note: Risk is shown relative to daily recommended maximum exposure to non-background radiation of 1000 µSv/year. Note that natural background radiation averages around 2400 µSv/year so in reality these risks are probably extremely overstated! With infrequent handling and safe storage natural radioactive minerals do not usually pose much risk.
Note: The mass selector refers to the mass of radioactive mineral present, not the full specimen, also be aware that the matrix may also be radioactive, possibly more radioactive than this mineral!
Activity: –
| Distance | Dose rate | Risk |
|---|---|---|
| 1 cm | ||
| 10 cm | ||
| 1 m |
The external dose rate (D) from a radioactive mineral is estimated by summing the gamma radiation contributions from its Uranium, Thorium, and Potassium content, disregarding daughter-product which may have a significant effect in some cases (eg 'pitchblende'). This involves multiplying the activity (A, in Bq) of each element by its specific gamma ray constant (Γ), which accounts for its unique gamma emissions. The total unshielded dose at 1 cm is then scaled by the square of the distance (r, in cm) and multiplied by a shielding factor (μshield). This calculation provides a 'worst-case' or 'maximum risk' estimate because it assumes the sample is a point source and entirely neglects any self-shielding where radiation is absorbed within the mineral itself, meaning actual doses will typically be lower. The resulting dose rate (D) is expressed in microsieverts per hour (μSv/h).
D = ((AU × ΓU) + (ATh × ΓTh) + (AK × ΓK)) / r2 × μshield
Fluorescence of Ashcroftine-(Y)
Other Information
Internet Links for Ashcroftine-(Y)
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References for Ashcroftine-(Y)
Localities for Ashcroftine-(Y)
Showing 4 localities.
Locality List
- This locality has map coordinates listed.
- This locality has estimated coordinates.
ⓘ - Click for references and further information on this occurrence.
? - 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.
Canada | |
| Grice (1989) +1 other reference |
Greenland (TL) | |
| Nature (1932) +2 other references |
Italy | |
| Anthony et al. (1995, reprinted 2003) +1 other reference |
Russia | |
| Krivovichev et al. (2026) |







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The
Poudrette quarry, Mont Saint-Hilaire, La Vallée-du-Richelieu RCM, Montérégie, Québec, Canada