Abelsonite is a nickel porphyrin mineral with chemical formula C31H32N4Ni. It was discovered in 1969 in the U.S. State of Utah and described in 1975. The mineral is named after geochemist Philip H. Abelson. It is the only known crystalline geoporphyrin.

Abelsonite
Abelsonite from the Green River Formation, Uintah County, Utah, US
General
CategoryOrganic minerals
Formula
(repeating unit)
C31H32N4Ni[1]
IMA symbolAbl[2]
Strunz classification10.CA.20
Dana classification50.4.9.1
Crystal systemTriclinic
Space groupP1 (No. 2)[3]
Unit cella = 8.508, b = 11.185 Å
c = 7.299 [Å], α = 90.85°
β = 114.1°, γ = 79.99°
Z = 1[1]
Identification
ColorPink-purple, dark greyish purple, pale purplish red, reddish brown
CleavageProbable on {111}[1]
FractureFragile[4]
Mohs scale hardness2–3
LusterAdamantine, sub-metallic
StreakPink
DiaphaneitySemitransparent[1]
Specific gravity1.45
Optical propertiesBiaxial[1]
Ultraviolet fluorescenceNon-fluorescent[4]
Absorption spectraStrong reddish brown to reddish black[1]
References[5]

Description

edit

Abelsonite is semitransparent and pink-purple, dark greyish purple, pale purplish red, or reddish brown in color.[1][5] The mineral occurs as thin laths or plates or small aggregates up to 1 cm (0.39 in).[1] The mineral is soluble in benzene and acetone and is insoluble in water, dilute hydrochloric acid, and dilute nitric acid.[6]

Occurrence and formation

edit

The mineral is known only from the Parachute Creek Member of the Green River Formation.[7] It has been known from the Uinta Basin in Utah since its discovery and from the Piceance Basin in Colorado since 1985.[7] Abelsonite occurs in association with albite, analcime, dolomite, mica, orthoclase, pyrite, and quartz.[1]

Abelsonite is a secondary mineral that formed in fractures, vugs, and bedding planes of oil shale.[1][7] The mineral probably formed from diagenesis of chlorophyll, likely chlorophyll a, which was transported as an aqueous solution into a favorable geologic setting. [7][8] Alternative source are Methanogen Archea, where close compound is used in Cofactor F430 critical for methane production.

In 2003, abelsonite was fully synthesized for the first time.[9]

Structure

edit
 
Structure of abelsonite

In 1989, abelsonite was the only known geoporphyrin to have a crystalline structure.[7][a] Most geoporphyrins occur as a series of homologues spanning a large range of carbon numbers.[7] The porphyrin which comprises abelsonite is common, but it does not usually occur in isolation from other porphyrins.[10]

The mineral is a deoxophylloerythroetioporphyrin (DPEP), with nickel occupying the center of the porphyrin ring. Most of the mineral consists of a C31 porphyrin with small quantities of a C30 norisomer.[11] The mineral crystallizes in the triclinic crystal system.[1]

History

edit

The mineral was first noted in 1969 in a core sample made by the Western Oil Shale Corporation in Uintah County, Utah.[12] It was described in 1975 in the journal Geological Society of America Abstracts with Programs.[13] The mineral was named after Philip H. Abelson (1913–2004), a long-time editor of the journal Science,[7] for his work in organic geochemistry.[14]

Type specimens are held in The Natural History Museum in London and the National Museum of Natural History in Washington, D.C.[1]

See also

edit

Notes

edit
  1. ^ So far as the authors were aware[7]

References

edit
  1. ^ a b c d e f g h i j k l Anthony, John W.; Bideaux, Richard A.; Bladh, Kenneth W.; Nichols, Monte C. (eds.). "Abelsonite" (PDF). Handbook of Mineralogy. Chantilly, VA: Mineralogical Society of America.
  2. ^ Warr, L.N. (2021). "IMA–CNMNC approved mineral symbols". Mineralogical Magazine. 85 (3): 291–320. Bibcode:2021MinM...85..291W. doi:10.1180/mgm.2021.43. S2CID 235729616.
  3. ^ Hummer et al. 2017, pp. 1129–1132.
  4. ^ a b "Abelsonite". Webmineral. Retrieved January 2, 2013.
  5. ^ a b "Abelsonite". Mindat. Retrieved December 21, 2012.
  6. ^ Milton et al. 1978, p. 932.
  7. ^ a b c d e f g h Mason, Trudell & Branthaver 1989, p. 585.
  8. ^ Mason, Trudell & Branthaver 1989, p. 594.
  9. ^ Zhang & Lash 2003, p. 7253.
  10. ^ Mason, Trudell & Branthaver 1989, p. 593.
  11. ^ Storm et al. 1984, p. 1075.
  12. ^ Milton et al. 1978, pp. 930–931.
  13. ^ Fleischer, Michael (May–June 1976). "New Mineral Names" (PDF). American Mineralogist. 61 (5–6): 502.
  14. ^ Milton et al. 1978, p. 931.
Bibliography
edit