Feldspars - Species, Crystal Chemistry, Textures, CL and Provenance Potential
Feldspars is the most abundant mineral in the crust
It forms in igneous, sedimentary and metamorphic rocks.
Consequently, it is a likely source for framework grains in detrital sedimentary rocks.
The challenge is to recognize the feldspar species, textures, chemistry that may be preserved in sedimentary rocks without alteration during burial and diagenesis
Feldspar species and crystallography
The feldspars are generally considered a ternary system among the following end-members:
Albite - NaAlSi3O8
Anorthite - CaAl2Si2O8
Orthoclase - KAlSi3O8
Uncommonly, the species Celsian (BaAl2Si2O8) is found
Other important cations, generally at trace element concentrations include: Li+, Rb+, NH4+, Sr2+, Eu2+, Pb2+, Mg2+, Mn2+, Fe2+, Fe3+, Eu3+ Ti4+
Crystallographically, the feldspar minerals are aluminosilicates whose structures are composed of corner-sharing AlO4 and SiO4 tetrahedra linked in an infinite 3D array with relatively large (1 A) charge-balancing cations in the irregular cavities of the tetrahedral framework.
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![]() The tetrahedral sites are unique and upon cooling partial-to-complete ordering of Al and Si in the tetrahedra may develop, depending on the T of crystallization and the cooling rate. For K-feldspar (KAlSi3O8) has several forms depending on tetrahedral ordering
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The ternary feldspars are typically considered in terms of two binary subsystems:
Albite - K-feldspar (NaAlSi3O8 - KAlSi3O8) - alkali feldspar series

Features:
large solvus that could theoretically be used as a geothermometer.
Practically, the alkali feldspar continue to exsolve on cooling and develop the common perthite texture (albite in K-feldspar) and anti-perthite texture (K-feldspar in albite)
change in structural state with temperature
Albite - Anorthite (NaAlSi3O8 - CaAl2Si2O8) - plagioclase series

Features:
continuous solid solution upon crystallization (plagioclase loop).
Ordering of the plagioclase structure and the development of 3 miscibility gaps - Peristerite, Boggild and Huttonlocher gaps.
The presence of these intergrowths in detrital feldspars have a provenance potential. E.g. Lee et al. (2003)
Feldspar ternary

The general systematics of the ternary feldspars form the basis for compositional criteria for provenance studies using feldspars
empirical source rock fields in the ternary system (Trevena and Nash, 1981)
Other textural features in feldspars:
Subsolidus
Alteration (low temperature and diagenetic)
saussaritization
CL in feldspars
Feldspars of the system orthoclase-albite-anorthite in crystalline rocks show variable luminescence
bright blue,
greenish yellow,
violet
red
Three broad emission bands can be distinguishedin feldspar CL:
a blue emission band (420–500 nm) - mostly due to intrinsic defects (O- hole centers, Al-O-Al centers and Si-O-Si centers), Ti4+, and possibly Eu2+ and Cu2+
one emission band in the green to yellow wavelength range (540–570 nm) - due to trace Mn2+

a red band at the edge of the infrared (690–760 nm) - due to Fe3+
several rare, narrow bands related to rare earth elements such as Sm3+, Dy3+, Eu3+, Tb3+, Nd3+)


Sandstones can have quite variable CL characteristics e.g. Zinkernagel (1975) found that the Verrucano-Sandstone of the central Alps contains five different CL-types of alkali feldspar:
a) homogeneous light blue,
b) patchy light blue-Prussian blue
c) patchy light blue-light brown
d) homogeneous light brown
e) homogeneous olive-greenish yellow.
Feldspar cements in sandstones and authigenic feldsparsshow no CL according to observations with a cold cathode equipment .
Using the hot cathode CL-microscope, responses have been observed.
Richter and Zinkernagel (1975) described microcline cements with grey-olive or middle to dark brown CL and albite-cements with middle to dark brown colours in Lower Triassic siliciclastics of the central Alps. According to a more recent CL-spectroscopic investigation, the dark olive luminescence of authigenic albite in different carbonate rocks with diagenetic to epimetamorphic overprint is caused by Mn2+- and Fe3+-activation