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| Leucite |
K [AlSi2O6] |
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| Morphology: |
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Isometric or
pseudo-isometric. Crystals are equant and commonly euhedral
developed in the trapezohedron {211}, rarely the dodecahedron {110},
habit. |
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| Physical
properties: |
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Cleavage: {110} very
poor.
Hardness: 5.5 - 6.
Density = 2.485 ± 0.015 gm./cm3.
Luster: vitreous.
Streak: white. |
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Leucite phenocrysts in leucite basanite lava,
Nyiragongo, Democratic Republic of the Congo. Width of view 3 cm. |
| Optical
properties: |
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Color: colorless to gray,
colorless in thin section.
Isotropic or very weakly anisotropic, n 1.508 - 1.511. δ 0.001
All leucite is twinned, appearing as cross-hatched lamellae parallel
to {110}, just visible in thin section with the weak birefringence. |
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| Crystallography: |
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Unit cell:
low temperature polymorph:
a 13.09, c 13.75 Å
Z = 16, Space Group I 41/a
high temperature polymorphs:
a 13.50, c 13.59 Å
Z = 16, Space Group I 41/acd
a 13.55 Å
Z = 16, Space Group I a3d |
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| Name: |
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Even though it is
isostructural with analcime, leucite has not been considered a
zeolite, because it is an igneous mineral, contains no H2O
molecules, and has very limited solid solution with other members of
the structural group. However, after revising and expanding the IMA
definition of zeolite Coombs et al. (1997) included
leucite in this mineral group.
Leucite was described by Blumenbachs (1791), attributing the name to
Werner, who had previously described the mineral as “white garnet”.
The type locality is Vesuvius, Italy, and the name is from the
Greek, leukos, meaning white.
The term pseudoleucite refers to cloudy spheroids,
consisting of granular or fibrous, radiating intergrowths of
potassium feldspar, granular nepheline, and commonly zeolites.
Because of the common trapezohedron shape, they are generally
considered to have crystallized as leucite, which then reacted with
the magma or with subsolidus fluids, to form the later phases. |
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| Crystal structure: |
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Wyart (1940) showed that
the framework of leucite is the same as that of analcime and that
the space group is I41/a, which was
confirmed by Náry-Szabó (1942). Wyart (1940) also described the
transition of high temperature, isometric leucite to the low
temperature tetragonal polymorph. The unquenchable inversion causes
tetragonal leucite to be intensely twinned, which has long been
known. To refine the structure of leucite, Peacor (1968) heated his
crystal until the cell parameters were all equal and collected X?ray
data at 635°C. Mazzi et al. (1976) were able to find a
crystal fragment with sufficiently little twinning, to refine the
tetragonal polymorph. The differences between these two structures
are illustrated in the figure here. At high temperatures the leucite
framework is fully extended. With decreasing temperature tetrahedra
rotate to partially collapse the cages, allowing shorter K-O bond
lengths.

Using differential thermal analysis (DTA) heating curves, Faust
(1963) showed that the transition is actually characterized by two
endothermic peaks, suggesting that there is an intermediate form.
Lange et al. (1986) used differential scanning calorimeter
(DSC) scans to show that the transitions occur over a span of 122 to
176 degrees. They assigned the space group, I41/acd
to the intermediate phase, because it could be related to the cubic
(Ia3d) form by pseudomerohedral twinning and to
the low temperature phase (I41/a) by
merohedral twinning. The crystallography of these twins are
described by Mazzi et al. (1976), and by Palmer et al.
(1988) and Putnis (1992), who illustrate twins with transmission
electron micrographs. Transition temperatures vary from sample to
sample, but the transition of cubic leucite (point group, m3m)
to tetragonal (point group, 4/mmm) is at about 665°C. The
transition to the 4/m form occurs at about 630°C. Palmer et
al. (1989) measured the cell parameters with temperature, to
illustrate thermal contraction and phase changes with decreasing
temperature. Upon compression, a first-order phase transition is
observed at P = 2.4 ± 0.2 GPa from tetragonal (I41/a) to triclinic
symmetry (analysis of diffraction intensities suggests the space group P1?),
accompanied by a drastic increase in density of about 4.7% (Gatta et al. 2008).
Elastic properties of leucite have been investigated using resonant ultrasound
spectroscopy (Atkas et al. 2015). |
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| Chemical composition: |
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A selection of analyses of
leucite were tabulated by Deer et al. (2004, p. 306). Many leucite
phenocrysts have fluid and solid inclusions, containing measurable
amounts of extraneous elements, such as Ti. These may contribute to
the relatively poor charge balance of some published analyses.
Framework sites are occupied mainly by Si and Al, but some Fe occurs
in most samples. It is most likely that this iron occurs as Fe3+ in
tetrahedral sites, because iron leucite KFe3+Si2O6
is easily synthesized (Gupta and Yagi 1980, Palmer et al.
1997). The Si content, expressed as Si/(Si+Al+Fe), is near 0.667 for
many samples, but some are higher. For example, Si in leucite from
Wyoming is 0.69 (33.0 Si per unit cell), which is expressed as the
K-feldspar component by some workers. The substitution of Na for K
is limited, although some analyses indicate amounts up to 2.4 atoms
per unit cell. It is not clear how much substitution can occur at
liquidus temperatures, but replacement of K by Na can be extensive
at subsolidus temperatures from altering fluids. Up to complete
replacement of leucite by analcime occurs in many areas, for
example, Roccamonfina, Italy (Luhr and Giannetti 1989). |
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| Occurrences: |
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Leucite is a
characteristic component of potassic, undersaturated, volcanic and
hypabyssal rocks, ranging in composition from ultramafic to felsic.
Because water pressure restricts the stability field of leucite, it
does not occur in most plutonic rocks of the same compositions.
Because of the tendency of leucite to be altered by low temperature
processes, most leucite is found in young lavas and pyroclastic
rocks. It is, however, present in the 1240 Ma lamproite dikes in
west Greenland (Thy et al. 1987) and southern Baffin
Island, Canada (Hogarth 1997). Much of the following description of
occurrences is from Deer et al. (2004).
Trachybasalt-basanite-tephrite-leucitite series
Leucite phenocrysts occur with plagioclase and titanaugite
in trachybasalt lavas on Tristan da Cunha (Baker et al.
1964). These lavas with SiO2 about 48%, Na2O
4-5%, and K2O 3.4-3.9% are midway in the fractionation
series alkali basalt, trachyandesite, and trachyte that have been
erupted from the islands’ volcanoes.
Leucite basanite has been erupted from Holocene vents (e.g.
Nyiragongo) in the Virunga Mountains, Democratic Republic of
Congo-Uganda-Rwanda (Holmes and Harwood 1937, Bell and Powell 1969,
Sahama 1973), from numerous vents in the Eifel District of western
Germany (Duda and Schminke 1978), and from several volcanic centers
in the Roman Province (Washington 1906, Savelli 1967, Luhr and
Giannetti 1989), and Somma-Vesuvius, Italy (Rittmann 1933). Even
with the compositional variation between eruptive areas, leucite
basanite lavas have SiO2 between 46 and 48%, Na2O about
3%, and K2O about 4%. Phenocryst minerals in these lavas
are commonly leucite, labradorite, olivine, and diopsidic augite,
with leucite also crystallizing in the groundmass.
Leucite-bearing tephritic to phonolitic lavas have been erupted in
the volcanic fields of the Roman Province, Italy. For example, the
composition of lavas and tuffs from Roccamonfina has SiO2
in the range 50 to 56%, Na2O about 2.4%, and K2O
nearly 9% (Appleton 1972, Luhr and Gianetti 1987). A typical mode is
leucite phenocrysts 40%, labradorite 20%, sanidine 20% augite and
minor olivine 15%, and various accessory minerals including
nepheline 5%. In a different setting a series of leucite-bearing
mafic lavas, tuffs and breccia of mostly leucite shonkinite and
leucite tephrite, from Mt. Mouriah volcano, northeast Java, have
been described by Rittmann (1951). Pyroclastic kamafugite near
L’Aquila, Abruzzo, in the Umbrium-Latjum ultralkaline district of
central Italy contains diopside, leucite, haüyne, Mg-mica,
andraditic garnet, apatite, magnetite, kalsilite and olivine (Stoppa
et al. 2002).
Leucitite is a volcanic rock, strongly undersaturated with respect
to silica, in which leucite is the sole or dominant felsic mineral
(feldspars do not exceed 10 modal per cent). Leucite occurs both as
phenocrysts, accompanied by diopsidic augite and olivine, and in the
groundmass. The phenocryst abundances of leucite in leucitite in the
Roman Province have a considerable range. In flows of the Colli
Albani volcanic field leucite and augite occur in roughly equal
proportions, while some ejecta blocks consist of about 90% leucite.
Also in the Alban Hill the 561 ka Trigoria-Tor de' Cenci tuff
resulted from a pyroclastic flow from an unusually energetic
eruption (Palladino et al. 2001). The magma (SiO2,
42-45 wt. %) had crystallized only leucite, clinopyroxene, and
phogopite before the eruption. Lavas erupted in the Toro-Ankole and
Bufumbira province are olivine leucitite with ultramafic
compositions (SiO2 between 35-40% and K2O about 9 %).
An unusual rock suite of ultrapotassic, but silica saturated, lavas
are generally known by such names as wyomingite, as well as many
others of local origin. These occur in small volumes in the Leucite
Hills, Wyoming, USA (Carmichael 1967, Lange et al. 2000),
and west Kimberly, New South Wales, Australia (Cundari 1973). SiO2
contents range between 50-55, and K2O up to 12%.
Wyomingite is porphyritic with phenocrysts of phlogopite,
microphenoscryts of diopsidic augite in a groundmass of leucite.
Some varieties contain sanidine in the form of large phenocrysts.
The lavas of West Kimberly contain less K2O (about 8-9%)
than those of the Leucite Hills, and therefore, lack phlogopite
phenocrysts; otherwise mineral assemblages are similar.
Preservation of leucite crystallized in sub-surface magma is very
rare, and only occurs in unusual circumstances. In Proterozoic
lamproite dikes in the Sisiuit area, central West Greenland (Thy et
al. 1987) and at Napolean Bay, Baffin Island, Canada, leucite
crystallized early, and was preserved as microphenocrysts in the
chilled dike margins (Hogarth 1997). More commonly pseudomorphs
after leucite with euhedral outlines consist of tabular kalsilite
interleaved with sanidine. These pseudomorphs are similar to those
in the Sisimiut lamproite dikes of Greenland, illustrated by Thy et
al. (1987). Ejecta blocks from the 1944 eruption of Mt.
Vesuvius are highly crystalline rocks consisting of leucite,
clinopyroxene, plagioclase, olivine, apatite, oxides and glass
(Fulignati et al. 2000). These rocks formed by sidewall
accumulation of crystals from the potassic tephritic-phonolitic
magma resident in the chamber, and were ejected by the
phreatomagmatic eruptions.
Pseudomorphs of leucite
There are four kinds of pseudomorphs of leucite retaining
an outline characteristic of sections through trapezohedral crystals
consisting of (a) intergrowths of granular nepheline and potassium
feldspar, with analcime in some cases, to which the term pseudoleucite
refers, (b) tabular kalsilite interleaved with sanidine, (c)
granular analcime, and (d) aluminous clays and hydroxides.
Pseudoleucite. Pseudoleucite was first described
by Hussak (1890) from Serra de Tingua, Brazil, and has since been
found in many other localities, including the Bearpaw (Zies and
Chayes 1960) and Highwood Mountains (Larsen and Buie 1938) of
Montana; Magnet Cove, Arkansas, USA (Knight 1906); Spotted Fawn
Creek, Yukon Territory, Canada (Knight 1906), (Tempelman-Kluit
1969); Loch Borolan Laccolith, Scotland (Shand 1939); Laacher See
district, Germany; Tzu Shin Shan, Shansi, China (Yagi 1954);
Tezharsk, Armenia (Yagi and Gupta 1977); Vesuvius area, Italy
(Rittmann 1933); Lugingol Massif, Mongolia (Kononova et al.
1982); and the Sakun Massif in the western Aldan area, Russia
(Kononova et al. 1997). In descriptions of these and other
occurrences the usage of the term has not been uniformly consistent.
The clearest examples are those in volcanic and hypabyssal rocks,
where the pseudomorph boundaries and shapes are well defined.
Potassium feldspar and nepheline intergrowths in some plutonic rocks
are less well defined, having rounded margins which merge into the
other rock constituents. In some localities, e.g. Tzu Chin Shan
(Yagi 1954), pseudoleucite “crystals” have an internal structure, a
narrow outer zone of randomly oriented orthoclase and nepheline
covers an inner zone in which crystals are oriented with their
longer dimensions perpendicular to the pseudomorph boundary. Gittins
et al. (1980) argue that some intergrowths of nepheline and
potassium, to which the name pseudoleucite has also been applied,
are interstitial to other minerals of the rock or have grown on
nepheline grains during late stage magmatic crystallization and are
not related to leucite crystallization.
Over the past century the several processes proposed for the origin
of pseudoleucite, have been the subject of on-going discussion,
which has been reviewed by Guta and Yagi (1980) and Gittins et
al. (1980). In all cases the assumption has been that the
intergrowths with good crystal form initially crystallized as
leucite and were subsequently replaced. Knight (1906) suggested that
after the magma had solidified and cooled below the stability limit
of leucite, it was transformed into the stable assemblage of
nepheline and potassium feldspar. The principal argument against
this hypothesis is that the original leucite would have had to be
considerably more Na-rich than any phenocrysts known. Fudali (1963)
showed that at 1 atm leucite can accommodate up to 40 wt. % of
NaAlSi2O6 and up to 27 wt. % at P(H2O)
= 1 Kbar at 800°C. These compositions are unstable at lower
temperatures and breakdown to nepheline and potassium feldspar. Roux
and MacKenzie (1978) found that extensive solid solution of NaAlSi2O6
in leucite is metastable or unstable. They suggest that
potassium-rich analcime may be the precursor to pseudoleucite. In
fact, Larsen and Buie (1938) found such an analcime in the Highwood
Mountains. However, similar analcime compositions from Roccamonfina
have resulted from analcime replacement of leucite (Luhr and Kyser
1989).
Based on the phase diagram of the system nepheline-kalsilite-SiO2
(Schairer and Bowen 1935), Bowen and Ellestad (1937) suggested that
pseudoleucite forms at the reaction point, leucite + L = K-feldspar
+ nepheline. The main argument against this mechanism is that such
reactions show dissolution of the reacting phase resulting in
embayments in the crystal outline. However, it is the only mechanism
that accounts for pseudoleucite formation at liquidus temperatures,
thus accounting for pseudoleucite is young lava flows.
Taylor and MacKenzie (1975) proposed that ion exchange between
early-formed leucite and sodium-rich glass or sodium-rich vapour
under subsolidus conditions may account for most occurrences of
pseudoleucite. Given the ease of Na-replacement of leucite by
Na-containing fluids (Barrer and Hinds 1953), the suggestion that
pseudoleucite formation occurs by subsolidus reaction is receiving
increasing support, see for example Ryka (1998). Edgar (1978), using
sub-solidus phase relations along the join NaAlSi2O6-KAlSi2O6
at 1 kb P(H2O), suggests that pseudoleucite may form in
the analcime+nepheline+feldspar field at temperatures below 500°C
without the necessity of Na-bearing fluids.
Kalsilite-potassium feldspar intergrowths. In the
lamproite dikes of southern Baffin Island, Canada (Hogarth 1997) and
Sisimuit area, West Greenland (Thy et al. 1987) leucite
microphencrysts not quenched in the chilled margins are replaced by
sandine and kalsilite. These pseudomorphs consist of tabular
kalsilite interleaved with sanidine, and commonly display several
different orientations per “crystal”. Hogarth (1997) suggests that
these packets may present different domains in the original
tetragonal leucite. Similar intergrowths with a texture, termed
sympletitic, occur in the layered rocks of the southern Sakun
Massif, western Aldan area, on the Siberian platform, Russia
(Kononova et al. 1997).
Analcime pseudomorphs. In Italy analcime
replacement of leucite is widespread in the potassic lavas in the
region around Lago di Vico (northwest of Rome). Cundari and Graziani
(1964) have documented the process in tephritic lavas, some of which
contain partially replaced leucite phenocrysts. Luhr and Giannetti
(1987) describe analcime that has completely replaced
centimeter-sized leucite phenocrysts in a 385 Ka leucite tephrite
lava flow from the Quaternary volcano, Roccamonfina (northwest of
Naples). These analcime pseudomorphs are milky white apparently from
cracking of crystals, caused by the nearly 10% volume increase in
the conversion of leucite to analcime, and are richer in K than
crystals from other occurrences. Karlsson and Clayton (1991), among
others, have proposed that most igneous-appearing analcime is
replaced by leucite.
Clay pseudomorphs. Other pseudomorphs of leucite
are known such as those replaced by kaolinite and aluminum
hydroxides including gibbsite (Cassedanne and Menezes 1989). Such
pseudomorphs likely form by low temperature hydrothermal alteration.
Pseudoleucite from Loucná, Hory Mtns., Czech Republic (Pivec and
Ulrych 1982) consists of potassium feldspar and illite. |
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| References: |
| |
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Updated: August 2025.
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