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Pegmatites
Pegmatites
Pegmatites
Keystone pegmatite,
Pennington County,
South Dakota, USA.
Named in honor
ern.
of Petr C
SOURCE : M. SCOTT;
PHOTO : R OBERT D OWNS
Petr Cern,
David London,2 and Milan Novk3
1811-5209/12/0008-0289$2.50
DOI: 10.2113/gselements.8.4.289
E LEMENTS , V OL . 8,
PP.
289294
FOR PEGMATITES
The current system for classifying pegmatites (TABLE 1)
begins with a subdivision of pegmatite classes (Ginsburg
et al. 1979). The pegmatite classes are distinguished on
the basis of the metamorphic environment of their host
rocks (the abyssal class), mineralogy (the muscovite class),
elemental composition (the rare-element class), and texture
(the miarolitic class). Most of the pegmatite classes carry
an implied connotation of their environment of emplacement, more or less equivalent to depth of formation. The
pressures (depths) at which pegmatites crystallize, however,
are poorly constrained by any chemical or textural features
of the pegmatites themselves. Most pegmatites are intrusive
bodies, and hence postdate their immediately adjacent host
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Class
Subclass
Abyssal
HREE
Type
Subtype
Family
NYF
LREE
NYF
LCT
U
BBe
Muscovite
Muscovite
rare element
REE
NYF
Li
Rare element
REE
LCT
allanite
monazite
euxenite
NYF
gadolinite
Li
beryl
berylcolumbite
berylcolumbitephosphate
complex
spodumene
petalite
lepidolite
LCT
elbaite
amblygonite
albite
spodumene
albite
Miarolitic
REE
topazberyl
NYF
gadolinitefergusonite
Li
beryltopaz
spodumene
LCT
petalite
lepidolite
ern and
The pegmatite classification scheme of C
Ercit (2005), modified to show the correlation
between pegmatite classes and families. NYF = niobiumyttrium
fluorine family (green); LCT = lithiumcesiumtantalum
family (yellow); HREE = heavy rare earth elements; LREE = light rare
earth elements
TABLE 1
Cern
(1991) and Cern
and Ercit (2005) expanded the classification of granitic pegmatites to include ten subclasses,
four of which are subdivided into thirteen types, and two
types are further broken down into seven subtypes. All
of these categories are based on the trace element signatures of the pegmatites as reflected in their mineralogy and
mineral chemistry. TABLE 1 shows the hierarchy of classifi
cation, beginning, as did Cern
and Ercit (2005), with the
pegmatite classes. Color bars illustrate how the pegmatite
subclasses and their constituents fit into an overarching
classification of two pegmatite families.
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Cern
and Ercit (2005) now ascribe a small fraction of the
LCT and NYF pegmatites to I-type sources. I-type granites
are usually affi liated with subduction-related magmatism,
but they can be generated from the metamorphic products
of any mafic to intermediate igneous rocks or volcaniclastic
sedimentary rocks.
White mica (muscoviteparagonitephengite solid solutions) and dark mica (biotite-group solid solutions) carry
most of the trace elements that defi ne the signature of
the LCT pegmatites (e.g. Dahl et al. 1993). The abundant
white mica in schist of marine sedimentary origin reacts
extensively at the onset of anatexis (London et al. 2012).
The initial extent of melting is small, because it is limited
by the low sodium content of the rock. Consequently, a
large fraction of the rare-element content of mica schist is
transferred to a small volume of partial melt. The melting
reactions of white and dark mica also produce K-feldspar
+ aluminosilicate + spinel as products, especially when
the concentration of H 2O in the melt is well below that
of saturation (e.g. Acosta-Vigil et al. 2003). Rubidium is
slightly incompatible in K-feldspar, whereas Li and Cs are
almost perfectly incompatible. Hence, the formation of
K-feldspar at the source, and its continued crystallization
from the granitic melt, leads the liquid line of descent
toward a composition in which the Cs/Rb and Li/Rb ratios
become highly elevated. This fractionation trend results
in the pattern of rare-alkali enrichment found in the
LCT pegmatites.
In TABLE 1, Cerns
(1991) pegmatite families are identified by their diagnostic trace element signatures. If these
signatures were substituted for the classes, the classification
of granitic pegmatites would be purely on their chemical
attributes, without genetic inferences for depth of emplacement or an implied tectonic setting.
(e.g. Cern
et al. 1985), when the distributions of these
elements are controlled by major and accessory minerals
in which Nb and Ta are nonessential trace constituents.
London (2008) reviewed the published data on partitioning
of Nb and Ta among rutile, ilmenite, titanite, amphiboles, and biotite. There was no consistent pattern in the
partitioning data; that is, the phases in question did not
consistently incorporate one element over another. Thus,
the factors that fractionate Ta from Nb in granites are not
yet fully known.
Chappell and White (2001) observed that an elevated phosphorus content is as diagnostic of the S-type granites as
is their peraluminous composition. Both chemical attributes are positively correlated with the derivation of melt
from metapelite protoliths and with the H 2O content of
those melts (London et al. 1999; Acosta-Vigil et al. 2003).
Phosphorus- and Cs-rich lithium pegmatites are truly diagnostic of S-type sources for the LCT family of pegmatites
(Martin and De Vito 2005).
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Cern
and Ercit (2005) suggested that some rare-element
pegmatites in both families might be sourced from I-type
granites. However, the I-type granites that are clearly
associated with subduction zones (mostly Phanerozoic in
age) tend to lack significant pegmatitic aureoles at their
margins, which is a hallmark of the S-type and A-type
granites. As an example, the granitic porphyries of Tertiary
age that generated large hydrothermal cells and copper
mineralization in the western Cordillera of North America
are devoid of pegmatitic textures. These igneous bodies are
thought to have exsolved a saline aqueous fluid early in
the history of their magmatic consolidation, and hence,
according to the Jahns-Burnham model (see London and
Morgan 2012), should have been prime candidates for
developing a pegmatitic facies (cf Nabelek et al. 2010).
Granite and pegmatite dikes in tonalite along the Piute Pass Trail
between Piute Pass and Hutchinson Meadow, central Sierra Nevada,
California. The thicker central dike shown here possesses pegmatitic borders, in
which feldspar crystals are elongate and branch toward the dike center, followed
inwardly by aplitic texture, and then a return to coarse-grained pegmatitic texture
in the central zone. Pencil for scale. PHOTO : JAMES T. G UTMANN
FIGURE 1
E LEMENTS
HYBRIDIZATION VIA
LOCAL CONTAMINATION
Pegmatite-forming magmas contain negligible heat to
promote melting of rafted inclusions of solid rock. However,
the fractionated compositions of pegmatite magmas and
their fi nal aqueous fluids are highly reactive with other,
less-evolved, common host lithologies (e.g. Morgan and
London 1987; Novk et al. 2012). Local contamination of
pegmatites occurs principally along dike margins during
emplacement, and again at the transition into subsolidus
conditions. Alteration of host rocks by pegmatite-derived
fluids occurs late in the history of consolidation.
Mafic Components
The process of crystallization and separation of mafic
minerals from granitic magmas leaves their derivative
pegmatites depleted in Fe and Mg. In LCT pegmatites, the
crystallization of tourmaline can reduce Fe and Mg in the
melt to trace levels (Wolf and London 1997). The A-type
sources of NYF pegmatites are also poor in Fe and especially in Mg. It is common, however, for evolved pegmatites of both types to contain spectacular concentrations
of biotite or tourmaline along their margins (FIG. 2A, B).
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B
(A) Tourmaline-rich fringe along the margins of a
thin pegmatite dike hosted by metaconglomerate,
from Capoeira 2, Borborema Pegmatitic Province, Brazil.
PHOTO : JAN LOUN
FIGURE 2
Alkaline Earths
Contamination of LCT pegmatites by metacarbonates
appears to have modified the sources of some pegmatites
in central Madagascar and the Czech Republic (Novk et
al. 2012). These pegmatites possess strong enrichment in
Li and B (as spodumene, lepidolite, or elbaite) and locally
Cs (as londonite, CsBe4 Al4 [B11Be]O28 ), but they contain
primary assemblages that include diopside, danburite
(CaB2 Si 2O8 ), uvite (CaMg tourmaline), and liddicoatite
(CaLi tourmaline).
Alkalis
Within a given large group of pegmatites (LCT or NYF),
a general trend in the fractionation of alkalis begins with
chemically primitive K-rich pegmatites closest to their
source, followed by Na-rich pegmatites at the distal end of
CONCLUDING REMARKS
The compositions of pegmatites reflect an association
mostly with two granite types: the S- and the A-types.
Pegmatites of the LCT family, especially those enriched
in Li, Cs, B, and P, greatly predominate over all others.
This indicates that the metamorphosed juvenile sediments from which S-type granites arise are particularly
prone to yielding pegmatite-forming melts. Considering
what makes S-type and A-type sources distinct from I-type
sources, the difference comes down to their abundance
of fluxing components, that is, ligands other than silica
and alumina that profoundly influence the properties of
pegmatite-forming melts. S-type sources are enriched in B
and P, but also F, which is derived from the micas. A-types
are enriched in F, which is contributed by the eventual
melting of amphiboles and biotite. The archetypal I-type
granites found in subduction zones, as the sources of arc
volcanism and base-metal mineralization, are notably rich
in Cl and are hydrous, but they are largely devoid of the
fluxing components noted here (see London and Morgan
2012). They generate enormous volumes of quartz veins but
lack pegmatites to any significant extent. This distinction
points to an essential role for fluxing components like B,
P, and F, along with H 2O, in the formation of pegmatites,
as has been evident to most petrologists for over a century.
ACKNOWLEDGMENTS
Many colleagues and students discussed with us the topics
covered here in the field and laboratory, and Karen Ferreira
contributed to pulling the diverse contributions together,
including the reviewerss comments.
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REFERENCES
Acosta-Vigil A, London D, Morgan GB,
Dewers TA (2003) Solubility of excess
alumina in hydrous granitic melts
in equilibrium with peraluminous
minerals at 700800 C and 200 MPa:
applications of the aluminum saturation
index. Contributions to Mineralogy and
Petrology 146: 100-119
Bebout GE, Bebout AE, Graham CM
(2007) Cycling of B, Li, and LILE (K,
Cs, Rb, Ba, Sr) into subduction zones:
SIMS evidence from micas in highP/T metasedimentary rocks. Chemical
Geology 239: 284-304
ern P
Linnen RL, Van Lichtervelde M, C
(2012) Granitic pegmatites as sources of
strategic metals. Elements 8: 275-280
London D (2008) Pegmatites. Canadian
Mineralogist Special Publication 10,
347 pp
London D, Morgan GB VI (2012) The
pegmatite puzzle. Elements 8: 263-268
London D, Wolf MB, Morgan GB VI,
Gallego Garrido M (1999) Experimental
silicatephosphate equilibria in peraluminous granitic magmas, with a case
study of the Albuquerque batholith at
Tres Arroyos, Badajoz, Spain. Journal of
Petrology 40: 215-240
London D, Morgan GB VI, Acosta-Vigil
A (2012) Experimental simulations of
anatexis and assimilation involving
metapelite and granitic melt. Lithos, in
press, http://dx.doi.org/10.1016/j. lithos
.2012.04.006
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