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Metamorphic Systems and Phase Rule Analysis

The document discusses metamorphic facies and minerals. It describes key minerals that form under different pressure-temperature conditions, including aluminosilicates like andalusite, kyanite, and sillimanite. It discusses the classification of metamorphic facies series proposed by Miyashiro, including contact, Barrovian, Sanbagawa, and Franciscan facies series. It also describes isograds, which mark the appearance or disappearance of index minerals, indicating changing metamorphic grade across a region.

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Salman Ahmad
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0% found this document useful (0 votes)
272 views29 pages

Metamorphic Systems and Phase Rule Analysis

The document discusses metamorphic facies and minerals. It describes key minerals that form under different pressure-temperature conditions, including aluminosilicates like andalusite, kyanite, and sillimanite. It discusses the classification of metamorphic facies series proposed by Miyashiro, including contact, Barrovian, Sanbagawa, and Franciscan facies series. It also describes isograds, which mark the appearance or disappearance of index minerals, indicating changing metamorphic grade across a region.

Uploaded by

Salman Ahmad
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PPT, PDF, TXT or read online on Scribd

The Phase Rule in Metamorphic Systems

Consider the following three scenarios:


C = 1 (Al2SiO5)

F = 1 common

F = 2 rare

F = 3 only at the
specific P-T
conditions of the
invariant point
(~ 0.37 GPa and
500oC)
Figure 21-9. The P-T phase diagram for the system Al2SiO5
calculated using the program TWQ (Berman, 1988, 1990,
1991). Winter (2001) An Introduction to Igneous and
Metamorphic Petrology. Prentice Hall.
Representing Mineral Reactions
• albite  jadeite + quartz
From Hacker, B.R.,
Let’s put it all together…
• What if we had staurolite and andalusite
together? What conditions would that indicate?
Metamorphic facies
• P-T conditions, presence of fluids induces
different metamorphic mineral assemblages
(governed by thermodynamics/ kinetics)
• These assemblages are lumped into
metamorphic facies (or grades)
Aluminosilicate Minerals
• SILLIMANITE: Orthorhombic: Octahedral Al chains (6-fold) are
crosslinked by both Si and Al tetrahedra (4-fold).
• ANDALUSITE: Orthorhombic: 5-coordinated Al; Same octahedral (6-
fold) chains.
• KYANITE: Triclinic: All the Al is octahedrally coordinated (6- and 6-
fold).

Andalusite Kyanite Sillimanite

•Clearly, changes in structure are in response to changing P and T. Result is


changes in Al coordination.
•Phase transformations require rebonding of Al. Reconstructive polymorphism
requires more energy than do displacive transformations. Metastability of these 3
are therefore important (Kinetic factors limit equilibrium attainment).
•All 3 are VERY important metamorphic index minerals.
Aluminosilicate Minerals
• 3 polymorphs of Al2SiO5 are important
metamorphic minerals

Andalusite Kyanite Sillimanite


Topaz
• Aluminosilicate mineral as well, one oxygen
substituted with OH, F
• Al2SiO4(F,OH)2
• Where do you think Topaz forms??
Serpentine Minerals
• Mg3Si2O5(OH)4 minerals (principally as
antigorite, lizardite, chrysotile polymorphs)
• Forms from hydration reaction of magnesium
silicates
– Mg2SiO4 + 3 H2O  Mg3Si2O5(OH)4 + Mg(OH)2
forsterite serpentine brucite

• Asbestosform variety is chrysotile (accounts


for 95% of world’s asbestos production 
MUCH LESS DANGEROUS than crocidolite)
Phyllosilicates

T
Yellow = (OH) O
- vdw

Serpentine: Mg3 [Si2O5] (OH)4 T


O
T-layers and triocathedral (Mg2+) layers - vdw
(OH) at center of T-rings and fill base of VI layer  T
weak van der Waals bonds between T-O groups O
Serpentine
Antigorite maintains a
sheet-like form by
alternating segments of
opposite curvature

Chrysotile does not do this


and tends to roll into tubes

Octahedra are a bit larger than tetrahedral


match, so they cause bending of the T-O
layers (after Klein and Hurlbut, 1999).
Serpentine Veblen and Busek, 1979,
Science 206, 1398-1400.

S = serpentine T = talc
Nagby and Faust (1956) Am.
Mineralogist 41, 817-836.

The rolled tubes in chrysotile resolves the apparent


paradox of asbestosform sheet silicates
Chlorite
• Another phyllosilicate, a group of difficult
to distinguish minerals
• Typically green, and the dominant and
characteristic mineral of greenschist
facies rocks
• Forms from the alteration of Mg-Fe
silicates (pyroxenes, amphiboles, biotite,
garnets)
• Clinochlore, chamosite,
pennantite, nimmite – end members
• Chloritoid - Similar in appearance to
chlorite, but different 2V and relief
Prehnite-Pumpellyite
• Low-grade metamorphic minerals
• Minerals related to chlorite, form at slightly
lower P-T conditions
• Prehnite is also green, pumpellyite green
too, varies based on Fe content

• Prehnite + chlorite  pumpellyite + quartz


Micas
• Biotite and Muscovite are also important
metamorphic minerals (muscovite often the
principle component of schists)
• Phlogopite – similar to biotite, but has little
iron, forms from Mg-rich carbonate deposits
and a common mineral in kimberlites
(diamond-bearing material)
• Sericite – white mica (similar to muscovite)
– common product of plagioclase feldspar
alteration at low grades
Zeolites
• Diverse group of minerals forming at lower
metamorphic grades
• Framework silicas, but characteristically
containing large voids and highly variable
amounts of H2O
– Name is from the greek – meaning to boil stone as
the water can de driven off with heat
– Voids can acts as molecular sieves and traps for
many molecules
– Diversity of minerals in this group makes a for a
wide variety of sieve and trapping properties
selective for different molecules
Epidote Group

• Sorosilicates (paired silicate tetrahedra)


• Include the mineral Epidote Ca2FeAl2Si3O12(OH),
Zoisite (Ca2Al3Si3O12(OH) and clinozoisite
(polymorph)
Garnets
Garnet: A2+3 B3+2 [SiO4]3

“Pyralspites” - B = Al
Pyrope: Mg3 Al2 [SiO4]3
Almandine: Fe3 Al2 [SiO4]3
Spessartine: Mn3 Al2 [SiO4]3
“Ugrandites” - A = Ca
Uvarovite: Ca3 Cr2 [SiO4]3
Grossularite: Ca3 Al2 [SiO4]3
Andradite: Ca3 Fe2 [SiO4]3

Occurrence:
Mostly metamorphic
Some high-Al igneous
Also in some mantle peridotites
Garnet (001) view blue = Si purple = A turquoise = B
Staurolite
• Aluminosilicate - Fe2Al9Si4O22(OH)2
• Similar structure to kyanite with tetrahedrally
coordinated Fe2+ easily replaced by Zn2+ and Mg2+
• Medium-grade metamorphic mineral, typically
forms around 400-500 C
– chloritoid + quartz = staurolite + garnet
– chloritoid + chlorite + muscovite = staurolite + biotite +
quartz + water
• Degrades to almandine (garnet at higher T)
– staurolite + muscovite + quartz = almandine +
aluminosilicate + biotite + water
Metamorphic chain silicates
• Actinolite and tremolite are chain silicates
derived from dolomite and quartz and
common in low-mid grade metamorphic
rocks
• Riebeckite and Glaucophane are also
chain silicates – higher grade minerals,
often a blue color
• These minerals usually lower P, higher T
conditions
Metamorphic Facies
• Where do we find
these regimes of P-
T ‘off’ of the typical
continental
isotherms??
• How is the
environment that
forms a blueschist
facies rock different
from one forming a
hornfels?
Metamorphic Facies
• Table 25-1. The definitive mineral assemblages
that characterize each facies (for mafic rocks).
Let’s put it all together…
Facies Series
• Miyashiro (1961) initially proposed five facies series,
most of them named for a specific representative
“type locality” The series were:
1. Contact Facies Series (very low-P)
2. Buchan or Abukuma Facies Series (low-P
regional)
3. Barrovian Facies Series (medium-P
regional)
4. Sanbagawa Facies Series (high-P,
moderate-T)
5. Franciscan Facies Series (high-P, low T)
Fig. 25-3.
Temperature-
pressure diagram
showing the three
major types of
metamorphic
facies series
proposed by
Miyashiro (1973,
1994). Winter
(2001) An
Introduction to
Igneous and
Metamorphic
Petrology.
Prentice Hall.
Isograds
• Lines (on a map) or Surfaces (in the 3D
world) marking the appearance or
disappearance of the Index minerals in
rocks of appropriate composition
e.g. the ‘garnet-in isograd’; the ‘staurolite-
out isograd’
Complicated by the fact that most of these
minerals are solid solutions
• Isograds for a
single shale unit
in southern
Vermont
• Which side
reflects a higher
grade, or higher
P/T environment?

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