marbles and metaperidotites; geothermobarometry...
TRANSCRIPT
1
Marbles and Metaperidotites;
Geothermobarometry
GEOL 13.53
Metamorphic Lecture 5
Typical Composition of Peridotitesand
Carbonate Rocks 0.05
0.24
0.34
K2O
0.03
0.07
0.49
Na2O
32.87
53.06
5.05
CaO
21.88
1.59
31.24
MgO
0.05
0.07
0.41
MnO
0.60
1.15
11.19
FeO
0.13
0.98
4.23
Al 2O3
0.41
3.64
42.26
SiO
2
Dolostone
Limestone
Peridotite
Metaperidotitesand Marbles
Low Grade Reactions in
Metaperidotites
2
Metamorphism of Calcareous Rocks
Figure 29-1. Winter (2001) An Introduction to Igneous and M
etamorphic Petrology. Prentice Hall.
Isogradsin Marbles
Figure 29-5. Metamorphic zones developed in regionally m
etamorphosed dolomitic rocks of the Lepontine Alps, along the Swiss-Italian border. After
Trommsdorff (1966) Schweiz. Mineral. Petrogr. Mitt., 46, 431-460 and (1972) Schweiz. Mineral. Petrogr. Mitt., 52, 567-571. Winter (2001) An
Introduction to Igneous and M
etamorphic Petrology. Prentice H
all.
Figure 29-2. A portion of the Alta aureole in Little Cottonwood Canyon, SE of Salt Lake City, UT, where talc, tremolite, forsterite, and periclase isograds were
mapped in m
etacarbonates by M
oore and K
errick(1976) Amer. J. Sci., 276, 502-524. Winter (2001) An Introduction to Igneous and M
etamorphic Petrology.
Prentice Hall.
3
Figure 29-4. After Spear (1993) Metamorphic Phase Equilibria and Pressure-Temperature-Time Paths
Isogradsin Marbles
Mixed
Volatile
Reactions
Mixed
Volatile
Reactions
Internal vsExternal Buffering
4
Intersecting Isograds
Figure 29-7b. Isograds mapped in the field. Note that isograd (5) crosses the others in a m
anner sim
ilar to that in part (a). This behavior is attributed to infiltration
of H
2O from the syn-m
etamorphic pluton in the area, creating a gradient in X
H2Oacross the area at a high angle to the regional temperature gradient, equivalent to
the T-X
diagram. After Carmichael (1970) J. Petrol., 11, 147-181.
1
234
Bt+Cc+Qz=
Ca-Amph+Kf
Intersecting Isograds
Figure 29-7a. T-X
H2Odiagram illustrating the shapes and relative locations of the reactions for the isograds mapped in the W
hetstone Lake area. Reactions 1, 2,
and 4 are dehydration reactions and reaction 3 is the Ky = Sil transition, all in m
etapelites. Reaction 5 is a dehydration-decarbonation in calcic rocks with a
temperature maxim
um at X
H2O= 0.25. After Carmichael (1970) J. Petrol., 11, 147-181,
Intersecting Isograds
Figure 29-7a. T-X
H2Odiagram illustrating the shapes and relative locations of the reactions for the isograds mapped in the W
hetstone Lake area. Reactions 1, 2,
and 4 are dehydration reactions and reaction 3 is the Ky = Sil transition, all in m
etapelites. Reaction 5 is a dehydration-decarbonation in calcic rocks with a
temperature maxim
um at X
H2O= 0.25. b. Isograds mapped in the field. Note that isograd (5) crosses the others in a m
anner similar to that in part (a). This behavior
is attributed to infiltration of H
2O from the syn-m
etamorphic plutonin the area, creating a gradient in X
H2Oacross the area at a high angle to the regional
temperature gradient, equivalent to the T-X
diagram. After Carmichael (1970) J. Petrol., 11, 147-181.
Geothermobarometry
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Geothermobarometry
•Metamorphic facies
and petrogenetic
grids allow us to
estimate PT
conditions based on
mineral assemblages
•Only requires field
and/or petrographic
data
Continuous Reactions
Figure 27-6. AFM
projections showing
the relative
distribution of Fe and
Mg in garnet vs.
biotite at
approxim
ately 500oC
(a) and 800oC (b).
Winter (2001) An
Introduction to
Igneous and
Metamorphic
Petrology. Prentice
Hall.
Ion Exchange
Reactions
Geothermobarometry
•Continuous and ion-
exchange reactions
require chemical
composition data from
coexisting minerals
•Can further limit PT
estimates
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Distribution Coefficient (K
D)
•The distribution coefficient (K
D) is the ratio
by which two elements are partitioned
between two minerals at equilibrium
•For example, the distribution coefficient of
Fe and Mg in garnet and biotite is:
KDGt-Bt = (Mg/Fe)Gt/ (Mg/Fe)Bt
The Garnet -Biotite Geothermometer
T oC
Initial
X(Fe-Bt)
Final
X(Fe-Bt)
Final
X(Fe-Grt)
Final
(Mg/Fe)Grt
Final
(Mg/Fe)Bt
KT
Kelvins
1/T
Kelvins
lnK
799
1.00
0.750
0.905
0.105
0.333
0.315
1072
0.00093
-1.155
799
0.50
0.710
0.896
0.116
0.408
0.284
1072
0.00093
-1.258
749
0.50
0.695
0.896
0.116
0.439
0.264
1022
0.00098
-1.330
738
1.00
0.730
0.906
0.104
0.370
0.281
1011
0.00099
-1.271
698
0.75
0.704
0.901
0.110
0.420
0.261
971
0.00103
-1.342
698
0.50
0.690
0.896
0.116
0.449
0.258
971
0.00103
-1.353
651
0.75
0.679
0.901
0.110
0.473
0.232
924
0.00108
-1.459
651
0.50
0.661
0.897
0.115
0.513
0.224
924
0.00108
-1.497
599
0.75
0.645
0.902
0.109
0.550
0.197
872
0.00115
-1.623
599
0.50
0.610
0.898
0.114
0.639
0.178
872
0.00115
-1.728
550
0.75
0.620
0.903
0.107
0.613
0.175
823
0.00122
-1.741
550
0.50
0.590
0.898
0.114
0.695
0.163
823
0.00122
-1.811
601
0.50
0.500
0.800
0.250
1.000
0.250
874
0.00114
-1.386
601
0.25
0.392
0.797
0.255
1.551
0.164
874
0.00114
-1.807
697
0.75
0.574
0.804
0.244
0.742
0.329
970
0.00103
-1.111
697
0.25
0.468
0.796
0.257
1.137
0.226
970
0.00103
-1.487
Table 27-2. Experimental results of Ferry and Spear (1978) on a Garnet-Biotite Geothermometer
The Garnet -Biotite Geothermometer
Figure 27-6. AFM projections showing the relative distribution of Fe and M
g in garnet vs. biotite at approxim
ately 500oC (a) and 800oC
(b). From Spear (1993) Metamorphic Phase Equilibria and Pressure-Temperature-Time Paths. M
ineral. Soc. Amer. M
onograph 1.
The Garnet -Biotite Geothermometer
Figure 27-7. Pressure-temperature diagram sim
ilar to Figure 27-4 showing lines of constant K
Dplotted using equation (27-35) for the
garnet-biotite exchange reaction. The Al 2SiO
5phase diagram is added. From Spear (1993) Metamorphic Phase Equilibria and Pressure-
Temperature-Time Paths. M
ineral. Soc. Amer. M
onograph 1.
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The GASP
Geobarometer
Figure 27-8. P-T phase diagram
showing the experimental results of
Kozioland New
ton (1988), and the
equilibrium curve for reaction (27-37).
Open triangles indicate runs in which
An grew, closed triangles indicate runs
in which G
rs + K
y + Q
tz grew, and
half-filled triangles indicate no
significant reaction. The univariant
equilibrium curve is a best-fit
regression of the data brackets. The
line at 650oC is Kozioland New
ton’s
estimate of the reaction location based
on reactions involving zoisite. The
shaded area is the uncertainty
envelope. After Kozioland New
ton
(1988) Amer. Mineral., 73, 216-233
The GASP Geobarometer
Figure 27-8. P-T diagram contoured for equilibrium curves of various values of K for the GASP geobarometer reaction: 3 An = G
rs + 2
Ky + Q
tz. From Spear (1993) Metamorphic Phase Equilibria and Pressure-Temperature-Time Paths. M
ineral. Soc. Amer. M
onograph 1.
Geothermobarometry
Figure 27-11. P-T phase diagram calculated by TQW 2.02 (Berman, 1988, 1990, 1991) showing the internally consistent reactions between garnet, muscovite,
biotite, Al 2SiO
5and plagioclase, when applied to the mineral compositions for sample 90A, Mt. M
oosilauke, NH. The garnet-biotite curve of Hodges and Spear
(1982) Amer. Mineral., 67, 1118-1134 has been added.
PTtPaths
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Figure 27-12. Chemically zoned
plagioclase and poikiloblastic
garnet from m
eta-pelitic sample 3,
WopmayOrogen, Canada. a.
Chem
ical profiles across a garnet
(rim
→ →→→rim). b. An-content of
plagioclase inclusions in garnet
and corresponding zonation in
neighboring plagioclase. After St-
Onge(1987) J. Petrol.28, 1-22 .
PTtPaths
PTtPaths
Figure 27-13. The results
of applying the garnet-
biotite geothermometer
of Hodges and Spear
(1982) and the GASP
geobarometer of Koziol
(1988, in Spear 1993) to
the core, interior, and
rim composition data of
St-Onge(1987). The
three intersection points
yield P-T estim
ates
which define a P-T-t
path for the growing
minerals showing near-
isothermal
decompression. After
Spear (1993).