exhumation of ultrahigh-pressure metamorphic oceanic crust
TRANSCRIPT
Exhumation of ultrahigh-pressure metamorphicoceanic crust from Lago di Cignana,
Piemontese zone, Western Alps
Dissertation
zur Erlangung des Grades eines
Doktors der Naturwissenschaften der
Fakultät für Geowissenschaften an
der Ruhr-Universität Bochum
vorgelegt von
Sebastiaan Nicolaas Gerardus Cornelis van der Klauw
aus Gouda (Niederlande)
Bochum 1998
Als Dissertation genehmigt von der Fakultät für
Geowissenschhaften der Ruhr-Universität Bochum
Tag der Disputation: 11. Mai 1999
Promotionskomission:
Vorsitzender: Prof. Dr. Dr. h.c. L. Dresen
Erster Gutachter: Prof. Dr. B. Stöckhert
Zweiter Gutachter: Prof. Dr. W. Schreyer
Fachfremder Gutachter: Prof. Dr. B. Marschner
iii
Kurzfassung
Zur Entschlüsselung der Exhumierungsgeschichte ehemaliger ozeanischer Kruste im Gebiet
des Lago di Cignana, Valtournanche, in den Westalpen wurden die hier vorkommenden ultrahoch-
druckmetamorphen Coesit-führenden Basalte und Sedimentgesteine untersucht. Unter Einbeziehung
von Altersbestimmungen aus der Literatur werden mögliche Exhumierungsprozesse eingegrenzt.
In den metabasischen Gesteinen ist folgende Geschichte aufgezeichnet: Unter ultrahochdruck-
metamorphen Bedingungen (ca. 600 °C, 2,7 GPa) wurden die Eklogite durch Versetzungskriechen
von Omphacit verformt. Scherbänder belegen eine Lokalisierung der Verformung. Für die ersten
50 km der Exhumierung existieren keine Aufzeichnungen, was suggeriert, dass die Verformung
außerhalb des Aufschlussbereiches lokalisiert war. Bei Druck- und Temperaturbedingungen von
1,2 GPa und 500 °C wurde ein kleiner Teil der ultrahochdruckmetamorphen Minerale statisch
ersetzt. Weitere statische Ersetzungen benötigte Fluid-Infiltration entlang von Zugrissen, die jetzt
als Quarzgänge vorliegen. Form und Orientierung der verschiedenen Generationen von Quarzgängen
deuten auf niedrige Differentialspannungen hin. Die Ganggenerationen können mit den Stadien
des Ersatzes der ultrahochdruckmetamorphen Minerale korreliert werden. So kann eine Änderung
in der Orientierung des Spannungsfeldes und eine Zunahme der Differentialspannung bei Tempera-
turen um 500 °C und Drücken um 0,8 GPa abgeleitet werden.
Bei Druck- und Temperaturbedingungen von unter 0,6 GPa und 450 °C wurden die meta-
sedimentären Gesteine durchgreifend verformt, wobei sämtliche früher angelegten Strukturen über-
prägt wurden. In den Eklogiten fand die Verformung lokal statt und führte zur Bildung von
Grünschiefern. Mikrostrukturen in den Quarzgängen belegen für dieses Ereigniss eine Verformung
durch Versetzungskriechen von Quarz. Weitere Verformung war lokalisiert und fand bei Tempera-
turen um 350 °C und höheren Differentialspannungen statt. Die Dichte von Fluideinschlüssen belegt
eine Abkühlung unter 300 °C bei Drücken zwischen 0,2 und 0,4 GPa. Eine spätere spröde Ver-
formung konnte mit dem Druck-Temperatur-Pfad nicht in Bezug gesetzt werden.
Der Vergleich von publizierten radiometrischen Altersbestimmungen mit der Entwicklungsge-
schichte zeigt, dass die Exhumierung in zwei Phasen ablief. Die Exhumierung aus einer Tiefe von
etwa 90 km bis auf etwa 25 km fand innerhalb weniger Millionen Jahre bei niedrigen Differential-
spannungen statt. Das Model eines Subduktionskanals mit einer Zone entgegengesetzt gerichteten
Flusses passt zu dieser Entwicklungsgeschichte. Die Exhumierung von etwa 25 km bis auf etwa 10
km Tiefe fand langsamer und bei höheren Differentialspannungen statt. Dieser Teil der Entwicklungs-
geschichte wird im Einklang mit Konzepten zur regionalen Geologie wie folgt interpretiert. Auf
eine Stapelung von Decken folgte die Exhumierung durch Extension der verdickten Kruste an
flach einfallenden Abschiebungen.
iv
Abstract
The metamorphic and structural history of coesite-bearing ultra high pressure metamorphic oceanic
crust at Lago di Cignana, Valtournanche, Western Alps, recorded during exhumation has been
resolved. The record of metamorphic oceanic crust consisting of metabasalts and metasedimentary
rocks combined with geochronologic data from the literature is used to constrain possible exhumation
mechanisms.
In the metabasic rocks following history has been recorded: At ultra high pressure metamorphic
conditions (ca. 600 °C, 2.7. GPa) the eclogites were deformed by dislocation creep of omphacite.
The deformation was progressively localised into shearbands. A gap in the record for the first
50 km of subsequent exhumation suggests that any deformation during this time was localised
outside the outcrop area. At pressure and temperature conditions of 1.2 GPa and 550 °C the record
shows static replacement of a minor part of the ultra high pressure metamorphic mineral assemblage
in small scale closed systems. Further static replacement required fluid infiltration, concentrated
along tensile fractures now represented by veins. Shape and orientation of the several vein generations
indicate relatively low differential stresses. The vein generations can be correlated with replacement
stages of the ultra high pressure metamorphic minerals. In this way, a change in the orientation of
the stress field and an increase of the differential stress can be inferred at a temperature of around
500 °C and a pressure of 0.8 GPa.
At pressure and temperature conditions below 0.6 GPa and 450 °C intense deformation wiped
out all structures that might have formed earlier in the metasedimentary rocks. Localised ductile
deformation transformed part of the eclogites to greenschists. Microstructures of quartz veins
deformed during this stage indicate deformation by dislocation creep of quartz. This was followed
by a period of low differential stress. Localised deformation occurred at temperatures of ca. 350 °C
and at higher differential stresses. The densities of fluid inclusion suggest cooling to below ca.
300 C° at pressures between 0.2 and 0.4 GPa. Later deformation that occurred in the brittle field
could not be correlated with the pressure and temperature path.
The combination of this pressure-temperature-deformation-record with published geochronologic
data indicates a two stage exhumation. Exhumation from depths of approx. 90 km to depths of
approx. 25 km took place in at maximum a few million years and with low differential stresses in
the rock. For this exhumation stage the concept of a subduction channel with a zone of reverse flow
remains within the constraints posed by the record. Exhumation from depths of approx. 25 km to
approx. 10 km was slower and differential stresses were higher. This part of the record is in
conjunction with the regional geologic framework interpreted to represent the stacking of thrust
slices, followed by extension along low angle normal faults to explain exhumation.
v
Acknowledgments
This study became possible due to financial support from the German Science Foundation as
part of the Research group „High-pressure metamorphism in nature and experiment“ at the Ruhr-
University Bochum. This study was initiated by Prof. Dr. Bernard Stöckhert and Dr. Thomas
Reinecke, who both through numerous discussions and critical comments focused my thinking
about exhumation of high pressure metamorphic rocks. I must also thank numerous other persons
at the Institute of Geology and the Institute of Mineralogy and will risk to forget more than a few by
mentioning some.
I will start with Mr Gilsing and Mr Eickhoff, who prepared, usually in remarkably short time, a
large number of thin sections for me. Next on the list are Dr. Bernhardt and Mr Köhler-Schnettger
who kept the electron microprobe in running order. For SEM and CL photographs I have to thank
Dr. Rolf Neuser and Dirk Habermann. Dirk and Peter Wagner-Zweigel are also thanked for the
good time we had in the Alps. Thanks are also due for Mr Reß and Mrs Aschenbrenner for numerous
quickly delivered photographs.
The many computerprograms written by Klaus Röller made data interpretation much easier. I
should not forget to thank all the colleagues who introduced me to different analytical methods.
I like to thank my former roommates at the institute Petra Heckhoff, Sybille Schwarz and Andreas
Toetz for their introduction to the Ruhr-University. Finally, all colleagues from Bochum and Jena,
who spent time for discussions with beer, coffee, etc., are also thanked.
vi
Contents
Kurzfassung iii
Abstract iv
Acknowledgments v
Contents vi
List of abbreviations ix
List of tables xii
List of photographs xv
List of figures xvi
1 Introduction 1
2 Regional Geology 2
2.1 The studied Area 5
3 The record in the metabasic rocks 6
3.1 Petrology of the metabasic rocks - eclogites and greenschists 6
3.1.1 Group 0 eclogites 8
3.1.1.1 Mineral compositions 8
3.1.1.2 Mineral paragenesis and PT-estimates 13
3.1.2 Group 1 eclogites 15
3.1.2.1 Mineral compositions 15
3.1.2.2 Mineral paragenesis and PT-estimates 19
3.1.3 Group 2 eclogites 22
3.1.3.1 Mineral compositions 22
3.1.3.2 Mineral paragenesis and PT- estimates 23
3.1.4 Group 3 eclogites 24
3.1.4.1 Mineral compositions 24
3.1.4.2 Mineral paragenesis and PT-estimates 25
3.1.5 Group 4 eclogites and greenschists 26
3.1.5.1 Mineral compositions 26
3.1.5.2 Mineral paragenesis and PT-estimates 26
3.2 Structures in the eclogites 27
3.3 Structures in the greenschists 33
vii
4 The record in the metasedimentary rocks 34
4.1 Petrology of the metasedimentary rocks 34
4.2 Structures in the metasedimentary rocks 34
5 Quartz veins (microstructures, fabrics and fluid inclusions) 38
5.1 Microstructures of vein quartz 38
5.2 Paleopiezometry 39
5.3 C-axis fabrics in quartz veins 41
5.3.1 Eclogites 41
5.3.2 Metasedimentary rocks 43
5.3.3 Summary 44
5.4 Fluid inclusions in vein quartz 44
5.4.1 Compositions and densities of the fluid inclusions. 47
6 The exhumation record of the rocks 50
6.1 The record during UHPM and early exhumation 50
6.2 The record between 575 and ca. 450 °C 52
6.3 The record between ca. 450 and 300 °C 54
6.4 Synthesis: A two stage exhumation for the UHPM rocks of Lago di Cignana 55
7 Discussion and Exhumation concepts 58
7.1 Exhumation theories 58
7.1.1 Exhumation through erosion 58
7.1.2 Exhumation by extension tectonics 59
7.1.2.1 The critical wedge concept 60
7.1.2.2 The lithospheric extension concept 61
7.1.2.3 The subduction zone roll back concept 62
7.1.2.4 Concepts that require a period of divergence 62
7.1.3 Upflow concepts 63
7.2 Evaluation of published exhumation scenarios for exhumation from depths of 65
approx. 90 km to 25 km
7.3 Scenario for exhumation from 90 to 25 km depth 66
7.4 The scenario for the later exhumation from depths of ca. 25 km to the surface 69
8 Conclusions 72
9 References 74
Curriculum vitae
viii
Appendix A Methods A-1
A1 Sampling A-1
A2 Preparation A-1
A3 Analytical methods A-2
Appendix B Geothermobarometry B-1
B1 Thermometers B-1
B1.1 Garnet clinopyroxene thermometry B-1
B1.2 Amphibole Plagioclase thermometry. B-3
B1.3 Calcite - Dolomite thermometry B-4
B2 Barometers B-4
Tables with calculated temperatures and pressures B-6
Appendix C Tables C-1
C1 Sample list C-1
C2 Whole rock analyses C-5
C3 Tables of mineral compositions C-6
ix
List of abbreviations
° degree
°C degree Celsius
α angle between surface of the orogenic wedge and the horizontal
β angle between the basal decollement of the orogenic wedge and the horizontal
∆-velocity difference between the velocity of the downgoing plate and the material in the subduction channel close
to the plate-channel interface
θ frontal angle of the orogenic wedge
µ shear modulus
µm micrometer, 10-6m
µm2 square micrometer
ρ density
σ sigma, standard deviation
σ1
largest principal stress
σ3
smallest principal stress
τb
shear stress along the basal decollement of the orogenic wedge
A&E87 Anovitz & Essene, 1987
A94 Ai, 1994
ab albite
acm acmite, or acmite component in clinopyroxene
adr andradite, or andradite component in garnet
ae aegerine, or aegerine component in clinopyroxene
aggr. aggregate
alm almandine, or almandine component in garnet
amp gln rims of blue-green amphibole around glaucophane
amp grt discontineous overgrowth of blue-green amphibole on garnet
amp amphibole
an anorthite, or anorthite component in plagioclase
ap apatite
app appendix
approx. approximately
arg aragonite
b burgers vector
B88 Berman, 1988
biot green brown mica
BSE back scattered electron
c core position
ca. circa
cal calcite
cf. confer
chl chlorite
CL cathodoluminescence
cm centimeter
cm3 cubic centimeter
cpx clinopyroxene
cs coesite
czo clinozoisite
x
D deformation
d grain size
D1e
first deformation stage in eclogites
D2g
second deformation stage in the greenschists
D2s
second deformation stage in the metasedimentary rocks
D3e
third deformation stage in the eclogites
D3g
third deformation stage in the greenschists
D3s
third deformation stage in the metasedimentary rocks
D4e
fourth deformation stage in the eclogites
D4e1
number one shearzone of the fourth deformation stage in the eclogites
D4e2
number two shearzone of the fourth deformation stage in the eclogites
D4g
fourth deformation stage in the greenschists
D4s
fourth deformation stage in the metasedimentary rocks
D5g
fifth deformation stage in the greenschists
D5s
fifth deformation stage in the metasedimentary rocks
DEDM Digital Element Distribution Map
diop diopide, or diopside component in clinopyroxene
dol dolomite
Dr. Doctor
E east
ein eclogite
E&G79 Ellis & Green, 1979
e.c.c. extensional crenulation cleavage
e.g. example given
ENE east-north-east
eq. equivalent
exhum. exhumation
Fig. figure
g gravity
gln glaucophane
GPa giga Pascal (109 Pascal, 10 kilobar)
gr gramm
grs grossular, or grossular component in garnet
grt garnet
h thickness of the orogenic wedge
H&B94 Holland & Blundy, 1994
H79 Holland, 1979
hed hedenbergite, or hedenbergite component in clinopyroxene
HP high pressure
HPM high pressure metamorphic
ilm ilmenite
J&P71 Johannes & Puhan, 1971
jd jadeite, or jadeite component in clinopyroxene
K Kelvin
K88 Krogh, 1988
km kilometer
Kn
constant in the recrystallised grain size paleopiezometer
kV kilovolt
xi
L1e
stretching lineation of the first deformation stage in eclogites
L2s
stretching lineation of the second deformation stage in the metasedimentary rocks
l-ab low albite
m meter
m.y. million years
m2 square meter
Ma million years before present
max. maximum
mc microcline
min. minimum
mm millimeter, 10-3 m
MORB mid ocean ridge basalt
MPa mega Pascal, (106 Pascal, 0,1 kbar)
n constant in the recrystallised grain size paleopiezometer
N north
NE north-east
NNE north-north-east
NNW north-north-west
NW north-west
omp omphacite, or omphacite component in clinopyroxene
P pressure
P&N89 Pattison & Newton, 1989
P85 Powell, 1985
Pa Pascal
Pf
pore fluid pressure
pfu per formula unit
pg paragonite
phe phengite
pl plagioclase
prp pyrope, or pyrope component in garnet
PT pressure and temperature
qtz quartz
quad quadrilateral pyroxene
r rim position
rt rutile
sin metasedimentary rock
s second
S south
s-1 per second
S1e
foliation of the first deformation stage in eclogites
S1g
foliation of the first deformation stage in the greenschists
S2e
foliation of the second deformation stage in eclogites
S2g
foliation of the second deformation stage in the greenschists
S2s
foliation of the second deformation stage in the metasedimentary rocks
S3e
foliation of the third deformation stage in the eclogites
S3s
foliation of the third deformation stage in the metasedimentary rocks
SE south-east
SEM scanning electron microscope
xii
sps spessartine, or spessartine component in garnet
SSW south-south-west
SW south-west
sympl symplectite
T temperature
t time
Te tensile strength
Teut
eutectic temperature
Thom
homogenisation temperature
tlc talc
Tm
melting temperature
tot total
ttn titanite
UHP ultra high pressure
UHPM ultra high pressure metamorphic
V volume
vol.% volume percent
W west
WNW west-north-west
WSW west-south-west
wt.% weight percent
X maximum principal strain axis
Y intermediate principal strain axis
Z minimal principal strain axis
zoi zoisite
Z-S Zermatt Saas
List of Tables
Table 1 2
Pressure and temperature estimates of different authors for the high pressure metamorphism and later reequilibration
of rocks from the Zermatt Saas zone.
Table 2 7
The UHPM mineral assemblage and the lower PT-replacement products formed at their expense in the different
eclogite groups.
Table 3 14
Temperatures (at 2.7. GPa) calculated with different calibrations of the grt-cpx thermometer for some representative
grt and omp combinations.
Table 4 20
Pressures (at 550 °C) calculated with the jad(in omp)+qtz=ab barometer of Holland (1980).
Table 5 22
Temperatures calculated with the calcite-dolomite thermometer of Anovitz & Essene (1987) for some representative
cal analyses in domains with different cl colours.
xiii
Table 6 27
Mineral compositions of the minerals used by Evans (1990) to construct his petrogenetic grid and the composition
of these minerals in the metabasic rocks at Lago di Cignana.
Table 7 48
Temperature ranges for observed phase transformations and inferred composition and densities of early and late
fluid inclusions from the investigated samples.
Table 8 53
Correlation between the degree of lower PT-replacement and the number of veins present in a rock volume.
Appendix B
Table B1 B-2
Parameters for the Pattison & Newton (1989) calibration of the garnet clinopyroxene thermometer
Table B2 B-6
Temperatures calculated with different calibrations of the garnet clinopyroxene thermometer for several garnet
clinopyroxene pairs
Table B3 B-7
Temperatures for the growth of albite-amphibole-symplectites calculated with the amphibole-plagioclase
thermometer (Holland & Blundy, 1994).
Table B4 B-4
Regression parameters for the Anovitz & Essenne (1987) calibration of the calcite dolomite solvus thermometer in
the system CaCO3 - MgCO
3 and the system CaCO
3 - MgCO
3-FeCO
3 .
Table B5 B-12
Temperatures for the onset of dolomite decomposition calculated with the calcite-dolomite solvus thermometer
(Anovitz & Essenne, 1987).
Table B6 B-14
Pressures for the onset of omphacite decomposition calculated with the jadeite quartz and albite barometer (Holland,
1980) at a temperature of 550 °C.
Appendix C
Table C1 C-1
list of samples
Table C2 C-5
Whole rock analyses for major and trace elements from samples of group 1 to 4 eclogites.
Table C3 C-6
omphacite compositions
Table C4 C-15
garnet compositions
xiv
Table C5 C-26
glaucophane compositions
Table C6 C-28
clinozoisite compositions
Table C7 C-33
zoisite compositions
Table C8 C-34
paragonite compositions
Table C9 C-37
phengite compositions
Table C10 C-40
rutile compositions
Table C11 C-41
dolomite compositions
Table C12 C-41
calcite compositions
Table C13 C-43
albite compositions
Table C14 C-45
compositions of amphibole around garnet
Table C15 C-47
compositions of amphibole around glaucophane
Table C16 C-48
compositions of amphibole in symplectite
Table C17 C-51
titanite compositions
Table C18 C-53
ilmenite compositions
Table C19 C-53
compositions of dark mica between garnet and phengite
Table C20 C-54
coarse grained green amphibole compositions
Table C21 C-55
chlorite compositions
Table C22 C-59
epidote compositions
xv
List of Photographs
Photo 1 12
Typical coesite inclusion in omphacite with a small rim of quartz between omphacite and coesite. Plane polarised
light, length of photograph 1.4 mm.
Photo 2 12
Coesite inclusion in omphacite, with a small rim of quartz between cs and omp. Plane polarised light, length of
photograph 1.4 mm.
Photo 3 15
A digital element distribution map for Mn in grt. Length of the picture ca. 5 mm.
Photo 4 16
Gln rimmed by blue-green amp (amp gln) in a matrix of omp. Plane polarised light, long side of the photograph is
1.4 mm.
Photo 5 16
B(ack)S(cattered)E(lectron) photograph of the rim of blue- green amp around gln.
Photo 6 19
Cathodoluminescence photograph of cal in a dolomite domain. Long side of the photograph is 3.8 mm.
Photo 7 19
Late replacement of grt by chl and epidote (czoV). Crossed polars, long side of the photograph is 7 mm.
Photo 8 36
A lens of high viscous eclogite in a matrix of low viscous metasedimentary rocks. The assymmetric structure
suggests a high degree of non coaxial deformation. N is up, length of eclogitic lens is ca. 0.5 m.
Photo 9 36
Dust trails in vein albite, define an older growth structure. Crossed polars, long side of photograph is 7 mm.
Photo 10 38
Microstructure of a type IIe quartz vein close to a late shearzone. Crossed polars, long side of the photograph is
7 mm.
Photo 11 38
Microstructure of quartz in a deformed type IIe vein. Crossed polars, long side of the photograph is 1.4 mm.
Photo 12 39
Microstructure of a quartz vein in a small shearzone (D4e1
) in an eclogite lens. Crossed polars, long side of the
photograph is 7 mm.
Photo 13 39
Core and mantle structure in a late intensively deformed quartz vein (D4e2
). Crossed polars, long side of the photograph
is 7 mm.
Photo 14 46
Fluid inclusions arranged along irregular planes in a recrystallised grain. Plane polarised light, length of scale bar
125 µm.
xvi
Table of figures
Figure 1 3
A Simplified geological map of the Central and Western Alps.
B Simpflied geological map of the northern part of the Western Alps.
C Simplified cross section through Figure 1B.
Figure 2 4
Simplified geological map of the vicinity of Lago di Cignana, based on 1.10000 mapping by Habermann (1992)
and Wagner-Zweigel (1993).
Figure 3 5
Simplified geological cross section through figure 2, showing the structure of the studied area.
Figure 4 6
The amount of individual reequilibration products plotted against the total amount of reequilibration products in
group 1 to 4 eclogites.
Figure 5 8
Compositions of clinopyroxene in eclogites from Lago di Cignana.
Figure 6 9
Compositional trends of zoned garnets in different eclogitic samples from Lago di Cignana.
Figure 7 11
Differences in phengite compositions in relation to grain size and position of the analyses in the grain for sample
Cig 91-1 and the compositions of phengites from other samples.
Figure 8 15
Drawing after a SEM image of a blue-green amp, ab symplectite at an omp-omp grain boundary.
Figure 9 17
Compositional differences of amphiboles in different textural position for all eclogite groups.
Figure 10 21
Histogram of temperatures calculated with the plagioclase-amphibole thermometer of Holland & Blundy (1994)
for ab-amp symplectites in group 1 to 4 eclogites
Figure 11 25
The composition of chlorite in relation to its microstructural position.
Figure 12 28
Microstructure of a group 1 eclogite.
Figure 13 29
Orientation of structural elements in eclogites, depicted in stereographic projections.
Figure 14 30
Histograms showing the abundance of measured angles between foliation and shortest dimension of minerals or
mineral aggregates for eclogites with different amounts of lower PT-replacement products.
xvii
Figure 15 31
Schematic diagram (not to scale) depicting orientation, crosscutting relations and aspect ratios of the different vein
types and their relation to orientation of foliation S1e and shearbands S2
e as seen on a horizontal plane.
Figure 16 32
Schematic sketch of mesoscopic structural relations between eclogites, greenschists and metasedimentary rocks at
Lago di Cignana.
Figure 17 35
Orientation of structural elements in the metasedimentary rocks, depicted in stereographic projections.
Figure 18 40
Several calibrations of the dynamically recrystallised grain size paleopiezometer for quartz.
Figure 19 42
Lattice preferred orientation of quartz (c-axes) in selected veins in eclogite, that underwent grain growth under low
differential stress after deformation (Bk 4,5,8,20,118) and a vein that deformed during D4e1
(Bk 119). Data are
presented as scatter plots and contour plots.
Figure 20 43
Lattice preferred orientation of quartz (c-axes) of veins deformed during D4e2
. Data are presented as scatter plots
and contour plots.
Figure 21 44
Lattice preferred orientation of quartz (c-axes) in veins subparallel to foliation S2s
. Data are presented as scatter
plots and contour plots.
Figure 22 45
Lattice preferred orientation of quartz (c-axes) in veins deformed in D3s
. Data are presented as scatter plots and
contour plots.
Figure 23 48
Melting temperatures against temperature of homogenisation for the fluid inclusions in the investigated samples
differentiated for the arrangement of the fluid inclusions.
Figure 24 49
Position of the isochores (equation of state of Brown & Lamb (1989) ) for the early and late fluid inclusions from
samples Bk 20 and Bk 100.
Figure 25 51
PT-d path for the exhumation of UHPM rocks of Lago di Cignana, Western Alps, Italy, modified after van der
Klauw et al., (1997).
Figure 26 55
Flow law „best choice 2“ of Paterson & Luan (1990) for dislocation creep in synthetically prepared wet quartzite
for geological relevant strain rates of 10-14 and 10-16 s-1.
Figure 27 56
Above: Cooling curve calculated for rocks of the Zermatt Saas-Fee zone.
Below: Decompression curve for the rocks of Lago di Cignana calculated by combining the cooling curve of the
Zermatt Saas-Fee zone and the PT-path of the rocks fom Lago di Cignana.
xviii
Figure 28 59
Schematic sketches illustrating the exhumation concept of Chemenda et al. (1995).
Figure 29 60
The plastic or Coulomb wedge in the concept of Platt (1986, 1987), with terms that describe the geometry of a
steady state wedge.
Figure 30 61
Tectonic evolution of the Western Alps after Platt (1987).
Figure 31 62
Schematic diagramm after Royden (1993) showing the response of the upper plate to different relative velocity
configurations of the subducting and overriding plate.
Figure 32 63
Simplified cross section illustrating successive positions and trajectories of identifiable points in the dynamic
scaled wedge model of Cowan & Silling (1978).
Figure 33 67
A tentative schematic sketch, illustrating some important points of the proposed exhumation scenario for the
UHPM rocks of Lago di Cignana.
The upper sketches show the configuration at UHPM conditions before exhumation.
The lower sketches show the configuration at the onset of exhumation.
Figure 34 70
A tentative schematic sketch, illustrating the proposed exhumation scenario for the UHPM rocks of Lago di Cignana
from depths of 25 km to ca. 10 km.
The upper sketches show the configuration just after break-off of the oceanic crustal slab.
The lower sketches shows the proposed exhumation scenario.
Appendix A
Figure A1 A-1
Distribution of the different lithologies at the southern shore of Lago di Cignana.
1
1 Introduction
Ultrahigh pressure metamorphic (UHPM) rocks have been described from a number of localities
(for reviews, see Schreyer, 1995; Harley & Carswell, 1995; Coleman & Wang, 1995). These crustal
rocks underwent metamorphism at depths well above the thickness of present-day crust, at
temperature-pressure ratios below 50 °C/100 MPa. The processes, during which such high pressures
at relatively low temperatures are produced, are generally accepted and a subduction mechanism
with thickening through thrusting in the overlying crust is usually postulated (e.g., Chopin, 1984;
Schreyer, 1995). The processes that returned UHPM rocks to the surface are still under discussion,
however (e.g., Platt, 1993; Harley & Carswell, 1995). Understanding of these processes constrains
kinematics and dynamics of convergent plate boundaries and several kinematic exhumation models
have been proposed (e.g., Platt, 1993; Chemenda et al., 1995; Davies & von Blanckenburg, 1995;
Thomson et al., 1998). To distinguish between these models, accurate information on P(ressure),
T(emperature), and structural evolution as well as unambigeous geochronological data for the UHPM
rocks must be available. For most UHPM rocks the outlines of the PT-paths are principally known
and continually improved (see Schreyer, 1995; Harley & Carswell, 1995), although the reconstruction
of complete PT-paths is hampered by the discontinuous record preserved in the rocks and the common
failure of rocks at attaining even small scale heterogeneous equilibrium during exhumation. Data
for the structural evolution of most UHPM terrains are scarce (see Michard et al., 1995), because
UHPM deformation fabrics and structures formed on the earlier part of the exhumation path are
seldom preserved, owing to intense distributed deformation under greenschist facies conditions.
The structural record acquired on the way to the surface provides vital information about the
exhumation process, however, and every proposed exhumation scenario should be based on an
analysis of this record (e.g., Wheeler, 1991; Henry et al., 1993; Michard et al., 1993 in Dora Maira
and Andersen et al., 1991, in south Norway). Geochronological data from several localities, indicate
that UHPM at depths of 100 km or more and a return to shallower crustal levels may take place in
a few million years (e.g., Tilton et al., 1991; Gebauer et al., 1997 in Dora Maira; Barnicoat et al.,
1995; Amato et al., 1999, in Zermatt Saas; Ames et al., 1996; Hacker & Wang, 1995 in Dabie Shan;
Shatsky et al., 1999 in Kazachstan).
This study concentrates on the exhumation of a small occurrence of UHPM oceanic crust at
Lago di Cignana, Valtournanche, Western Alps (Reinecke, 1991; Reinecke et al., 1994). Part of this
study, which deals with the petrologic, structural, and microstructural record of the metabasic rocks
at Lago di Cignana, was published in van der Klauw et al. (1997). The record of the metabasic rocks
will be correlated with the PT-record (Reinecke, 1995; 1998), and the (micro-)structural record of
the metasedimentary rocks and discussed in terms of state of stress, and mechanical behaviour
during successive stages of exhumation. These data provide the boundary conditions for a tentative
exhumation model for the UHPM rocks of Lago di Cignana.
2
2 Regional geology
The Alps are traditionally subdivided in four domains (Fig. 1A); the Helvetic and Penninic
domains both with mainly north vergent structures, derived from the European continent, respectively,
the European continent and oceanic crust; and the Austroalpine and Southalpine domains both
derived from the southern continent and with mainly north, respectively, south vergent structures
(e.g., Heim, 1922; Debelmas & Lemoine, 1970). The arrangement of these domains, with the
Austroalpine domain thrust on the Penninic domain and both thrust on the Helvetic domain, indicate
that convergence of the European plate and the Adriatic plate and SE directed subduction of
intervening oceanic crust, followed by continent-continent collision during the Cretaceous and
Tertiary, formed the Alps (e.g., Coward & Dietrich, 1989; Dewey et al., 1989; Polino et al., 1990).
Lago di Cignana is situated in the northern part of the Western Alps (Fig. 1B). The UHPM rocks
are part of the Penninic, Piemontese zone - a remnant of the former ocean. The Piemontese zone is
divided in the Combin zone, consisting mainly of calcschists (e.g., Deville et al., 1992) and in the
Zermatt Saas zone - a dismembered ophiolitic sequence - that is built up by peridotites, metabasalts
and subordinate oceanic metasedimentary rocks (e.g., Bearth, 1952; Barnicoat & Fry, 1986). The
UHPM rocks are part of the Zermatt Saas zone.
The mineral assemblages in the rocks of the Zermatt Saas zone reflect an eclogite facies meta-
morphic imprint of Early Tertiary age (52 ± 18 Ma, Bowtell et al., 1994; 40.6 ± 2.6 Ma, Amato et
al., 1999; 44.1 ± 0.7 Ma, Rubatto et al., 1998). The PT-conditions for this eclogite facies metamor-
phism have been estimated by several authors (Table 1). The large differences in the estimated PT-
conditions may reflect real differences in the metamorphic evolution of different parts of the Zermatt
Saas zone, but the discrepancies are for the earlier studies (Ernst & Dal Piaz, 1978; Oberhänsli, 1980)
certainly also due to the lack of well calibrated geothermobarometers at that time. The eclogite
facies mineral assemblages were partly reequilibrated during cooling and decompression (e.g.,
Meyer, 1983; Barnicoat & Fry, 1989). Locally an intense greenschist facies overprint developed
(Ernst & Dal Piaz, 1978; Barnicoat, 1988b). The K-Ar, Ar-Ar, and Rb-Sr ages of white micas range
from 45 to 30 Ma (Hunziker, 1974; Barnicoat et al., 1995). The oldest ages are interpreted as
Table 1
Pressure and temperature estimates of different authors for the high pressure metamorphism and laterreequilibration (exhum. P1; T1, exhum. P2; T2) of rocks from the Zermatt Saas zone.
3
cooling ages below the closure temperature of white mica (ca. 350 °C, Hodges, 1991). The younger
ages are interpreted as reset during later localised deformation (Barnicoat et al., 1995).
The rock units in the northern part of the Western Alps can be subdivided in units that experienced
an eclogite facies metamorphism (Zermatt Saas, Monte Rosa and parts of the Sesia zone) and units
Figure 1
A Simplified geological map of the Central and Western Alps.
B Simpflied geological map of the northern part of the Western Alps (modified after Ballèvre & Merle,1993). The arrow shows the approximate position of Lago di Cignana. Z-S = Zermatt-Saas.
C Simplified cross section through Figure 1B (modified after Ballèvre & Merle, 1993).
4
that experienced maximum pressures (< 1.4 GPa) of blueschist facies metamorphism (Grand Saint
Bernhard, Dent Blanche and Combin), during the alpine orogeny. In these last units, an early blueschist
facies metamorphic imprint (e.g., Ayrton et al., 1982; Desmons, 1992) is almost completely obliterated
by a greenschist facies overprint, associated with an usually penetrative ductile deformation (e.g.,
Wüst & Baehni, 1986; Dal Piaz & Ernst, 1978). Only for the Grand Saint Bernhard unit an age
estimate for the blueschist facies metamorphism is known (< 54 Ma, Monié, 1990). The later
greenschist facies overprint is estimated for all units to have occured between 45 - 35 Ma (Hunziker,
1986; Hunziker et al., 1989). Structures at the contacts between the blueschist units, indicate
juxtaposition of these units by NW-ward directed thrusting under greenschist facies conditions
(Mazurek, 1986; Wüst & Baehni, 1986; Ellis et al., 1989). The units with eclogite facies meta-
morphism experienced different maximum pressure and temperature conditions (e.g., Table 1; Chopin
& Monié, 1984) at different times. This shows that juxtaposition of these units did not occur at high
pressure conditions, as also suggested by the greenschist facies shearzones at the contacts between
the units (Ellis et al., 1989). A greenschist facies metamorphic overprint, estimated to have occurred
between 40 and 35 Ma (Chopin & Monié, 1984; Barnicoat et al., 1995; Inger et al., 1996), is locally
developed, often accompanied by penetrative ductile deformation (e.g., Williams & Compagnoni,
1983; Frey et al., 1976; van der Klauw et al., 1997).
The present day configuration, with the blueschist to greenschist facies metamorphic rocks on
top of the eclogite facies metamorphic rocks (Fig. 1C), developed between 36 and 30 Ma (Barnicoat
et al., 1995; Freeman et al., 1997), by SE directed thrusting of the blueschist facies rocks over the
eclogite facies metamorphic units, under lower greenschist facies conditions (Wheeler & Butler,
Figure 2
Simplified geological map of the vicinity ofLago di Cignana, based on 1.10000 mappingby Habermann (1992) and Wagner-Zweigel(1993).
Key: (1) eclogites and derived greenschists(Zermatt Saas zone), (2) UHPM metasedi-mentary rocks (Zermatt Saas zone), (3)serpen-tinised ultramafic rocks, (4)greenschists with minor calcschists (Combinzone), (5) calc- schists with minorgreenschists and marbles (Combin zone), (6)dolomite-calcite marbles (exotic decollementsheet, cf. Dal Piaz, 1988), (7) Austroalpine(undifferentiated), (8) scree, moraine depositsand wetlands, (9) tectonic contact, (10)normal faults.
5
1993). The zircon fission track ages of approx. 33 Ma observed in all rock units in this part of the
Alps indicate that at this time all units exposed at the surface today were at temperatures of ca.
225 °C (Hurford et al., 1991). The different apatite fission track ages within some units, suggest
differential uplift and cooling histories for parts of these units between the Oligocene and the present
(Hurford et al., 1991).
2.1 The studied area
The studied area is situated south of Lago di Cignana, Valtournanche. The rocks in this area
belong to the Zermatt Saas zone, the Combin Zone, and the Dent Blanche zone. A simplified
geologic map of the area (Habermann, 1992; Wagner-Zweigel, 1993) and a simplified section are
shown in figures 2 and 3. The lithological divisions are comparable to those proposed by other
authors in this area (Dal Piaz, 1988; Marthaler & Stampfli, 1989; Vannay & Allemann, 1990).
In the area, the lowermost rocks are serpentinites of the Zermatt Saas zone. The serpentinites are
overlain by eclogites with a strong greenschist facies metamorphic overprint, usually, without pre-
servation of the eclogite facies mineral assemblage (Habermann, 1992). The top of these overprinted
eclogites consists of well preserved coesite bearing eclogites and metasedimentary rocks of the
Zermatt Saas zone. Most of the work was done on these eclogites, which were extremely well
exposed at the southern shore of the lake.
The rocks of the Zermatt Saas zone are overlain by the rocks of the Combin zone that can be
divided in three parts. The lowermost part of the Combin zone consists of greenschists with minor
amounts of calcschists. The upper part of the Combin zone is dominated by calcschists with only
minor amounts of greenschists and dolomitic marbles. Between these parts, locally dolomitic and
calcitic marbles occur that are considered a separate unit by Dal Piaz (1988). The uppermost rocks
in the studied area are the gneisses and schists of the Dent Blanche zone.
The occurence of serpentinites as small lenses within all units and as large lenses at the contacts
between the units, suggests that not only the contacts between the units are tectonic, but that also
within the units tectonic contacts occur.
Figure 3
Simplified geological cross section through figure 2, showing the structure of the studied area. Key as infigure 2.
6
Figure 4
The amount of individual reequilibration products plotted against the total amount of reequilibration productsin group 1 to 4 eclogites. Minor amounts (< 2 vol.%) of titanite (± ilmenite) rims around rutile in all eclogitesare omitted. Key: sympl = symplectite of blue-green amphibole and albite, czo = clinozoisite, amp grt =discontineous overgrowth of blue-green amphibole on garnet, amp gln = rims of blue-green amphibolearound glaucophane, chl = chlorite, and ab = albite.
3 The record in the metabasic rocks
In this chapter the record preserved in the metabasic rocks will be presented in two parts, first the
petrological part and second the structural part. The record preserved in the veins of the metabasic
rocks will be presented in chapter 5.
3.1 Petrology of the metabasic rocks - eclogites and greenschists
The metabasic rocks are presumed to be derived from basalts of former oceanic crust. This inter-
pretation is supported by bulk rock analyses of seven samples with different degrees of lower PT-
replacement (Table C2 in app. C) that invariably indicate MORB affinity, and by relic pillow
structures. This was already established for other localities in the Zermatt Saas zone (Dal Piaz et al.,
1981; Beccaluva et al., 1984; Pfeifer et al., 1989 and Bearth, 1959; Oberhänsli, 1982).
Two principal types of metabasic rocks can be distinguished. The first type comprises eclogites
and transformed eclogites, where the original eclogitic microstructure is still discernable owing to
pseudomorphic replacement. This holds true, even where the replacement to a lower PT-paragenesis
has gone to completion. The second type is represented by schistose metabasic rocks devoid of
high-pressure relics and is subsequently called greenschist. Greenschists constitute the minor portion
(estimated < 5 vol.%) of the metabasic rock in the studied area. They occur frequently at the contacts
between metasedimentary rocks and eclogite bodies and as m-sized lenses in both eclogitic and
metasedimentary rocks.
7
Table 2
The UHPM mineral assemblage and the lower PT-replacement products formed at their expense in thedifferent eclogite groups. sympl. = symplectite, aggr. = aggregate.
The eclogites can be classified in 5 groups, based on the degree of their lower PT-replacement
(Fig. 4 and Table 2):
Group 0 eclogites represent an idealised eclogite with perfectly preserved UHPM paragenesis.
In fact, such eclogites lacking any lower PT-replacement have not been found.
Group 1 eclogites appear macroscopically fresh, but a moderate amount (estimated 15-20 vol.%)
of replacement products is visible under the microscope.
Group 2 eclogites appear macroscopically darker green, because of partial replacement of
omphacite by a symplectite of amphibole and albite. Garnet is macroscopically still fresh,
however. Under the microscope between 20 and 55 vol.% of lower PT-replacement products
are visible.
In group 3 eclogites the replacement of garnet through an aggregate of biotite, chlorite, and
epidote is macroscopically visible. Between 55 and 85 vol.% of replacement products are
visible under the microscope.
In group 4 eclogites the replacement reactions have gone to completion and the amount of
replacement products reaches up to 100 vol.%.
For all eclogite groups, appearence and compositions of its minerals will be presented, followed
by a discussion of potential equilibrium paragenesis and PT-estimates. The minerals of the green-
schists will be treated together with group 4 eclogites.
8
Figure 5
Compositions of clinopyroxene in eclogites from Lago di Cignana. Only analyses from sample Bk 39 areshown; the core and rim analyses of Bk 39 are representative for omphacites from all samples studied. Key:ae = aegerine, jd = jadeite, quad = quadrilateral pyroxene.
3.1.1 Group 0 eclogites
In group 0 eclogites, clinopyroxene (omphacite), garnet, blue amphibole (glaucophane), clino-
zoisite I, zoisite, white mica, rutile, coesite, and apatite occur in all samples, whereas dolomite
occurs only in a few samples. Because no group 0 eclogites have been found, the mineral compositions
given are of minerals of group 1 eclogites, that are not in contact with lower PT-replacement products.
3.1.1.1 Mineral compositions
omphacite (omp)
The amount of omphacite ranges from 50 to 80 vol.% of the rocks. The omp grains are anhedral;
their shape preferred orientation partly defines the foliation. The grain size ranges from ca. 40 µm
for matrix grains, to ca. 400 µm for grains in strain shadows and along shearbands. The matrix omp
often shows a patchy extinction due to compositional inhomogenities. Grain boundaries between
omp grains are serrated. Some of the larger grains have slightly blueish anomalous interference
colours.
The omp composition in all samples (Fig. 5, Table C3 in app. C) and within a single sample
varies between Na(0.4-0.6)
Ca(0.4-0.6)
Mg(0.28-0.48)
Fe2+(0.03-0.14)
Al(0.36-0.56)
Fe3+(0-0.14)
Si2O
6. Mean composition for
all samples is close to Na0.53
Ca0.47
Mg0.38
Fe2+0.09
Al0.47
Fe3+0.06
Si2O
6. The composition appears to be
unrelated to the kind of adjacent mineral. Individual grains are homogeneous or consists of an
irregular patchwork of domains with slightly different composition, but generally, do not show a
regular zoning pattern. The boundaries between these domains are sharp. Commonly, omp inclusions
in garnet have similar compositions as matrix omp. Only in samples Bk 39 and Cig 91/40, the
9
Figure 6
Compositional trends of zoned garnets in different eclogitic samples from Lago di Cignana. Key: c = coreposition, r = rim position, adr = andradite, alm = almandine, grs = grossular, prp = pyrope, sps =spessartine.
aegerine content in inclusions is slightly larger and the jadeite content in the inclusions is slightly
smaller than in the matrix (Fig. 5).
garnet (grt)
Garnet occurs as euhedral porphyroblasts of up to 1 cm in diameter. The amount of grt ranges
from 10 to 20 vol.% of the rock. The cores of garnets contain abundant inclusions of omp, quartz
single crystals, and composite clinozoisite/epidote; paragonite; and titanite inclusions - pseudomorphs
after lawsonite (Bearth, 1959). In the rim of grt inclusions occur less frequently and are smaller.
They consist of omp, rutile and rarely very small (< 10 µm) quartz pseudomorphs after coesite.
Garnets are almandine rich (50-65 mol%), with appreciable amounts of pyrope (10-35 mol%)
and grossular components (10-35 mol%) and only minor (< 5 mol%) amounts of spessartine and
andradite components (Table C4 in app. C). Between the samples, compositions differ mainly in
the amounts of pyrope and grossular component (Fig. 6). The compositional zoning pattern of
garnets from different samples is similar (Fig. 6). The core of grt is relatively grossular rich. Towards
the rim the grossular component decreases and the pyrope and almandine components increase.
The compositional trend changes abruptly in the outer rim, with a relative decrease in almandine
component and an increase in pyrope component. The highest pyrope content occurs in the grt rim.
This change in composition trend, coincides with the change from inclusion rich core to inclusion
poor rim (Photo 3, Fig. 12).
glaucophane (gln)
The amount of gln ranges between 5 to 15 vol.%. The grains are subhedral; their shape preferred
orientation partly defines the foliation and stretching lineation. Grain sizes range from 50 µm in
10
sections perpendicular to c-axis to 500 µm parallel to c-axis. The composition (Table C5 in app. C)
differs slightly between the samples, varying between
(Na0-0.1
,K0-0.1
)(Na1.55-1.90
,Ca0.10-0.45
)(Fe2+0.55-1.00
,Mg2.00-2.45
,Al1.60-1.85
,Fe3+0.10-0.30
)2(Si7.70-7.95
,Al0.05-0.30
)O22
(OH)2.
Within a sample, the compositional variation is small and gln grains have a homogeneous
composition.
clinozoisite I (czoI)
Clinozoisite I amounts to < 10 vol.% of the rock. The grains size is up to 200 µm, the grains are
subhedral and their shape preferred orientation partly defines foliation and stretching lineation. The
composition lies between Ca2Fe3+
(0.26-0.50)Al
(0.50-0.74)Al
2Si
3O
8(OH) with the smallest Al
2Fe3+ epidote
component in the cores of larger grains, increasing towards the rim (Table 6C in app. C). Differences
in Al2Fe3+ epidote component in relation to the adjacent mineral are not observed. Between samples,
the range in Al2Fe3+epidote component differs slightly (Table C6 in app. C).
zoisite (zoi)
The amount of zoi is in the order of 3 vol.% of the rock. It is present as large (up to 3 mm)
anhedral grains with a patchy extinction and as smaller (< 50 µm) subhedral grains with a homo-
geneous extinction. The shape preferred orientation of the zoi aggregates partly defines foliation
and stretching lineation. Large grains have numerous randomly orientated white mica inclusions.
Composition varies between Ca2Fe3+
(0.10-0.15)Al
(0.85-0.90)Al
2Si
3O
8(OH) (Table C7 in app. C), with the
higher Al2Fe3+ epidote component in contact with czoI.
white mica
The white micas in group 0 eclogites are paragonite (pg) and phengite (phe) and usually cannot
be distinguished optically. The presence of pg or phe was established with powder X-ray diffraction.
In most samples pg is the only white mica, in some samples powder X-ray diffraction showed the
presence of both pg and phe, however. Further investigation with the electron microprobe, indicated
that in these cases the white mica generally consists of pg with phe intergrowths; the width of the
phe layers is below the beam size of the microprobe (about 5 µm). Only a few samples have phe as
the only white mica.
paragonite (pg)
The amount of pg ranges from 4 to 8 vol.% of the rock. Pg grains are subhedral and their shape
preferred orientation partly defines the foliation. Grain size is about 40 µm. The composition varies
slightly around (Na1.9
,K0.1
)Al4[Si
6Al
2O
20](OH)
4. Pg in phe bearing samples can have up to 15 mol%
of phe solid solution (Table C8 in app. C).
phengite (phe)
The amount of phe can amount to ca. 10 vol.% of samples, where it is only white mica. Phe is
present as small (< 40 µm) grains in the matrix and as large (about 400 µm) porphyroblasts. The
grains of both varieties are subhedral and their shape preferred orientation partly defines the foliation.
The large phe have compositions (Fig.7, Table C9 in app. C) varying between
11
Figure 7
Differences in phengite compositions in relation to grain size and position of the analyses in the grain forsample Cig91-1 and the compositions of phengites from other samples.
(K0.94-0.98
,Na0.03-0.05
)(Mg0.40-0.47
,Fe2+0.02-0.07
)(Al1.40-1.46
,Fe3+0.03-0.08
)(Si3.45-3.51
,Al0.49-0.55
)O10
(OH)2. Similar
composition are found in a few small matrix phe. Most small matrix phe and the rims of the large
phe have compositions (Fig.7, Table C9 in app. C) varying between
(K0.89-0.94
,Na0.08-0.12
)(Mg0.29-0.35
,Fe2+0-0.04
)(Al1.50-1.56
,Fe3+0.08-0.14
)(Si3.28-3.38
,Al0.62-0.72
)O10
(OH)2. Which phe
composition belongs to the UHPM mineral paragenesis is not clear, because phe of both compositions
occurs in contact with UHPM minerals as well as with late PT-replacement products.
rutile (rt)
Rutile amounts to up to 2 vol.% of the rock. The grains are anhedral, rounded and about 30 µm
in size. In one sample (Bk 8) mm-sized anhedral rt grains occur. Composition is TiO2 without
significant amounts of other elements (Table C10 in app. C).
apatite (ap)
Apatite amounts to 0.5 vol.% of eclogitic rocks and is present as anhedral rounded grains. Its
grainsize is up to 50 µm, in some quartz veins large 5 mm sized ap grains occur, however. Ap
compositions were not analysed.
dolomite (dol)
Dolomite occurs only in metabasic rocks that are rich in gln and white mica and are considered
to be derived from pillow rims or interpillow material (e.g., Oberhänsli, 1982; Barnicoat, 1988a).
The amount of dol is below 4 vol.% of the rock. Dol is present as small (< 40 µm) anhedral grains.
and often occurs in elongated aggregates of max. 0.5 cm in length. The shape preferred orientation
of these aggregates partly defines the foliation. It also occurs as approximately equidimensional
aggregates in strain shadows at grt. Dol is easy distinguished optically from late calcite, due to
12
Photo 2
Coesite inclusion in omp, with a small rim of quartzbetween cs and omp. Note, that the diameter of theinclusion is more than half the diameter of theincluding omp grain. Plane polarised light, length ofphotograph 1.4 mm.
Photo 1
Typical coesite inclusion in omp with a small rim ofquartz between omp and cs. Note the cracks in omp,radiating away from the inclusion. Plane polarisedlight, length of photograph 1.4 mm.
numerous fine grains of an opaque mineral, resulting from the oxidation of the ankerite component
in dol, that are present along its cleavage planes. Dol is considered part of the UHPM mineral
assemblage, because it occurs in contact with all other UHPM minerals and has inclusions of gln
and rt. The composition varies between Ca(Mg0.75-0.80
Fe0.25-0.20
)(CO3)
2, with minor (< 2 mol%) amounts
of Mn substituting for Mg and Fe (Table C11 in app. C).
coesite (cs)
Coesite is found as inclusions in omp (up to 30 µm) and possibly in grt rims (< 10 µm). The cs
inclusions have the typical characteristics described by Chopin (1984) with radial cracks in the host
mineral and a rim of columnar quartz between cs and the host mineral (Photos 1, 2). Cs occurs as
colourless to slightly greenish grains with higher relief as the surrounding quartz. In several inclusions
in omp, the presence of cs was unequivocally proven with the electron microprobe, that showed a
SiO2 composition for phases in the inclusions and, respectively, blue and yellow luminesence colours
for cs and quartz (Schulze & Helmstaedt, 1988). The cs in the two small inclusions in grt could not
unequivocally be identified.
13
3.1.1.2 Mineral paragenesis and PT-estimates
All minerals of group 0 eclogites (omp, grt, gln, czoI, pg, zoi, cs, rt, and ap, with in some
samples that will not be discussed, dol and phe), with exception of gln and zoi, can be found
occuring in mutual contact, although lower PT-replacement products always occur at contacts
between some minerals (e.g., blue-green amphibole between grt and gln). Paragonite is considered
part of the UHPM mineral paragenesis of group 0 eclogites, although experimental investigations
(e.g., Holland, 1979), indicate that pg is not stable at the PT-conditions of UHPM (2.7 GPa at
625 °C, Reinecke 1991; 1995). At these conditions, pg should have reacted to jadeite (jd component
in cpx) and kyanite (Holland, 1979). However, kyanite has not been observed in the metabasic
rocks at Lago di Cignana and pg occurs without UHPM reaction textures in direct contact with the
other minerals of the UHPM paragenesis. Furthermore, pg occurs as inclusions in omp, that has the
same composition as omp with cs inclusions. Similar observations of the persistence of pg outside
its stability field are known from Dora Maira (Schertl et al., 1991) and from Dabie Shan (Okay, 1995).
That gln and zoi do not occur in mutual contact, but are always separated by other UHPM
minerals, suggests that in group 0 eclogites two local equilibrium assemblages, with slightly different
bulk rock compositions, occur. The first and most abundant assemblage consists of omp, grt, gln,
pg, czoI, cs, rt, and ap, the second assemblage consists of omp, grt, zoi, pg, czoI, cs, rt, and ap.
These assemblages are coupled by the reaction (in mol):
0.25 gln + 0.29 zo = 0.87 omp + 0.07 grt(rim) + 0.08 czoI + 0.14 pg + 0.07 cs/qtz + 0.22 H2O
calculated with the mineral compositions of sample Bk 39, which is representative for group 0
eclogites. Rutile and ap are the only Ti-, respectively, P-bearing minerals and, therefore, do not
appear in this reaction. A similar reaction is given by Reinsch (1977) and Ridley (1984), as the
reaction, that marks the temperature dependent transition from blueschist to eclogite in metabasic
rocks. This indicates that mm-scale compositional inhomogenities (the size of the smallest gln or
zoi domains) that were present in the blueschist precursor of the eclogite, were preserved during
UHPM.
The inhomogeneous composition of grt, czoI, and omp can be explained with partial equilibrium
that assummes that reaction with a disequilibrium phase is kinetically inhibited. The equilibrating
bulk composition is the original bulk composition minus the composition of the disequilibrium
phase (Loomis, 1983). In the case of the more or less concentrically zoned grt and czoI, it can be
argued that only the outer rim is in equilibrium with the other phases, and that the core region is no
longer part of the system, because of relatively slow intracrystaline diffusion in grt (e.g., Chakraborty
& Ganguly, 1990) and czoI at the temperature of 625 °C during UHPM. The variable omp
compositions cannot be attributed to partial equilibrium, however. Omphacite grains are either
homogeneous, or consist of irregular domains with different compositions. The formation of these
domains is attributed to localised compositional reequilibration during grain boundary migration
(chapter 3.2), due to deformation under changing PT-conditions. This process makes it impossible
to identify the omp composition in equilibrium with the other phases.
14
Table 3
Temperatures (at 2.7. GPa) calculated with different calibrations of the grt-cpx thermometer for somerepresentative grt and omp combinations. Key: E&G79 = Ellis & Green (1979), P85 = Powell (1985), K88= Krogh (1988), P&N89 = Pattison & Newton (1989) and A94 = Ai (1994)
PT-estimates
Equilibration temperatures for the UHPM mineral assemblage were obtained with garnet-
clinopyroxene Fe2+-Mg exchange thermometry (see appendix B for a discussion of the different
calibrations of the thermometer). The presence of cs inclusions in matrix omp and of small inclusions
of quartz (pseudomorphs after cs) in grt rims, indicates that grt rims must be combined with matrix
omp to obtain temperatures for the UHPM. The Powell (1985) calibration gives temperatures of
595 ± 35 °C (1 σ) for 27 grt (rim)-omp pairs from five samples, calculated at a pressure of 2.7 GPa.
The variation in exchange temperatures is larger within one sample (Table 3, Table B2 in app. B),
than between the samples. This large variation might have several causes:
* Analytical erors, that influence the calculation of the Fe2+ and Fe3+ content in grt and omp.
* The incomplete zoning pattern of grt. The Mg-richest rim of the normal zoned grt is often
missing, for example, where grt partly embays a matrix omp.
* The inhomogeneous omp composition in contact with the grt rim. As discussed earlier, it is
not possible to unequivocally determine the omp composition, that is in equilibrium with the
grt rim.
Analytical errors were minimised by measuring each mineral at least two times in direct contact
and by comparing these single analyses. Deviating analyses were discarded and temperatures were
calculated with the mean of the remaining analyses for every grt-omp pair.
To solve the other problems, digital element distribution maps (DEDM, Bernhardt et al., 1995)
were made of all garnets used for geothermometry. These maps show that a compositionally
homogeneous omp can be embayed in a zoned grt (Photo 3) and therefore, occurs in contact with a
range of grt compositions. The DEDM do not show a reversal of the prograde compositional zoning
trend in grt at grt-omp interfaces. Therefore, reequilibration of the Fe2+-Mg exchange on the
exhumation path and diffusive relaxation in grt rim and omp rim can be excluded. The impossibility
to define unique grt and omp equilibrium compositions, indicates that during UHPM Fe2+-Mg
exchange equilibrium between grt and omp was not reached at all grt-omp interfaces.
15
Photo 3
A digital element distribution map for Mn in grt. Mn-content decreases from green-yellow in the core overorange to pink and blue in the rim. Black islands ingarnet are mostly omp inclusions. Note in the lowerright and upper left corner of the grt, omp inclusionsin contact with grt core composition and grt rimcomposition. Length of the picture ca. 5 mm.
Figure 8
Drawing after a SEM image of a blue-green amp, absymplectite at an omp-omp grain boundary.
3.1.2 Group 1 eclogites
In group 1 eclogites several minerals have formed as partial replacement products of the UHPM
mineral assemblage (Table 2). These replacement minerals are restricted to specific UHPM minerals
and microstructural sites. A symplectite of albite and blue-green amphibole often replaces omp
along cracks and grainboundaries (Fig. 8). Blue-green amphibole develops as rims around gln
(Photo 4), at contacts of grt with pg and gln and is often also present at grt in contact with other
UHPM minerals and along cracks in grt. In phe-bearing samples a green-brown mica occurs as
lower PT-replacement product between grt and phe. Rims of ilmenite and/or titanite develop around
rt. Clinozoisite II partly replaces zoi and pg. Quartz replaces cs and in dol bearing samples, calcite
partly replaces dol.
The relative amounts of these replacement products are similar in all group 1 samples (Fig. 4).
Only during this replacement stage irregular overgrowths of blue-green amphibole formed around
grt and gln. During later replacement stages, the amount of these amphiboles remained constant, as
long as these could be recognised from their microstructural position (Fig. 4). Therefore, this
replacement stage is considered common to all eclogite groups.
3.1.2.1 Mineral compositions
albite (ab)
Albite amounts to between 50 and 70 vol.% of the symplectite that replaces omp. This symplectite
amounts to between 8 and 12 vol.% of group 1 eclogites. Albite forms grains of up to 50 µm in
16
Photo 5
B(ack)S(cattered)E(lectron) photograph of the rim ofblue- green amp around gln. Different shades of grayin the rim suggest slight compositional differencesin the blue-green amp.
Photo 4
Glaucophane rimmed by blue-green amp (amp gln)in a matrix of omp and rt with titanite (ttn) rims. Planepolarised light, long side of the photograph is 1.4 mm.
diameter that include the smaller amphibole grains. The anorthite (an) component of ab is below
5 mol% (Table C13 in app. C).
blue-green amphibole (amp)
Blue-green amphibole in group 1 eclogites can be divided in three groups with different micro-
structural positions and compositions (Fig. 9):
1. amphibole rims around garnet
2. amphibole rims around glaucophane
3. amphibole in symplectite
1. amphibole rims around garnet.
The amount of this amp ranges from 2 to 3 vol.% in group 1 and 2 eclogites. In group 3 and 4
eclogites with partly replaced grt, the amp around garnet is difficult to distinguish from other
amphiboles and its amount becomes less. This amp is present as thin (max. 30 µm) discontinuous
rims around grt and along fractures in grt. The grains are anhedral and up to 100 µm in length. The
17
Figure 9
Compositional differences of amphiboles in different textural position for all eclogite groups. Amp at grtand at gln only occur in group 1 and 2 eclogites, non pseudomorphic amphiboles and vein amphiboles onlyoccur in group 3 and 4 eclogites. Na
M1 is Na in the M1-position, pfu is per formula unit.
composition (Table C14 in app. C) ranges between magnesian-hastingite and magnesian-hastingitic-
hornblende (amp names after Leake, 1978).
2. amphibole rims around glaucophane
The amount of this amp ranges from 2 to 3 vol.% in group 1 and 2 eclogites. In group 3 and 4
eclogites, gln is completely transformed, and this amp cannot be identified. At grt-gln contacts a
transition in composition from amp around gln to the amp around grt is found. Back scattered
electron (BSE) images of amp rims indicate that these rims consist of patches (few µm2 in size)
with different compositions (Photo 5). The size of these patches is close to the beam size of the
microprobe and this is reflected by the highly variable measured compositions (Fig. 9, Table C15 in
app. C) for these amphiboles, between barroisite, actinolite and magnesio-hornblende (amp names
after Leake, 1978).
3. amphibole in symplectite (ampI)
The ampI comprises between 30 and 50 vol.% of the ab-amp symplectites (Fig. 8) that are the
lower PT-replacement products of omp. The grains are subhedral and small (< 20 µm). The
composition (Table C16 in app. C) ranges from magnesian-hornblende to actinolitic-hornblende
(amp names after Leake, 1978). In direct contact with quartz, ampI is always actinolite. This suggests
that after formation of the symplectite from omp, the ampI in contact with quartz has reequilibrated
according to the simplified reaction:
18
edenite + quartz = tremolite + albite (Holland & Blundy, 1994).
This is supported by the observations that i) symplectites after omp in quartz veins comprise a
larger amount of ab and ii) ampI adjacent to quartz aggregates is an actinolite at the symplectite-
quartz contact, but an actinolitic hornblende at the symplectite omp contact.
titanite (ttn)
Titanite amounts to up to 1.5 vol.% of group 1 eclogites. It forms anhedral grains up to 50 µm in
size, often with minor rt and ilmenite preserved in its core and also occurs as composite inclusions
with pg and czo in the core of garnets. Its composition is approximately Ca(Ti0.95
Al0.05
)
[SiO4](O,OH,F) (Table C17 in app. C).
ilmenite (ilm)
Ilmenite amounts to 0.5 vol.% of the rock. It forms small (< 20 µm) anhedral grains that usually
occur as discontinuous rims around rt. Ilmenite has also rarely been observed along cracks and as
inclusions in grt. The ilm composition in contact with rt is (Mg0.2
, Mn0.03
, Fe2+0.95
)TiO3, in grt its
composition (Mg0.01
, Mn0.1
, Fe2+0.89
)TiO3 is similar along cracks and in inclusions (Table C18 in
app. C).
clinozoisite II (czoII)
Clinozoisite II amounts to up to 3 vol.% of group 1 eclogites. It occurs as discontinuous rims
around large czoI grains in contact with lower PT-replacement products and as small (about 20 µm)
euhedral grains in aggregates of white mica. The composition of czoII (Table C6 in app. C) lies
between Ca2Fe3+
(0.40-0.55)Al
(0.45-0.60)Al
2Si
3O
8(OH). Between samples, the range in Al
2Fe3+epidote
component differs slightly.
quartz (qtz)
Quartz amounts to up to 2 vol.% of metabasic rocks. It is present as anhedral grains of max.
40 µm or as aggregates of several grains of up to 100 µm in size. It is also present as small (< 30 µm)
grains along shearbands and as vein filling material. Quartz is always completely surrounded by
lower PT-replacement products. Quartz also occurs as monomineralic inclusions in grt and seldom
in omp.
calcite (cal)
Calcite is present in only few samples of the metabasic rocks. In one group 1 eclogite, cal occurs
as a rim around dol grains and it amounts to < 2 vol.% of the rock. The composition varies slightly
between (Fe, Mg, Mn)<0.1
Ca>0.9
CaCO3 (Table C12 in app. C). Cathodoluminesence (CL) investigations
of cal, have shown that the CL colours depend on the relative amounts of Mn and Fe (Marshall,
1988). High Mn- and low Fe-contents result in bright yellow CL colours; High Fe- and low Mn-
contents result in a dark CL colour. In the group 1 eclogites, the Mn-content of cal is almost constant
at approx. 1 mol% (Table C12 in app. C). The Mg- and Fe-content is positively correlated. Therefore,
the CL colours of cal give an indication of the relative amounts of Mg and Fe in calcite. Dark
19
Photo 7
Late replacement of grt by chl and epidote (czoV).Crossed polars, long side of the photograph is 7 mm.
Photo 6
Cathodoluminescence photograph of cal in a dolomitedomain. Different shades of orange (cal1, cal2)represent cal with different amounts of Mn, Mg andFe. Long side of the photograph is 3.8 mm.
orange-red CL colours (high Mg- and Fe-contents) occur at the rim zone away from dol in the cal
overgrowths on dol, whereas towards dol the cal becomes brighter orange (Photo 6). In contact with
dol, cal has yellow-orange CL colours (low Mg- and Fe-contents). This change in CL colours is
present in all carbonate aggregates, but the absolute amounts of Mg and Fe differ slightly between
the aggregates.
green-brown mica
This green-brown mica occurs as small anhedral grains between phe and grt. It amounts to
< 1 vol.% and its composition is approximately (Na0.06
K0.94
)(Mg1.23
Fe1.18
)Al1.8
Si2.67
O10
(OH)2
(Table C19 in app. C).
3.1.2.2 Mineral paragenesis and PT-estimates
In the group 1 eclogites several minerals have formed as partial replacement products of minerals
of the UHPM assemblage. The amount of these replacement products is similar in all group 1
eclogites, independent of the relative amounts of the UHPM minerals. This suggests that these
replacement products formed simultaneous. However, the minerals of this first replacement stage
20
Table 4
Pressures (at 550 °C) calculated with the jd (in omp)+qtz=ab barometer of Holland (1980), using the methodof Holland (1990) for the calculation of jadeite activity in omp, for extreme omp compositions. Key:X(jd,acm,diop,hed) = resp. jadeite, acmite, diopside and hedenbergite component in cpx, a(jd) = jadeiteactivity, max. X(xx) = cpx analysis with highest xx component, min. X(xx) = cpx analysis with lowest xxcomponent, the analyses with min. X(jd) and min. X(diop) have also, resp., max. X(diop) and max. X(hed).
are not an equilibrium paragenesis, because three amp at different textural sites have different
compositions. The observation, that the lower PT-replacement products are restricted to specific
minerals of the UHPM mineral assemblage (Table 2), suggests local equilibrium. The local
equilibrium domains were defined by the different chemical compositions of the UHPM minerals
and the size of the domains was the grain size of the UHPM minerals.
PT-estimates
Pressures and temperatures for the onset of this lower PT- replacement can be obtained from two
independent domains: the omp (symplectite) domain present in all samples and the carbonate domain
present in one sample only.
The omphacite domain
The reaction inferred for this domain is:
omphacite = amphibole + albite
This reaction can be used to calculate temperatures and pressures according to partial reactions
(discussion of these thermo-barometers in Appendix B):
jadeite (in omp) + quartz = albite (barometer, Holland, 1980)
edenite (in amp) + quartz = tremolite (in amp) + albite (thermometer, Holland & Blundy, 1994).
A prerequisite, to obtain equilibrium temperatures and pressures with these reactions for omp
decomposition, is that qtz and omp occurred in mutual contact. Quartz is only seldom found in
partly replaced eclogites and never in mutual contact with omp. Therefore, the calculated pressures
of 1.2 to 1.3 GPa (Table 4, Table B6 in app. B) and temperatures of 525-575 °C (Fig. 9A, Table B3
in app. B) are maximum pressures and temperatures for the omp decomposition reaction. When qtz
is present, it occurs in veins or it is completely surrounded by lower PT-replacement products. This
21
Figure 10
Histogram of temperatures calculated with the plagioclase-amphibole thermometer of Holland & Blundy(1994) for ab-amp symplectites in group 1 to 4 eclogites, calculated at a pressure of 1.2 GPa. N is number ofsamples
suggest that the decomposition reaction ceased, when all qtz present in the reaction domain was
used up. Another suggestion is that the reaction ceased, when qtz was no longer available in the
reaction domains due to its rim of lower PT-replacement products.
The large range of temperatures (Fig. 10, Table B3 in app. B), partly results from the inhomo-
geneous compositions of educt and product phases. Omphacite has 0.6 > Xjd > 0.45 and, therefore,
the onset of symplectite formation will occur at different pressures and temperatures. Consequently,
the varying ampI compositions reflect different formation temperatures. The varying ampI composi-
tions could also result from contamination of the analyses of these fine grained ampI with ab, re-
sulting in higher Si, Al and Na content in the ampI and in a lower calculated formation temperature.
The carbonate domain
Pressure and temperature estimates for this domain are obtained with the cal-dol solvus thermo-
meter (Anovitz & Essene, 1987, see Appendix B for discussion), from calcite in contact with
dolomite, which shows temperatures of 575-450 °C for cal in aggregates with dol (Table 5, Table B5
in app. B). Combined CL and electron microprobe investigations of the carbonate aggregates, show
that the calculated temperature depends on the position in the carbonate aggregate (Photo 6). This
suggests that the reaction of dol to cal started at the rim of the dol grain and that the earliest cal
formed in equilibrium with dol was relatively Mg and Fe rich (dark orange-red CL colours). Further
reaction of dol to cal occurred at the interface between the earlier formed cal and dol. This new cal,
which formed in equilibrium with dol, was less Mg and Fe rich (orange CL colours). Again further
reaction occurred at the interface between the younger cal and dol. The cal formed at this stage in
equilibrium with dol, was relatively Fe and Mg poor (yellow-orange CL colours). This zoning trend
22
Table 5
Temperatures calculated with the calcite-dolomite thermometer of Anovitz & Essene (1987) for somerepresentative cal analyses in domains with different cl colours. T1 and T2 are, resp., calculated for systemCa2+-Mg2+ and Ca2+-Mg2+-Fe2+.
is contrary to a trend expected for diffusional reequilibration for cal in contact with dol. This means
that temperatures calculated with the compositions of cal with dark orange-red CL colours (575-
525 °C) mark the upper limit for the onset of the reaction of dol to cal.
Because aragonite does not contain appreciable amounts of Mg, Fe and Mn, the Mg-Fe-Mn rich
cal must have formed in the stability field of cal. Therefore, the maximum pressure for the onset of
the reaction of dol to cal at 550 °C, is limited to 1.1-1.2 GPa by the aragonite-calcite univariant
equilibrium (Johannes and Puhan, 1971).
The PT-conditions for the onset of lower PT-replacement in group 1 eclogites obtained from
two independant domains are estimated at P < 1.2 GPa and T < 550 °C.
3.1.3 Group 2 eclogites
In group 2 eclogites the mineral assemblage is the same as in group 1 eclogites, but the amounts
of ab-amp symplectites, czo and ttn formed at the expense of omp and gln, pg and rt, respectively,
are increased. In carbonate bearing samples, cal is the only carbonate mineral present.
3.1.3.1 Mineral compositions
albite (ab)
In group 2 eclogites ab is present in symplectite that amounts to up to 45 vol.% of group 2
eclogites. The only difference from ab in group 1 eclogites is the grain size of up to 80 µm.
amphibole in symplectite II (ampII)
Amphibole II occurs in the ab-amp symplectites, that are the lower PT-replacement products of
omp and gln. The ampII grains are subhedral and often slightly larger (< 30 µm) than ampI grains in
group 1 eclogites. However, it is not unequivocally possible in a group 2 eclogite to distinguish
between ampI and ampII. The composition of amphibole (ampI + ampII) in group 2 eclogites (Fig. 9,
Table C16 in app. C) ranges from magnesio-hornblende to actinolite (amp names after Leake,
1978).
23
clinozoisite III (czoIII)
Clinozoisite III amounts to up to 3 vol.% of group 2 eclogite and occurs as discontinuous rims
around large czoI and czoII grains in contact with lower PT-replacement products, and as rims
around the smaller euhedral czoII grains in aggregates of white mica. The composition (Table C6 in
app. C) lies between Ca2Fe3+
(0.45-0.60)Al
(0.40-0.55)Al
2Si
3O
8(OH).
titanite (ttn)
Titanite amounts to up to 2 vol.% of the rock in group 2 eclogites. The ttn formed during this
stage of lower PT-replacement has the same composition as earlier formed ttn and can not be
distinguished from earlier formed ttn.
calcite (cal)
Calcite occurs as untwinned anhedral grains of up to 4 mm in their longest dimension, interpreted
to be pseudomorphs after dol aggregates and as small (< 30 µm) anhedral grains along shearbands.
Calcite in group 2 and later eclogites has lower amounts of Mn, Fe and Mg substituting for Ca than
cal in group 1 eclogites (Table C12 in app. C), but because of the differing amounts of Mn in the cal,
the CL colours can no longer be directly correlated with the amount of Mg and Fe in cal.
3.1.3.2 Mineral paragenesis and PT- estimates
In the group 2 eclogites the mineral assemblage is similar to the assemblage in group 1 eclogites.
Some of the lower PT-replacement products that formed during this stage, however, have compo-
sitions different from similar replacement products in group 1 eclogites. The replacement minerals
that formed earlier did not change their composition in these samples. Therefore, the compositional
range of lower PT-replacement products is larger in group 2 eclogites than in group 1 eclogites. The
localised occurrence of the newly formed minerals, suggest that similar to group 1 eclogites, the
reaction products were in local equilibrium only. Therefore, the size of the equilibrium domains is
still similar to the grain size of the UHPM minerals.
PT-estimates
In group 2 eclogites dol is no longer present and therefore, the cal-dol thermometer cannot be
applied. Temperatures for this lower PT-replacement stage can be obtained from the omp (sym-
plectite) domain with the Holland & Blundy (1994) plagioclase-amphibole-quartz-thermometer.
Temperatures range from 500 to 575 °C (Fig. 10, Table B3 in app. B). This large range in calculated
temperatures is due to the presence in group 2 eclogite samples of 2 generations of symplectitic
amp (Fig. 9). Higher temperatures are calculated with amphiboles inherited from the earlier lower
PT-replacement stage and lower temperatures (500-525 °C) are calculated with newly formed more
actinolitic amphiboles. Because ampII is coarser grained than ampI, contamination of these analyses
with albite is improbable. Therefore, the higher Si-content in ampII compared to ampI suggests
decreasing temperatures (500 -525 °C) during later replacement in group 2 eclogites. A pressure
estimate for this stage is not possible.
24
3.1.4 Group 3 eclogites
In group 3 eclogites the replacement of gln and omp through ab-amp symplectites is completed.
The remaining pg is partly replaced by chlorite. Garnet is partly decomposed to an aggregate of
chlorite, dark mica, epidote (czoIV) and ab (Photo 7). Symplectitic amp partly grows to a coarser
amphibole.
3.1.4.1 Mineral compositions
albite (ab)
Albite occurs in two textural positions in group 3 eclogites. It occurs in symplectites that amount
to up to 55 vol.% of group 3 eclogites. This ab differs only in its grain size of up to 120 µm from
earlier formed ab in symplectite. Albite also occurs in the aggregates of several minerals replacing
grt. This ab forms anhedral grains of up to 100 µm in size and has between 8 and 10 mol% an
(Table C13 in app. C).
amphibole in symplectite III (ampIII)
The ampIII grains are subhedral with a grainsize larger (< 50 µm) than ampI and ampII in group 1
and 2 eclogites. In a group 3 eclogite, it is not unequivocally possible to distinguish between ampIII
and earlier ampI and ampII. The composition of amphibole (ampI + ampII + ampIII) in group 3
eclogites ranges (Fig. 9, Table C16 in app. C) from magnesio-hornblende to actinolite (amp names
after Leake, 1978), with a larger number of actinolites than in group 2 eclogites.
coarse amphibole
This amphibole forms large (up to 100 µm) subhedral grains and amountsto up to 5 vol.%. It
develops at the cost of small symplectitic amphiboles and has inclusions of ab, czo and ttn. The
composition (Table C20 in app. C) varies from actinolitic hornblende to actinolite (names after
Leake, 1978).
clinozoisiteIV (czoIV)
Clinozoisite IV amounts to nearly 3 vol.% and occurs in two textural positions. It occurs as
discontinuous rims around earlier czo grains with a composition (Table C6 in app. C) between
Ca2Fe3+
(0.50-0.70)Al
(0.30-0.70)Al
2Si
3O
8(OH) and also as large, up to 80 µm, anhedral grains in mineral
aggregates replacing grt, with a composition between Ca2Fe3+
(0.62-0.78)Al
(0.22-0.38)Al
2Si
3O
8(OH).
chlorite (chl)
Chlorite amounts to up to 5 vol.% of group 3 eclogites. It is present as randomly oriented stacks
in large (up to 1 cm) aggregates. The aggregates are approximately circular for chl formed at the
expense of grt and “stick” like for chl formed at the expense of white mica. The composition varies
between (Mg4.5-6.5
,Fe2+1.7-4.0
,Fe3+0.80-0.95
,Al2.1-2.5
)(Si5.3-5.6
,Al2.4-2.6
)(OH)16
(Table C21 in app. C) and depends
on textural position. The chl formed at the expense of white mica has XMg
, Mg/(Mg+Fe2+) between
0.7-0.8, whereas chl formed at the expense of grt has XMg
between 0.5-0.6 (Fig. 11). In the matrix
chl, that cannot be attributed to white mica or grt, has intermediate XMg
.
25
Figure 11
The composition of chlorite in relation to its microstructural position. pfu, per formula unit.
dark mica
This dark mica amounts to up to 1.5 vol.% of the rock and occurs as a fine grained intergrowth
with chlorite in aggregates replacing garnet. It was not possible to obtain reliable analyses of this
dark mica.
3.1.4.2 Mineral paragenesis and PT-estimates
In the group 3 eclogites the mineral assemblage is the assemblage of group 1 and 2 eclogites
with chlorite and a dark mica added. Some of the replacement products formed during this stage
have a different composition from similar, earlier formed, replacement products. However, the
minerals that formed during these earlier stages retained their composition (e.g., Fig. 9). The localised
occurrence of the newly formed minerals, suggest that similar to group 1 and 2 eclogites, the reaction
products were in local equilibrium only. However, the presence of chlorite with intermediate
composition and the growth of large amphiboles, indicate that at least locally the size of the
equilibrium domains was larger than the grain size of the original UHPM minerals.
PT-estimates
Temperatures for this replacement stage can be obtained from the omp (symplectite) domain
with the Holland & Blundy (1994) plagioclase amphibole thermometer. Calculated temperatures
range from 475 to 575 °C (Fig. 11, Table B3 in app. B). Some of the ampIII has a composition with
Si > 7.7 per formula unit (pfu) and is outside the compositional limit of the thermometer (Holland
& Blundy, 1994). These compositions, however, still point to formation temperatures below 475 °C.
The large range in calculated temperatures is, as in group 2 eclogites, due to preservation of earlier
formed amp(I and II). Therefore, a temperature below 500 °C is a reasonable estimate for stage 3
replacement. A pressure estimate for this stage is not possible.
26
3.1.5 Group 4 eclogites and greenschists
In group 4 eclogites the replacement of the UHPM mineral assemblage goes to completion and
a new paragenesis comprising chl, green amp, czoV, ttn, and ab has formed. The earlier replacement
products that formed pseudomorphs after the UHPM paragenesis and thereby, preserved the original
microstructure, are partly replaced by the new paragenesis; hence, the original microstructure is
largely obscured. The greenschists are rocks, where replacement and recrystallisation have gone to
completion. The composition of the greenschist minerals is the same as the minerals of the group 4
eclogites.
3.1.5.1 Mineral compositions
albite (ab)
Albite amounts to < 50 vol.% of the rock. It occurs in symplectite, in the aggregates replacing
grt, and as latest replacement product of remaining white mica. Locally, cm-sized poikiloblasts of
ab occur. In symplectite ab has < 5 mol% an, in other position an contents are between 5 and
10 mol% (Table 13C in app. C).
coarse amphibole
This amphibole forms large (up to 100 µm) subhedral grains and amounts to up to 10 vol.%. It
develops at the cost of small symplectitic amphiboles and has inclusions of ab, czo and ttn. The
composition (Table C20 in app. C) varies from actinolitic-hornblende to actinolite (names after
Leake, 1978).
epidote (czoV)
Clinozoisite V and czoIV amount to up to 5 vol.% of the rocks and have the same composition.
Clinozoisite V occurs as large up to 100 µm anhedral grains in the mineral aggregates replacing
garnet.
chlorite (chl)
Chlorite amounts to up to 10 vol.% in group 4 eclogites. Composition, distribution and textural
position are the same as in group 3 eclogites. The difference between group 3 and 4 eclogites lies
mainly in the larger amount of chl that cannot be attributed to grt or pg in group 4 eclogites.
titanite (ttn)
Titanite amounts to nearly 4 vol.% of group 4 eclogites. It occurs as anhedral grains of up to
100 µm in size, often with some rt or ilm in its core. It also occurs as euhedral (up to cm-sized)
grains in the host rock of some ttn-bearing quartz veins. Its composition (Table C17 in app. C) is
Ca(Ti0.95
Al0.05
)[SiO4](O,OH,F).
3.1.5.2 Mineral paragenesis and PT-estimates
In the group 4 eclogites the mineral assemblage is ab, green amp, chl, czoV, and ttn. Green amp,
chl, and CzoV still have large variations in their compositions, partly due to formation at different
27
Table 6
Mineral compositions of the minerals used by Evans (1990) to construct his petrogenetic grid and thecomposition of these minerals in the metabasic rocks at Lago di Cignana.
textural sites and partly inherited from earlier replacement stages. However, compared to group 3
eclogites the amount of these two minerals with intermediate compositions has increased. This
indicates that the size of the local equilibrium domains has increased, but is still below the size of
a thin section. In the greenschists, the size of the equilibrium domains is larger than the thin section.
PT-estimates
No reliable geothermobarometers exist for this low temperature mineral assemblage (e.g. Essenne,
1989; Evans, 1990) and one has to rely on petrogenetic grids to obtain pressure and temperature
estimates for these rocks. In the petrogenetic grid of Evans (1990), for a similar bulk rock composition
as the Lago di Cignana metabasic rocks (Table 6), the assemblage actinolitic amphibole, albite,
epidote, chlorite and quartz is stable at pressures below 0.7 GPa, relatively independant of
temperature. A reliable temperature for this replacement stage cannot be obtained with the Holland
& Blundy (1994) plagioclase amphibole thermometer, because even more amphiboles than in group 3
eclogites have compositions with Si > 7.7 pfu and are outside the compositional limit of the thermo-
meter (Holland & Blundy, 1994). These amphiboles, however, indicate formation at temperatutes
below 475 °C. Consequently, the mineral paragenesis of group 4 eclogites and the greenschists
probably formed at temperatures below 475 °C and pressures below 0.7 GPa.
3.2 Structures in the eclogites
The only primary structures discernible in the metabasic rocks from Lago di Cignana are deformed
pillows, which have been described from many locations within the Zermatt Saas zone (e.g., Bearth,
1959; Oberhänsli, 1982). Where preserved, they consist of omp-rich cores grading into gln-rich
rims. The interstices between individual pillows are filled by a gln-rich matrix with qtz and carbonate.
In most cases, however, the group 1 eclogites reveal a compositional banding of alternating gln-
and omp-rich layers. This banding, presumably, originated from extreme flattening of pillows. This
interpretation is supported by the observation of structures resembling isoclinal fold hinges in gln-
rich layers, always with gln poorer eclogite in the core, as well as by the discontinuous compositional
banding and the gradual changes in gln-content.
28
Figure 12
Microstructure of a group 1 eclogite: Grt poikiloblast in a matrix of omp, gln with rims of blue-green amp,rt with ttn rim, czo and pg. Strain shadows at grt filled with omp. The foliation S
1e, defined by the shape
preferred orientation of omp, gln, pg and czo aggregates lies horizontal. Shear bands S2e
(indicated bydashed lines) follow the boundaries of the strain shadows. Note the irregular, patchy distribution of blue-green amp-ab symplectites on intergranular fractures and along omp high-angle grain boundaries and ampovergrowths on grt. The thin dashed line in grt indicates the change of the trend in compositional zoning(Fig. 6). Grt contains inclusions of omp, rt and box-shaped czo-pg ± ttn pseudomorphs after lawsonite.
The compositional banding, together with a shape preferred orientation of omp, gln, pg, and
elongated (clino-)zoisite aggregates (Fig. 12) defines the foliation (S1e
) that strikes approximately
NE and dips with an angle between 20 and 50° towards the NW (Fig. 13). The orientation of S1e
varies between different outcrops, but the spread usually overlaps. On this foliation, a stretching
lineation (L1e
) is defined by the long axes of gln crystals and elongated aggregates of (clino-)zoisite.
The stretching lineation plunges with around 15° to the WNW (Fig. 13). The foliation S1e
flows
around garnets with symmetric strain shadows filled with coarse-grained (400 µm) omp (Fig. 12).
This shows that grt had grown before deformation D1e
. The finer grained (40 µm) matrix omp has
serrated grain boundaries. This indicates that omp deformed plastically by a combination of
dislocation creep and dynamic recrystallisation by grain boundary migration (Buatier et al., 1991;
Godard & van Roermund, 1995). In rocks completely transformed to a lower grade paragenesis, the
compositional banding is no longer discernible. The foliation S1e
is, however, preserved due to
pseudomorphic replacement of the UHPM minerals by lower PT-replacement products (Fig. 14).
The czo aggregates after zoi and pg, and the symplectites of ab and blue-green amp after omp and
gln, preserve the shape of the precursor mineral grains and, in this way, the foliation.
29
Figure 13
Orientation of structural elements in eclogites, depicted in stereographic projections (lower hemisphere,equal area). Left: foliation S
1e, lineation L
1e and shearbands S
2e. Center: π-pole construction of D
3e open
folds. Right: orientation of veins.
Locally, S1e
is crosscut by extensional shearbands (e.c.c.´s = extensional crenulation cleavage,
S2e
) (Figs. 12, 13). The distribution of S2e
is heterogeneous. Zones with closely spaced shearbands
alternate with zones were they are rare. Orientation of S2e
varies between the outcrops, as does the
foliation S1e
. Usually, two sets of shearbands form a conjugate system with one of the orientations
dominating in one outcrop. Shearbands nucleated at garnets following the S1e
strainshadow interface
and developed by coalescence of these domains. S2e
is defined by a shape preferred orientation of
omp. The coarser grainsize (up to 400 µm) of omp along S2e
compared to the matrix, indicates that
S2e
had formed before transformation of the eclogite to a lower grade mineral paragenesis had
started. There is no systematic difference in compositions between matrix omp and coarse grains in
S2e
. Furthermore, a quartz pseudomorph after coesite has been found in one of the coarse omphacites.
All these evidences suggest that S2e
(e.c.c.) formed under UHP metamorphic conditions. In eclogites
transformed to lower grade paragenesis, S2e
was preserved, because symplectites of ab and blue-
green amp preserve the shape of precursor omp grains. The frequently observed concentration of
minerals formed during lower PT-replacement along S2e
is attributed to later fluid infiltration focused
along these discontinuities. Fluid infiltration is also suggested by the relative abundance of quartz
and calcite along S2e
compared to the host rocks.
Later localisation of deformation in the eclogites is revealed by several generations of veins of
various kind and scale and by other structures. Veins will be presented first, because they can be
used as a reference frame for later deformation stages. The microstructures, fabrics, and fluid
inclusions data from veins will be presented in chapter 5. Veins in the eclogites can be classified
into four groups (Fig. 15).
30
Figure 14
Histograms showing the abundance of measured angles between foliation and shortest dimension of mineralsor mineral aggregates for eclogites with different amounts of lower PT-replacement products. Mineralaggregates that formed at the expense of UHP minerals approximately preserve the shape preferred orientationof this mineral and in this way the foliation. In group 3 and 4 eclogites, growth of a amphibole at the expenseof symplectitic amphibole partly destroys this pattern.
Type Ie veins are orientated sub-parallel to the foliation S
1e (Fig. 13, 15). They exhibit low aspect
ratios (< 5) and the opposing flanks do not fit. The vein mineralisation is composed of czo or
qtz often accompanied by minor amounts of omp, gln, ap, and rt, or by minor amounts of ttn,
and czo. Quartz in these veins is completely recrystallised. Other minerals are usually subhedral,
without any obvious lattice or shape preferred orientation. Where abundant, czo forms fibers
perpendicular to the vein flanks. The least transformed host rocks of type Ie veins are the
group 1 eclogites.
Type IIe veins are orientated sub-parallel to the foliation S
1e or sub-parallel to the shearband
foliation S2e
(Fig. 13, 15). Their aspect ratio ranges up to 10. There is no fit between the
31
Figure 15
Schematic diagram (not to scale) depicting orientation, crosscutting relations and aspect ratios of the differentvein types and their relation to orientation of foliation S1
e and shearbands S2
e as seen on a horizontal plane.
Chronological relations between type Ie and type II
e veins could not be deduced. Strike of the foliation is NE
with 20-50° dip to the NW. The trace of UHPM extensional shearbands cuts the foliation at a low angle.Late shear zones possibly synchronous with type IV
e veins are not shown.
opposing flanks. The vein mineralogy is qtz, often associated with czo or ttn. The qtz is partly
to completely recrystallised. Other minerals present in these veins occur as subhedral grains
without shape preferred orientation. The least transformed host rocks of type IIe veins are the
group 2 eclogites.
Type IIIe veins are orientated at a higher angle (> 30°) to the foliation S
1e and the shearbands S
2e
(Fig. 13, 15). They have aspect ratios up to 40. Usually, there is no fit between the opposing
flanks. Their mineralogy is qtz with green amp, with ttn or with czo. The qtz is partly to
completely recrystallised. Other minerals present in these veins occur as subhedral grains,
without obvious shape preferred orientation. The host rocks of type IIIe veins are mainly the
group 3 and 4 eclogites.
Type IVe veins are also orientated at a high angle to foliation S
1e and shearbands S
2e (Fig. 13, 15).
These veins have a high (> 30) aspect ratio and the opposing flanks fit. Their mineralogy is
ab, often with green amp and rarely epidote. The primary vein filling structure is preserved,
32
Figure 16
Schematic sketch of mesoscopic structural relations between eclogites, greenschists and metasedimentaryrocks at Lago di Cignana. Late shearzones in eclogite (D
4e1, D
4e2) and veins in eclogites and metasedimentary
rocks are not shown.
with fibrous ab, amp and epidote, oriented perpendicular to the vein flank. Crosscutting
relations between ab veins, indicate that at least three generations of ab veins exist. The host
rock of type IVe ab veins are the group 4 transformed eclogites.
Locally, foliation S1e
is folded on an m to 10 m scale, clearly discernible on stereographic
projections of the foliation poles (Fig. 13). On the outcrop scale, open folds with a corresponding
orientation (E-W trending fold axes) and a wavelength in the dm- to cm-range are observed. Initial
stages of an axial plane crenulation cleavage (S3e
) are developed in places. The fold limbs of these
microfolds are enriched in amphibole when compared to the fold hinges, indicating that dissolution
precipitation creep was involved. A type Ie or II
e qtz vein has also been folded. The folding of
foliation S1e
in some group 4 transformed eclogites, suggest that deformation D3e
took place at
T < 475 °C and P < 0.7 GPa.
Late shear zones (D4e1
) occur in an eclogitic lens within the metasedimentary rocks. The
continuation of the shear zones into the metasedimentary rocks is not exposed. The shearzones
strike between E-W and NE-SW and dip with 60° NNW. They acted as normal faults with a dextral
strike slip component. Each zone is 30 to 40 cm wide; with the spacing in between ranging from 1.5
to 3 m. The displacement across each individual shear zone is in the order of a few cm as indicated
by displaced early albite veins. These shearzones are crosscut by late ab veins.
Another shear zone (D4e2
) occurs in a qtz-ab vein in eclogite. Deformation concentrated in the
10-15 cm wide vein, with the wall rock of the vein, consisting of group 4 transformed eclogite,
33
remaining undeformed. The vein strikes NNE-SSW and dips with 60° W. The exposed length is
approx. 10 m; the magnitude of displacement is unknown. The sheared vein is crosscut by late ab
veins.
3.3 Structures in the greenschists
More intensive deformation led to the transformation of the pseudomorphically replaced group 4
eclogite into a true greenschist. Therefore, deformation of the greenschists must have occurred at T
< 475 °C and P < 0.7 GPa. The foliation of the greenschists (S1g
, strike NE, dip 30° NW) is defined
by alternating layers of amp or ab and by a shape preferred orientation of green amp (grainsize ca.
100 µm) and epidote, and developed out of S3e
. The main foliation is isoclinally folded (D2g
), with
transposition of S1g
to S2g
, but without development of a new foliation in the fold hinges. Amphibole
has partly recrystallised in the fold hinges. Locally, this foliation (S1g
/S2g
) is folded on an m- to cm-
scale around E-W trending fold axes with a steep axial plane striking approximately E-W (D3g
).
Furthermore, open folds with vertical N-S (D4g
) and E-W (D5g
) striking axial planes occur. The
orientation of the folds in the greenschists is similar to the orientation of the folds in the
metasedimentary rocks (Fig. 16, 17). The greenschists are devoid of veins.
34
4 The record of the metasedimentary rocks
In this chapter the petrologic and structural records of the metasedimentary rocks will be presented.
The record preserved in the veins of the metasedimentary rocks is presented in chapter 5.
4.1 Petrology of the metasedimentary rocks
The petrology of the metasedimentary rocks is a summary of the results of Reinecke (1991;
1995; 1998). The metasedimentary rocks are mainly garnet-phengite-quartz-schists, with variable
amounts of dolomite, calcite, paragonite, and epidote. Subordinately, garnet-clinopyroxene-quartzites
and piemontite-phengite-quartz-schists occur. The bulk rock composition is very heterogeneous
and often changes on a cm-scale. Some samples show up to three stages of garnet growth, associated
with varied low-variance inclusion assemblages as well as compositionally zoned phases (e.g.,
phengite, dolomite, calcite) and distinct reaction textures in the matrix. These rocks provide ample
information for the reconstruction of their PT-path. Combining results derived by methods of absolute
(geo-Calc-Software: Brown et al., 1988, database of Berman, 1988) and relative thermobarometry
(Spear, 1988; Spear & Menard, 1989; Spear, 1993) from three different bulk rock compositions,
Reinecke (1995; 1998) has produced a well constrained PT-path of the metasedimentary rocks at
Lago di Cignana. The principal results are given below:
Maximum pressures of about 2.8-3.0 GPa were attained at about 600 °C. The thermal peak was
reached at 30-45 °C higher temperatures and 0.2-0.3 GPa lower pressures.
Early denudation to approx. 2.3 GPa, into the stability field of quartz, was accompanied by a
significant (about 50 °C) temperature decrease.
Decompression from 1.7-1.9 GPa to 1.1-1.2 GPa was almost isothermal (at 500-550 °C).
Further decompression from about 1.1 GPa to 0.6 GPa was accompanied by a temperature decrease
from 550 to 450 °C.
A late greenschist facies overprint occurred at 350-420 °C and 0.2-0.5 GPa.
4.2 Structures in the metasedimentary rocks
The compositional banding in the metasedimentary rocks is interpreted as bedding. Sub-parallel
to this banding a foliation is developed. Isoclinal folds in compositional bands and foliation prove
that the dominant schistosity is at least the second foliation (S2s
, strike NE, dip 20° SE, Fig. 17).
The foliation is defined by alternating layers rich in quartz and mica, and by the shape preferred
orientation of phengite, clinozoisite/epidote, and albite-amphibole symplectites. The stretching
lineation (L2s, trend WNW, plunge subhorizontal, Fig. 17) is defined by the shape preferred orientation
of clinozoisite/epidote. Boudins of metabasic and quartzitic rocks in a matrix of mica rich rocks are
observed in this foliation. The width of the boudins is up to 30 cm and their length up to 40 cm. The
boudin necks are filled with quartz and clinozoisite. The quartzitic boudins are slightly rotated
along N-S striking, 20° E dipping shearzones. The asymmetric strain shadows at the eclogitic boudins
suggest non coaxial deformation and top to the N displacement (Photo 8). Because S2s
always flows
35
around garnets, these must have been mechanically effective during formation of foliation S2s
.
Reinecke (1995) calculated the PT-path of the metasedimentary rocks from profiles of zoned garnets.
Therefore, S2s
must have formed after the last garnet growth at T < 450 °C and P < 0.6 GPa (Reinecke,
1995). In some rock types, the foliation S2s
is partly defined by the shape preferred orientation of
fine grained aggregates of tremolite + microcline + albite + hematite ± jadeite poor aegerineaugite,
that replace UHPM aegerineaugite with jd26-37
(Reinecke, 1995). These fine grained aggregates are
undeformed, indicating that the replacement occurred after formation of the foliation. Therefore,
S2s
must have formed before the late greenschist reequilibration at 350-420 °C and 0.2-0.5 GPa
inferred by Reinecke (1995) from these aggregates.
Locally, the foliation S2s
is folded on a mm- to 10-m scale (figure 19). A first generation of ap-
proximately N-verging folds (D3s
) developed an axial plane crenulation cleavage (S3s
strike E-W,
dip vertical) in mica rich layers. Foliation S3s
is defined by a shape preferred orientation of mica and
clinozoisite. Foliation S2s
and S3s
are locally folded on a cm- to m-scale. The relative timing of for-
mation of the later generations of open folds (D4s
and D5s
) is unclear, because an axial plane cleavage
has not developed. Axial planes of D4s
and D5s
folds strike approximately NE-SW and N-S,
respectively, and are almost vertical. Distinction between small scale D3s
and D4s or 5s
folds is only
possible, when both generations occur in close contact and can be correlated with m-scale folds.
These deformation phases could not be correlated with petrologic observations.
In the metasedimentary rocks, veins can be classified into four groups using their relation to
foliations S2s
and S3s
, vein mineralogy and microstructure. The deformation microstructures and
fabrics of veins will be presented in chapter 5.
Figure 17
Orientation of structural elements in the metasedimentary rocks, depicted in stereographic projections (lowerhemisphere, equal area). Left: Poles of foliation S
2s and stretching lineation L
2s, Right: Poles of foliation S
3s
and axial planes to smal scale D4s or 5s
folds
36
Type Is veins are oriented sub-parallel to the foliation S
2s. They often form lenses in the foliation
that are the hinges of (refolded) isoclinal folds. The veins are mineralised with quartz, often
associated with garnet and white mica. In some veins, garnet is the main vein filling mineral.
Quartz in the veins is completely recrystallised. Garnet and white mica are euhedral and
white mica has a shape preferred orientation parallel to the foliation outside the vein. In one
garnet from these veins, an inclusion of coesite was unequivocally identified. This suggests
that at least some of the earliest veins were formed at UHPM conditions or prior to UHPM
and recrystallised during UHPM.
Type IIs veins are oriented at an angle (> 10°) to foliation S
2s and are sometimes folded by D
3s.
Aspect ratios of unfolded veins are high (> 20) and opposing vein flanks fit. These veins are
mineralised with quartz and clinozoisite. Quartz in those veins is partly recrystallised. Clino-
zoisite grains are subhedral and often broken.
Type IIIsveins crosscut S
2s and (where present) S
3s. These veins have high aspect ratios (> 30)
and opposing flanks fit. They are mineralised with quartz and clinozoisite and/or green
amphibole. A vein filling structure is preserved with large (cm-sized) quartz grains, that often
Photo 8
A lens of high viscous eclogite in a matrix of lowviscous metasedimentary rocks. The assymmetricstructure suggests a high degree of non coaxialdeformation. N is up, length of eclogitic lens is ca.0.5 m.
Photo 9
Dust trails in vein albite, define an older growthstructure. Long side of photograph is 7 mm.
37
enclose mm-sized amphibole needles. When clinozoisite is present, it forms cm-sized, sub-
hedral grains.
Type IVs veins are oriented at an angle to S
2s and (where present) S
3s. These veins have high
aspect ratio (> 30) and opposing flanks fit. They are mineralised with albite. A vein filling
structure is preserved, with mm-sized subhedral albite grains, that extend from the vein flanks
to the vein centre. The centre of the vein is often an open cavity. Fine dust trails in the albite
grains trace the outlines of older minerals (Photo 9).
38
5 Quartz veins (microstructures, fabrics and fluid inclusions)
Microstructure and fabrics of the veins give information about the stress and strain history of the
host rock after vein formation and are presented first. Fluid inclusions in the veins can give
thermobarometric information (e.g., Sheperd et al., 1985) and are presented at the end of the chapter.
5.1 Microstructures of vein quartz
In most quartz veins in the eclogites and the metasedimentary rocks, the primary microstructure
is destroyed due to subsequent deformation by dislocation creep, that caused partial to complete
recrystallisation. Locally, relic grains with a diameter of up to several millimetres are preserved in
the veins; they are composed of subgrains (Photo 10).
Most quartz veins in eclogite and type Is veins in the metasedimentary rocks have a recrystallised
grain size ranging from 70 to 125 µm. The presence of other minerals, especially of white mica in
some veins in the metasedimentary rocks, locally influenced size and shape of the recrystallised
grains. Usually, the recrystallised grains are elongated and have a slight shape preferred orientation.
Photo 11
Microstructure of quartz in a deformed type IIe vein.
The straight grain boundaris and the 120° angle atthe grain edges indicate that recrystallisation wasfollowed by grain growth under low differentialstress. Crossed polars, long side of the photograph is1.4 mm.
Photo 10
Microstructure of a type IIe quartz vein close to a
late shearzone. The polygonisation and subgrainformation of the large grain and the recrystallisationat its rim are inferred to be due to an earlierdeformation stage. Sutured grain boundaries andundulatory extinction in the recrystallised grains aredue to an overprint at lower temperatures. Crossedpolars, long side of the photograph is 7 mm.
39
The grain boundaries are straight and meet with angles near 120° at grain edges (foam structure,
Photo 11), indicating that the deformation was followed by normal grain growth under low differential
stress.
This foam microstructure has been overprinted near the later shear zones in the eclogites (D4e
)
and in type Is and II
s veins in the metasedimentary rocks folded during D
3s(Photos 10, 12, 13).
Deformation by dislocation creep under lower temperatures and higher differential stress is reflected
by undulatory extinction and irregularly serrated high angle grain boundaries and small recrystallised
grains. The recrystallised grain size is around 40 µm in shearzone 1 (Photo 12) and the folded veins
in the metasedimentary rocks and around 10 µm in shearzone 2 (Photo 13).
5.2 Paleopiezometry
In the material science, it was noted early that the differential stress during steady state creep of
metals and alloys could be related to the recrystallised grain size (e.g., Bird et al., 1969; Luton &
Sellars, 1969; Glovers & Sellars, 1973). This relation was later applied to geological materials,
mainly quartz and olivine (e.g., Mercier et al., 1977; Twiss, 1977; 1986). Derby & Ashby (1987)
and Derby (1991) propose that the steady state grain size at constant differential stress results from
Photo 13
Core and mantle structure in a late intensivelydeformed quartz vein (D
4e2). Crossed polars, long
side of the photograph is 7 mm.
Photo 12
Microstructure of a quartz vein in a small shearzone(D
4e1) in an eclogite lens. Note the bimodal grain size
distribution. In the upper right of the picture aglaucophane with small quartz inclusions occurs.Crossed polars, long side of the photograph is 7 mm.
40
a balance between the speed of recrystallisation and the rate of nucleation of new grains. This
theory explains the general relation between differential stress and recrystallised grain size:
d/b = Kn ((σ
1 - σ
3)/ µ)-n,
with d grainsize, b burgers vector, (σ1 - σ
3) differential stress, µ shear modulus and K
n and n constants.
Twiss (1977), derived values for these constants theoretically. Other authors determined these
constants by fitting the general relation to experimental data. This can be done by inserting b and µ
values for one mineral (e.g., quartz) in the formula and fitting this formula to data from experiments
on this mineral (e.g., Mercier et al., 1977; Koch, 1983; Ord & Christie, 1984), or by normalising the
experimental data from several minerals and metals (d/b and (σ1 -σ
3)/µ) and fitting the normalised
formula to the data (e.g., Skrotzki, 1992). The various calibrations of the recrystallised grainsize
paleopiezometer for quartz (e.g., Twiss, 1977; Mercier et al., 1977; Koch, 1983; Ord & Christie,
1984; Skrotzki, 1992), yield highly differing results (Fig. 18). The calibrations based on experiments,
yield for a given grainsize the highest differential stresses. These experiments were performed in a
Griggs-Blacic solid-medium deformation apparatus (Griggs, 1967; Blacic, 1972), with either talc,
pyrhophyllite, AlSiMag or copper as confining medium (e.g., Koch et al., 1989). Green & Borch
(1989; 1990) showed that the strength of the materials used as confining medium could result in a
large overestimate of the flow stress and recommended the use of salt as confining medium to
Figure 18
Several calibrations of the dynamically recrystallised grain size paleopiezometer for quartz, from Twiss(1977), Mercier et al. (1977), Koch (1983), Ord & Christie (1984), Skrotzki (1992). The barred line representsthe range of recrystallised grain sizes found in a completely recrystallised sample deformed at ca. 200 MPaby Gleason et al. (1993).
41
minimise this problem. The experiments of Gleason et al. (1993) using salts as confining medium,
provide independent data to check the different calibrations. These authors report for one sample
with a pre-deformation grain size of about 50 µm, a recrystallised grain size between 5 and 10 µm
after 75 % shortening. The differential stress in this experiment was ca. 200 MPa (Gleason et al.,
1993). This data point corresponds very well with the calibration of Twiss (1977) (Fig. 18). Therefore,
the Twiss (1977) calibration of the recrystallised grainsize paleopiezometer will be used in this
study.
In veins in eclogites and metasedimentary rocks, where the recrystallised grains show indications
of normal grain growth, the recrystallised grain size ranges between 70 and 125 µm. The micro-
structure changed after deformation and does not reflect the differential stresses during deformation
any longer. However, the preservation of a shape preferred orientation, suggests that the increase in
grainsize was only moderate. The paleopiezometer of Twiss (1977) indicates minimal differential
stresses for this deformation of 25 to 35 MPa. In the group IIs veins in the metasedimentary rocks
and the veins deformed during D4e1
, quartz is only partly recrystallised with grain sizes ranging
from 20 to 40 µm. In this case, the paleopiezometer should not be used, because it is not certain that
a steady state microstructure is reached. The recrystallised grain sizes of ca. 10 µm of completely
recrystallised veins deformed during D4e2
, points to differential stresses of ca. 125 MPa.
5.3 C-axis fabrics in quartz veins
For all recrystallised quartz veins, the c-axis fabrics were measured with standard universal
stage techniques (e.g., Turner & Weiss, 1963).
5.3.1 Eclogites
The development of foliation and lineation in the eclogitic host rock predated formation and
deformation of the quartz veins. Thus, these structural elements cannot be used as kinematic
framework. Therefore, the textures are referred to the finite strain axes, assumed to be parallel and
normal to the foliation and lineation defined by the shape preferred orientation of the recrystallised
grains (Price, 1985). The measured c-axis fabrics range from point maxima, to single girdles, and
weakly developed type I cross girdles (Lister, 1977), oriented at a high angle to this foliation (Fig. 19).
Owing to the isolated position of the veinlets in essentially undeformed eclogites, accumulation of
a large strain is precluded. Hence, the lattice preferred orientation developed during deformation is
probably influenced by the orientation of the pre-existing grains. In fact, point maxima are
characteristic for veins with mm-sized relic grains and better defined c-axis girdles occur in
completely recrystallised veins. As such, the variation in lattice preferred orientation seemingly
reflects the intensity of deformation.
For a vein deformed in shear zone 1 (D4e1
) the shear zone boundaries are taken as the kinematic
framework. The c-axis fabric is diffuse (Fig. 19, Bk 119). Taking into account the small amount of
displacement along this shearzone and the bimodal recrystallised grainsize distribution, the diffuse
c-axis fabric probably reflects the overprinting of two stages of low finite strain deformation.
42
For the veins deformed during D4e2
, the shear zone boundaries are not found and the textures are
referred to the finite strain axes, assumed to be parallel and normal to the foliation and lineation
Figure 19
Lattice preferred orientation of quartz (c-axes) in selected veins in eclogite, that underwent grain growthunder low differential stress after deformation (Bk 4,5,8,20,118) and a vein that deformed during D
4e1 (Bk 119).
Data are presented as scatter plots and contour plots. The orientation with respect to mesoscopic structuresis for all veins only approximate. Bk 5 and Bk 8 are type I
e veins, Bk 4 and Bk 20 are type II
e veins and Bk
118 is a type IIIe vein. See text for discussion.
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43
defined by the shape preferred orientation of the recrystallised grains (Price, 1985). The c-axis
fabrics for these veins are single girdles, tending towards type I crossed girdles (Fig. 20).
5.3.2 Metasedimentary rocks
For type Is veins the foliation S
2s and the stretching lineation were taken as kinematic framework.
The c-axis fabrics of the type Is veins (Fig. 21) are double point maxima with one maximum approxi-
mately normal to X and Z and the other maximum at a high angle to X and Y. These could be inter-
preted as single girdles at a high angle to the foliation. Sample Bk 77 has large variations in c-axis
orientations. This sample is from an isoclinally folded quartz vein that was refolded by D3s
. The
large spread in c-axes reflects an overprinting of an earlier fabric by a stage of low finite strain
deformation.
For type IIs veins the foliation S
3s and the direction normal to the fold axis were taken as kinematic
framework, where S3s
had developed. In the other cases (Bk 46, Bk 99) the textures are referred to
the finite strain axes that are assumed to be parallel and normal to the foliation and lineation defined
by the shape preferred orientation of the recrystallised grains (Price, 1985). The c-axis fabrics of the
type IIs veins (Fig. 22) are broad point maxima tending to weakly developed single girdles. The
broad point maxima probably reflect the influence of the orientation of the large pre-existing grains
on the developing lattice preferred orientation. It seems, that D3s
deformation of the veins was not
intense enough to produce a complete new c-axis fabric. This is supported by sample Bk 77, where
the earlier c-axis fabric is only slightly modified by later D3s
deformation.
Figure 20
Lattice preferred orientation of quartz (c-axes) of veins deformed during D4e2
. Data are presented as scatterplots and contour plots. The orientation with respect to mesoscopic structures is for all veins only approximate.
Z
X
Z
X
Bk 131A N = 250
Z
X
Z
X
��������
������
Z
X
Z
X
Bk 130 N = 250
44
5.3.3 Summary
The c-axis fabrics for most veins in eclogites and metasedimentary rocks are not well enough
developed to estimate strain ratios or sense of shear from these fabrics (e.g., Price, 1985). Only
veins deformed in shear zone (D4e2
) have well-developed c-axis fabrics that suggests non coaxial
deformation in this shearzone with a dextral sense of shear (Price, 1985). The c-axis girdles
approximately normal to the foliation, indicate that <a> glide on various lattice planes (e.g., Schmid
& Casey, 1986) was the predominant deformation mechanism. The predominance of <a> glide on
various lattice planes, suggests deformation at relatively low temperatures (Hobbs, 1985).
5.4 Fluid inclusions in vein quartz
Fluid inclusions are samples of a fluid phase that may be present during a certain moment in the
history of the rock. They are the only direct evidence for the presence of a fluid phase and the only
possibility to physically analyse the composition of this fluid phase (e.g., Roedder, 1984). In this
study, it is more important that under certain conditions thermobarometric data can be obtained
from these inclusions (e.g., Roedder, 1984; Shepherd et al., 1985). Fluid inclusions can be used as
thermobarometer, when their composition and density can be determined and when P(ressure)-
V(olume)-T(emperature)-data for this composition are available. If the composition and volume of
the inclusion did not change after formation, PT-conditions for the formation of the fluid inclusion
can be inferred (e.g., Roedder, 1984).
Figure 21
Lattice preferred orientation of quartz (c-axes) in veins subparallel to foliation S2s
. Data are presented asscatter plots and contour plots.
������
�����
X
X
Z
Z
�����
������
���� ��
�������
X
X
X
X
Z
Z
Z
Z
45
To interpret these PT-data the origin of the fluid inclusion must be known. Usually, a distinction
between primary inclusions that formed during the growth of the host mineral and secondary inclu-
sions that formed after the growth of the host mineral is made (Roedder, 1972).
Fluid inclusions were studied in partly to completely recrystallised type Ie and II
e quartz veins.
The arrangement of the high angle grain boundaries of the recrystallised grains in these samples
suggests late grain growth under low differential stress. In the recrystallised and relic grains four
types of fluid inclusions are recognised:
1. Single fluid inclusions in the recrystallised grains are considered to have formed during
recrystallisation (e.g., Wilkins & Barkas, 1978).
2. Fluid inclusions arranged along irregular planes in the recrystallised grains (Photo 14) are
interpreted as relics of a grain boundary porosity in an originally finer grained microstructure
and thus must have formed during recrystallisation (e.g., Wilkins & Barkas, 1978).
3. Fluid inclusions arranged along planes delineating subgrainboundaries in the relic grains are
considered to have formed during polygonisation (e.g., Wilkins & Barkas, 1978).
4. Fluid inclusions arranged along planes that crosscut grain boundaries are interpreted as healed
microcracks (e.g., Sprunt & Nur, 1979) and considered to have formed after recrystallisation.
This allows subdivision of the fluid inclusions in two main groups:
Early inclusions of the type 1, 2, and 3 that formed during deformation and recrystallisation of
the original vein filling material and are secondary inclusions after Roedder (1972) with
Figure 22
Lattice preferred orientation of quartz (c-axes) in veins deformed in D3s
. Data are presented as scatter plotsand contour plots.
������
������
������
���� ���
������
�������
x x x
x x x
z z z
z z z
46
respect to the relic grains. These inclusions, however, formed during the formation of the
recrystallised grains and are, therefore, primary inclusion for the recrystallised grains.
Late inclusions of type 4, that formed after formation of the recrystallised grains are true secondary
inclusions after Roedder (1972).
The composition of fluid inclusions is determined through observation of phase transitions at
low temperatures. Most fluid inclusions at Lago di Cignana can be described in the relative simple
system H2O-salt and only the phase transformations, that are observed upon heating of a frozen
inclusion in this system, will be described.
The first phase transition upon heating after cooling, which is only sometimes observed, is the
onset of melting (temperature of eutectic between solid and liquid phase). This temperature indicates
which cations might be dissolved in the fluid phase (e.g., Hollister & Crawford, 1981). Because the
amount of first melt is very small, the temperature at which this transition is observed will always
be higher than the real temperature of eutectic (Küster, 1994).
The next phase transition that occurs in this system, is the melting of the last ice. From the
freezing point depression the salinity of the fluid can be calculated (Roedder, 1984).
The density of a fluid inclusion of known composition is determined by measuring the homo-
genisation temperature. Homogenisation occurs when the vapour bubble in the inclusion disappears.
In the fluid inclusions from Lago di Cignana homogenisation was always in the fluid phase (inclusions
have a supercritical density); upon heating the vapour bubble becomes smaller and finally disappears
(Roedder, 1984). With these observations and if P-V-T-data for these compositions are known, the
positions of isochors in the PT-field can be determined (e.g., Haas, 1976; Potter & Brown, 1977).
Photo 14
Fluid inclusions arranged along irregular planes in a recrystallised grain, are interpreted as relics of a grainboundary porosity in an originally fine grained structure. In the lower left corner of the photograph a trail ofsecondary inclusions occurs. Plane polarised light, length of scale bar 125µm.
47
The temperatures determined for all observed phase transitions must be corrected according to
the calibration curve for the heating-freezing stage used (Roedder, 1984). Compositions and densities
can then be calculated with the program FLINCOR 1.2.1. using the corrected Tm H
2O and T
hom H
2O.
The position of the isochores in the PT-field was calculated with the equation of state of Brown &
Lamb (1989) in the system H2O-NaCl. Other equations of state for this system (e.g., Haas, 1976;
Potter & Brown, 1977; Zhang & Frantz, 1987) give similar results. Graphical representation of the
isochores in a PT-diagram was facilitated with the program FCP of Dr. Röller.
A problem is that the composition (salinity) of the inclusion is inferred from the freezing point
depression. The depression depends on the amount and on the kind of anions and cations in the
solution. The eutectic temperature suggests which cations might be solved. It gives, however, no
indication of the amounts of these cations in the solution. Furthermore, P-V-T-data are not known
for more complex salts solved in a fluid phase. Therefore, the salinity of the fluid is approximated
in wt.% NaCl-equivalent, because Na+ and Cl- are usually the dominant ions in the fluid phase
(Roedder, 1962). Because the eutectic temperature of the H2O-NaCl system is -20.8 °C, fluid
inclusions with melting temperatures below this temperature cannot be processed. Melting
temperatures at Lago di Cignana were, however, all above this temperature.
5.4.1 Compositions and densities of the fluid inclusions
Fluid inclusions were analysed in three quartz veins that are partly to completely recrystallised.
Bk 20 is a type IIe quartz clinozoisite vein in a group 3 eclogite. Bk 100 is a type I
e quartz omphacite
segregation in a group 1 eclogite. Bk 101 is a type IIe quartz vein in a group 3 eclogite that is part of
a swarm of veins parallel to the foliation in eclogite, that occur within 0.5 m from the contact
between eclogite and metasedimentary rock.
All measured inclusions in these quartz veins were at room temperature 2-phased and contained
an aqueous fluid of low salinity. At room temperature single phase inclusions were not measured,
while even at very low temperatures, usually, no phase transformations were observed. These
inclusions contain a low density vapour or a high density fluid phase. The absence of a vapour
bubble in a fluid phase could also be due to metastable behaviour of the inclusion (Roedder, 1967).
Metastable behaviour was observed in several inclusions that were initially 2-phased, but were
single phase after one or more cooling and heating cycles.
For the early inclusions, observed temperatures of eutectic range between -30 and -25 °C, indi-
cating the presence of other cations besides Na+ in the solution (Hollister & Crawford, 1981). The
temperatures of melting range from -1 to -11 °C (between 1.6 and 15 wt.% NaCl-equivalent).
Temperatures of homogenisation (in the fluid phase) range from 80 to 190 °C, corresponding to
densities between 0.94 and 1.07 gr/cm3 (equation of state of Brown & Lamb, 1989) (Table 7, Fig. 23).
For the late inclusions, observed temperatures of eutectic are also ca. -30 °C, indicating the
presence of other cations besides Na+ in the solution (Hollister & Crawford, 1981). The temperatures
of melting range from -1 to -11 °C (between 1.6 and 15 wt.% NaCl-equivalent). Temperatures of
48
homogenisation (in the fluid phase) range from 100 to > 250 °C, corresponding to densities between
< 0.87 and 1.05 gr/cm3 (equation of state of Brown & Lamb, 1989) (Table 7, Fig.23).
The large spread in homogenisation temperatures found in sample Bk 101 can, perhaps, be
explained by necking down of larger inclusions (Lemmlein & Kliya, 1952). In this sample fluid
inclusions were observed consisting of two spheres connected by a thin tube, indicative for necking
down. Because necking down changes the density of the fluid inclusions, only the data of samples
Bk 20 and Bk 100 are interpreted. The isochores for the fluid inclusions in these samples are depicted
in figure 24.
The thermobarometric interpretation of the fluid inclusion data assumes constant volume (density)
and constant composition for the inclusion. Several studies have shown that fluid inclusions that
from geological reasoning formed at peak metamorphic conditions, have densities and compositions,
Table 7
Temperature ranges for observed phase transformations and inferred composition and densities of early andlate fluid inclusions from the investigated samples.
Figure 23
Melting temperatures against temperature of homogenisation for the fluid inclusions in the investigatedsamples differentiated for the arrangement of the fluid inclusions.
49
that suggest pressures and temperatures of formation below these conditions (e.g., Hollister et al.,
1979; Küster, 1994 on Crete; Swanenberg, 1980, in Rogaland; Kreulen, 1980 on Naxos). Therefore,
the fluid inclusions changed after formation, either their density, or their composition. Experimental
investigations on fluid inclusions in quartz have also shown that fluid inclusions can change their
density and/or their composition (e.g., Pecher, 1981; Pecher & Bouillier, 1984; Sterner & Bodnar,
1989; Bouillier et al., 1989; Bakker & Janssen, 1990; Bakker, 1994). Compositional changes in
fluid inclusions can be explained with diffusion of material out of the inclusion at relatively high
(T > 600 °C) temperatures (e.g., Bakker, 1994). A theory, that explains the density decrease observed
for fluid inclusions in quartz at lower temperatures (T > 300 °C), has been proposed by Küster
(1994) and Küster & Stöckhert (1997). They show that at the low rate of change in P and T in
metamorphic rocks, very low strain rates are sufficient for volume adaptation of the inclusions by
dislocation creep of the host quartz. Dislocation creep is driven by the differential stresses, that
develop in the host mineral around the inclusions, when cooling and decompression does not follow
the isochor of the fluid inclusion. Therefore, they suggest that as long as the host mineral behaves
ductile, fluid inclusions will change their volume. The density of the fluid inclusions reflects the
PT-conditions at which plastic stretching of the host mineral is no longer possible. Experimentally
derived flow laws for quartz (e.g., Paterson & Luan, 1990; Koch et al., 1989) suggest that for
relevant strain rates (10-15, 10-16 s-1, Küster & Stöckhert, 1997) the flow stress drastically increases
at temperatures of about 300 °C or somewhat below.
Following the model of Küster & Stöckhert (1997), the densities of the early fluid inclusions
measured in two quartz veins at Lago di Cignana suggest a pressure between 0.2 and 0.4 GPa at
temperatures around 300 °C (Fig. 24).
Figure 24
Position of the isochores (equation of state of Brown & Lamb (1989)) for the early and late fluid inclusionsfrom samples Bk 20 and Bk 100.
50
6 The exhumation record of the rocks
Metamorphic rocks are sometimes thought of as flight recorders, black boxes recovered from
the wreckage of an orogen, that tell us something of that orogens history (Haugerud & Zen, 1991).
They differ, however, from flight recorders in that the recording is not continuous and that often
parts of the recordings are erased. The record preserved in the rock, generally depends on an incom-
plete and spatially distributed response of the rock to the changing conditions. During large parts of
the exhumation history the rocks have remained essentially passive, without undergoing discernible
modification and the exhumation history is, therefore, only partly recorded.
Two general remarks can be made concerning the record found in the rocks:
1. All orientations and directions mentioned in the text are as they occur today. During later
deformations earlier structures have been rotated.
2. Uncertainties of absolute PT-estimates pertaining to some well-calibrated geothermobaro-
meters are on the order of 50 K (1 σ) and 500 MPa (Kohn & Spear, 1991a). Differences in P
and T, however, calculated with the same thermobarometer from different samples have much
smaller uncertainties, that are commonly about a few tens of Kelvin and tens of MPa (Kohn
& Spear, 1991a; 1991b; Hodges & McKenna, 1987). This means that absolute PT-conditions
mentioned in this study have uncertainties of at least 50 K and 500 MPa, whereas relative
changes in PT-conditions are relatively well constrained, but the exact positions of these
segments of the PT-path are subject to similar errors as the absolute thermobarometry.
The metabasic and the metasedimentary rocks preserved different parts of the exhumation history.
The petrological record (Fig. 25) is nearly complete in the metasedimentary rocks (e.g., Reinecke,
1998) and a similar, but more fragmentary record is found in the metabasic rocks (this study). A
comparison of the structural records shows that in the metasedimentary rocks only the last part of
this record is preserved, but that the metabasic rocks preserved the UHPM and later parts of the
record (Fig. 25). The records of both rock types will now be combined and discussed for several
intervals.
6.1 The record during UHPM and early exhumation
In the metabasic rocks deformation under UHPM conditions (Fig. 25; T 575-625 °C;
P 2.5-2.8 GPa) is indicated by the foliation (S1e
) defined by omphacite. This deformation was
heterogeneous, as evident by the variable distortion of pillow structures. The bulk rock rheology
was controlled by omp, with the other minerals essentially acting as rigid bodies. This interpretation
is supported by the irregulary distributed composition domains found in individual omp grains,
attributed to compositional reequilibration during grain boundary migration (e.g., Buatier et al.,
1991; Godard & van Roermond, 1995), that contrast with the compositional homogeneity of other
minerals and the regular zoning pattern in garnet. Differential stresses must have been high enough
to drive deformation by dislocation creep in omphacite at temperatures of about 600 °C. Extrapolation
of laboratory data on diopside (e.g., Boland & Tullis, 1986), assumming geological relevant strain
51
Figure 25
PTD-path for the exhumation of UHPM rocks of Lago di Cignana, Western Alps, Italy, modified after vander Klauw et al., (1997). The continuous segments of the PT-path were derived by Reinecke (1995; 1998)from absolute and relative thermobarometric methods applied to compositional zoning and inclusion patternsin garnet, combined with compositional information from other zoned matrix phases of the metasedimentary
52
rates (10-14–10-16 s-1), provides an upper limit of about 200-250 MPa for the differential stress to
drive steady state creep of diopside at these conditions. Preliminary results on the deformation
behaviour of jadeite (Stöckhert & Renner, 1998) suggest that at ca. 600 °C and a strain rate of
10-14 s-1, the flow stress may be as low as a few MPa. The strength of omp is probably not the same
as that of jadeite at these conditions, but possibly well below that of diopside.
The extensional shearbands (S2e
) in the metabasic rocks indicate localisation of deformation.
Quartz pseudomorphs after coesite in omp grains on these bands, suggest that S2e
formed as the
rocks were in the stability field of coesite. The shearbands are inferred to have nucleated at the
interface between strain shadows at garnets and matrix, and thus result from the contrasts in
mechanical properties of the rock forming minerals.
Subsequent to the formation of S2e
at P > 2.7 GPa and T > 575 °C, no further deformation and
mineral reactions took place in the metabasic rocks prior to the onset of the replacement of the
UHPM mineral assemblage at 1.2 GPa and 550-575 °C. Net-transfer and exchange reactions are
probably not detected, because the mineral assemblage omp + grt + rt + gln/zoi + czoI is stable over
a large range of PT-conditions and minor possible relaxation of Fe-Mg exchange between ferro-
magnesian minerals was impeded by slow rates of volume diffusion, due to the relatively low
temperatures. Veins parallel to the foliation may have formed, but cannot be distinguished from
other vein types. Along this part of the PT-path, the differential stress remained too low to allow for
notable deformation of the metabasic rocks. Any deformation during this stage must have been
localised into weak shearzones that were not observed or located in the overlying metasedimentary
rocks. The metasedimentary rocks preserved the UHPM and early exhumation PT-record, as minerals
included in garnet, as minerals in strain shadows or as zoned minerals (Reinecke, 1995; 1998). All
structures that might have formed under these conditions were either completely transposed, or
wiped out by intense later deformation and the structural record was not preserved. The structural
record in the metasedimentary rocks starts at T > 450 °C and P > 0.6 GPa.
6.2 The record between 575 and ca. 450 °C
In the metasedimentary rocks the PT-record of Reinecke (1995; 1998) shows a change from
almost isothermal decompression to pronounced cooling with decompression in this temperature
interval (Fig. 25). In the metabasic rocks, omp in contact with qtz became unstable at PT-conditions
below ca. 1.2 GPa and 575 °C and recording resumed, showing similar PT-changes as the
metasedimentary rocks.
The spatial and implied temporal relationship between the late vein types and the extent of lower
PT-replacement in the metabasic rocks (Table 8), allows the reconstruction of the trend in the
evolution of relative fluid pressures Pf and differential stress on this part of the exhumation path
(Fig. 25).
Type Ie qtz veins were formed before or during UHPM and deformed together with their metabasic
host rock, probably as coesite veins. Therefore, they give no information about the exhumation
history, apart from structures superimposed during post UHPM deformation. According to the
53
correlation with the type of lower PT-replacement, type IIe qtz veins were formed at temperatures of
about 550 to 500 °C and type IIIe qtz veins at T < 500 °C. Shape and aspect ratio of type II
e and III
e
qtz veins, and the lack of fit between the vein flanks, indicate that the host rock deformed plastically
at the time of vein formation. In contrast, the shape of most type IVe ab veins, formed at temperatures
below ca. 475 °C, indicates that the host rocks exhibited brittle behaviour at the time of vein formation.
The orientation of the veins with respect to pre-existing structures and discontinuities can be
used to place some qualitative constraints on the magnitude of differential stress (Etheridge, 1983;
Sibson, 1985). Type IIe qtz veins are oriented parallel to foliation S
1e or S
2e; these are interpreted to
represent planes of low tensile strength. Differential stress was too low to allow formation of new
cracks in other orientations. Hence, σ3 was oriented at a large angle, but not necessarily normal to
the veins. Furthermore, formation of veins in these orientations requires that Pf exceeded the normal
stress acting across these planes; hence, Pf was larger than σ
3. This limits the magnitude of the
differential stress to very low values (Jaeger & Cook, 1979). The later formation of type IIIe qtz
veins at a high angle to the pre-existing discontinuities, requires a reorientation of the principal
stress directions to prevent cracks following pre-existing discontinuities. The three generations of
type IVe ab veins, indicate that conditions favouring the formation of open cracks at a high angle to
pre-existing discontinuities, were realised several times during later deformation history.
An upper limit for the magnitude of the differential stress during formation of tensile fractures is
given by Jaeger & Cook (1979) as σ1-σ
3 < 4Te, where Te denotes the tensile strength of the rock.
For this, Etheridge (1983) proposes 10 MPa as an upper limit in unfractured rocks under metamorphic
PT-conditions. It is expected that this magnitude is drastically reduced along pre-existing discon-
tinuities. According to these considerations, the magnitude of differential stress during formation
of type IIIe and IV
e veins is limited to less than 40 MPa, and may have been significantly lower for
the formation of type IIe veins.
Table 8
Correlation between the degree of lower PT-replacement and the number of veins present in a rock volume.
54
6.3 The record between ca. 450 and 300 °C
In the metasedimentary rocks the PT-record (Reinecke, 1995; 1998) shows a slight decomp-
ression with decreasing temperature from ca. 0.6 GPa at 450 °C to 0.2-0.5 GPa at 350-420 °C
(Fig. 25). This fits well with the PT-estimate of 0.2–0.4 GPa at around 300 °C, inferred with the
method of Küster & Stöckhert (1997) from fluid inclusions in quartz veins in the metabasic rocks.
The structural record in the metabasic rocks shows localised folding of foliation S1e
in pseudo-
morphic replaced eclogite with a greenschist facies mineral assemblage at T < 475 °C and
P < 0.7 GPa. Localisation and more intense deformation led to the development of the foliated
(S1g
/S2g
) greenschists. Lenses of metabasic rocks in the metasedimentary rocks have their foliation
(S1e
, S2e
) at varying angles to foliation S2s
of the metasedimentary rocks, if they consist of (pseudo-
morphic) eclogite; the foliation (S2g
) is parallel to S2s
, if they consist of greenschists, indicating that
S2g
and S2s
formed during the same deformation event. At this stage, also the quartz veins in the
metabasic rocks and type Is veins were deformed by dislocation creep of quartz. The recrystallised
grainsize in those veins ranges between 70 and 125 µm, indicating minimal differential stresses of
25 and 35 MPa (Twiss, 1977) for this deformation. In combination with experimentally determined
“best choice 2” flow law of Paterson & Luan (1990), these differential stresses indicate for assumed
strain rates of 10-14-10-16 s-1 temperatures between 400 and 450 °C during deformation (Fig. 26).
These temperatures are in good accordance with temperatures for D2s
inferred from petrologic
observations.
The arrangement of high angle grain boundaries in the quartz veins indicates interfacial free
energy control. This microstructure can only be attained, if no driving force for grain boundary
migration is exerted by contrasting dislocation densities. Different dislocation densities are produced
during dislocation creep deformation, that at these temperatures requires only low differential stresses
(e.g., Stöckhert et al., 1997). Consequently, the magnitude of differential stress must have been low
subsequent to this (D2s
, D2g
, D3e
) deformation event.
After this period of low differential stress, only localised deformation occurred, suggesting a
heterogeneous stress field. Similarities in microstructures of quartz veins folded in D3s
/D3g
and
deformed in D4e
shearzones suggest that they were deformed under similar conditions. The weakly
developed lattice preferred orientation and incomplete recrystallisation in most veins deformed
during this stage suggest that a steady state microstructure had not developed. Only one quartz vein
in eclogite deformed in a shear zone (D4e2
) shows irregular serrated grain boundaries of quartz and
a strong lattice preferred orientation, suggesting development of a new steady state microstructure
during this deformation. The 10 µm recrystallised grain size indicates a differential stress of ca.
125 MPa (Twiss, 1977) during deformation of this vein. In combination with the “best choice 2”
flow law of Paterson & Luan (1990), this suggests, for the assumed geological strain rates of 10-14-
10-16 s-1, temperatures between 325 and 375 °C (Fig. 26). The localised more intense deformation
(D4e2
), however, could indicate that the deformation was strongly localised (e.g., Küster & Stöckhert,
1999) and the rock deformed with a faster strain rate. This would require higher temperatures
55
during deformation. There is no independent evidence for the temperature during this deformation
stage.
The later deformation stages in the metasedimentary rocks and greenschists (D4s-g
and D5s-g
)
could not be correlated with deformed veins or petrologic information and inferences about PT-
conditions during these deformations are not possible.
6.4 Synthesis: A two stage exhumation for the UHPM rocks of Lago diCignana
A combination of the PT-path with published geochronological data allows an approximate
reconstruction of the PTt-evolution (Fig. 27). An Sm-Nd garnet age of 40.6 ± 2.6 (2 σ) Ma is given
by Amato et al. (1999) for the eclogitic rocks of Lago di Cignana. The closure temperature of the
Sm-Nd system in garnet is ca. 600 °C (Hodges, 1991) and the age of 41 Ma can be considered to
date the UHPM. A similar age, 44.1 ± 0.7 (95 % confidence interval) Ma was obtained with SHRIMP,
U-Pb dating of zircons (closure temperature > 700 °C, Hodges, 1991) in the eclogites (Rubatto et
al., 1998). The later greenschist facies overprint was dated between 40 and 45 Ma with Rb-Sr in
Figure 26
Flow law „best choice 2“ of Paterson & Luan (1990) for dislocation creep in synthetically prepared wetquartzite for geological relevant strain rates of 10-14 and 10-16 s-1. Also depicted are differential stress estimatesfor quartz veins deformed during D
2s and D
4e, as determined with the Twiss (1977) quartz recrystallised
grainsize paleopiezometer. This suggests temperatures between 375 and 450 °C during D2s
and of ca. 330 °Cduring D
4e.
56
newly grown phengites and with U-Pb in titanite by Barnicoat et al. (1995). The fission track ages
in the units above and below the Zermatt Saas eclogites indicate cooling to below 300 - 250 °C
(Tagami & Dumitru, 1996; Wagner et al.,1997) at ca. 33 Ma and cooling to below ca. 125 °C
(Hodges, 1991) at ca. 12 Ma (Hurford et al., 1991).
The earliest exhumation from 2.6 to ca. 0.8 GPa occurred in at maximum 4 m.y. and the minimal
time for this exhumation can be < 1 m.y., because the ages for UHPM and greenschistfacies
Figure 27
Above: Cooling curve calculated for rocks of the Zermatt Saas-Fee zone, calculated with the published agesof Amato et al., (1999), Rubatto et al., (1998), Barnicoat et al., (1995) and Hurford et al., (1991), withclosure temperatures of Hodges (1991).
Below: Decompression curve for the rocks of Lago di Cignana calculated by combining the cooling curve ofthe Zermatt Saas-Fee zone and the PT-path of the rocks fom Lago di Cignana.
57
metamorphism are identical within the limits of error. This results in a minimum average
decompression rate of 450 MPa/m.y. (ca. 15 mm/year for a mean rock density of 3 gr/cm3) and a
maximum average decompression rate of > 1800 MPa/m.y. (> 54 mm/year). The second part of the
exhumation path requires decompression from 0.8 to 0.3 GPa in, at maximum 11 and, at minumum
7 m.y. and results in a minimum average decompression rate of 45 MPa/m.y. (1.3 mm/year) and a
maximum average decompression rate of 70 MPa/m.y. (2.1 mm/year) (Fig. 27).
The large change in decompression rate at pressures around 0.8 GPa, that coincides with a
reorientation of the stress field, indicates a change in the exhumation mechanism at a depth of ca.
25 km for the UHPM rocks of Lago di Cignana. The first exhumation mechanism brings the rocks
very fast (> 8 mm/year) from depths of ca. 90 km to depths of ca. 25 km and with a small decrease
in temperature and low differential stresses. The transition to a different exhumation mechanism
occurs at depths of around 25 km. At this depth, stages with high pore fluid pressures and low
differential stresses alternated with stages with low pore fluid pressures and differential stresses of
up to 40 MPa. The second exhumation mechanism brings the rocks slower (ca. 1-2 mm/year) from
depths of ca. 25 km to depths of ca. 10 km. During this part of the exhumation path the stress field
was very heterogeneous and periods with relatively high (40 to 125 MPa) differential stresses and
low pore fluid pressures alternated with stages with almost lithostatic pore fluid pressure and low
differential stress, as indicated by several generations of late albite veins. For the last part of the
exhumation path, from depths of ca. 10 km to surface conditions, this study provides no constraints.
58
7 Discussion and Exhumation concepts
In this chapter concepts for the exhumation of HPM rocks to normal crustal levels will be intro-
duced and compared to the constraints obtained for the first part of the exhumation path. On this
basis, a tentative scenario for the the two stage exhumation from 90 to ca. 10 km depth of the
UHPM rocks of Lago di Cignana will be proposed.
7.1 Exhumation theories
Before introducing exhumation concepts, some terms must be defined, because exhumation and
uplift are often used in a confusing way in the geological literature (e.g., Behrmann & Ratschbacher,
1989). In this study, exhumation means the vertical movement of rocks with respect to the Earth’s
surface, whereas uplift is vertical movement of rocks or surface with respect to the Geoid (England
& Molnar, 1990). In principle, there are three possible ways to bring rocks closer to the surface:
1. removal of the overburden by erosion,
2. removal of the overburden by extensional tectonic processes,
3. transport of the rocks to the surface in a flowing matrix.
These three exhumation principles are used in all exhumation concepts for HPM rocks and will
be discussed, where relevant, with concepts proposed for the Western Alps as illustration.
7.1.1 Exhumation through erosion
Erosion is an important exhumation process. It is, however, difficult to quantify the effect of
erosion on exhumation. Recent erosion rates are locally upto 13 mm/year, but over a larger area
maximum rates are usually not above 2 mm/year (Allen, 1997). Erosion rates are controlled by
surface elevation and by climate (rainfall) (England & Molnar, 1990; Koons, 1990). The last factor
is often ignored, but may influence erosion rates by one order of magnitude. Surface elevation is
dependent on surface uplift and a high erosion rate can only be maintained, when erosion rate is
approximately balanced by the rate of surface uplift. Therefore, postulation of exhumation through
erosion should always be accompanied by a hypothesis that explains the continuous surface uplift.
Older literature about exhumation in the Western Alps (e.g., Dal Piaz et al., 1971; Hsü, 1991;
Gillet et al., 1985; 1986), usually combines erosion with thrusting, to provide the continuous surface
uplift. These concepts rely heavily on a ca. 100 Ma old ultra high pressure metamorphism at depths
of 80 km or more and a return to midcrustal levels of these HPM rocks at ca. 40 Ma, to be able to
exhume these rocks with reasonable erosion rates. The 41 Ma age for UHPM at Lago di Cignana
(e.g., Amato et al., 1999) requires for the first part of the exhumation path a minimum decompression
rate of 15 mm/year. Therefore, exhumation through erosion is not feasible for the first part of the
exhumation path. It might, however, be important for the second part of the exhumation path with
decompression rates between 1 and 2.1 mm/year.
The concept of Chemenda et al. (1995) differs from the standard concepts, in that it combines
normal faulting with localised erosion and thrusting and only requires locally high erosion rates,
59
Figure 28
Schematic sketches illustrating the exhumation concept of Chemenda et al. (1995). See text for discussion.
but has not yet been applied to the Alps. Chemenda et al. (1995) assume subduction of the continental
crust. When the crust is subducted to depths of approx. 250 km, the buoyant upper crust ”delaminates”
from the weak lower crust and is thrusted on the foreland (Fig. 28A). Ongoing subduction will
further underthrust the continental crust and result in isostatic uplift of this thrust stack and
concomitant erosion. The delaminated upper crust is bounded by two relatively weak zones; the
upper weak zone is the former subduction channel and the lower weak zone is the weak lower crust
or the new subduction channel. The erosional unloading causes this buoyant segment of subducted
upper crust to move upward along the weak lower crust (Fig. 28B). This movement results in faster
movement along the lower thrust and produces normal movement and exhumation along the upper
surface of the slice. However, the low strength of the continental material at UHPM conditions
(Stöckhert & Renner, 1998) precludes the exhumation of large coherent slices of UHPM material
as suggested by Chemenda et al. (1995). Hence, this concept appears unrealistic.
7.1.2 Exhumation by extension tectonics
Exhumation by extension tectonics brings rocks with different metamorphic grade in contact or
will result in large changes of pressure and temperature over a small area. This situation is often
observed in orogens like the Alps (e.g., Selverstone, 1985; Ratschbacher et al, 1989; Blake &
Jayko, 1990), the Franciscan, (Harms et al., 1992), Betics, (Platt & Behrmann, 1986), the Aegean
(e.g., Jolivet et al., 1996; Thomson et al., 1998). This observation alone is not necessarily an indication
for extensional tectonics, because a similar configuration can be obtained by reimbrication of a
nappe pile, or by juxtaposition of rocks that experienced metamorphism at different times (e.g.,
Wheeler & Butler, 1994).
60
Figure 29
The plastic or Coulomb wedge in the concept of Platt(1986, 1987), with terms that describe the geometryof a steady state wedge (modified after Platt, 1993).
For extensional tectonics to take place one has to postulate a period of plate divergence or a
concept to explain extension in a convergent plate tectonic setting. Three concepts exist at present
to explain extension in a convergent plate tectonic setting:
1. the critical wedge (Platt, 1986; 1987).
2. lithospheric extension through gravitational collapse (e.g., Dewey, 1988; England & Houseman,
1989; Lister & Davis, 1989).
3. subduction roll back (e.g., Royden, 1993; Thomson et al., 1998).
These three concepts will be introduced first and concepts that postulate a period of divergence
will be discussed at the end of this section.
7.1.2.1 The critical wedge concept
This concept of Platt (1986; 1987) is based on the work of Chapple (1978), Davis et al. (1983),
and Dahlen et al. (1984) on thrust belts. Platt (1987; 1986) gives a general analysis of an orogenic
wedge with only one rheological assumption, viz. that in a orogenic wedge temperatures and fluid
content will be high enough for ductile flow to occur and to prevent build up of a high stress (e.g.,
Rutter, 1976; 1983; Etheridge, 1983; Atkinson, 1980). Assuming a wedge that has achieved a dynamic
equilibrium, the stable form of the wedge is described by:
τb = ρ g h α
with τb shear stress along the basal decollement, ρ density, g gravity, h thickness of the wedge and
α surface slope (Fig. 29). The significance of this formula is, that it allows to predict the reaction of
the wedge to external modification of its geometry.
If the values of α and/or h are decreased the basal traction exerted by τb (unchanged) is no longer
compensated by the gravity sliding (ρ g h α) and the wedge will shorten. If the wedge shortens αand h become larger and a stable configuration is restored. The values of α and h can be decreased
by erosion at the rear of the wedge or by frontal accretion.
If the values of α and/or h are increased the gravity sliding force (ρ g h α) becomes larger than
the drag force exerted by τb and the wedge will extend. Extension occurs by brittle normal faulting
close to the surface and by horizontal ductile extension at depth. This extension decreases the
values of α and/or h and a stable wedge configuration is restored. The values of α and h can be
increased by underplating at the rear of the wedge or by sedimentation on the wedge.
The combination of underplating below the wedge, with extension in the upper part of the wedge,
elegantly explains formation, preservation and exhumation of HPM rocks. Scenarios for the exhum-
61
Figure 30
Tectonic evolution of the Western Alps after Platt (1987). In the late Cretaceous (70 Ma) upper Penninic andSesia zone rocks have been subducted and experienced HP metamorphism, ongoing subduction of oceaniccrust keeps temperature in these rocks low. Continued underplating till early Oligocene (35 Ma) of lowerPenninic rocks resulted in oversteepening of the wedge and in extension in the overlying Austro-Alpine andupper Penninic rocks, allowing the HPM rocks to rise towards the surface.
ation of the HPM rocks of the Western Alps using this concept are given by Platt (1986) (Fig. 30)
and Polino et al. (1990).
7.1.2.2 The lithospheric extension concept
This is derived from the metamorphic core complex concept (e.g., Lister & Davis, 1989). It
suggests that metamorphic rocks are exhumed through lithospheric extension, involving low-angle
(listric) normal faults (e.g., Lister & Davis, 1989). The concept requires thickening of the continental
lithosphere and isostatic uplift of the surface. The vertical stress generated through this topographic
elevation is balanced by a horizontal stress through continuing convergence. Upsetting of this force
balance in favour of the vertical stress will result in horizontal extension with the development of
low-angle normal faults (e.g., England & Houseman, 1986). The force balance can be disturbed
through removal of a gravitational unstable high density lithospheric root (e.g., England & Houseman,
1989; Dewey, 1988). A variant of this concept is the slab breakoff concept of Davies & von
Blanckenburg (1995), that results in a localised disturbance of the force balance.
62
Figure 31
Schematic diagramm after Royden (1993) showing the response of the upper plate to different relativevelocity configurations of the subducting and overriding plate.
These concepts, however, cannot be used for the exhumation of the HPM rocks of the Western
Alps, because replacement of the relatively cold material at the base of the crust by relatively hot
asthenosphere results in a temperature increase at the base of the crust (e.g., Sonder et al., 1987;
Davies & von Blanckenburg, 1995). The HPM rocks in the Western Alps do, however, not reflect a
significant temperature increase prior or during exhumation (e.g., Schertl et al., 1991, this study).
7.1.2.3 The subduction zone roll back concept
This concept suggests that extension in the upper plate occurs when the subduction rate exceeds
the convergence rate of the plates (Fig. 31). The high subduction rate is thought to be caused by the
slab pull exerted by the sinking of heavy oceanic lithosphere in the mantle (Royden, 1993). Typical
features expected in this situation are, regional extension in the overriding plate, topographical low
mountains and a low erosion rate, low grade to no metamorphism, almost no involvement of
crystalline basement in thrusting and continuous flysch sedimentation (Royden, 1993; Thomson et
al., 1998). The Western Alps clearly do not display these features and therefore, this concept cannot
be used to explain the exhumation of HPM rocks in the Western Alps.
7.1.2.4 Concepts that require a period of divergence
Several authors have attributed exhumation of HPM rocks in the Western Alps through extension,
to a period of divergence between the European and African plates (e.g., Butler, 1986; Ballevre &
Merle, 1993). These scenarios require a middle to late Cretaceous (100- 80 Ma) HP metamorphism
and a period of extension sometime between 80 and 60 Ma (e.g., Butler, 1986; Ballevre & Merle,
63
Figure 32
Simplified cross section illustrating successivepositions and trajectories of identifiable points inthe dynamic scaled wedge model of Cowan &Silling (1978).
1993) to partly exhume these HPM rocks. The newer radiometric ages between 70 and 35 Ma (e.g.,
Inger et al., 1996; Gebauer et al., 1997) for the UHP metamorphism leave, however, not enough
time for a period of plate divergence to exhume HPM rocks.
7.1.3 Upflow concepts
Exhumation by upflow requires the high pressure metamorphic rocks to be embedded in a low
viscosity matrix (Cloos, 1982; Emerman & Turcotte, 1983; Platt, 1993). The HPM rocks themselves
cannot have a low viscosity, because the intense deformation that low viscous rock would experience
during exhumation, would probably result in complete reequilibration of the mineral paragenesis
(e.g., Rutter & Brodie, 1985). Two endmember flow processes can be postulated:
· Buoyant upflow of material driven by density contrasts.
· Upflow of material driven by forced flow.
The first process requires that the high pressure rocks and their matrix have a relatively low bulk
density compared to the surrounding rocks. It was proposed by England & Holland (1979) to exhume
eclogitic blocks in a carbonate rich matrix and by Takasu (1989) to exhume blocks of HPM rocks in
a serpentinite matrix. This mechanism cannot be used to exhume continuous large sections of HPM
rocks.
The second process is based on the corner flow concept of Cowan & Silling (1978), who used a
dynamic scaled model to study the development of an accretionary prism. They found the expected
underthrusting at the toe of the prism (e.g., Karig, 1974), but also that appreciable amounts of
sediments were carried below the wedge and were accreted there, and that material began to flow
upward from the deepest part of the accretionary prism (Fig. 32). If the rocks in an accretionary
prism behave as a viscous fluid, this forced flow could bring material from the deepest part of the
accretionary prism to shallower levels in the wedge. This can be considered as an initial stage in the
development of an accretionary wedge that, with ongoing subduction and accretion, will develop in
a critical tapered wedge (e.g., Platt, 1986; 1987).
The subduction channel concept is a modification of the corner flow model for a narrowing
channel and was proposed by Cloos (1982) to explain observations in the Franciscan subduction
complex. It was further developed (Shreve & Cloos, 1986; Cloos & Shreve, 1988 a; 1988b) to
describe the processes of prism accretion, sediment subduction and melange formation.
The concept assumes that subducting sediments deform approximately as a viscous fluid, when
they are dragged by the descending plate beneath the overriding plate and the accretionary prism.
This layer of deforming sediments forms a shear zone, called the subduction channel. The subduction
64
channel has a certain width, that depends on the velocity and angle of subduction, as well as on
surface slope and material in the hanging wall. The width of the subduction channel determines its
capacity, the amount of sediment that can be transported downwards along the subduction channel.
If enough sediment is available at the inlet of the subduction channel, it will be filled to capacity.
Where the dip of the descending plate changes or where the rear of an accretionary wedge abuts
basement rock the subduction channel changes its width (control point). At the control point the
capacity of the subduction channel decreases. If the subduction channel was filled to capacity, not
all incoming material can pass the control point. Material will accumulate at the control point and
the channel thickens. When this happens, the upward directed force due the adverse pressure gradient
and the buoyancy of the sediment, becomes larger as the downward directed force due to shearing
and a zone of reverse flow or upflow will develop. The material that flows up consists of low
viscous metasedimentary rocks that are intensely deformed. In this low viscous matrix, small blocks
of high viscous material that have retained their HPM imprint, that is almost completely wiped out
in the low viscous material, can be included and brought to shallow crustal levels (concept of
Cloos, 1982). The flowing material exerts a viscous drag (shear stress) on the walls of the channel
(Shreve & Cloos, 1986). Without reverse flow this viscous drag is downward directed for the hanging
wall and can result in incorporation of hanging wall material in the subduction channel (subduction
erosion). In a zone of reverse flow the viscous drag on the hanging wall is upward directed and
could move larger sheets of previously accreted (HPM) rocks to the surface (Cloos & Shreve,
1988a).
The weak point of the subduction channel concept is the nature and the deformation mechanism
of the low viscous material in the channel. In the quantitative subduction channel models of Shreve
& Cloos (1986), water saturated sediment is taken as the low viscosity material. This may be valid
for the upper few kilometres of the subduction channel, but at depths of 90 km or more, necessary
to exhume UHPM rocks with this concept, a different yet unspecified material and deformation
mechanism operating in this material are required.
Forced flow concepts were proposed to explain the exhumation of (U)HPM rocks in the Western
Alps by Fry & Barnicoat (1987) for the Zermatt Saas zone and by Michard et al. (1993) for the Dora
Maira Massif. The interpretation of Michard et al. (1993) postulates, the oldest HP metamorphism
for ca. 100 Ma old and a period of ca. 60 m.y. of subduction, but can be readily adapted to younger
HP metamorphism and a shorter subduction time span.
These concepts (Fig. 33) assume onset of subduction of oceanic crust (rocks of the Zermatt Saas
zone) with offscraping of parts of the southern continent (Sesia zone). To accrete parts of the sub-
ducting oceanic crust to the overlying plate, Fry & Barnicoat (1987) suggest geometric irregularities
along the subducting slab or rheological irregularities in the slab, to cause detachment from the
subducting slab. With the onset of continental collision, fragments of the thinned continental margin
(Monte Rosa, Dora Maira) are also subducted. The density contrast between the deeply subducted
continental rocks (3.09 gr/cm3) and the surrounding mantle rocks (3.3 gr/cm3) adds buoyant uprise
to the forces that can cause detachment from the subducting slab and accretion to the overlying
65
plate (Michard et al., 1993). Exhumation occurs by forced return flow in a narrowing subduction
channel driven by continuing continental collision. During exhumation UHPM rocks become mixed
with rocks that experienced HP metamorphism at lower pressures (Michard et al., 1993). After
forced flow exhumation to mid crustal levels, further exhumation was achieved by other mechanisms.
7.2 Evaluation of published exhumation scenarios for exhumation fromdepths of approx. 90 km to 30 km
Only the upflow (e.g., Fry & Barnicoat, 1987; Michard et al., 1993) and the critical wedge (Platt,
1986; 1987) concepts, stay within the limits posed by the PTD-path of this study and geochronological
data (e.g., Amato et al., 1999; Barnicoat et al., 1995). Essential for a scenario that uses extensional
tectonics to explain the exhumation of HPM rocks, is the identification of extensional structures
that were active during the exhumation of the HPM rocks. In the area around Valtournanche the
only described extensional structure is the ”Combin fault”, that is considered part of the Mischabel
backfold/backthrust system (e.g., Wheeler & Butler, 1993; Barnicoat et al., 1995). On this fault
system extensional activity under lower greenschist facies PT-conditions took place at ca. 40 Ma
(Barnicoat et al., 1995), post-dating the greenschist facies overprint of the HPM rocks in the Zermatt
area (Barnicoat et al., 1995). Therefore, this structure was active as the HPM rocks of the Zermatt
Saas zone were already at a midcrustal level. In its present configuration this fault cannot be
responsible for the exhumation of the HPM rocks. As long as from the Northern part of the Western
Alps no extensional structures are described, that predate the greenschist facies overprint of the
HPM rocks, the critical wedge model of Platt (1986; 1987) is not applicable to the exhumation of
the UHPM rocks of Lago di Cignana.
The forced flow concept requires that during exhumation, the UHPM rocks are embedded in a
matrix of low viscous material that precludes the buildup of higher differential stresses at depth in
the subduction channel (Shreve & Cloos, 1986). Low differential stresses at depth in subduction
zones are inferred from geological evidence (e.g., Stöckhert et al., 1997; 1999) and from geophysical
reasoning (e.g., Pacheco et al., 1993; Wang et al., 1995). The nature of the material in the subduction
channel and the deformation processes operating in this material are unknown (e.g., Platt, 1993). At
Lago di Cignana the serpentinites, that occur in large volumes in the Zermatt Saas zone and the
locally preserved HP metasedimentary rocks of the Zermatt Saas zone, could have been these low
viscosity rocks. The metasedimentary rocks of the Zermatt Saas zone consist mainly of quartz-
phengite-garnet schists, that locally have preserved their HPM imprint as inclusions in rigid minerals
(e.g., Reinecke, 1995). During the later exhumation, however, microstructures in the rock were
completely modified and inferences about deformation processes during UHPM conditions can no
longer be made. The same holds for the serpentinites that have preserved deformation structures
(e.g., Vogler, 1987), but because of the PT insensitive mineral paragenesis, these cannot be unequivo-
cally attributed to specific segments of the PT-path.
A subduction channel is characterised by high strain rates at relatively low temperatures and the
deformation process operating should preclude high differential stresses. Most geologic materials
66
require for deformation by dislocation creep at these conditions (e.g., Carter & Tsenn, 1986),
differential stresses that are much too high for the postulated viscosities (10-17-10-18 Pa s, Shreve &
Cloos, 1986). Altough most minerals in crustal rocks deforming by dislocation creep are weaker
then expected (Stöckhert & Renner, 1998), they are still not weak enough. Diffusional flow
deformation mechanisms can achieve deformation at low differential stress, but at the relatively
low temperature conditions only diffusion precipitation creep in the presence of a fluid phase is a
feasible mechanism. Stöckhert et al. (1999) estimated for the HPM phyllite quarzite unit of Crete,
which deformed mainly by dissolution precipitation creep (Schwarz & Stöckhert, 1996), a bulk vis-
cosity of ca. 10–19 Pa s, still a factor 10 higher as the viscosity in normal subduction channel models
(e.g., Shreve & Cloos, 1986), although Mancktelow (1995) used viscosities between 10-17-10-19 Pa
s to model tectonic overpressures in a subduction channel setting. A deformation process, similar to
liquid phase sintering is considered feasible to explain the inferred low strenghth of UHPM rocks
by Stöckhert & Renner (1998), but microstructural evidence in geologic materials for this process
has not yet been presented.
Although the nature of the material and the deformation mechanism operating in this material in
the subduction channel are not unequivocally identified, a forced flow subduction channel concept
can be applied to explain the exhumation from 90 km to 25 km depth of the UHPM rocks of Lago
di Cignana. A forced flow subduction channel scenario for the UHPM rocks of Lago di Cignana
will be presented and discussed in the next section.
7.3 Scenario for exhumation from ca. 90 km to ca. 25 km depth
In a forced flow subduction channel scenario for the UHPM rocks of Lago di Cignana, several
points must be discussed. A short description of the scenario is given and the numbered points will
be discussed.
The oceanic crust at Lago di Cignana was subducted down to depths of ca. 90 km. Deformation
during subduction was concentrated in the weak subduction channel above the oceanic crust (Fig. 33).
At this depth, a part of the oceanic crust was detached from the downgoing slab (1) and incorporated
in the subduction channel. Assumming a control point in ca. 90 km depth (2) and a subduction
channel filled over the capacity of the control point (3), the oceanic slab was transported upward
along the subduction channel (4) through a forced return flow in a low viscous material. Where the
drag force of the hanging wall became larger than the driving force of the return flow, the material
was either accreted to the hanging wall (5) or the material flowed down again.
Point (1), detachment of the downgoing plate, requires localised deformation of the downgoing
slab at or close to maximum PT-conditions. At first, this seems to contradict the subduction channel
model, because deformation is assummed to be concentrated in the weak material of the subduction
channel. The record of the eclogites at Lago di Cignana, however, shows at maximum PT-conditions
deformation of the rock by dislocation creep of omphacite. At these conditions jadeite may flow at
differential stresses of a few MPa (Stöckhert & Renner, 1998) and omphacite probably flows at
somewhat higher stresses. This is a similar magnitude as the differential stress that in subduction
67
Figure 33
A tentative schematic sketch illustrating some important points of the proposed exhumation scenario for theUHPM rocks of Lago di Cignana.
The upper sketches show the configuration at UHPM conditions before exhumation. In the right sketch thesituation in the subduction channel is shown. The velocity distribution in the subduction channel is qualitativelyonly and adapted from England & Holland (1979). ∆-velocity is the difference between the velocity of thedowngoing plate and the material in the subduction channel close to the plate-channel interface and a measurefor the magnitude of the viscous drag, that is assummed to have caused deformation by dislocation creep inomphacite. Localisation of deformation results in the development of a shearzone in the downgoing plateand in detachment of UHP metamorphic rocks from this plate.
The lower sketches show the configuration at the onset of exhumation. The right sketch shows the situationin the subduction channel at the control point. The width of the subduction channel at the control point,determines the amount of material that can pass. In the sketch, all material below the dashed line can passthe control point and is subducted. Material between the dashed and dotted lines is downflowing material inthe subduction channel, that cannot pass the control point and will follow a path given by the arrow. Betweendotted line and the mantle wedge of the overlying plate a zone of reverse flow occurs, that allows forexhumation of material.
channel models (e.g., Shreve & Cloos, 1986) is produced by viscous drag of the flowing material
on the walls of the channel. The magnitude of the viscous drag in these models depends on the
vicosity of the material in the subduction channel, the channel width, the velocity of the downgoing
plate, and on the change in hydraulic potential and channel width in direction of subduction (Shreve
& Cloos, 1986). Most of these parameters are only approximately known, but varying the parameters
within reasonable limits (factor 10 higher or lower viscosities, plate velocities between 1 and
10 cm/year, subduction channel thickness between 300-5000 m) gives similar magnitudes for the
differential stress (e.g., Shreve & Cloos, 1986; Mancktelow, 1995). This suggests that at maximum
PT-conditions the eclogites at Lago di Cignana were deformed, because of the viscous drag of the
68
material flowing in the subduction channel on the downgoing plate. Detachment of the rocks from
the downgoing plate requires localisation of the deformation in a shear zone below these rocks. The
heterogeneous deformation at UHPM conditions at Lago di Cignana (this study) is also observed at
other UHPM localities (e.g., Michard et al., 1993; 1995), therefore, localisation of deformation has
to be expected. Because the shear zone rocks could not be identified, nothing can be said about
deformation mechanisms in the shear zone. Possible mechanisms are dissolution precipitation creep
as inferred from microstructures by Stöckhert et al., (1997) for rocks from the Tauern Window
deformed under HPM conditions or grain size sensitive flow that, however, would require an extreme
grainsize reduction in the shear zone (e.g., Walker et al., 1990).
Point (2) concerns the control point in ca. 90 km depth. At the control point, the width of the
subduction channel changes. Cloos & Shreve (1988a; 1988b) propose a change of material in the
overlying plate (e.g. accretionary wedge to crystalline basement) or a change of dip in the downgoing
plate as possible causes for the development of a control point. The only possible material change
in the overlying plate in this depth range is the crust mantle transition. Present day crustal thickness
in mountain belts, however, rarely exceeds 70 km (e.g., Tanimoto, 1995) and a crustal thickness of
90 km implies extreme thickening of the overlying plate and this seems improbable, because large
scale continental collision is considered to occur later (e.g., Steck & Hunziker, 1994). The alternative
is, that the downgoing plate changes its dip at ca. 90 km depth. According to Jarrard (1986), the
greatest change in dip in the downgoing plates in present day subduction zones occurs between
depths of 60 and 100 km. From his data, it is not clear which parameter influence the depth of the
dip change, therefore, it cannot be ascertained whether or not the plate tectonic configuration of the
Western Alps at ca. 44 Ma could produce a change of dip in the downgoing plate at approx. 90 km
depth. It is, however, the most probable explanation for the existence of a control point at approx.
90 km depth.
Point (3) is concerned with the amount of material in the subduction channel above the control
point. If this amount is smaller than the capacity at the control point, return flow and exhumation
cannot occurr. The amount of material in the subduction channel cannot be estimated. The schistes
lustres or Bundnerschiefer (calcschists and greenschists of the Combin zone), however, are interpreted
to have formed in an accretionary wedge (e.g., Deville et al., 1992). The formation of an accretionary
wedge requires a certain amount of sediment on the downgoing plate (e.g., Pavlis & Bruhn, 1983).
This does not prove that parts of this sediments were subducted to great depths, but it shows at least
that at shallower depths enough material was available to fill the subduction channel to capacity
(e.g., Cloos & Shreve, 1988b).
Point (4), the upward transport along the subduction channel in a matrix of low viscous rocks,
explains the almost isothermal decompression with slight cooling and no notable deformation, as
recorded in the UHPM rocks of Lago di Cignana, because thermal models for subduction zones
(e.g., Peacock, 1987; 1996), show that isotherms are subparallel to the subduction channel. These
models, however, cannot be quantitatively applied, because they do not account for the return flow
of material. Qualitatively the return flow of hotter material from below, will result in higher
69
temperatures at given depth as expected from thermal modelling without return flow. The magnitude
of this temperature rise will depend on the velocity and the amount of material flowing back. The
presence of cold material below the zone of return flow, will qualitatively result in cooling of this
material during exhumation, as for example recorded by the rocks of Lago di Cignana.
Point (5) is the accretion of the upward transported slice of UHPM material to the hanging wall.
The material in the hanging wall has a non-negligible strength and can transmit higher stresses.
This results in deformation of the accreted rock during further exhumation as described for example
by Stöckhert et al. (1997) for HPM rocks of the Tauern window. The change in decompression rate
in the UHPM rocks of Lago di Cignana that coincides with a change in orientation of the stress field
and an increase in maximum differential stress, suggests that the rocks became accreted to the
overlying plate at temperatures of ca. 500 °C and a depth of ca. 25 km.
7.4 The scenario for the later exhumation from depths of ca. 25 km to thesurface
This part of the exhumation path is also divided in two parts, exhumation from depths of ca.
25 km to depths of ca. 10 km and from there towards the surface. For this last part, this study offers
no constraints and it will not be discussed.
A comparison with published data for the Northwestern Alps (e.g., Mazurek, 1986; Ellis et al.,
1989; Wust & Silverberg, 1989; Sartori, 1990; Wheeler & Butler, 1993; Barnicoat et al., 1995)
allows the integration of the data of Lago di Cignana in the regional framework and the development
of an exhumation scenario for this part of the exhumation path. Formation of the greenschists (D3e
)
in the metabasic and D2s
in the metasedimentary rocks are tentatively correlated with top to the NW
movement of several regional faults under greenschist facies conditions (e.g., Ellis et al., 1989;
Barnicoat et al., 1995). This deformation is related to the onset of nappe stacking due to SE directed
underthrusting of the European continental crust below the Adriatic or Apulian continental crust
(e.g., Butler, 1986; Steck & Hunziker, 1994). In this thrusting event that occurred between 43 Ma
(age of static greenschist facies overprint, Barnicoat et al., 1995) and 40 Ma (age of SE directed
fault zone, Barnicoat et al., 1995), the rocks of the Zermatt Saas zone were juxtaposed between the
rocks of the Monte Rosa unit and the rocks of the Combin zone (Fig. 34A). The thrusts bounding
the Zermatt Saas zone then became inactive and new thrusts developed further north.
The localised D3s
and D4e
deformation at Lago di Cignana is tentatively correlated with top to the
SE movement. This late top to the SE movement is traditionally interpreted as backthrusting or
backfolding (e.g., Steck, 1990; Sartori, 1987), because it often stacks external units on top of internal
units. Recently, some late structures with top to the SE and E displacement have been interpreted as
hinterland dipping extensional shearzones (e.g., Phillipot, 1990; Wheeler & Butler, 1993). The
contradictionary interpretations for these shearzones, result from possible reorientation of these
structures through later deformation (Wheeler & Butler, 1993). If these shears are interpreted as
backthrusts (e.g., Steck, 1994), the main exhumation mechanism must have been erosion, which
would require relative high erosion rates (Allen, 1997) of between 2 and 3 mm/year. Therefore, I
70
Figure 34
A tentative schematic sketch illustrating the proposed exhumation scenario for the UHPM rocks of Lago diCignana from depths of 25 km to ca. 10 km.
The upper sketches show the configuration just after breakoff of the oceanic crustal slab (see text fordiscussion). The crust at the former subduction zone was already thickened by thrusting and is furtherthickened by buoyant uprise of deeply subducted slabs of continental material along former thrusts. Theright sketch shows, that at this stage the already exhumed UHPM rocks in the subduction channel material,become juxtaposed between underthrusted continental crust (Monte Rosa unit) and serpentinites and materialfrom the accretionary wedge (Combin zone).
The lower sketches shows the proposed exhumation scenario. See text for discussion. During extensionalshearing, favourably orientated thrust were reactivated as low angle normal faults. Where thrusts were notfavourably orientated they were cut off by low angle normal faults.
prefer to interpret most of theses shears as extensional shears. A tentative interpretation of these top
to the SE shears as extensional shearzones in combination with top to the NW thrusting after the
interpretation of Wheeler & Butler (1993) is shown in figure 34B.
The described features can be explained in a scenario that combines features from the critical
wedge concept of Platt (1986; 1987) and the slab breakoff concept of von Blankenburg & Davies
(1995). Prior to subduction of buoyant continental crust, slab pull of the downgoing slab is the
force, that mainly determines the configuration of a subduction zone (e.g., Royden, 1993). With the
onset of subduction of continental crust, buoyancy disturbs the force balance and will lead to a
changed stress situation in the downgoing slab. Ultimately, the heavy oceanic slab will break off
(Davies & von Blanckenburg, 1995). Because further subduction of buoyant continental crust is not
possible, the ongoing convergence between the plates must be accommodated otherwise. The inter-
face between continental crust (quartzo-feldspatic rocks) and mantle (olivine rocks) is, due to the
compositional change, also a rheologic interface between relatively weak crustal rocks and strong
71
mantle rocks (e.g., Kusznir & Park, 1986). Therefore, crust and mantle can decouple along this
interface (e.g., van den Beukel, 1992). With ongoing convergence the mantle part of the lithosphere
will be subducted and convergence in the crust is taken up by thrusting (e.g., Laubscher, 1990). At
the same time, however, already subducted continental crust, rises along the subduction zone, and
this results in extreme thickening of the crust and in reorientation of the older thrust surfaces, which
are no longer favourably orientated for thrusting. Further shortening of the crust is taken up in new
thrust zones that developed further to the North. The thickening of the continental crust results in
isostatic uplift of the surface. The vertical stress generated by this uplift is, however, no longer
balanced by a horizontal stress and the result is horizontal extension with the development of low-
angle normal faults (e.g., von Blanckenburg & Davies, 1994).
For the exhumation from a depth of ca. 10 km as the rocks had a temperature close to 300 °C to
surface conditions, this study offers no constraints. Discontinuous uplift of discrete blocks with
different erosion rates caused by dextral transpression is discussed as possibility in the literature
(e.g., Laubscher, 1990; Hurford et al., 1991; Steck & Hunziker, 1994; Escher et al., 1997; Marchant
& Stampfli, 1997).
72
8 Conclusions
The PTD- path for the exhumation of UHPM rocks of Lago di Cignana can be partly reconstructed
by combining petrological and (micro)structural observations. This PTD-path combined with
published radiometric ages, divides the exhumation history in two parts. The first part of the
exhumation is very fast, almost isothermal decompression from depths of approx. 90 km to depths
of approx. 25 km, with differential stresses too low to drive deformation in the metabasic rocks. At
around 500 °C and 0.8 GPa, the slope of the PT-path as well as the orientation of the stress field
changes. The second part of the exhumation is slower, with pronounced cooling during uplift from
depths of approx. 25 km to depths of approx. 10 km and deformation at higher differential stresses.
The exhumation mechanism for this first part of the exhumation path that obeys most constraints
imposed by the PTDt-path is a modified forced flow/subduction channel model, as proposed by
Shreve & Cloos (1986) and Cloos & Shreve (1988 a; 1988b). For the second part of the exhumation
path a modified slab break off model (e.g., Davies & von Blanckenburg, 1995) is feasible.
For the UHPM rocks of Lago di Cignana following scenario is considered. The oceanic rocks
were subducted to depths of about 90 km and metamorphosed at pressures of 2.6-2.8 GPa and a
temperature of ca. 600 °C. Under these conditions, the eclogites were heterogeneously deformed
with differential stresses, high enough to drive deformation by dislocation creep in omphacite. This
deformation is tentatively attributed to the viscous drag between the material flowing in the subduction
channel and the foot wall. At these conditions the material must have been transferred from the
downgoing plate to the subduction channel, possibly by further localisation of deformation in a
shear zone that is no longer preserved. Subsequently, differential stress was too low to drive further
deformation in the metabasic rocks. Exhumation of the slice of UHP material to depths of approx.
25 km is attributed to a forced return flow in a matrix of weak material. For the forced return flow
to occur a control point at approx. 90 km depth has to be assummed.
Accretion of the slice of UHP material to the hanging wall occured at a depth of approx. 25 km
and a temperature of ca. 500 °C. Accretion was closely followed by wholesale continent-continent
collision. At this stage the subduction channel became inactive and the Zermatt Saas zone probably
became a coherent unit, composed of several subunits that had followed slightly different PT-paths
before (e.g., Ellis et al., 1989; Barnicoat & Fry, 1986; Meyer, 1983; Reinecke, 1991; 1995; this
study). After accretion, higher stresses were possible, resulting in development of the greenschists
in the metabasic rocks and intensive deformation D2s in the metasedimentary rocks. This deformation
is correlated with NW directed overthrusting under greenschistfacies conditions between 43 and
40 Ma (Barnicoat et al., 1995).
Exhumation of the UHPM rocks from Lago di Cignana from depths of ca. 25 km to depths of ca.
10 km between 40 and 33 Ma under lower greenschist facies conditions is attributed to hinterland-
directed shears (e.g., Steck & Hunziker, 1994; Wheeler & Butler, 1993), that are tentatively correlated
with the late localised deformation in the rocks of Lago di Cignana.
73
An important objekt for further study are the deformation mechanisms in the weak material in
the subduction channel. Stöckhert & Renner (1998) propose a mechanism similar to liquid phase
sintering in the presence of a highly saline fluid phase or a melt, as possible deformation mechanism,
but also state that microstructures indicative for this process have not been observed and that
experimental evidence on geologic materials for this mechanism is also not available.
Another subject is the regional study of structures, active under greenschist facies conditions
and with top to the SE movement. These structures are traditionally interpreted as backthrusts (e.g.,
Steck & Hunziker, 1994), but must be reeinterpreted as rotated extensional shear zones (e.g., Wheeler
& Butler, 1993) to validate the postulated model for exhumation from 25 to 10 km depth.
74
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Lebenslauf
Name: Sebastiaan Nicolaas Gerardus Cornelis van der Klauw
Geburtsdatum: 28. September 1966
Geburtsort: Gouda
Staatsangehörigkeit: Niederländisch
Familienstand: Ledig
Akademischer Werdegang
08.78 - 05.84 St. Willibrord Gymnasium in Deurne
05.84 Abitur
09.84 - 11.90 Geologiestudium an der Rijksuniversiteit Utrecht
30.11.90 Examen zum Diplom-Geologen
04.91 - 03.94 Wissenschaftlicher Mitarbeiter am Institut für Geologie der Ruhr-Universität
Bochum (Promotionsstelle)
04.94 - 09.94 Wissenschaftlicher Hilfskraft am Institut für Geologie der Ruhr-Universität
Bochum
04.96 - Wissenschaftlicher Mitarbeiter am Institut für Geowissenschaften des
Friedrich-Schiller-Universität Jena
A-1Appendix A methods
APPENDIX A Methods
A1 Sampling
Mapping in the area around Lago di Cignana (unpublished Diplomkartierung, Habermann, 1992,
Wagner-Zweigel, 1993) showed that the UHPM rocks are extremely well exposed on the southern
shore of the lake. All of the about 120 samples (Table C1) for this study were taken from this well
exposed area (Fig. A1). Due to these good exposures the lower PT-overprint could be correlated
with m- to dm- scale structures in the metabasic rocks and several series of samples were taken to
investigate the relation between structures and lower PT-overprint. Due to the very heterogeneous
bulk rock composition of the metasedimentary rocks, such a correlation was not possible for that
material and sampling was concentrated on small scale folds and veins.
A2 Preparation
From all samples thin sections were made to study with a polarising microscope; usually one
thin section was made approximately parallel to the stretching lineation and normal to the foliation,
and another thin section normal to the stretching lineation and the foliation. In samples with no
apparent stretching lineation a thin section normal to the foliation was cut. From vein samples, thin
sections with both vein and host rock were made.
Figure A1
Distribution of the different lithologies at the southern shore of Lago di Cignana.
Appendix A methodsA-2
A small part of most samples was finely grounded for investigation with X-ray diffractometry to
distinguish between paragonitic and phengitic white mica. From selected samples thin sections
polished on both sides and without cover slip were made for investigation with the electron
microprobe (EMP, Table C3 -C22), Scanning electron microscope (SEM) and cathodoluminesence
microscope (CL). From several vein samples, 200 µm thick sections were made for the investigation
of fluid inclusions by microthermometry. After study of the thin sections a series of seven samples
from fresh (group 1) to completely overprinted (group 4) eclogite was selected for X-ray fluorescence
(XRF) whole rock chemistry (Table C2).
A3 Analytical methods
In order to determine the phases and their compositions in the metabasic and the metasedimentary
rocks as well as to determine the relative volumes and shape preferred orientations of some of these
phases, and for fluid inclusion studies, the following analytical methods were used:
· polarising microscopy
· powder X-ray diffractometry
· electron microprobe analysis
· X-ray fluorescence spectroscopy,
· scanning electron microscopy,
· cathodoluminesence microscopy
· image analysis
· microthermometry
A3.1 Polarising microscopy
A polarising microscope allows determination of phases present in a thin section and also to
establish the spatial relations between these phases. Furthermore, it allows observation of deformation
microstructures for the different phases.
Polarising microscopes of Zeiss, Leitz and Olympus were used in this study. Important
observations were photographed with an Olympus OM 10 camera mounted on an Olympus polarising
microscope. A Leitz microscope with long working distance objectives was used for Universal
stage measurements.
A3.2 powder X- ray diffraction
For powder X-ray diffraction a representative part of the sample is finely grounded (1- 10 µm),
to obtain a large amount of grains of the different minerals, so that it is likely that all grain orientations
for all minerals are present. The powdered specimen is brought into a beam of monochromatic
parallel X-rays and slowly rotated. The incident X-rays will be scattered by the atomic planes in the
specimen. These diffracted X-rays will usually interfere destructively with each other and no signal
will be produced. For specific incedent angles however, the spacing of the atomic planes is such,
A-3Appendix A methods
that the diffracted X-rays interfere positively with each other and a signal can be recorded. This is
Braggs law, in formula
n λ = 2 d sinθwith λ wavelength of the X-rays, d distance between the atomic planes, θ incident angle of the X-
ray beam and n an integer (usually taken as 1). When the wavelength of the X-rays is known and the
different incident angles at which a signal occurred are recorded, the d values for the unknown
specimen may be calculated. These d-values together with the intensities of the signals are material
specific. By comparing the recorded values with reference values in the A.S.T.M. powder data file,
the unknown material(s) may be identified. More information on X-ray diffraction may be found in
Zussmann (1977) and Putnis (1992).
Philips X-ray diffractometers at the “Institut für Mineralogie” and the “ Institut für Geologie” at the
Ruhr-University Bochum were used in this study. All scans were made with Cu Kα X-rays over a
range of θ angles from 5° to 50° with steps of 0.1° and 2 seconds counting time.
A3.3 Electron microprobe and X-ray fluorescence spectroscopy
Electron microprobe and X-ray fluorescence use the same principles, but different excitating
media to produce X-rays. When an electron with sufficient energy strikes matter, X-rays are produced.
X-rays may also be produced, when these primary X-rays strike matter. These secondary X-rays are
called fluorescence. The X-ray spectrum produced by incedent electrons may be divided in a
continuous spectrum (background) and a characteristic spectrum. Excitation by primary X-rays
differs from excitation by electrons in that no continuous spectrum is formed. The characteristic
spectrum is produced when the incident electrons remove an electron from the inner shells of an
atom. The X-ray photons that are produced when outer electrons fall back have an energy that is
characteristic for a particular element. The energies (or wavelengths) and intensities of the excited
X-rays are measured in a spectrometer. From the measured wavelengths the different elements that
are present in the material can be inferred. By comparing the intensities of the X-rays with intensities
obtained from materials with known composition, the absolute amounts of the different elements
may be obtained. More about these techniques may be found in Zussman (1977), Smith (1976), and
Reed (1996).
A3.3.1 The electron microprobe (EMP)
The EMP uses a beam of electrons to produce characteristic X-rays. This beam is focused using
magnetic lenses, without loss of intensity. Therefore, the electron microprobe can be used to obtain
spot analyses (1 µm diameter) from a material. However due to the superposition of continuous and
characteristic X-ray spectra the accuracy of the EMP is not as high as the accuracy of the XRF. To
prevent the build up of heat and electrical charge on the specimen, samples must be coated with a
conductive thin carbon or gold film. In this study the electron microprobe was used to measure the
composition of minerals in thin section in specific microstructural settings.
A Camebax microprobe in WDS mode at the “Bereich Zentrale Elektronen-Mikrosonde” of the
Ruhr-University Bochum was used. Operating conditions were 15 kV accelerating voltage and a
Appendix A methodsA-4
14 nA beam current for most minerals. For albite and mica the beam was slightly defocused and a
12 nA beam current was used to yield better results for the alkali elements. A 12 nA beam current
was also used for carbonates. Natural and synthetic minerals were used as standards and the PAP
(Pouchou & Pichoir, 1984) correction procedure was used.
A3.3.2 X-ray fluorescence spectroscopy (XRF)
X-ray fluorescence spectroscopy uses X-rays to produce characteristic X-rays. X-rays cannot be
focused without loss of intensity. Therefore, XRF gives information about the composition of a
larger area. To ensure that this area is homogeneous and representative of the sample, part of the
sample is dissolved in lithium borate glass and the glass is analysed or the sample is finely grounded
and a pressed powder tablet is analysed. These analyses give information about the bulk composition
of a sample. A more detailed description of the XRF technique can be found in Zussmann (1977).
A Philips PW 1400 X-ray fluoresence spectrometer at the “Institut für Mineralogie” at the Ruhr
university Bochum was used for XRF-analyses.
A3.4 Scanning electron microscopy (SEM)
When electrons with sufficient energy strike matter, not only X-rays are produced but also other
signals. In the SEM, the signals provided by the backscattered electrons and the secondary electrons
are used. Secondary electrons are the electrons that are removed from the electron shells around an
atom by the incident electrons. Their energy ranges from 0 to about 50 eV, partly depending on the
material. Backscattered electrons are electrons of the incident beam that are rebounded in the
specimen. They have generally higher energies than the secondary electrons, ranging between zero
and the energy of the incident electrons. Their intensity is related to the mean atomic number of the
material under the beam. Both signals can be detected when they leave the surface of the specimen
and give information about the surface topography of the sample and some qualitative information
about the material under the beam. When the sample has a smooth surface the SEM can be used
much the same way as a normal light optical microscope, with the advantages that the range of
possible magnification is larger and that SEM has a better depth of focus. More information about
this technique can be found in Reed (1996).
In this study SEM was used to provide images of the symplectitic intergrowths in the metabasic
rocks. SEM images were made with a Cambridge Stereoscan 250 Mk III at the “Bereich Zentrales
Rasterelektronenmikroskop” of the Ruhr University Bochum. Accelerating voltage for the
electronbeam varied between 15 and 20 kV. SEM images were made with assistance of Dr. Neuser.
A3.5 Cathodoluminescence (CL)
Another signal that may be emitted when a material is struck by electrons is light in the visible
wavelength area. This may be an intrinsic property of the material under the beam, for example in
scheelite or benthonite, but may also be due to the presence of trace impurities in the mineral e.g.,
Mn and REE in calcite or defects in crystal structure e.g., quartz (Marshall, 1988).
In this study CL was used to image the zoning of calcite around dolomite, that could not be seen
A-5Appendix A methods
in polarisation microscope. A cathodoluminescence microscope HC1-LM at the “Institut für
Geowissenschaften Ruhr Universität Bochum”, developed by Dr. Neuser (Neuser, 1995) was used
in this study. A standard camera mounted on the microscope was used to obtain photographs of the
CL-images. Dr. Neuser and Dipl.-Geol Habermann assisted with the CL investigations.
A3.6 Image analysis
Image analysis was used to obtain qualitative information on shape, area, and shape preferred
orientation of minerals in thin sections or on back scattered electron images. The image is digitised
and a computer program approximates area, perimeter, longest dimension, direction of longest
dimension, and other parameters from this image.
The VIDS IV image analysis system (AI-Tektron) combined with a videocamera (JVC BY-110)
mounted on a Zeiss microscope and a digitising tablet were used in this study.
A3.7 Microthermometry
With the microthermometry it is possible to obtain information about density and composition
of fluid inclusions without destroying the inclusions. A heating-freezing stage installed on a
microscope allows to observe phase transitions in the fluid inclusionsas a function of temperature.
Two heating-freezing stages were used, a Linkam THM 600, described in Sheperd (1981) and
Roedder (1984) and a stage specially for low temperature measurements, constructed by W. Harbott
at the “Institut für Geologie der Ruhr Universität Bochum”. This last stage is described by Harbott
et al. (1990) and Küster (1994).
Both stages were calibrated with natural standards (e.g. Calanda Quartz provided by J. Mullis)
in the low temperature region and with the melting point of several pure chemicals (Fa. Merck) in
the high temperature region.
B-1Appendix B geothermobarometry
Appendix B Geothermobarometry
In this study several different methods were used to estimate pressures and temperatures during
UHP metamorphism and exhumation. A short description of these methods is presented below.
B1 Thermometer
B1.1 Garnet clinopyroxene thermometry
This thermometer is based on Fe, Mg exchange between garnet and clinopyroxene as defined in
the following reaction
1/3Pyrope + Hedenbergite = 1/3Almandine + Diopside
Mg3Al
2Si
3O
12 CaFeSi
2O
6 Fe
3Al
2Si
3O
12 CaMgSi
2O
6
with equilibrium constant K (Banno, 1970) defined as
(agrtFe
)1/3 (acpxMg
)K = * *
(agrtMg
)1/3 (acpxFe
)
with agrtFe
the activity of Fe in garnet, acpxMg
the activity of Mg in clinopyroxene etc. At equilibrium,
taking a standard state of pure solids at the temperature and pressure of interest ∆G°(P,T) = 0,
∆H° - T∆S° + (P-1)∆V° = -RTlnK
assuming ideal solid solution for the minerals (a = x) gives
(XGtFe
) (XCpxMg
)K = * = Kd
(XGtMg
) (XCpxFe
)
This last assumption is not completely valid and a correct treatment requires knowledge of the
mixing properties of garnet and pyroxene.
First experiments to calibrate this thermometer were made by Raheim & Green, (1974). Ellis
and Green (1979) experimentally evaluated the effect of the grossular component in garnet and
assuming that the non-ideal mixing behaviour of garnet and clinopyroxene was concentrated in XCa
of garnet proposed following empirical calibration:
3104 XGtCa
+ 3030 + 10.86 P(kb)T(K) = .
ln Kd + 1.9034 .
The same data set was used by Powell (1985) using robust regression and regression diagnostics
to give the calibration a better statistical fundament. He derived following relation:
3140 XGtCa
+ 2790 + 10 P(kb)T(K) = .
ln Kd + 1.735 .
Another calibration using this data set is Krogh’s (1988). Here the dependence of Kd on XCa
was
assumed to be curvilinear instead of linear as in the previous calibrations. He derived following
relation:
Appendix B geothermobarometryB-2
-6173(XGtCa
)2 + 6731XGtCa
+ 1879 + 10 P(kb)T(K) = .
ln Kd + 1.393 .
All these three calibrations assume an independence of Kd from the Mg number of garnet,
which was postulated by Ellis & Green (1979). A new experimental calibration of this thermometer
by Pattison & Newton, (1989), not only shows a dependence of Kd on XCa
but also on the Mg
number of garnet. Their calibration has the general form
a´X3 + b´X2 + c´X +d´T(K) = + 5.5 (P(kb)-15),
ln Kd + a0X3 + b
0X2 +c
0X4 +d
0
where the constants a´, a0, etc. depend on X
Ca in garnet (Table B1). X is the Mg number in garnet
(Mg/(Mg+Fe2+)).
The experimental data from these studies together with data from other studies were used by Ai
(1994) to propose a different calibration with a curvilinear dependence of Kd on Ca and a linear
dependence of Kd on the Mg-number of garnet. His calibration has the form:
-1629(XGtCa
)2 + 3648.55XGtCa
- 6.59 XGtMg
+ 1987.98 + 17.66 P(kb)T(K) = .
ln Kd + 1.076 .
The experimental data of Pattison & Newton (1989) were evaluated and thermodynamically
analysed by Aranovich & Pattison (1995) and Berman, Aranovich & Pattison (1995). These authors
tried to take the mixing properties of garnet and pyroxene into account and proposed a different
calibration of the garnet-clinopyroxene thermometer, that gives similar results to the Ai (1994)
calibration.
None of the calibrations takes the jadeite content of clinopyroxene into account. It was, however,
shown by Koons (1984), that jadeite contents up to Xcpx jd <0.6 do not affect temperatures calculated
with the Ellis & Green (1979) calibration.
Results calculated for all calibrations are presented in table B2. The Pattison and Newton (1989)
calibration gives consistently the lowest temperatures for the eclogites of Lago Cignana. Since the
authors suggest application of their calibration only in high grade amphibolite and eclogite facies
rock as well as in granulite facies rocks this calibration is discarded. The Ellis and Green (1979)
calibration gives always the highest temperatures and is discarded, because other studies (e.g. Green
& Adam, 1991) have shown that this calibration gives temperatures that are often 50 to 150 ° too
high. From the remaining three calibrations the Powell (1985) calibration is preferred, because it
gives an adequate description of the experimental data with a minimum number of variables.
Table B1
Parameters for the Pattison & Newton (1989) calibration of the garnet clinopyroxene thermometer.
B-3Appendix B geothermobarometry
B1.2 Amphibole-plagioclase thermometer (Holland & Blundy, 1994)
This thermometer or better these two thermometers are based on the reactions:
A) 1 edenite + 4 quartz = tremolite + albite
NaCa2Mg
5Si
4(AlSi
3)O
22(OH)
2 SiO
2 Ca
2Mg
5Si
8O
22(OH)
2NaAlSi
3O
8
B) 2 edenite + albite = richterite + anorthite
NaCa2Mg
5(AlSi
3)Si
4O
22(OH)
2 NaAlSi
3O
8 Na(CaNa)Mg
5Si
8O
22(OH)
2CaAl
2Si
2O
8
Only the thermometer based on the first reaction is discussed here, because the second reaction
requires plagioclase compositions with Xan
> 0.1, that are not found in the metabasic rocks of Lago
di Cignana.
The thermometer was calibrated using an experimental data set (Blundy & Holland, 1990), com-
bined with data from natural samples to expand the compositional relatively small range of the
experimental data set.
To use the first reaction as a thermometer, activity models for plagioclase and amphibole are
needed. For plagioclase a simplified version of the DQF (Darkens Quadratic Formalism) model
given by Holland & Powell (1992) is used. For amphibole the situation is more complicated, because
different non ideal interactions are important. Using a symmetrical form of non ideal interaction to
model the multi-site-solid-solution in amphibole and using a relative simple system involving
distribution of [ ]-K-Na-Ca-Mg-Fe2+-Fe3+-AlSi over the A, M4, M1, M2, M3 and T1 crystallographic
sites in amphibole, the number of non ideal interaction terms is reduced to 8. These 8 terms do not
have thermodynamic meaning but are a simplification useful for developing the thermometric
expression (Holland & Blundy, 1994).
The equilibrium condition for the first reaction is given by:
∆µA = 0 = ∆H°
A - T∆S°
A + P∆V°
A + RTlnK(Ed-Tr
id) + RTlnγ
ab + RTlnγ
trem - RTlnγ
ged
with KEd - Tr id = 27/256 * ((XA
[ ] * XT1
Si)/(XA
Na * XT1
Al)) * Xplag
An
and RTlnγab
= Yab
= 0 for Xab
> 0.5
and Wplag
(1-Xab
)2 + Iab
for Xab
< 0,5
Wplag
= 12 Kj, Iab
= -3,0 Kj
and Y(ed-tr)
= RTlnγed
-RTlnγtrem
= XANa
*A1 + XA
K * A
2 +XM4
Na * A
3+ XM13
Fe * A
4 + XM2
Al *A
5 +
XM2Fe
* A6 + XM2
Fe3+ *A
7 + XT1
Al * A
8 * A
9
The result is a thermometric expression for the Edenite-Tremolite thermometer:
∆H°A + P∆V°
A + Y
ab + Y
(ed-tr)T(K) = .
∆S°A - R lnK Ed - Tr
id
values for ∆H°A, ∆V°
A, ∆S°
A and for A
1 to A
9 were determined by regression of the experimental
and the natural amphibole plagioclase pairs. A9 was incorporated in ∆H°
A. A
3, A
4, A
6, A
7 and A
8
had regression values within 1 σ from zero and were removed from the regression. Following
values were determined:
Appendix B geothermobarometryB-4
∆H*(kJ) = -76.95, ∆S°(kJ K-1) = -0.065, ∆V°(kJ kbar-1) = 0.79, A1(kJ) = 39.4, A
2(kJ) = 22.4,
A5(kJ) = 41.5 - P(kbar) * 2.89. This thermometer can be used in a temperature range between 400
and 900 °C, with amphiboles that have NaA > 0.02 pfu, Alvi < 1.8 pfu and Si between 6.0 and 7.7
pfu, plagioclase must have Xan
< 0.9. Typical temperature uncertainty due to the calibration lies
around 40 °C. Results for this thermometer are presented in Table B3.
Calcite - Dolomite solvus thermometry
For this thermometer the calibration of Anovitz & Essene (1987) was used. These authors used
all available reversed experimental data on binary solvi in the system CaCO3-MgCO
3-FeCO
3 and
analyses of natural carbonates to model ternary activity/composition relationships for calcite and
dolomite structure carbonates. These data were used to model the mole fraction of MgCO3 in calcite
as a function of temperature along the calcite dolomite solvus. The least squares fit for the solvus
between 200 °C and 900 °C has the form:
TMg
(K) = A(XMgCO3
) + B/(XMgCO3
) + C(XMgCO3
)2 + D(XMgCO3
)0.5 + E
with XMgCO3
the MgCO3 concentration in Calcite. The values of the regression parameters are given
in Table B4. This thermometer and further data were used to develop a thermometer in the ternary
system CaCO3 - MgCO
3 - FeCO
3. This thermometer has the form:
TFeMg
(K) = TMg
+ a(XFeCO3
) + b(XFeCO3
)2 + c(XFeCO3
/ XMgCO3
) + d(XFeCO3
* XMgCO3
) +
e(XFeCO3
/ XMgCO3
)2 + f(XFeCO3
* XMgCO3
)2 .
with XFeCO3
and XMgCO3
respectively the FeCO3 and MgCO
3 concentrations in Calcite. The values
of the regression parameters can also be found in Table B4.
Comparison of the results of this calibration (Table B5) with results of the calibration of Powell
et al. (1984) shows no significant temperature differences.
B2 Barometer
In this study three reactions were used to estimate pressures. Two polymorphic transition reactions
that divide the P-T field in two parts were either one or the other polymorph is the stable phase. One
net transfer reaction gives a pressure estimate that depends on the composition of the reacting
phases.
The polymorphic transition reaction Coesite - Quartz gives a minimum pressure for the UHP
metamorphism. This equilibrium has been well located as a function of P and T (e.g., Mirwald &
Massonne, 1980; Bohlen & Boettcher, 1982).
Table B4
Regression parameters for the Anovitz & Essenne (1987) calibration of the calcite dolomite solvusthermometer in the system CaCO
3 - MgCO
3 and the system CaCO
3 - MgCO
3-FeCO
3 .
B-5Appendix B geothermobarometry
The polymorphic reaction Calcite-Aragonite gives a maximum pressure for the onset of lower
PT-transformation of the eclogitic mineral assemblage. This equilibrium has been well located as a
function of P and T (e.g., Johannes & Puhan, 1971; Goldsmith & Newton, 1969).
The net transfer reaction used for geobarometry is the reaction (Holland, 1980):
NaAlSi2O
6+ SiO
2= NaAlSi
3O
8
Jadeite + Quartz = Albite
The equilibrium condition for this reaction is given by
∆µ = 0 = ∆H° - T∆S° + P∆V° + RTlnK
with
aQz
* aJd
K = . a
Ab
The position of this reaction in the PT-field was calculated using the PTX-programm of Brown
et al. (1988) with the Bermann (1988) data base. Albite and quartz activities were taken as 1. The
jadeite activity in omphacite was calculated, with the method of Holland (1990) using Landau
theory to mixture according to the formula:
RT ln ajd
= RT ln (XNaM1
*XAlM2
) + RT ln γNaAl
with
RT ln γNaAl
= XCaM2
*(XMgM1
WA + X
Fe2+M1W
B + X
Fe3+M1W
C),
WA = 26 kJ, W
B = 25 kJ and W
C = 0 and with Na and Ca on the M2 site and Al, Mg, Fe2+ and Fe3+
on the M1 site. A main uncertainty factor is the ordering state of omphacite. The calculated activity
is for disordered omphacite. At the temperatures in the studied rocks between 400 and 600 °C,
omphacite should be ordered (Carpenter et al., 1990). The activity for ordered omphacites should
be lower as for disordered omphacites (Holland et al., 1990) and the pressures calculated with this
barometer (Table B6) are therefore maximum pressures only.
B-6 Appendix B Table B2 grt-cpx thermometer
GroupPositionSample
XgrtMg
XgrtCa
XgrtMg
E&GPowellKroghP&NAi
A1rBk 7
0,3230,1710,833
633607560522614
A2rBk 7
0,3540,1480,846
625599540513604
A3iBk 7
0,2580,1990,837
584559521470556
Temperaturen (°C) at 2.7 GPa
B2rBk 7
0,2930,1770,828
616591545514594
B3iBk 7
0,2560,2440,782
688665643560680
B4iBk 7
0,2760,2500,827
652629606507636
B5iBk 7
0,2290,2080,816
588563527472560
B6iBk 7
0,2880,1660,849
574547497474543
B7iBk 7
0,2690,2220,833
616592562488594
B8iBk 7
0,2690,2130,803
652627596535636
GroupPositionSample
XgrtMg
XgrtCa
XgrtMg
E&GPowellKroghP&NAi
C1rBk 7
0,2160,2620,834
587564539436558
D1rBk 7
0,3220,1770,801
685661618582678
D2iBk 7
0,2790,2380,787
704681659576700
A1rBk 8
0,3700,1410,850
628602540511607
A1rBk 39
0,2050,2680,821
595572548440567
B1rBk 39
0,2630,2390,862
580556528439551
B2iBk 39
0,1860,2510,816
570547519418539
B3iBk 39
0,1980,2170,750
635611580516616
B4alliBk 39
0,2330,2080,780
637613579529619
C1rBk 39
0,2490,2470,810
644621597507626
GroupPositionSample
XgrtMg
XgrtCa
XgrtMg
E&GPowellKroghP&NAi
C4rBk 39
0,2590,2510,872
568544517420536
C5rBk 39
0,2660,2580,844
622599575472599
C6rBk 39
0,2710,2320,842
613589560477589
D1iBk 39
0,2240,2360,797
626602575496605
D2rBk 39
0,2580,2410,817
641617592506622
A1rCig 91-1
0,3460,1350,815
658632567571644
B1iCig 90\40\2
0,1500,2310,695
632608581477613
B2iCig 90\40\2
0,2060,2410,766
645621596512627
B3iCig 90\40\2
0,1510,2270,750
579554523422550
B4iCig 90\40\2
0,1540,2230,697
631607577484611
GroupPositionSample
XgrtMg
XgrtCa
XgrtMg
E&GPowellKroghP&NAi
B5iCig 90\40\2
0,1770,2320,712
657633607523643
Temperaturen (°C) at 2.7 GPa
Temperaturen (°C) at 2.7 GPa
Temperaturen (°C) at 2.7 GPa
B-7Appendix B Table B3 amphibole-plagioclasethermometer
SampleAnalysisDate
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2OTotal
H2O
SiAlt
AloFe3CrTiMgFe2MnZn
CaNa
NaK
sum
OH
T in °C
Bk 10 B918.10.93
52,290,085,180,032,959,170,1614,7510,750,181,620,1597,31
2,09
7,5030,4978,000
0,3790,3180,0030,0063,1551,1000,0190,0195,000
1,6530,3472,000
0,1030,0280,131
15,131
2,000
497
SampleAnalysisDate
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2OTotal
H2O
SiAlt
AloFe3CrTiMgFe2MnZn
CaNa
NaK
sum
OH
T in °C
Bk 10 B1618.10.93
51,720,026,180,023,378,160,1215,3010,930,201,930,1798,12
2,11
7,3530,6478,000
0,3880,3600,0020,0023,2420,9700,0140,0215,000
1,6650,3352,000
0,1970,0310,228
15,228
2,000
540
Bk 10 B1718.10.93
53,180,025,120,004,997,261,1515,2211,010,261,530,1599,89
2,14
7,4420,5588,000
0,2860,5260,0000,0023,1740,8490,1360,0275,000
1,6510,3492,000
0,0660,0270,093
15,093
2,000
491
Bk 10 B2018.10.93
49,600,058,460,004,799,350,1712,749,930,372,410,2698,13
2,09
7,1310,8698,000
0,5640,5180,0000,0042,7301,1240,0210,0395,000
1,5300,4702,000
0,2010,0490,250
15,250
2,000
565
Bk 10 B2118.10.93
50,500,108,080,004,948,330,0913,189,580,162,180,2297,37
2,09
7,2460,7548,000
0,6120,5340,0000,0082,8191,0000,0110,0175,000
1,4730,5272,000
0,0790,0410,120
15,120
2,000
513
Bk 10 B3318.10.93
52,090,075,490,003,336,700,0016,1210,820,701,930,1797,41
2,10
7,4210,5798,000
0,3430,3570,0000,0053,4230,7980,0000,0745,000
1,6520,3482,000
0,1850,0320,216
15,216
2,000
529
Bk 10 B3418.10.93
53,010,115,000,010,928,820,0015,9711,180,071,530,1496,76
2,10
7,5820,4188,000
0,4240,0990,0010,0083,4041,0550,0000,0075,000
1,7130,2872,000
0,1370,0260,164
15,164
2,000
489
Bk 10 B3918.10.93
53,500,114,690,222,418,230,1416,0211,210,201,460,1698,35
2,12
7,5510,4498,000
0,3320,2560,0250,0083,3700,9710,0170,0215,000
1,6950,3052,000
0,0950,0290,124
15,124
2,000
486
Bk 10 B4218.10.93
51,840,096,040,063,507,070,0915,7510,860,101,680,1997,27
2,10
7,3870,6138,000
0,4020,3750,0070,0073,3450,8430,0110,0115,000
1,6580,3422,000
0,1220,0350,158
15,158
2,000
521
Bk 10 B4718.10.93
50,450,078,470,004,018,120,0513,779,730,022,390,2597,33
2,10
7,2180,7828,000
0,6460,4320,0000,0052,9370,9720,0060,0025,000
1,4920,5082,000
0,1550,0470,201
15,201
2,000
542
Bk 10 B4918.10.93
49,790,106,990,003,318,720,0014,5311,060,001,660,3096,46
2,06
7,2300,7708,000
0,4260,3620,0000,0083,1451,0590,0000,0005,000
1,7210,2792,000
0,1880,0570,245
15,245
2,000
554
Bk 10 B5018.10.93
52,180,105,460,004,397,080,1115,7210,970,251,510,2297,99
2,11
7,4050,5958,000
0,3190,4690,0000,0083,3250,8410,0130,0265,000
1,6680,3322,000
0,0840,0410,124
15,124
2,000
505
Bk 10 B5118.10.93
50,950,068,450,005,207,210,0914,049,780,092,250,2498,36
2,12
7,2030,7978,000
0,6110,5530,0000,0052,9590,8530,0110,0095,000
1,4810,5192,000
0,0980,0440,142
15,142
2,000
529
Bk 10 B5218.10.93
50,370,086,490,004,628,970,1014,1811,080,251,580,3098,02
2,09
7,2400,7608,000
0,3390,5000,0000,0063,0381,0780,0120,0275,000
1,7060,2942,000
0,1470,0560,203
15,203
2,000
550
Bk 10 B5318.10.93
46,300,1311,180,003,5110,230,1511,9710,460,202,670,4397,23
2,05
6,7741,2268,000
0,7010,3860,0000,0102,6101,2520,0190,0225,000
1,6400,3602,000
0,3970,0820,479
15,479
2,000
594
Bk 10 B5418.10.93
50,520,036,700,044,817,460,1314,6510,820,501,710,2597,62
2,09
7,2460,7548,000
0,3780,5190,0050,0023,1320,8950,0160,0535,000
1,6630,3372,000
0,1380,0470,185
15,185
2,000
547
Bk 10 B5518.10.93
50,260,057,060,092,729,230,0814,5511,180,351,970,2997,83
2,09
7,2230,7778,000
0,4190,2940,0100,0043,1171,1090,0100,0375,000
1,7210,2792,000
0,2700,0540,325
15,325
2,000
556
Bk 10 B5718.10.93
51,240,168,230,004,817,570,0013,328,630,192,680,2297,04
2,10
7,3230,6778,000
0,7090,5170,0000,0122,8370,9040,0000,0205,000
1,3210,6792,000
0,0640,0410,105
15,105
2,000
487
Bk 10 B5818.10.93
49,810,138,330,006,076,770,0413,799,740,172,130,2397,21
2,09
7,1440,8568,000
0,5520,6550,0000,0102,9480,8120,0050,0185,000
1,4970,5032,000
0,0890,0430,132
15,132
2,000
535
Bk 10 B219.10.93
47,240,029,240,006,947,110,0013,5710,780,001,830,3797,09
2,06
6,8591,1418,000
0,4400,7580,0000,0022,9370,8630,0000,0005,000
1,6770,3232,000
0,1920,0700,262
15,262
2,000
605
Bk 10 B319.10.93
50,200,055,580,004,178,020,1515,0611,260,251,500,2796,52
2,06
7,2990,7018,000
0,2550,4570,0000,0043,2640,9760,0180,0275,000
1,7540,2462,000
0,1770,0510,228
15,228
2,000
551
Bk 10 B419.10.93
50,940,065,320,025,706,790,2415,4311,310,301,240,2397,58
2,09
7,3050,6958,000
0,2040,6160,0020,0053,2980,8140,0290,0325,000
1,7380,2622,000
0,0830,0430,126
15,126
2,000
524
norm 23 oxygen, Fe3 over Si+Ti+Al+Cr+Fe+Mg+Mn+Zn = 16
norm 23 oxygen, Fe3 over Si+Ti+Al+Cr+Fe+Mg+Mn+Zn = 16
B-8 Appendix B Table B3 amphibole plagioclasethermometer
Bk 10 B1619.10.93
51,550,086,840,051,758,690,0414,7110,610,151,770,1796,41
2,08
7,4180,5828,000
0,5780,1890,0060,0063,1551,0450,0050,0165,000
1,6360,3642,000
0,1300,0320,161
15,161
2,000
511
Bk 10 B1226.11.93
51,710,135,870,043,838,250,1014,7410,630,181,620,1797,26
2,09
7,4120,5888,000
0,4040,4130,0050,0103,1490,9890,0120,0195,000
1,6330,3672,000
0,0830,0320,115
15,115
2,000
501
SampleAnalysisDate
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2OTotal
H2O
SiAlt
AloFe3CrTiMgFe2MnZn
CaNa
NaK
sum
OH
T in °C
SampleAnalysisDate
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2OTotal
H2O
SiAlt
AloFe3CrTiMgFe2MnZn
CaNa
NaK
sum
OH
T in °C
Bk 10 B1326.11.93
49,990,146,830,024,488,560,2013,9310,650,161,730,2196,90
2,07
7,2440,7568,000
0,4110,4880,0020,0113,0091,0370,0250,0175,000
1,6540,3462,000
0,1400,0400,179
15,179
2,000
548
Bk 172725.7.94
51,720,114,230,043,1410,410,1814,2810,890,011,500,1696,68
2,06
7,5260,4748,000
0,2520,3440,0050,0123,0971,2670,0220,0015,000
1,6980,3022,000
0,1210,0300,151
15,151
2,000
507
Bk 172825.7.94
52,210,093,780,023,6010,370,2014,3010,950,001,290,1396,94
2,07
7,5740,4268,000
0,2200,3930,0020,0103,0921,2580,0250,0005,000
1,7020,2982,000
0,0650,0250,089
15,089
2,000
483
Bk 172925.7.94
52,440,073,890,014,0410,350,2714,0810,630,021,500,1397,42
2,08
7,5740,4268,000
0,2360,4390,0010,0083,0311,2500,0330,0025,000
1,6450,3552,000
0,0650,0240,090
15,090
2,000
482
Bk 173025.7.94
52,810,082,860,002,4411,290,2714,7311,670,051,010,1197,31
2,07
7,6510,3498,000
0,1390,2660,0000,0093,1811,3670,0330,0055,000
1,8110,1892,000
0,0950,0210,116
15,116
2,000
480
Bk 17513.7.94
46,910,097,810,073,8112,340,3611,8711,530,021,730,2996,83
2,02
6,9741,0268,000
0,3430,4260,0080,0102,6301,5350,0450,0025,000
1,8370,1632,000
0,3350,0560,392
15,392
2,000
577
Bk 17523.7.94
47,420,2110,630,014,379,750,1311,559,030,063,140,3096,60
2,05
6,9321,0688,000
0,7640,4800,0010,0232,5171,1920,0160,0065,000
1,4140,5862,000
0,3040,0570,362
15,362
2,000
563
Bk 17533.7.94
47,180,2010,350,014,369,610,1411,969,250,003,210,3296,59
2,05
6,9071,0938,000
0,6930,4800,0010,0222,6101,1760,0170,0005,000
1,4510,5492,000
0,3620,0610,423
15,423
2,000
559
Bk 17543.7.94
48,700,167,680,035,949,770,3012,319,720,002,470,2697,35
2,06
7,1020,8988,000
0,4220,6520,0030,0182,6761,1920,0370,0005,000
1,5190,4812,000
0,2170,0490,267
15,267
2,000
569
Bk 17553.7.94
46,870,259,160,046,0710,130,3211,019,170,122,750,3396,23
2,02
6,9481,0528,000
0,5480,6770,0050,0282,4331,2560,0400,0135,000
1,4560,5442,000
0,2470,0640,310
15,310
2,000
577
Bk 1719.7.94
52,390,051,950,003,7810,370,3515,0812,080,000,500,0796,62
2,05
7,6510,3498,000
0,0000,4160,0000,0053,2831,2660,0430,0005,013
1,8900,1102,000
0,0320,0130,045
15,058
2,000
447
Bk 1769.7.94
51,880,125,410,035,088,890,2913,629,560,122,080,1497,22
2,08
7,4720,5288,000
0,3900,5510,0030,0132,9241,0710,0350,0135,000
1,4750,5252,000
0,0560,0260,082
15,082
2,000
491
Bk 1789.7.94
51,770,124,020,055,2711,100,2112,9510,000,081,790,1797,54
2,06
7,5250,4758,000
0,2140,5770,0060,0132,8061,3500,0260,0095,000
1,5570,4432,000
0,0620,0320,094
15,094
2,000
493
Bk 1799.7.94
49,390,214,800,023,4014,190,4011,8611,610,041,260,2097,38
2,02
7,3220,6788,000
0,1600,3800,0020,0232,6211,7590,0500,0045,000
1,8440,1562,000
0,2060,0390,245
15,245
2,000
551
Bk 17109.7.94
50,820,156,730,155,299,050,2112,969,150,002,470,1697,14
2,08
7,3380,6628,000
0,4840,5750,0170,0162,7891,0930,0260,0005,000
1,4160,5842,000
0,1070,0300,137
15,137
2,000
527
Bk 17129.7.94
50,790,113,340,002,1815,280,5011,9311,830,070,880,1797,09
2,02
7,5470,4538,000
0,1320,2440,0000,0122,6421,8990,0630,0085,000
1,8830,1172,000
0,1370,0330,170
15,170
2,000
509
Bk 17419.7.94
43,530,1211,090,054,3813,540,3210,2911,700,002,270,5197,80
2,01
6,5081,4928,000
0,4620,4920,0060,0132,2931,6930,0410,0005,000
1,8740,1262,000
0,5320,0990,631
15,631
2,000
575
Bk 17429.7.94
46,450,2510,090,056,1811,220,1510,429,300,032,850,3997,38
2,04
6,8401,1608,000
0,5910,6850,0060,0282,2871,3820,0190,0035,000
1,4670,5332,000
0,2810,0750,356
15,356
2,000
581
Bk 17439.7.94
45,160,2111,600,046,7012,030,119,088,760,113,290,4697,55
2,03
6,6841,3168,000
0,7080,7460,0050,0232,0031,4900,0140,0125,000
1,3890,6112,000
0,3330,0890,422
15,422
2,000
580
Bk 17489.7.94
49,010,187,680,024,2911,210,3411,919,910,002,340,2697,15
2,05
7,1700,8308,000
0,4950,4730,0020,0202,5971,3710,0420,0005,000
1,5530,4472,000
0,2170,0500,267
15,267
2,000
555
norm 23 oxygen, Fe3 over Si+Ti+Al+Cr+Fe+Mg+Mn+Zn = 16
norm 23 oxygen, Fe3 over Si+Ti+Al+Cr+Fe+Mg+Mn+Zn = 16
B-9Appendix B Table B3 amphibole-plagioclasethermometer
SampleAnalysisDate
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2OTotal
H2O
SiAlt
AloFe3CrTiMgFe2MnZn
CaNa
NaK
sum
OH
T in °C
SampleAnalysisDate
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2OTotal
H2O
SiAlt
AloFe3CrTiMgFe2MnZn
CaNa
NaK
sum
OH
T in °C
Bk 17499.7.94
47,240,159,610,014,7410,920,3111,149,360,002,900,3796,74
2,04
6,9591,0418,000
0,6270,5250,0010,0172,4461,3450,0390,0005,000
1,4770,5232,000
0,3060,0710,377
15,377
2,000
559
Bk 17509.7.94
50,600,146,680,034,3110,420,4412,539,390,002,550,1997,28
2,07
7,3410,6598,000
0,4830,4700,0030,0152,7091,2650,0540,0005,000
1,4600,5402,000
0,1770,0360,213
15,213
2,000
533
Bk 17519.7.94
50,270,167,380,024,879,390,3212,899,460,032,560,2097,55
2,08
7,2510,7498,000
0,5060,5290,0020,0172,7711,1320,0390,0035,000
1,4620,5382,000
0,1780,0380,216
15,216
2,000
547
Bk 183625.7.94
52,080,154,400,002,1512,420,2513,1410,450,001,750,1796,96
2,06
7,5920,4088,000
0,3480,2360,0000,0162,8551,5140,0310,0005,000
1,6320,3682,000
0,1270,0320,159
15,159
2,000
489
Bk 183825.7.94
51,850,163,020,052,6111,300,2414,1711,270,001,070,1095,84
2,04
7,6330,3678,000
0,1570,2890,0060,0183,1091,3910,0300,0005,000
1,7780,2222,000
0,0830,0190,102
15,102
2,000
480
Bk 185025.7.94
52,360,034,470,071,318,850,1616,1011,820,221,290,1296,80
2,08
7,5310,4698,000
0,2880,1420,0080,0033,4511,0650,0190,0235,000
1,8210,1792,000
0,1810,0220,204
15,204
2,000
510
Bk 185125.7.94
50,250,075,450,023,868,390,2314,8711,330,301,480,1596,40
2,06
7,3200,6808,000
0,2560,4230,0020,0083,2291,0220,0280,0325,000
1,7680,2322,000
0,1860,0280,215
15,215
2,000
550
Bk 185225.7.94
49,570,048,160,064,408,680,2413,159,690,322,580,2597,14
2,07
7,1700,8308,000
0,5610,4790,0070,0042,8351,0500,0290,0345,000
1,5020,4982,000
0,2250,0470,272
15,272
2,000
552
Bk 185325.7.94
51,680,065,440,074,007,980,2014,8310,390,211,820,1696,84
2,08
7,4400,5608,000
0,3630,4340,0080,0063,1820,9600,0240,0225,000
1,6030,3972,000
0,1110,0300,141
15,141
2,000
516
Bk 185525.7.94
52,850,054,970,044,057,930,2314,749,920,241,830,1396,98
2,09
7,5670,4338,000
0,4060,4360,0050,0053,1460,9490,0280,0255,000
1,5220,4782,000
0,0300,0240,054
15,054
2,000
454
Bk 185625.7.94
51,720,076,720,045,357,710,2913,388,710,262,560,1596,96
2,09
7,4230,5778,000
0,5600,5780,0050,0082,8620,9250,0350,0285,000
1,3390,6612,000
0,0520,0280,080
15,080
2,000
490
Bk 185725.7.94
52,960,055,660,032,416,720,1115,839,870,132,090,1295,98
2,10
7,5730,4278,000
0,5270,2590,0030,0053,3740,8040,0130,0145,000
1,5120,4882,000
0,0920,0220,114
15,114
2,000
480
Bk 185825.7.94
48,730,067,140,063,918,970,2213,7510,880,281,940,1896,12
2,04
7,1520,8488,000
0,3870,4310,0070,0073,0081,1020,0270,0305,000
1,7110,2892,000
0,2630,0340,297
15,297
2,000
566
Bk 3952 24.6.92
49,030,116,990,032,858,680,0914,7610,560,002,680,1995,97
2,05
7,1760,8248,000
0,3810,3140,0030,0093,2201,0620,0110,0005,000
1,6560,3442,000
0,4160,0360,453
15,453
2,000
552
Bk 3953 24.6.92
49,010,107,840,002,889,060,0813,869,630,003,180,1995,84
2,05
7,1760,8248,000
0,5290,3180,0000,0083,0251,1100,0100,0005,000
1,5110,4892,000
0,4140,0360,450
15,450
2,000
543
Bk 392513.3.93
50,530,176,630,021,088,170,0815,8310,780,112,550,2296,17
2,07
7,3120,6888,000
0,4430,1170,0020,0133,4140,9890,0100,0125,000
1,6710,3292,000
0,3870,0410,428
15,428
2,000
528
Bk 392713.3.93
51,450,086,460,023,287,470,1115,5710,250,212,670,1897,76
2,11
7,3260,6748,000
0,4100,3520,0020,0063,3040,8900,0130,0225,000
1,5640,4362,000
0,3010,0330,334
15,334
2,000
540
Bk 392813.3.93
48,340,1010,460,023,0310,050,1611,908,260,114,150,2696,83
2,06
7,0320,9688,000
0,8250,3310,0020,0082,5801,2220,0200,0125,000
1,2870,7132,000
0,4580,0490,507
15,507
2,000
540
Bk 39.143 27.8.92
48,820,058,820,024,049,710,1812,738,650,004,050,1897,25
2,07
7,0870,9138,000
0,5960,4410,0020,0042,7551,1790,0220,0005,000
1,3450,6552,000
0,4850,0340,519
15,519
2,000
541
Bk 772 6.7.92
47,980,0810,230,063,809,500,1611,447,740,003,990,1895,16
2,03
7,0780,9228,000
0,8570,4220,0070,0062,5161,1720,0200,0005,000
1,2230,7772,000
0,3650,0350,399
15,399
2,000
550
Bk 773 6.7.92
47,210,0311,720,073,4711,230,1910,247,660,004,410,2296,45
2,04
6,9331,0678,000
0,9620,3840,0080,0022,2421,3790,0240,0005,000
1,2050,7952,000
0,4610,0420,503
15,503
2,000
548
Bk 71 7.7.92
49,750,057,780,003,409,410,1612,878,550,003,430,1595,55
2,05
7,2920,7088,000
0,6360,3750,0000,0042,8121,1530,0200,0005,000
1,3430,6572,000
0,3170,0290,346
15,346
2,000
533
norm 23 oxygen, Fe3 over Si+Ti+Al+Cr+Fe+Mg+Mn+Zn = 16
norm 23 oxygen, Fe3 over Si+Ti+Al+Cr+Fe+Mg+Mn+Zn = 16
B-10 Appendix B Table B3 amphibole plagioclasethermometer
Bk 77 7.7.92
40,820,0715,520,003,2015,400,246,818,720,004,450,5595,78
1,96
6,2581,7428,000
1,0630,3690,0000,0061,5561,9740,0310,0005,000
1,4320,5682,000
0,7550,1100,865
15,865
2,000
665
Bk 755 7.7.92
46,900,1510,550,041,7210,490,1812,079,280,003,580,2495,20
2,02
6,9551,0458,000
0,7990,1920,0050,0122,6681,3020,0230,0005,000
1,4750,5252,000
0,5040,0460,550
15,550
2,000
545
Bk 7437.8.92
46,570,069,650,033,0510,180,1912,4410,010,203,220,2195,82
2,02
6,9061,0948,000
0,5930,3410,0040,0052,7501,2630,0240,0225,000
1,5900,4102,000
0,5160,0410,557
15,557
2,000
565
Bk 7477.8.92
47,260,049,510,003,379,640,2112,8610,100,153,100,2096,44
2,04
6,9391,0618,000
0,5840,3720,0000,0032,8141,1840,0260,0165,000
1,5890,4112,000
0,4710,0380,510
15,510
2,000
569
Bk 7487.8.92
52,240,014,930,061,496,940,1517,0311,310,231,930,0896,40
2,09
7,4870,5138,000
0,3200,1610,0070,0013,6380,8320,0180,0245,000
1,7370,2632,000
0,2730,0150,288
15,288
2,000
519
Bk 7497.8.92
51,520,077,560,014,846,640,2214,028,270,243,260,1496,80
2,10
7,3650,6358,000
0,6390,5210,0010,0052,9870,7940,0270,0255,000
1,2670,7332,000
0,1700,0260,196
15,196
2,000
525
Bk 81514.3.93
49,980,158,950,083,048,070,1213,809,200,163,190,2496,98
2,09
7,1790,8218,000
0,6950,3290,0090,0122,9550,9700,0150,0175,000
1,4160,5842,000
0,3040,0450,349
15,349
2,000
548
Bk 81714.3.93
51,230,036,460,000,628,830,1115,5310,700,192,520,1696,37
2,08
7,3930,6078,000
0,4920,0670,0000,0023,3401,0650,0130,0205,000
1,6540,3462,000
0,3590,0300,390
15,390
2,000
516
Bk 81814.3.93
48,240,0510,670,002,868,180,1013,269,370,233,380,2696,60
2,07
6,9801,0208,000
0,7990,3110,0000,0042,8600,9890,0120,0255,000
1,4530,5472,000
0,4010,0490,450
15,450
2,000
560
Bk 81914.3.93
52,130,054,870,001,716,670,1117,1711,570,171,550,1696,16
2,09
7,4820,5188,000
0,3060,1840,0000,0043,6730,8010,0130,0185,000
1,7790,2212,000
0,2110,0300,241
15,241
2,000
521
Bk 9623.2.94
52,040,124,990,040,879,150,0515,6211,430,191,390,1396,02
2,07
7,5350,4658,000
0,3860,0950,0050,0093,3711,1080,0060,0205,000
1,7730,2272,000
0,1630,0250,188
15,188
2,000
505
SampleAnalysisDate
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2OTotal
H2O
SiAlt
AloFe3CrTiMgFe2MnZn
CaNa
NaK
sum
OH
T in °C
SampleAnalysisDate
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2OTotal
H2O
SiAlt
AloFe3CrTiMgFe2MnZn
CaNa
NaK
sum
OH
T in °C
Bk 9823.2.94
51,450,086,810,001,978,110,1114,7410,050,142,150,1495,75
2,07
7,4360,5648,000
0,5960,2140,0000,0063,1750,9800,0130,0155,000
1,5560,4442,000
0,1590,0260,185
15,185
2,000
513
Bk 91223.2.94
53,630,054,350,040,089,280,0816,2511,490,111,420,0896,86
2,10
7,6610,3398,000
0,3930,0080,0050,0043,4601,1090,0100,0125,000
1,7590,2412,000
0,1520,0150,167
15,167
2,000
476
Bk 91323.2.94
50,360,128,090,031,788,800,1213,9510,030,232,370,1896,06
2,07
7,2950,7058,000
0,6760,1940,0030,0093,0121,0660,0150,0255,000
1,5570,4432,000
0,2220,0340,256
15,256
2,000
536
Bk 92023.2.94
45,270,1511,040,054,4510,600,1711,0410,020,122,770,2895,96
2,01
6,7411,2598,000
0,6790,4980,0060,0122,4501,3200,0210,0135,000
1,5990,4012,000
0,3980,0540,453
15,453
2,000
604
Bk 91424.2.94
47,260,3010,260,013,2610,010,0912,039,720,072,810,2696,09
2,04
6,9491,0518,000
0,7270,3610,0010,0242,6361,2310,0110,0085,000
1,5310,4692,000
0,3320,0500,382
15,382
2,000
579
Bk 91524.2.94
48,160,289,900,043,269,960,1411,799,040,173,030,2395,99
2,04
7,0660,9348,000
0,7770,3600,0050,0222,5781,2220,0170,0185,000
1,4210,5792,000
0,2830,0440,327
15,327
2,000
564
Bk 91624.2.94
48,380,408,340,103,309,700,1212,9010,250,182,270,2396,17
2,04
7,1020,8988,000
0,5450,3650,0120,0322,8221,1910,0150,0205,000
1,6120,3882,000
0,2580,0440,302
15,302
2,000
572
Bk 92524.2.94
45,990,2210,270,003,4411,090,1411,4610,160,162,780,2995,99
2,02
6,8411,1598,000
0,6420,3850,0000,0182,5411,3790,0180,0185,000
1,6190,3812,000
0,4210,0560,477
15,477
2,000
587
Bk 92624.2.94
46,740,049,890,023,3010,470,1112,0410,180,102,680,2895,85
2,02
6,9221,0788,000
0,6480,3680,0020,0032,6571,2970,0140,0115,000
1,6150,3852,000
0,3850,0540,439
15,439
2,000
580
Bk 92724.2.94
49,400,008,100,062,737,980,0514,5610,570,112,310,1496,00
2,07
7,1720,8288,000
0,5580,2980,0070,0003,1510,9690,0060,0125,000
1,6440,3562,000
0,2940,0260,321
15,321
2,000
561
Bk 92924.2.94
49,440,148,460,001,719,580,0713,459,990,122,540,2195,71
2,05
7,2230,7778,000
0,6800,1880,0000,0112,9291,1710,0090,0135,000
1,5640,4362,000
0,2830,0400,323
15,323
2,000
544
norm 23 oxygen, Fe3 over Si+Ti+Al+Cr+Fe+Mg+Mn+Zn = 16
norm 23 oxygen, Fe3 over Si+Ti+Al+Cr+Fe+Mg+Mn+Zn = 16
B-11Appendix B Table B3 amphibole-plagioclasethermometer
SampleAnalysisDate
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2OTotal
H2O
SiAlt
AloFe3CrTiMgFe2MnZn
CaNa
NaK
sum
OH
T in °C
Bk 9224.3.94
48,770,149,260,053,7010,280,1512,309,960,202,600,2597,66
2,07
7,0610,9398,000
0,6410,4030,0060,0112,6541,2450,0180,0215,000
1,5450,4552,000
0,2750,0470,322
15,322
2,000
572
Bk 9234.3.94
48,770,178,580,002,8510,570,1512,6710,270,162,450,2596,90
2,05
7,1160,8848,000
0,5920,3130,0000,0132,7561,2900,0190,0175,000
1,6060,3942,000
0,2990,0480,346
15,346
2,000
564
Cig 91-17317.6.93
47,670,288,820,000,989,380,0915,0511,680,002,660,3396,94
2,06
6,9391,0618,000
0,4530,1080,0000,0223,2651,1410,0110,0005,000
1,8220,1782,000
0,5720,0630,635
15,635
2,000
556
Cig 91-17417.6.93
45,180,2612,610,021,6310,110,1212,4010,240,003,550,4096,51
2,04
6,6401,3608,000
0,8240,1800,0020,0212,7161,2420,0150,0005,000
1,6120,3882,000
0,6240,0770,701
15,701
2,000
574
norm 23 oxygen, Fe3 over Si+Ti+Al+Cr+Fe+Mg+Mn+Zn = 16
B-12 Appendix B Table B5 calcite-dolomite solvusthermometer
sampleanalysisdateCL colour
CaOMgOFeOMnO
Sum
CO2
total
CaMgFeMn
CO3
T(Mg)°CT(Fe,Mg)°C
Bk 7726.4.93yellow
52,391,972,130,65
57,14
44,97
102,11
0,9140,0480,0290,009
1,000
518538
Bk 7826.4.93brown
50,902,552,410,65
56,51
44,61
101,12
0,8950,0620,0330,009
1,000
572577
Bk 72126.4.93yellow
51,102,392,190,56
56,24
44,40
100,64
0,9030,0590,0300,008
1,000
560568
Bk 72226.4.93yellow
50,552,432,450,53
55,96
44,15
100,11
0,8980,0600,0340,007
1,000
564571
Bk 76326.4.93yellow
53,281,311,470,63
56,69
44,53
101,22
0,9390,0320,0200,009
1,000
442470
Bk 76426.4.93yellow
51,921,301,570,57
55,36
43,48
98,84
0,9370,0330,0220,008
1,000
445475
Bk 726.7.92yellow
63,611,241,400,86
67,11
52,66
119,77
0,9480,0260,0160,010
1,000
400429
Bk 746.7.92yellow
62,281,682,111,06
67,13
52,66
119,79
0,9280,0350,0250,012
1,000
457488
Bk 7106.7.92orange
59,982,182,721,29
66,17
51,92
118,09
0,9070,0460,0320,015
1,000
510533
Bk 7336.7.92yellow
62,601,011,871,07
66,55
52,04
118,59
0,9440,0210,0220,013
1,000
362407
Bk 7Th311.6.94yellow
54,901,851,200,64
58,59
46,24
104,83
0,9320,0440,0160,009
1,000
501516
Bk 7Th411.6.94yellow
54,281,771,540,68
58,27
45,90
104,17
0,9280,0420,0210,009
1,000
494513
sampleanalysisdateCL colour
CaOMgOFeOMnO
Sum
CO2
total
CaMgFeMn
CO3
T(Mg)°CT(Fe,Mg)°C
Bk 7Th711.6.94orange
53,651,971,850,73
58,20
45,84
104,04
0,9180,0470,0250,010
1,000
515533
Bk 7Th1611.6.94yellow
51,421,751,430,50
55,10
43,45
98,55
0,9290,0440,0200,007
1,000
502520
Bk 7Th1711.6.94orange
51,381,832,120,96
56,29
44,21
100,50
0,9120,0450,0290,013
1,000
507530
Bk 7Th1811.6.94orange
52,791,962,520,82
58,09
45,62
103,71
0,9080,0470,0340,011
1,000
515537
Bk 7Th1911.6.94yellow
51,541,301,770,72
55,33
43,40
98,73
0,9320,0330,0250,010
1,000
446479
Bk 7Th2011.6.94yellow
52,911,261,730,71
56,61
44,40
101,01
0,9350,0310,0240,010
1,000
435469
Bk 7Th2111.6.94orange
49,871,661,960,74
54,23
42,61
96,84
0,9190,0430,0280,011
1,000
496520
Bk 7Th2211.6.94orange
50,591,621,900,68
54,79
43,06
97,85
0,9220,0410,0270,010
1,000
489514
Bk 7Th2311.6.94orange
50,051,701,800,69
54,24
42,66
96,90
0,9210,0440,0260,010
1,000
500522
Bk 7Th2411.6.94yellow
50,211,411,790,54
53,95
42,37
96,32
0,9300,0360,0260,008
1,000
465495
Bk 7Th2511.6.94orange
49,401,691,980,74
53,81
42,29
96,10
0,9170,0440,0290,011
1,000
501524
Bk 7Th2611.6.94yellow
51,131,341,570,59
54,63
42,92
97,55
0,9350,0340,0220,009
1,000
453482
Bk 7Th2811.6.94orange
49,921,762,270,62
54,57
42,87
97,44
0,9140,0450,0320,009
1,000
506530
Bk 7Th2911.6.94orange
50,641,711,940,70
54,99
43,23
98,22
0,9190,0430,0270,010
1,000
499522
Bk 7Th3011.6.94yellow
50,641,752,130,67
55,19
43,37
98,56
0,9160,0440,0300,010
1,000
502526
Bk 7Th3111.6.94orange
50,921,381,970,60
54,87
43,05
97,92
0,9280,0350,0280,009
1,000
458492
Bk 7Th3311.6.94yellow
50,631,502,020,46
54,61
42,89
97,50
0,9260,0380,0290,007
1,000
475505
Bk 7Th3411.6.94yellow
52,621,051,600,55
55,82
43,76
99,58
0,9440,0260,0220,008
1,000
403441
Bk 7Th3311.6.94yellow
50,631,502,020,46
54,61
42,89
97,50
0,9260,0380,0290,007
1,000
475505
Bk 7Th3411.6.94yellow
52,621,051,600,55
55,82
43,76
99,58
0,9440,0260,0220,008
1,000
403441
Bk 7Th3611.6.94brown
50,981,601,940,70
55,22
43,38
98,60
0,9220,0400,0270,010
1,000
485512
sampleanalysisdateCL colour
CaOMgOFeOMnO
Sum
CO2
total
CaMgFeMn
CO3
T(Mg)°CT(Fe,Mg)°C
B-13Appendix B Table B5 calcite-dolomite solvusthermometer
sampleanalysisdateCL colour
CaOMgOFeOMnO
Sum
CO2
total
CaMgFeMn
CO3
T(Mg)°CT(Fe,Mg)°C
sampleanalysisdateCL colour
CaOMgOFeOMnO
Sum
CO2
total
CaMgFeMn
CO3
T(Mg)°CT(Fe,Mg)°C
Bk 7Th3711.6.94brown
50,371,641,790,66
54,46
42,83
97,29
0,9230,0420,0260,010
1,000
492516
Bk 7Th3811.6.94brown
50,521,601,930,60
54,65
42,95
97,60
0,9230,0410,0280,009
1,000
487513
Bk 7Th4011.6.94brown
51,271,511,690,68
55,15
43,34
98,49
0,9280,0380,0240,010
1,000
474500
Bk 7Th4111.6.94yellow
53,030,720,750,69
55,19
43,29
98,48
0,9610,0180,0110,010
1,000
329355
Bk 7Th4211.6.94yellow
52,140,980,970,65
54,74
42,99
97,73
0,9520,0250,0140,009
1,000
393419
Bk 7Th4311.6.94yellow
53,130,710,730,62
55,19
43,30
98,49
0,9630,0180,0100,009
1,000
326352
Bk 7Th4411.6.94yellow
51,721,330,930,55
54,53
42,95
97,48
0,9450,0340,0130,008
1,000
452470
Bk 7Th4511.6.94yellow
52,471,220,980,75
55,42
43,58
99,00
0,9450,0310,0140,011
1,000
433454
Bk 7Th5011.6.94orange
52,241,431,460,64
55,77
43,85
99,62
0,9350,0360,0200,009
1,000
462487
Bk 7Th5111.6.94orange
51,581,411,190,52
54,70
43,07
97,77
0,9400,0360,0170,007
1,000
462484
Bk 7Th5211.6.94orange
52,051,401,160,64
55,25
43,48
98,73
0,9390,0350,0160,009
1,000
459480
Bk 7Th4611.6.94yellow
52,241,000,870,58
54,69
42,98
97,67
0,9540,0250,0120,008
1,000
397420
Bk 7Th4711.6.94yellow
53,380,720,920,56
55,58
43,59
99,17
0,9610,0180,0130,008
1,000
328359
Bk 7Th4811.6.94yellow
51,471,601,450,70
55,22
43,46
98,68
0,9290,0400,0200,010
1,000
485506
Bk 7Th4911.6.94orange
51,191,521,290,71
54,71
43,06
97,77
0,9330,0390,0180,010
1,000
477497
B-14 Appendix B Table B6 jadeite-quartz-albitebarometer
sampleanalysisdate
SiAlt
AloFe3Ti
MgFe2MnCaNaK
sum
at T (K)
P (Gpa)
Bk 391,34.5.92
1,9950,0052,000
0,4740,0330,0010,509
0,4310,0830,0000,4740,5030,0011,491
2,000
823
1,30
Bk 399,24.5.92
1,9980,0022,000
0,4450,0290,0010,475
0,4560,0800,0010,5130,4740,0001,525
2,000
823
1,30
Bk 3910,24.5.92
2,002-0,0022,000
0,4520,0240,0010,477
0,4510,0880,0000,5030,4800,0001,523
2,000
823
1,30
Bk 3912,24.5.92
1,9990,0012,000
0,4320,0410,0010,473
0,4510,0910,0000,5120,4720,0011,527
2,000
823
1,28
Bk 3913,24.5.92
1,9880,0122,000
0,4640,0660,0010,530
0,4200,0570,0010,4730,5190,0001,470
2,000
823
1,27
Bk 3914,24.5.92
1,9930,0072,000
0,4290,0650,0010,496
0,4420,0690,0010,5020,4890,0001,504
2,000
823
1,27
Bk 39823.3.92
1,9730,0272,000
0,4350,1560,0000,591
0,3850,0160,0000,4430,5640,0001,409
2,000
823
1,21
Bk 39923.3.92
1,9360,0642,000
0,4470,0560,0010,504
0,4310,2690,0030,3520,4390,0031,496
2,000
823
1,26
BK 391023.3.92
1,9450,0552,000
0,4260,0550,0010,482
0,4400,1770,0020,4720,4260,0011,518
2,000
823
1,27
BK 392,34.5.92
1,9970,0032,000
0,4810,0390,0000,521
0,4130,0760,0010,4710,5180,0001,479
2,000
823
1,29
Bk 391,15.5.92
1,9890,0112,000
0,4670,0770,0010,545
0,3680,1100,0010,4400,5340,0011,455
2,000
823
1,27
sampleanalysisdate
SiAlt
AloFe3Ti
MgFe2MnCaNaK
sum
at T (K)
P (Gpa)
Bk 392,15.5.92
1,9930,0072,000
0,4500,0570,0010,508
0,4250,0740,0020,4900,5020,0001,492
2,000
823
1,28
Bk 393,25.5.92
1,9980,0022,000
0,4600,0740,0010,536
0,3900,0840,0000,4550,5350,0001,464
2,000
823
1,27
Bk 394,25.5.92
2,001-0,0012,000
0,4630,0570,0010,523
0,3870,0930,0000,4720,5250,0001,477
2,000
823
1,28
Bk 395,15.5.92
1,9970,0032,000
0,4680,0680,0010,538
0,3930,0720,0000,4610,5350,0001,462
2,000
823
1,27
Bk 396,15.5.92
1,9950,0052,000
0,4790,0660,0010,546
0,3850,0780,0000,4500,5410,0001,454
2,000
823
1,28
Bk 398,15.5.92
2,002-0,0022,000
0,5310,0780,0010,611
0,3060,0930,0000,3750,6130,0011,389
2,000
823
1,28
Bk 3910,15.5.92
1,9870,0132,000
0,4690,0700,0010,539
0,4060,0970,0000,4300,5260,0011,461
2,000
823
1,27
Bk 3911,15.5.92
1,9920,0082,000
0,4640,0940,0010,559
0,3770,0690,0010,4430,5510,0001,441
2,000
823
1,26
Bk 39124.6.92
1,9900,0102,000
0,4930,1020,0000,596
0,3420,0760,0020,3980,5860,0001,404
2,000
823
1,26
Bk 39324.6.92
2,012-0,0122,000
0,4900,0210,0010,513
0,3950,1340,0020,4300,5260,0001,487
2,000
823
1,30
Bk 39424.6.92
1,9850,0152,000
0,4700,0730,0010,545
0,3890,0830,0000,4520,5300,0001,455
2,000
823
1,27
Bk 393824.6.92
1,9970,0032,000
0,4120,0620,0010,476
0,4250,1100,0000,5150,4740,0001,524
2,000
823
1,27
sampleanalysisdate
SiAlt
AloFe3Ti
MgFe2MnCaNaK
sum
at T (K)
P (Gpa)
Bk 396124.6.92
2,0000,0002,000
0,4790,0290,0010,511
0,4140,0930,0000,4720,5110,0001,489
2,000
823
1,30
Bk 39428.8.92
1,9880,0122,000
0,4710,0860,0010,557
0,3810,0760,0010,4390,5450,0001,443
2,000
823
1,26
Bk 39528.8.92
1,9770,0232,000
0,4510,1230,0010,576
0,3830,0400,0000,4450,5530,0011,424
2,000
823
1,24
Bk 391028.8.92
1,9910,0092,000
0,4520,1020,0010,555
0,3850,0610,0000,4490,5460,0001,445
2,000
823
1,25
Bk 391128.8.92
1,9760,0242,000
0,4280,1730,0010,603
0,3260,0740,0000,4160,5800,0001,397
2,000
823
1,20
Bk 391328.8.92
1,9950,0052,000
0,4650,0810,0030,549
0,3780,0910,0010,4330,5470,0001,451
2,000
823
1,26
Bk 391428.8.92
1,9890,0112,000
0,4610,0670,0010,530
0,3870,0910,0000,4720,5190,0001,470
2,000
823
1,27
Bk 392928.8.92
1,9850,0152,000
0,4650,0580,0010,525
0,4110,0800,0010,4720,5100,0001,475
2,000
823
1,28
Bk 3930 28.8.92
1,9880,0122,000
0,4420,0480,0000,490
0,4560,0610,0010,5140,4780,0001,510
2,000
823
1,28
Bk 393128.8.92
1,9850,0152,000
0,4470,0580,0010,507
0,4520,0460,0000,5010,4910,0011,493
2,000
823
1,28
B-15Appendix B Table B6 jadeite-quartz-albitebarometer
sampleanalysisdate
SiAlt
AloFe3Ti
MgFe2MnCaNaK
sum
at T (K)
P (Gpa)
Bk 393228.8.92
1,9820,0182,000
0,4440,0630,0010,507
0,4470,0560,0000,5010,4890,0011,493
2,000
823
1,27
Bk 393328.8.92
1,9770,0232,000
0,3880,0720,0010,461
0,5020,0430,0010,5530,4380,0001,539
2,000
823
1,25
Bk 393428.8.92
1,9810,0192,000
0,4440,0690,0020,515
0,4480,0380,0000,5010,4960,0011,485
2,000
823
1,27
Bk 393528.8.92
1,9840,0162,000
0,4450,0510,0010,496
0,4580,0520,0000,5120,4810,0011,504
2,000
823
1,28
Bk 393628.8.92
1,9850,0152,000
0,4290,0620,0010,493
0,4600,0480,0010,5190,4790,0001,507
2,000
823
1,27
Bk 393728.8.92
1,9820,0182,000
0,3950,0980,0000,495
0,4460,0650,0020,5110,4770,0011,505
2,000
823
1,24
Bk 393928.8.92
1,9900,0102,000
0,3950,0730,0010,469
0,4510,0870,0000,5330,4590,0011,531
2,000
823
1,25
Bk 394028.8.92
1,9900,0102,000
0,4570,0430,0000,500
0,4420,0630,0020,5010,4900,0011,500
2,000
823
1,29
Bk 394128.8.92
1,9880,0122,000
0,4700,0410,0010,513
0,4370,0640,0020,4830,5020,0001,487
2,000
823
1,29
Bk 394228.8.92
1,9880,0122,000
0,4590,0420,0010,503
0,4430,0670,0010,4930,4900,0011,497
2,000
823
1,29
Bk 395328.8.92
1,9790,0212,000
0,3850,1260,0010,512
0,4060,0870,0020,4980,4890,0021,488
2,000
823
1,21
Bk 395428.8.92
1,9770,0232,000
0,3910,1180,0010,510
0,3980,0880,0030,5130,4860,0011,490
2,000
823
1,22
sampleanalysisdate
SiAlt
AloFe3Ti
MgFe2MnCaNaK
sum
at T (K)
P (Gpa)
Bk 395528.8.92
1,9690,0312,000
0,3930,1120,0010,506
0,4160,0880,0020,5100,4740,0021,494
2,000
823
1,22
Bk 395528.1.93
1,9730,0272,000
0,4210,1390,0010,563
0,3880,0500,0110,4480,5350,0011,437
2,000
823
1,22
Bk 395728.1.93
1,9950,0052,000
0,4610,0650,0010,527
0,3950,0860,0010,4650,5220,0001,473
2,000
823
1,27
Bk 396028.1.93
1,9820,0182,000
0,4360,0830,0010,521
0,4300,0570,0010,4790,4980,0051,479
2,000
823
1,26
Bk 73825.6.92
1,9860,0142,000
0,4140,0700,0010,486
0,4260,0850,0020,5280,4730,0001,514
2,000
823
1,26
Bk 7126.7.92
1,9950,0052,000
0,4620,0760,0010,540
0,3770,0870,0010,4580,5370,0001,460
2,000
823
1,27
Bk 7236.7.92
1,9940,0062,000
0,4940,0620,0010,556
0,3800,0690,0010,4440,5490,0011,444
2,000
823
1,28
Bk 7556.7.92
1,9860,0142,000
0,4170,1080,0010,528
0,3870,0950,0040,4700,5150,0001,472
2,000
823
1,24
Bk 7686.7.92
1,9780,0222,000
0,4200,1010,0010,523
0,3980,0830,0000,4940,5020,0001,477
2,000
823
1,24
Bk 7746.7.92
1,9990,0012,000
0,4510,0510,0000,503
0,4080,0970,0010,4870,5030,0001,497
2,000
823
1,28
sampleanalysisdate
SiAlt
AloFe3Ti
MgFe2MnCaNaK
sum
at T (K)
P (Gpa)
Bk 737.7.92
1,9940,0062,000
0,4530,0480,0010,503
0,3980,1020,0000,4980,4980,0001,497
2,000
823
1,28
Bk 747.7.92
1,9870,0132,000
0,4340,0620,0000,496
0,4120,0840,0020,5220,4830,0011,504
2,000
823
1,27
Bk 767.7.92
1,9810,0192,000
0,4310,0800,0000,512
0,4110,0720,0020,5090,4940,0001,488
2,000
823
1,26
Bk 7427.7.92
1,9950,0052,000
0,5180,0560,0010,576
0,3570,0740,0010,4210,5710,0001,424
2,000
823
1,29
Bk 7457.7.92
1,9810,0192,000
0,4330,0920,0010,526
0,3970,0650,0000,5060,5070,0001,474
2,000
823
1,25
Bk 7467.7.92
1,9780,0222,000
0,4610,0660,0010,530
0,3910,1130,0030,4540,5080,0011,470
2,000
823
1,27
Bk 7507.7.92
1,9770,0232,000
0,4330,0910,0010,525
0,4010,0590,0030,5090,5020,0001,475
2,000
823
1,25
Bk 7577.7.92
2,006-0,0062,000
0,4520,0390,0010,494
0,4070,1200,0030,4760,5000,0001,506
2,000
823
1,29
Bk 71527.8.92
1,9770,0232,000
0,4250,0900,0010,518
0,4130,0600,0020,5080,4940,0011,482
2,000
823
1,25
Bk 71727.8.92
1,9770,0232,000
0,4290,0830,0010,515
0,4090,0660,0010,5090,4930,0001,485
2,000
823
1,25
Bk 71827.8.92
1,9930,0072,000
0,4410,0340,0010,476
0,4060,1190,0020,5170,4690,0001,524
2,000
823
1,29
B-16 Appendix B Table B6 jadeite-quartz-albitebarometer
Bk 81229.1.93b
1,9950,0052,000
0,5650,0180,0020,586
0,3430,0870,0010,3920,5810,0011,414
2,000
823
1,32
Bk 72827.8.92
1,9890,0112,000
0,4490,0270,0000,478
0,4340,0940,0020,5220,4670,0001,522
2,000
823
1,30
sampleanalysisdate
SiAlt
AloFe3Ti
MgFe2MnCaNaK
sum
at T (K)
P (Gpa)
Bk 73027.8.92
1,9750,0252,000
0,3800,0720,0000,455
0,4770,0560,0020,5710,4310,0001,545
2,000
823
1,25
Bk 73527.8.92
1,9800,0202,000
0,4450,0550,0010,503
0,4270,0720,0010,5100,4820,0011,497
2,000
823
1,28
Bk 73727.8.92
1,9750,0252,000
0,3830,0770,0000,462
0,4580,0650,0010,5710,4360,0011,538
2,000
823
1,25
Bk 74127.8.92
1,9650,0352,000
0,3660,1070,0000,473
0,4860,0250,0020,5690,4370,0011,527
2,000
823
1,22
Bk 74227.8.92
1,9810,0192,000
0,4040,0510,0010,456
0,4620,0780,0020,5600,4350,0011,544
2,000
823
1,27
Bk 75127.8.92
1,9800,0202,000
0,4490,0750,0000,524
0,4050,0660,0020,4930,5030,0011,476
2,000
823
1,26
Bk 75327.8.92
1,9840,0162,000
0,4280,0630,0010,491
0,4110,0920,0010,5230,4760,0001,509
2,000
823
1,27
Bk 81414.3.93
1,9850,0152,000
0,5380,0650,0010,605
0,3580,0430,0010,3960,5640,0261,395
2,000
823
1,28
Bk 83614.3.93
1,9840,0162,000
0,4570,0610,0010,519
0,4010,0710,0020,5000,5030,0011,481
2,000
823
1,27
Bk 83714.3.93
1,9830,0172,000
0,4680,0600,0010,529
0,3990,0730,0000,4810,5110,0011,471
2,000
823
1,28
Bk 83814.3.93
1,9920,0082,000
0,4390,0270,0020,468
0,4350,1070,0020,5220,4620,0001,532
2,000
823
1,30
sampleanalysisdate
SiAlt
AloFe3Ti
MgFe2MnCaNaK
sum
at T (K)
P (Gpa)
Bk 83914.3.93
1,9950,0052,000
0,4570,0240,0000,481
0,4230,1020,0020,5090,4760,0011,519
2,000
823
1,30
Bk 84214.3.93
1,9920,0082,000
0,4380,0660,0000,504
0,4050,0890,0020,5000,4960,0011,496
2,000
823
1,27
Bk 84314.3.93
1,9950,0052,000
0,4530,0490,0010,504
0,3810,1100,0020,4960,4990,0011,496
2,000
823
1,28
Bk 8329.1.93a
1,9910,0092,000
0,5130,0160,0080,538
0,4030,0820,0000,4290,5290,0071,462
2,000
823
1,31
Bk 8429.1.93a
2,0000,0002,000
0,5120,0040,0060,523
0,3970,1100,0020,4360,5280,0011,477
2,000
823
1,32
Bk 8529.1.93a
1,9970,0032,000
0,4870,0140,0040,505
0,3850,1250,0070,4680,5060,0001,495
2,000
823
1,31
Bk 81429.1.93a
1,9800,0202,000
0,4520,0630,0010,516
0,4130,0730,0020,4950,4960,0011,484
2,000
823
1,27
Bk 82029.1.93a
1,9860,0142,000
0,5560,0600,0010,618
0,3410,0540,0010,3760,6040,0011,382
2,000
823
1,29
Bk 82129.1.93a
1,9920,0082,000
0,4750,0790,0000,555
0,3810,0810,0010,4330,5470,0011,445
2,000
823
1,27
Bk 82329.1.93a
1,9830,0172,000
0,4700,0530,0000,523
0,4050,0790,0010,4800,5050,0021,477
2,000
823
1,28
sampleanalysisdate
SiAlt
AloFe3Ti
MgFe2MnCaNaK
sum
at T (K)
P (Gpa)
Cig90/40/2456.1.91
2,0030,0002,003
0,5020,0480,0010,550
0,3680,1030,0010,4180,5570,0001,447
1,997
823
1,29
Cig90\40\133?
1,9980,0022,000
0,5070,0600,0010,568
0,3620,0860,0000,4170,5670,0001,432
2,000
823
1,28
Cig90\40\148?
2,0030,0002,003
0,5110,0430,0010,555
0,3690,0920,0000,4190,5630,0001,441
1,997
823
1,30
Cig90\40\165?
1,9930,0072,000
0,4290,0830,0010,513
0,3620,1360,0000,4820,5070,0001,487
2,000
823
1,25
Cig90\40\166?
1,9810,0192,000
0,4710,1110,0010,583
0,3760,0400,0000,4340,5650,0001,417
2,000
823
1,25
Cig90\40\167?
1,9950,0052,000
0,4790,0760,0010,556
0,3760,0810,0000,4360,5520,0001,444
2,000
823
1,27
Cig90\40\168?
2,0000,0002,000
0,4650,0750,0000,540
0,3830,0880,0000,4490,5400,0001,460
2,000
823
1,27
C-1Appendix C
Table C1
List of samples, XRD is powder X-ray diffraction, EMP is electron microprobe, CL is cathodoluminescence,SEM is scanning electron microscopy, XRF is X-ray fluorescence spectroscopy, UST is universal stage, IAis image analysis, FIS is microthermometry
C-2 Appendix C
Table C1 continued
List of samples, XRD is powder X-ray diffraction, EMP is electron microprobe, CL is cathodoluminescence,SEM is scanning electron microscopy, XRF is X-ray fluorescence spectroscopy, UST is universal stage, IAis image analysis, FIS is microthermometry
C-3Appendix C
Table C1 continued
List of samples, XRD is powder X-ray diffraction, EMP is electron microprobe, CL is cathodoluminescence,SEM is scanning electron microscopy, XRF is X-ray fluorescence spectroscopy, UST is universal stage, IAis image analysis, FIS is microthermometry
C-4 Appendix C
Table C1 continued
List of samples, XRD is powder X-ray diffraction, EMP is electron microprobe, CL is cathodoluminescence,SEM is scanning electron microscopy, XRF is X-ray fluorescence spectroscopy, UST is universal stage, IAis image analysis, FIS is microthermometry
C-5Appendix C
Table C2
Whole rock analyses fpr major and trace elementsfrom samples of group 1 to 4 eclogites
C-6 Appendix C Table C3 omphacite
normed to 4 cations, Fe3 over charge balance (12+)
normed to 4 cations, Fe3 over charge balance (12+)
position means analysis of: i(x), inclusion of cpx in mineral x, core is core position in a cpx grain, mineral x, rimposition in cpx grain in contact with mineral x, mineral x(i), cpx at an inclusion of mineral x in cpx
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2Ototal
SiAlt
AloFe3CrTi
MgFe2MnCaZnNaK
sum
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2Ototal
SiAlt
AloFe3CrTi
MgFe2MnCaZnNaK
sum
Bk 398,213.3.93i (gnt)
55,790,0410,800,036,552,310,025,9710,630,158,610,03100,93
1,9820,0182,000
0,4350,1750,0010,0010,611
0,3160,0690,0010,4050,0040,5930,0011,389
4,000
Bk 399,213.3.93i (gnt)
55,850,0610,750,135,372,640,076,3011,050,178,320,00100,71
1,9870,0132,000
0,4370,1440,0040,0010,586
0,3340,0780,0020,4210,0040,5740,0001,414
4,000
Bk 39623.3.92i (gnt)
55,550,0312,360,053,722,320,035,909,98n.a8,790,0198,74
1,9930,0072,000
0,5160,1000,0010,0010,618
0,3160,0700,0010,384-0,6110,0001,382
4,000
Bk 39723.3.92i (gnt)
55,880,0312,670,002,243,240,045,909,82n.a8,720,0198,54
2,0050,0002,005
0,5410,0600,0000,0010,602
0,3160,0970,0010,377-0,6070,0001,398
4,000
Bk 39823.3.92i (gnt)
54,930,0010,900,005,780,540,017,1911,50n.a8,100,0198,96
1,9730,0272,000
0,4350,1560,0000,0000,591
0,3850,0160,0000,443-0,5640,0001,409
4,000
Bk 391223.3.92core
55,120,0410,460,045,031,120,027,2811,58n.a7,970,0198,66
1,9870,0132,000
0,4310,1360,0010,0010,570
0,3910,0340,0010,447-0,5570,0001,430
4,000
Bk 391323.3.92core
55,560,0210,670,002,841,190,038,4013,13n.a7,210,0099,05
1,9870,0132,000
0,4360,0760,0000,0000,513
0,4480,0360,0010,503-0,5000,0001,487
4,000
Bk 391723.3.92i (gnt)
55,200,0311,970,043,872,580,006,1010,33n.a8,470,0298,61
1,9890,0112,000
0,4970,1050,0010,0010,603
0,3280,0780,0000,399-0,5920,0011,397
4,000
Bk 391923.3.92core
55,190,0210,840,034,531,580,007,1511,58n.a7,940,0198,87
1,9850,0152,000
0,4450,1230,0010,0000,569
0,3830,0480,0000,446-0,5540,0001,431
4,000
Bk 392023.3.92core
55,350,0510,340,022,401,590,028,5713,40n.a6,930,0198,68
1,9890,0112,000
0,4270,0650,0010,0010,493
0,4590,0480,0010,516-0,4830,0001,507
4,000
Bk 39124.6.92gnt
55,210,0211,850,003,782,520,066,3610,31n.a8,390,0098,50
1,9900,0102,000
0,4930,1020,0000,0000,596
0,3420,0760,0020,398-0,5860,0001,404
4,000
Bk 39424.6.92i (gnt)
55,230,0511,460,032,682,770,017,2611,74n.a7,610,0198,85
1,9850,0152,000
0,4700,0730,0010,0010,545
0,3890,0830,0000,452-0,5300,0001,455
4,000
Bk 391524.6.92i (gnt)
54,860,0510,560,063,503,490,086,5111,55n.a7,690,0098,35
1,9950,0052,000
0,4480,0960,0020,0010,546
0,3530,1060,0020,450-0,5420,0001,454
4,000
Bk 391624.6.92i (gnt)
54,570,0010,670,033,733,530,106,5111,64n.a7,570,0098,35
1,9870,0132,000
0,4450,1020,0010,0000,548
0,3530,1080,0030,454-0,5340,0001,452
4,000
Bk 393824.6.92cpx
54,850,049,670,042,263,610,017,8313,21n.a6,710,0098,23
1,9970,0032,000
0,4120,0620,0010,0010,476
0,4250,1100,0000,515-0,4740,0001,524
4,000
Bk 396124.6.92gnt
55,700,0511,330,051,073,090,007,7312,26n.a7,340,0198,63
2,0000,0002,000
0,4790,0290,0010,0010,511
0,4140,0930,0000,472-0,5110,0001,489
4,000
Bk 391128.1.93i (gnt)
55,290,0110,580,054,003,260,066,8411,870,207,590,0199,76
1,9860,0142,000
0,4330,1080,0010,0000,543
0,3660,0980,0020,4570,0050,5280,0001,457
4,000
Bk 391328.1.93i (gnt)
55,180,0711,300,052,235,040,026,0310,350,007,970,0098,24
2,0060,0002,006
0,4900,0610,0010,0010,554
0,3270,1530,0010,4030,0000,5620,0001,446
4,000
Bk 391428.1.93i (gnt)
55,150,0611,500,083,982,910,026,2910,870,138,140,0299,15
1,9840,0162,000
0,4720,1080,0020,0010,583
0,3370,0870,0010,4190,0030,5680,0011,417
4,000
Bk 391528.1.93i (gnt)
55,070,0711,240,056,013,310,045,249,560,218,780,0299,60
1,9850,0152,000
0,4620,1630,0010,0010,628
0,2820,1000,0010,3690,0060,6140,0011,372
4,000
Bk 391628.1.93i (gnt)
54,600,039,820,067,073,160,035,6510,580,328,220,0399,57
1,9820,0182,000
0,4020,1930,0020,0010,597
0,3060,0960,0010,4110,0090,5790,0011,403
4,000
Bk 391728.1.93i (gnt)
54,210,059,330,026,474,640,065,3910,600,137,940,0198,86
1,9900,0102,000
0,3940,1790,0010,0010,574
0,2950,1430,0020,4170,0040,5650,0001,426
4,000
C-7Appendix C Table C3 omphacite
normed to 4 cations, Fe3 over charge balance (12+)
normed to 4 cations, Fe3 over charge balance (12+)
position means analysis of: i(x), inclusion of cpx in mineral x, core is core position in a cpx grain, mineral x, rimposition in cpx grain in contact with mineral x, mineral x(i), cpx at an inclusion of mineral x in cpx
Bk 39428.8.92cpx
55,370,0311,420,003,192,530,027,1311,420,007,830,0198,95
1,9880,0122,000
0,4710,0860,0000,0010,557
0,3810,0760,0010,4390,0000,5450,0001,443
4,000
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2Ototal
SiAlt
AloFe3CrTi
MgFe2MnCaZnNaK
sum
Bk 39528.8.92cpx
54,850,0611,160,034,521,330,017,1311,530,047,910,0398,60
1,9770,0232,000
0,4510,1230,0010,0010,576
0,3830,0400,0000,4450,0010,5530,0011,424
4,000
Bk 39628.8.92coes (i)
55,430,0310,970,031,961,760,048,4413,160,077,010,0198,91
1,9850,0152,000
0,4480,0530,0010,0010,502
0,4500,0530,0010,5050,0020,4870,0001,498
4,000
Bk 39828.8.92coes (i)
55,470,0412,130,003,073,370,006,0610,790,038,260,0199,23
1,9890,0112,000
0,5020,0830,0000,0010,585
0,3240,1010,0000,4150,0010,5740,0001,415
4,000
Bk 39928.8.92core
55,900,0411,780,022,242,880,016,9311,480,087,940,0199,31
1,9960,0042,000
0,4920,0600,0010,0010,553
0,3690,0860,0000,4390,0020,5500,0001,447
4,000
Bk 391028.8.92cpx
55,780,0310,940,023,792,060,007,2411,750,107,890,0199,61
1,9910,0092,000
0,4520,1020,0010,0010,555
0,3850,0610,0000,4490,0030,5460,0001,445
4,000
Bk 391128.8.92cpx
54,970,0510,670,036,392,470,006,0910,800,038,320,0099,82
1,9760,0242,000
0,4280,1730,0010,0010,603
0,3260,0740,0000,4160,0010,5800,0001,397
4,000
Bk 391328.8.92cpx
55,550,1711,080,022,993,020,037,0611,250,017,860,0199,05
1,9950,0052,000
0,4650,0810,0010,0030,549
0,3780,0910,0010,4330,0000,5470,0001,451
4,000
Bk 391428.8.92cpx
55,240,0711,130,002,473,010,007,2212,240,017,440,0198,84
1,9890,0112,000
0,4610,0670,0000,0010,530
0,3870,0910,0000,4720,0000,5190,0001,470
4,000
Bk 392928.8.92sympl
55,510,0611,390,022,162,680,027,7212,330,007,360,0199,26
1,9850,0152,000
0,4650,0580,0010,0010,525
0,4110,0800,0010,4720,0000,5100,0001,475
4,000
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2Ototal
SiAlt
AloFe3CrTi
MgFe2MnCaZnNaK
sum
Bk 392228.1.93i (gnt)
55,270,0111,390,053,783,160,076,1110,530,268,230,0398,89
1,9940,0062,000
0,4790,1030,0010,0000,583
0,3290,0950,0020,4070,0070,5760,0011,417
4,000
Bk 392428.1.93i (gnt)
55,190,0110,950,124,482,640,036,7011,380,207,880,0399,61
1,9810,0192,000
0,4440,1210,0030,0000,569
0,3580,0790,0010,4380,0050,5480,0011,431
4,000
Bk 392528.1.93i (gnt)
54,990,2210,990,043,902,950,036,5911,280,207,840,0699,09
1,9840,0162,000
0,4520,1060,0010,0040,563
0,3540,0890,0010,4360,0050,5480,0031,437
4,000
Bk 392928.1.93i (gnt)
54,560,479,220,126,844,050,026,0411,020,187,850,01100,37
1,9750,0252,000
0,3680,1860,0030,0090,567
0,3260,1230,0010,4270,0050,5510,0001,433
4,000
Bk 393128.1.93i (gnt)
55,460,0711,000,025,632,490,056,039,730,088,730,0299,30
1,9940,0062,000
0,4600,1520,0010,0010,614
0,3230,0750,0020,3750,0020,6090,0011,386
4,000
Bk 393428.1.93i (gnt)
55,410,1110,990,066,012,400,565,8310,100,168,590,02100,23
1,9830,0172,000
0,4460,1620,0020,0020,612
0,3110,0720,0170,3870,0040,5960,0011,388
4,000
Bk 395528.1.93gnt
54,660,0510,540,075,111,660,357,2211,590,147,650,0299,06
1,9730,0272,000
0,4210,1390,0020,0010,563
0,3880,0500,0110,4480,0040,5350,0011,437
4,000
Bk 395728.1.93gnt
56,550,0311,210,002,442,930,037,5212,300,127,630,01100,77
1,9950,0052,000
0,4610,0650,0000,0010,527
0,3950,0860,0010,4650,0030,5220,0001,473
4,000
Bk 396028.1.93gnt
55,590,0610,820,023,091,910,028,0912,540,367,210,1199,82
1,9820,0182,000
0,4360,0830,0010,0010,521
0,4300,0570,0010,4790,0090,4980,0051,479
4,000
Bk 397228.1.93i (gnt)
54,860,0010,020,005,643,580,055,7810,580,298,150,0298,98
1,9960,0042,000
0,4260,1540,0000,0000,580
0,3130,1090,0020,4120,0080,5750,0011,420
4,000
Bk 39328.8.92coes (i)
55,560,0311,190,050,862,770,048,2112,790,007,030,0198,54
1,9950,0052,000
0,4690,0230,0010,0010,494
0,4390,0830,0010,4920,0000,4890,0001,506
4,000
Bk 393028.8.92cpx
55,850,0210,830,001,792,040,048,5913,480,006,930,0099,57
1,9880,0122,000
0,4420,0480,0000,0000,490
0,4560,0610,0010,5140,0000,4780,0001,510
4,000
C-8 Appendix C Table C3 omphacite
normed to 4 cations, Fe3 over charge balance (12+)
normed to 4 cations, Fe3 over charge balance (12+)
position means analysis of: i(x), inclusion of cpx in mineral x, core is core position in a cpx grain, mineral x, rimposition in cpx grain in contact with mineral x, mineral x(i), cpx at an inclusion of mineral x in cpx
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2Ototal
SiAlt
AloFe3CrTi
MgFe2MnCaZnNaK
sum
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2Ototal
SiAlt
AloFe3CrTi
MgFe2MnCaZnNaK
sum
Bk 393128.8.92cpx
55,550,0310,990,052,151,550,018,4813,090,077,090,0299,07
1,9850,0152,000
0,4470,0580,0010,0010,507
0,4520,0460,0000,5010,0020,4910,0011,493
4,000
Bk 393228.8.92cpx
55,560,0410,980,002,341,860,008,4013,100,007,070,0299,37
1,9820,0182,000
0,4440,0630,0000,0010,507
0,4470,0560,0000,5010,0000,4890,0011,493
4,000
Bk 393328.8.92cpx
55,420,049,790,012,681,430,049,4514,460,036,340,0199,70
1,9770,0232,000
0,3880,0720,0000,0010,461
0,5020,0430,0010,5530,0010,4380,0001,539
4,000
Bk 393428.8.92cpx
55,660,0911,060,002,571,260,018,4513,150,007,190,0399,48
1,9810,0192,000
0,4440,0690,0000,0020,515
0,4480,0380,0000,5010,0000,4960,0011,485
4,000
Bk 393528.8.92cpx
55,690,0610,970,001,891,750,008,6213,410,006,960,0299,37
1,9840,0162,000
0,4450,0510,0000,0010,496
0,4580,0520,0000,5120,0000,4810,0011,504
4,000
Bk 393628.8.92cpx
55,800,0610,580,032,321,610,028,6713,620,006,950,0099,66
1,9850,0152,000
0,4290,0620,0010,0010,493
0,4600,0480,0010,5190,0000,4790,0001,507
4,000
Bk 393728.8.92cpx
55,130,019,750,053,632,150,058,3213,270,136,840,0299,35
1,9820,0182,000
0,3950,0980,0010,0000,495
0,4460,0650,0020,5110,0030,4770,0011,505
4,000
Bk 393828.8.92core
55,470,0511,260,002,542,730,027,2411,990,057,600,0298,96
1,9920,0082,000
0,4680,0680,0000,0010,537
0,3870,0820,0010,4610,0010,5290,0011,463
4,000
Bk 393928.8.92cpx
55,330,049,540,002,712,890,008,4213,820,016,580,0299,36
1,9900,0102,000
0,3950,0730,0000,0010,469
0,4510,0870,0000,5330,0000,4590,0011,531
4,000
Bk 394028.8.92cpx
55,680,0111,070,021,602,120,058,3013,090,017,070,0299,04
1,9900,0102,000
0,4570,0430,0010,0000,500
0,4420,0630,0020,5010,0000,4900,0011,500
4,000
Bk 394128.8.92cpx
55,720,0611,450,021,542,140,068,2112,630,007,250,0199,09
1,9880,0122,000
0,4700,0410,0010,0010,513
0,4370,0640,0020,4830,0000,5020,0001,487
4,000
Bk 394228.8.92cpx
55,810,0511,230,031,562,250,038,3412,920,107,100,0299,44
1,9880,0122,000
0,4590,0420,0010,0010,503
0,4430,0670,0010,4930,0030,4900,0011,497
4,000
Bk 395328.8.92gnt
55,120,049,590,014,662,890,067,5812,950,157,030,05100,13
1,9790,0212,000
0,3850,1260,0000,0010,512
0,4060,0870,0020,4980,0040,4890,0021,488
4,000
Bk 395428.8.92gnt
54,360,039,670,004,322,910,107,3513,170,006,890,0398,82
1,9770,0232,000
0,3910,1180,0000,0010,510
0,3980,0880,0030,5130,0000,4860,0011,490
4,000
Bk 391,34.5.92gnt
56,000,0511,420,021,232,780,008,1112,41n.a.7,290,0299,32
1,9950,0052,000
0,4740,0330,0010,0010,509
0,4310,0830,0000,474-0,5030,0011,491
4,000
Bk 392,24.5.92i (gnt)
55,420,0411,450,023,352,940,016,5911,02n.a.8,070,0298,93
1,9930,0072,000
0,4780,0910,0010,0010,570
0,3530,0880,0000,425-0,5630,0011,430
4,000
Bk 392,34.5.92gnt
56,090,0111,540,041,462,550,027,7812,36n.a.7,500,0199,36
1,9970,0032,000
0,4810,0390,0010,0000,521
0,4130,0760,0010,471-0,5180,0001,479
4,000
Bk 396,24.5.92i (gnt)
55,090,0210,480,093,803,080,046,7911,86n.a.7,650,0098,90
1,9910,0092,000
0,4380,1030,0030,0000,544
0,3660,0930,0010,459-0,5360,0001,456
4,000
Bk 397,24.5.92i (gnt)
55,170,0211,030,053,853,290,056,4811,24n.a.7,900,0299,10
1,9890,0112,000
0,4580,1040,0010,0000,564
0,3480,0990,0020,434-0,5520,0011,436
4,000
Bk 398,24.5.92i (gnt)
55,200,0412,010,003,402,240,056,4310,78n.a.8,290,0198,45
1,9880,0122,000
0,4980,0920,0000,0010,591
0,3450,0670,0020,416-0,5790,0001,409
4,000
Bk 399,24.5.92gnt
55,830,0610,610,011,072,680,048,5513,38n.a.6,830,0199,07
1,9980,0022,000
0,4450,0290,0000,0010,475
0,4560,0800,0010,513-0,4740,0001,525
4,000
Bk 3910,24.5.92gnt
55,640,0410,630,010,882,920,018,4113,06n.a.6,880,0098,49
2,0020,0002,002
0,4520,0240,0000,0010,477
0,4510,0880,0000,503-0,4800,0001,523
4,000
C-9Appendix C Table C3 omphacite
normed to 4 cations, Fe3 over charge balance (12+)
normed to 4 cations, Fe3 over charge balance (12+)
position means analysis of: i(x), inclusion of cpx in mineral x, core is core position in a cpx grain, mineral x, rimposition in cpx grain in contact with mineral x, mineral x(i), cpx at an inclusion of mineral x in cpx
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2Ototal
SiAlt
AloFe3CrTi
MgFe2MnCaZnNaK
sum
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2Ototal
SiAlt
AloFe3CrTi
MgFe2MnCaZnNaK
sum
Bk 3913,24.5.92gnt
55,750,0311,310,012,451,920,037,9012,37n.a.7,500,0199,28
1,9880,0122,000
0,4640,0660,0000,0010,530
0,4200,0570,0010,473-0,5190,0001,470
4,000
Bk 3914,24.5.92gnt
55,470,0310,290,052,422,290,038,2613,05n.a.7,020,0198,92
1,9930,0072,000
0,4290,0650,0010,0010,496
0,4420,0690,0010,502-0,4890,0001,504
4,000
Bk 392,15.5.92par
55,320,0510,740,002,102,450,057,9212,68n.a.7,180,0198,50
1,9930,0072,000
0,4500,0570,0000,0010,508
0,4250,0740,0020,490-0,5020,0001,492
4,000
Bk 393,15.5.92core
55,490,0712,600,002,803,510,045,509,76n.a.8,730,0298,52
1,9990,0012,000
0,5330,0760,0000,0010,611
0,2950,1060,0010,377-0,6100,0011,389
4,000
Bk 393,25.5.92clz
55,450,0510,900,052,722,780,017,2611,78n.a.7,660,0098,65
1,9980,0022,000
0,4600,0740,0010,0010,536
0,3900,0840,0000,455-0,5350,0001,464
4,000
Bk 394,15.5.92core
55,720,0412,560,012,563,670,015,639,69n.a.8,720,0398,64
2,0030,0002,003
0,5350,0690,0000,0010,605
0,3020,1100,0000,373-0,6080,0011,395
4,000
Bk 394,25.5.92clz
55,520,0710,870,042,103,090,007,2012,22n.a.7,510,0198,63
2,0010,0002,001
0,4630,0570,0010,0010,523
0,3870,0930,0000,472-0,5250,0001,477
4,000
Bk 395,15.5.92cpx
55,340,0411,090,042,522,390,017,3111,92n.a.7,650,0198,31
1,9970,0032,000
0,4680,0680,0010,0010,538
0,3930,0720,0000,461-0,5350,0001,462
4,000
Bk 396,15.5.92cpx
55,500,0311,430,002,452,600,007,1811,69n.a.7,760,0198,65
1,9950,0052,000
0,4790,0660,0000,0010,546
0,3850,0780,0000,450-0,5410,0001,454
4,000
Bk 397,15.5.92core
55,540,0612,230,002,142,850,006,3310,63n.a.8,340,0198,12
2,0020,0002,002
0,5210,0580,0000,0010,580
0,3400,0860,0000,410-0,5830,0001,420
4,000Bk
398,15.5.92cpx
55,570,0712,460,042,873,090,005,709,71n.a.8,780,0398,32
2,0020,0002,002
0,5310,0780,0010,0010,611
0,3060,0930,0000,375-0,6130,0011,389
4,000
Bk 399,15.5.92core
55,510,0611,140,031,302,410,028,0512,73n.a.7,180,0198,44
1,9950,0052,000
0,4670,0350,0010,0010,504
0,4310,0730,0010,490-0,5000,0001,496
4,000
Bk 3910,15.5.92par
54,970,0411,300,012,563,210,017,5411,09n.a.7,510,0298,27
1,9870,0132,000
0,4690,0700,0000,0010,539
0,4060,0970,0000,430-0,5260,0011,461
4,000
Bk 3911,15.5.92par
55,330,0311,130,033,462,300,047,0211,48n.a.7,890,0198,73
1,9920,0082,000
0,4640,0940,0010,0010,559
0,3770,0690,0010,443-0,5510,0001,441
4,000
Bk 73825.6.92gnt
54,910,0310,040,042,562,820,087,9013,62n.a.6,740,0098,74
1,9860,0142,000
0,4140,0700,0010,0010,486
0,4260,0850,0020,528-0,4730,0001,514
4,000
Bk 7226.4.93gnt
56,240,0311,670,031,832,720,087,4711,560,297,770,0299,70
1,9980,0022,000
0,4870,0490,0010,0010,537
0,3960,0810,0020,4400,0080,5350,0011,463
4,000
Bk 7326.4.93gnt
56,070,1512,230,130,733,720,077,0911,260,227,770,0299,46
1,9980,0022,000
0,5110,0200,0040,0030,537
0,3760,1110,0020,4300,0060,5370,0011,463
4,000
Bk 73826.4.93i (gnt)
55,970,1110,270,001,403,860,067,7112,390,097,200,0099,06
2,0120,0002,012
0,4350,0380,0000,0020,475
0,4130,1160,0020,4770,0020,5020,0001,512
4,000
Bk 74026.4.93i (gnt)
56,310,0412,120,102,422,420,026,9910,720,158,310,0299,62
1,9980,0022,000
0,5050,0650,0030,0010,574
0,3700,0720,0010,4080,0040,5720,0011,426
4,000
Bk 74126.4.93i (gnt)
55,340,0410,910,032,003,870,097,4611,530,127,320,0498,75
1,9970,0032,000
0,4610,0540,0010,0010,517
0,4010,1170,0030,4460,0030,5120,0021,483
4,000
Bk 74226.4.93i (gnt)
55,100,0710,890,032,224,010,097,1211,960,217,240,0298,96
1,9900,0102,000
0,4540,0600,0010,0010,516
0,3830,1210,0030,4630,0060,5070,0011,484
4,000
Bk 71527.8.92par
54,970,0410,570,073,332,010,077,7013,190,137,090,0299,19
1,9770,0232,000
0,4250,0900,0020,0010,518
0,4130,0600,0020,5080,0030,4940,0011,482
4,000
C-10 Appendix C Table C3 omphacite
normed to 4 cations, Fe3 over charge balance (12+)
normed to 4 cations, Fe3 over charge balance (12+)
position means analysis of: i(x), inclusion of cpx in mineral x, core is core position in a cpx grain, mineral x, rimposition in cpx grain in contact with mineral x, mineral x(i), cpx at an inclusion of mineral x in cpx
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2Ototal
SiAlt
AloFe3CrTi
MgFe2MnCaZnNaK
sum
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2Ototal
SiAlt
AloFe3CrTi
MgFe2MnCaZnNaK
sum
Bk 71627.8.92core
55,870,0613,120,081,482,840,006,7710,410,278,260,0299,18
1,9880,0122,000
0,5390,0400,0020,0010,581
0,3590,0850,0000,3970,0070,5700,0011,419
4,000
Bk 71727.8.92par
55,180,0510,690,063,092,210,037,6613,260,267,090,0199,59
1,9770,0232,000
0,4290,0830,0020,0010,515
0,4090,0660,0010,5090,0070,4930,0001,485
4,000
Bk 71827.8.92par
55,030,0410,510,001,253,920,067,5313,330,396,680,0198,74
1,9930,0072,000
0,4410,0340,0000,0010,476
0,4060,1190,0020,5170,0100,4690,0001,524
4,000
Bk 72827.8.92gl
55,520,0210,900,031,003,130,068,1213,610,136,720,0199,25
1,9890,0112,000
0,4490,0270,0010,0000,478
0,4340,0940,0020,5220,0030,4670,0001,522
4,000
Bk 73027.8.92cpx
54,740,029,520,092,651,840,068,8614,760,346,160,0099,05
1,9750,0252,000
0,3800,0720,0030,0000,455
0,4770,0560,0020,5710,0090,4310,0001,545
4,000
Bk 73527.8.92par
54,930,0510,960,052,042,400,037,9513,220,106,900,0398,66
1,9800,0202,000
0,4450,0550,0010,0010,503
0,4270,0720,0010,5100,0030,4820,0011,497
4,000
Bk 73727.8.92par
54,610,019,570,032,832,150,028,5014,720,256,220,0298,93
1,9750,0252,000
0,3830,0770,0010,0000,462
0,4580,0650,0010,5710,0070,4360,0011,538
4,000
Bk 73827.8.92core
55,350,0511,110,031,163,040,058,0313,290,276,790,0299,20
1,9850,0152,000
0,4540,0310,0010,0010,487
0,4290,0910,0020,5110,0070,4720,0011,513
4,000
Bk 73927.8.92core
54,800,0510,990,032,311,880,058,0513,590,306,810,0198,87
1,9720,0282,000
0,4380,0630,0010,0010,503
0,4320,0570,0020,5240,0080,4750,0001,497
4,000
Bk 74027.8.92core
54,330,019,760,012,522,010,058,7314,710,156,100,0398,40
1,9720,0282,000
0,3890,0690,0000,0000,459
0,4720,0610,0020,5720,0040,4290,0011,541
4,000
Bk 74127.8.92par
54,670,029,470,013,960,840,069,0814,770,246,270,0399,42
1,9650,0352,000
0,3660,1070,0000,0000,473
0,4860,0250,0020,5690,0060,4370,0011,527
4,000
Bk 7446.7.92i (gnt)
55,340,049,820,062,693,800,067,6212,99n.a.6,920,0199,35
1,9950,0052,000
0,4130,0730,0020,0010,488
0,4100,1140,0020,502-0,4840,0001,512
4,000
Bk 74227.8.92cpx
54,510,039,900,001,852,580,068,5414,390,176,180,0398,25
1,9810,0192,000
0,4040,0510,0000,0010,456
0,4620,0780,0020,5600,0050,4350,0011,544
4,000
Bk 75127.8.92gl
55,320,0111,130,002,792,190,057,5912,860,267,250,0299,47
1,9800,0202,000
0,4490,0750,0000,0000,524
0,4050,0660,0020,4930,0070,5030,0011,476
4,000
Bk 75327.8.92clz
54,910,0510,430,002,303,030,047,6413,500,226,790,0198,92
1,9840,0162,000
0,4280,0630,0000,0010,491
0,4110,0920,0010,5230,0060,4760,0001,509
4,000
Bk 776.7.92core
55,380,0511,700,022,202,160,007,3111,95n.a.7,710,0098,48
1,9900,0102,000
0,4850,0590,0010,0010,546
0,3920,0650,0000,460-0,5370,0001,454
4,000
Bk 786.7.92core
55,080,0310,730,031,453,740,057,3613,08n.a.6,940,0198,51
1,9940,0062,000
0,4520,0400,0010,0010,493
0,3970,1130,0020,507-0,4870,0001,507
4,000
Bk 7126.7.92gnt
55,650,0611,060,022,832,920,027,0511,93n.a.7,720,0099,25
1,9950,0052,000
0,4620,0760,0010,0010,540
0,3770,0870,0010,458-0,5370,0001,460
4,000
Bk 7136.7.92i (gnt)
55,810,0612,850,021,562,330,026,7410,77n.a.8,320,0198,50
1,9950,0052,000
0,5370,0420,0010,0010,581
0,3590,0700,0010,413-0,5770,0001,419
4,000
Bk 7146.7.92i (gnt)
55,230,0512,350,033,021,860,006,7310,94n.a.8,240,0098,44
1,9830,0172,000
0,5060,0820,0010,0010,589
0,3600,0560,0000,421-0,5740,0001,411
4,000
Bk 7186.7.92amph
54,040,018,180,003,673,350,088,1814,97n.a.5,910,0198,40
1,9830,0172,000
0,3370,1010,0000,0000,438
0,4470,1030,0020,588-0,4200,0001,562
4,000
Bk 7236.7.92gnt
55,600,0311,830,002,292,300,047,1111,55n.a.7,900,0298,67
1,9940,0062,000
0,4940,0620,0000,0010,556
0,3800,0690,0010,444-0,5490,0011,444
4,000
C-11Appendix C Table C3 omphacite
normed to 4 cations, Fe3 over charge balance (12+)
normed to 4 cations, Fe3 over charge balance (12+)
position means analysis of: i(x), inclusion of cpx in mineral x, core is core position in a cpx grain, mineral x, rimposition in cpx grain in contact with mineral x, mineral x(i), cpx at an inclusion of mineral x in cpx
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2Ototal
SiAlt
AloFe3CrTi
MgFe2MnCaZnNaK
sum
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2Ototal
SiAlt
AloFe3CrTi
MgFe2MnCaZnNaK
sum
Bk 7456.7.92i (gnt)
54,990,029,990,102,873,290,137,6813,22n.a.6,840,0099,14
1,9860,0142,000
0,4110,0780,0030,0000,493
0,4130,1000,0040,512-0,4790,0001,507
4,000
Bk 7476.7.92i (gnt)
55,510,0211,860,022,652,180,046,9711,30n.a.8,030,0198,60
1,9920,0082,000
0,4940,0720,0010,0000,567
0,3730,0660,0010,435-0,5590,0001,433
4,000
Bk 7556.7.92gnt
54,750,0310,080,083,973,140,127,1612,09n.a.7,320,0198,75
1,9860,0142,000
0,4170,1080,0020,0010,528
0,3870,0950,0040,470-0,5150,0001,472
4,000
Bk 7646.7.92i (gnt)
55,100,0410,380,082,992,910,027,2512,16n.a.7,430,0198,37
1,9970,0032,000
0,4400,0820,0020,0010,525
0,3920,0880,0010,472-0,5220,0001,475
4,000
Bk 7686.7.92gnt
55,030,0310,430,043,752,760,007,4312,83n.a.7,200,0099,50
1,9780,0222,000
0,4200,1010,0010,0010,523
0,3980,0830,0000,494-0,5020,0001,477
4,000
Bk 7746.7.92sympl
55,140,0210,580,031,883,210,037,5612,55n.a.7,150,0098,15
1,9990,0012,000
0,4510,0510,0010,0000,503
0,4080,0970,0010,487-0,5030,0001,497
4,000
Bk 737.7.92amph
55,390,0610,820,011,763,400,007,4212,92n.a.7,130,0198,93
1,9940,0062,000
0,4530,0480,0000,0010,503
0,3980,1020,0000,498-0,4980,0001,497
4,000
Bk 747.7.92calcit
54,820,0110,450,002,282,780,077,6213,43n.a.6,870,0298,35
1,9870,0132,000
0,4340,0620,0000,0000,496
0,4120,0840,0020,522-0,4830,0011,504
4,000
Bk 767.7.92amph
54,850,0210,570,012,962,380,057,6413,14n.a.7,050,0198,68
1,9810,0192,000
0,4310,0800,0000,0000,512
0,4110,0720,0020,509-0,4940,0001,488
4,000
Bk 7217.7.92i (gnt)
55,190,0611,300,073,481,780,087,3312,07n.a.7,680,0199,05
1,9790,0212,000
0,4570,0940,0020,0010,554
0,3920,0530,0020,464-0,5340,0001,446
4,000
Bk 7247.7.92i (gnt)
55,310,0212,030,002,262,760,006,9711,24n.a.7,880,0198,48
1,9890,0112,000
0,4990,0610,0000,0000,560
0,3740,0830,0000,433-0,5490,0001,440
4,000
Bk 7287.7.92i (gnt)
55,140,0711,390,073,731,460,017,1811,88n.a.7,870,0098,80
1,9800,0202,000
0,4620,1010,0020,0010,566
0,3840,0440,0000,457-0,5480,0001,434
4,000
Bk 7297.7.92i (gnt)
54,710,0410,340,064,112,940,066,7812,39n.a.7,430,0198,87
1,9830,0172,000
0,4240,1120,0020,0010,539
0,3660,0890,0020,481-0,5220,0001,461
4,000
Bk 7327.7.92i (gnt)
54,450,0810,050,013,773,120,087,1512,50n.a.7,160,0098,37
1,9840,0162,000
0,4150,1030,0000,0020,520
0,3880,0950,0020,488-0,5060,0001,480
4,000
Bk 7427.7.92par
55,810,0512,410,022,092,490,026,7010,99n.a.8,240,0198,83
1,9950,0052,000
0,5180,0560,0010,0010,576
0,3570,0740,0010,421-0,5710,0001,424
4,000
Bk 7457.7.92gnt
55,100,0410,670,003,402,160,007,4013,13n.a.7,270,0199,18
1,9810,0192,000
0,4330,0920,0000,0010,526
0,3970,0650,0000,506-0,5070,0001,474
4,000
Bk 7467.7.92gnt
54,950,0711,380,052,453,750,097,2911,76n.a.7,280,0399,11
1,9780,0222,000
0,4610,0660,0010,0010,530
0,3910,1130,0030,454-0,5080,0011,470
4,000
Bk 7507.7.92gnt
54,720,0410,700,003,351,960,097,4513,15n.a.7,170,0198,65
1,9770,0232,000
0,4330,0910,0000,0010,525
0,4010,0590,0030,509-0,5020,0001,475
4,000
Bk 81414.3.93cpx
56,340,0313,310,052,461,470,036,8210,500,218,260,57100,09
1,9850,0152,000
0,5380,0650,0010,0010,605
0,3580,0430,0010,3960,0050,5640,0261,395
4,000
Bk 83614.3.93gnt
55,360,0611,210,002,272,360,057,5013,030,157,240,0299,25
1,9840,0162,000
0,4570,0610,0000,0010,519
0,4010,0710,0020,5000,0040,5030,0011,481
4,000
Bk 83714.3.93gnt
55,560,0311,520,002,252,430,017,5012,580,237,390,0299,51
1,9830,0172,000
0,4680,0600,0000,0010,529
0,3990,0730,0000,4810,0060,5110,0011,471
4,000
Bk 83814.3.93gnt
55,250,1010,510,001,013,540,058,0913,520,136,610,0198,82
1,9920,0082,000
0,4390,0270,0000,0020,468
0,4350,1070,0020,5220,0030,4620,0001,532
4,000
C-12 Appendix C Table C3 omphacite
normed to 4 cations, Fe3 over charge balance (12+)
normed to 4 cations, Fe3 over charge balance (12+)
position means analysis of: i(x), inclusion of cpx in mineral x, core is core position in a cpx grain, mineral x, rimposition in cpx grain in contact with mineral x, mineral x(i), cpx at an inclusion of mineral x in cpx
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2Ototal
SiAlt
AloFe3CrTi
MgFe2MnCaZnNaK
sum
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2Ototal
SiAlt
AloFe3CrTi
MgFe2MnCaZnNaK
sum
Bk 83914.3.93gnt
55,830,0110,960,000,903,410,077,9413,290,216,870,0299,51
1,9950,0052,000
0,4570,0240,0000,0000,481
0,4230,1020,0020,5090,0060,4760,0011,519
4,000
Bk 84014.3.93core
56,070,0412,370,032,662,360,006,5710,690,218,410,0499,45
1,9950,0052,000
0,5140,0710,0010,0010,586
0,3480,0700,0000,4080,0060,5800,0021,414
4,000
Bk 84114.3.93core
55,970,0510,990,001,833,030,017,6813,070,157,140,0899,99
1,9920,0082,000
0,4530,0490,0000,0010,503
0,4070,0900,0000,4980,0040,4930,0041,497
4,000
Bk 84214.3.93cpx
55,560,0110,550,042,432,950,057,5713,010,167,130,0299,51
1,9920,0082,000
0,4380,0660,0010,0000,504
0,4050,0890,0020,5000,0040,4960,0011,496
4,000
Bk 84314.3.93cpx
55,700,0510,860,011,823,680,077,1412,930,267,180,0299,74
1,9950,0052,000
0,4530,0490,0000,0010,504
0,3810,1100,0020,4960,0070,4990,0011,496
4,000
Bk 84414.3.93core
56,310,0212,190,021,162,570,077,4611,310,327,880,0399,35
2,0010,0002,001
0,5100,0310,0010,0000,542
0,3950,0770,0020,4310,0080,5430,0011,457
4,000
Bk 8329.1.93arut
55,960,4112,460,030,612,770,007,6011,260,427,670,1699,35
1,9910,0092,000
0,5130,0160,0010,0080,538
0,4030,0820,0000,4290,0110,5290,0071,462
4,000
Bk 8429.1.93arut
55,550,3012,070,030,163,640,057,3911,290,147,570,0298,22
2,0000,0002,000
0,5120,0040,0010,0060,523
0,3970,1100,0020,4360,0040,5280,0011,477
4,000
Bk 8529.1.93aap
55,120,1911,470,020,504,140,237,1212,060,127,200,0198,18
1,9970,0032,000
0,4870,0140,0010,0040,505
0,3850,1250,0070,4680,0030,5060,0001,495
4,000
Bk 8629.1.93acore
55,660,1112,400,090,933,200,356,9811,340,177,740,0298,99
1,9920,0082,000
0,5140,0250,0030,0020,544
0,3720,0960,0110,4350,0040,5370,0011,456
4,000
Bk 81429.1.93agnt
55,370,0411,190,022,352,430,077,7412,910,177,150,0399,48
1,9800,0202,000
0,4520,0630,0010,0010,516
0,4130,0730,0020,4950,0040,4960,0011,484
4,000
Bk 82029.1.93agnt
55,980,0513,640,042,231,830,026,459,900,198,780,0299,13
1,9860,0142,000
0,5560,0600,0010,0010,618
0,3410,0540,0010,3760,0050,6040,0011,382
4,000
Bk 82129.1.93agnt
55,320,0211,380,032,912,670,047,1011,210,077,830,0298,60
1,9920,0082,000
0,4750,0790,0010,0000,555
0,3810,0810,0010,4330,0020,5470,0011,445
4,000
Bk 82329.1.93agnt
55,480,0211,560,001,962,640,037,6012,530,187,290,0499,33
1,9830,0172,000
0,4700,0530,0000,0000,523
0,4050,0790,0010,4800,0050,5050,0021,477
4,000
Bk 82629.1.93ai (rut)
55,660,2713,240,000,143,320,036,8310,120,198,190,0398,02
1,9990,0012,000
0,5590,0040,0000,0050,568
0,3660,1000,0010,3890,0050,5700,0011,432
4,000
Bk 8129.1.93bi (rut)
56,240,2613,880,002,191,350,056,609,910,208,910,0299,61
1,9830,0172,000
0,5590,0580,0000,0050,622
0,3470,0400,0010,3740,0050,6090,0011,378
4,000
Bk 81129.1.93bcore
56,270,1612,540,012,211,660,017,2810,990,118,310,0199,56
1,9910,0092,000
0,5140,0590,0000,0030,576
0,3840,0490,0000,4170,0030,5700,0001,424
4,000
Bk 81229.1.93bsympl
56,230,0813,650,060,672,950,036,4910,320,288,450,0399,24
1,9950,0052,000
0,5650,0180,0020,0020,586
0,3430,0870,0010,3920,0070,5810,0011,414
4,000
Bk 83629.1.93bcore
55,980,0012,200,000,942,870,027,3510,870,207,940,0198,37
2,0060,0002,006
0,5210,0250,0000,0000,546
0,3930,0860,0010,4170,0050,5520,0001,454
4,000
Bk 83729.1.93bcore
55,840,0412,140,040,333,390,047,4811,370,007,650,0098,31
2,0040,0002,004
0,5170,0090,0010,0010,528
0,4000,1020,0010,4370,0000,5320,0001,472
4,000
Bk 83829.1.93bcore
56,020,0312,220,032,951,090,017,5411,270,547,970,1999,87
1,9830,0172,000
0,4920,0790,0010,0010,572
0,3980,0320,0000,4270,0140,5470,0091,428
4,000
Bk 83929.1.93bcore
56,210,0312,250,050,004,150,037,1610,950,217,760,0398,35
2,0170,0002,017
0,5350,0000,0010,0010,524
0,3830,1250,0010,4210,0060,5400,0011,476
4,000
C-13Appendix C Table C3 omphacite
normed to 4 cations, Fe3 over charge balance (12+)
normed to 4 cations, Fe3 over charge balance (12+)
position means analysis of: i(x), inclusion of cpx in mineral x, core is core position in a cpx grain, mineral x, rimposition in cpx grain in contact with mineral x, mineral x(i), cpx at an inclusion of mineral x in cpx
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2Ototal
SiAlt
AloFe3CrTi
MgFe2MnCaZnNaK
sum
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2Ototal
SiAlt
AloFe3CrTi
MgFe2MnCaZnNaK
sum
Cig 90/40456.1.91cpx
55,680,0411,830,001,783,410,046,8610,84n.a.7,980,0198,49
2,0030,0002,003
0,5020,0480,0000,0010,550
0,3680,1030,0010,418-0,5570,0001,447
4,000
Cig 90/40536.1.91i (gnt)
53,180,0310,680,024,325,360,086,8412,16n.a.6,550,0199,22
1,9420,0582,000
0,4020,1190,0010,0010,522
0,3720,1640,0020,476-0,4640,0001,478
4,000
Cig 90/40556.1.91i (gnt)
55,380,0611,220,002,323,890,107,2412,28n.a.7,240,0299,75
1,9830,0172,000
0,4560,0630,0000,0010,520
0,3860,1160,0030,471-0,5030,0011,480
4,000
Cig 90/4036.1.91ai (gnt)
55,290,0411,390,032,473,100,046,8911,31n.a.7,800,0098,50
1,9960,0042,000
0,4800,0670,0010,0010,549
0,3710,0930,0010,437-0,5460,0001,451
4,000
Cig 90/4046.1.91ai (gnt)
54,690,059,430,032,435,070,017,0512,79n.a.6,760,0098,41
2,0020,0002,002
0,4070,0670,0010,0010,476
0,3850,1550,0000,502-0,4800,0001,523
4,000
Cig 90/4026.1.91bi (gnt)
54,870,039,280,041,896,000,026,8612,86n.a.6,660,0198,52
2,0090,0002,009
0,4000,0520,0010,0010,454
0,3740,1840,0010,505-0,4730,0001,536
4,000
Cig 90/4036.1.91bi (gnt)
54,370,048,930,054,584,340,066,5912,26n.a.7,150,0198,38
1,9970,0032,000
0,3830,1270,0010,0010,512
0,3610,1330,0020,482-0,5090,0001,488
4,000
Cig 90/4066.1.91bi (gnt)
54,820,059,750,052,624,940,006,9812,80n.a.6,860,0098,86
1,9950,0052,000
0,4140,0720,0010,0010,488
0,3790,1500,0000,499-0,4840,0001,512
4,000
Cig 90/4076.1.91bi (gnt)
54,770,058,450,073,015,460,027,5113,74n.a.6,260,0099,40
1,9960,0042,000
0,3590,0830,0020,0010,445
0,4080,1660,0010,537-0,4420,0001,555
4,000
Cig 90/40436.1.91bcoes (i)
55,140,0510,640,011,903,950,007,3711,73n.a.7,300,0098,09
2,0020,0002,002
0,4550,0520,0000,0010,508
0,3990,1200,0000,456-0,5140,0001,489
4,000
Cig 90/40446.1.91bcoes (i)
55,740,0311,490,002,402,960,047,1311,33n.a.7,860,0098,98
1,9970,0032,000
0,4830,0650,0000,0010,548
0,3810,0890,0010,435-0,5460,0001,452
4,000
Cig 90/4031?coes (i)
55,800,0411,000,002,623,040,007,3011,70n.a.7,700,0099,20
1,9990,0012,000
0,4640,0710,0000,0010,535
0,3900,0910,0000,449-0,5350,0001,465
4,000
Cig 90/4032?coes (i)
55,600,0511,300,003,262,370,007,1011,60n.a.7,900,0099,18
1,9910,0092,000
0,4680,0880,0000,0010,557
0,3790,0710,0000,445-0,5480,0001,443
4,000
Cig 90/4033?par
56,000,0412,100,002,242,880,006,8010,90n.a.8,200,0099,16
1,9980,0022,000
0,5070,0600,0000,0010,568
0,3620,0860,0000,417-0,5670,0001,432
4,000
Cig 90/4043?par (i)
55,200,0510,300,001,933,260,007,9013,40n.a.6,800,0098,84
1,9920,0082,000
0,4300,0530,0000,0010,483
0,4250,0980,0000,518-0,4760,0001,517
4,000
Cig 90/4044?par (i)
55,800,0410,700,001,673,500,007,6013,10n.a.7,100,0099,51
1,9970,0032,000
0,4490,0450,0000,0010,495
0,4050,1050,0000,502-0,4930,0001,505
4,000
Cig 90/4046?coes (i)
55,500,0511,700,003,531,630,007,1011,00n.a.8,200,0098,70
1,9890,0112,000
0,4840,0950,0000,0010,580
0,3790,0490,0000,422-0,5700,0001,420
4,000
Cig 90/4047?coes (i)
55,700,0511,500,003,132,280,007,1011,40n.a.8,000,0099,16
1,9920,0082,000
0,4770,0840,0000,0010,562
0,3780,0680,0000,437-0,5550,0001,438
4,000
Cig 90/4048?i (gnt)
55,900,0512,100,001,613,050,006,9010,90n.a.8,100,0098,61
2,0030,0002,003
0,5110,0430,0000,0010,555
0,3690,0920,0000,419-0,5630,0001,441
4,000
Cig 90/4063?i (gnt)
55,600,0411,900,003,392,350,076,6010,80n.a.8,300,0099,05
1,9910,0092,000
0,4930,0910,0000,0010,585
0,3520,0700,0020,414-0,5760,0001,415
4,000
Cig 90/4064?i (gnt)
55,500,0512,000,003,361,680,007,0011,10n.a.8,200,0098,89
1,9850,0152,000
0,4910,0900,0000,0010,583
0,3730,0500,0000,425-0,5690,0001,417
4,000
Cig 90/4065?cpx
54,900,0510,200,003,044,470,006,7012,40n.a.7,200,0098,95
1,9930,0072,000
0,4290,0830,0000,0010,513
0,3620,1360,0000,482-0,5070,0001,487
4,000
C-14 Appendix C Table C3 omphacite
normed to 4 cations, Fe3 over charge balance (12+)
normed to 4 cations, Fe3 over charge balance (12+)
position means analysis of: i(x), inclusion of cpx in mineral x, core is core position in a cpx grain, mineral x, rimposition in cpx grain in contact with mineral x, mineral x(i), cpx at an inclusion of mineral x in cpx
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2Ototal
SiAlt
AloFe3CrTi
MgFe2MnCaZnNaK
sum
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2Ototal
SiAlt
AloFe3CrTi
MgFe2MnCaZnNaK
sum
Cig 90/4066?cpx
55,700,0611,700,004,161,360,007,1011,40n.a.8,200,0099,68
1,9810,0192,000
0,4710,1110,0000,0010,583
0,3760,0400,0000,434-0,5650,0001,417
4,000
Cig 90/4067?cpx
55,400,0511,400,002,792,690,007,0011,30n.a.7,900,0098,53
1,9950,0052,000
0,4790,0760,0000,0010,556
0,3760,0810,0000,436-0,5520,0001,444
4,000
Cig 90/4068?cpx
55,300,0010,900,002,772,910,007,1011,60n.a.7,700,0098,28
2,0000,0002,000
0,4650,0750,0000,0000,540
0,3830,0880,0000,449-0,5400,0001,460
4,000
Cig 91-1516.6.93cpx
56,340,0310,680,021,423,440,048,0712,940,157,070,01100,21
2,0000,0002,000
0,4470,0380,0010,0010,486
0,4270,1020,0010,4920,0040,4870,0001,514
4,000
Cig 91-1716.6.93gnt
56,690,0411,710,001,983,040,007,1611,330,078,040,05100,11
2,0060,0002,006
0,4880,0530,0000,0010,542
0,3780,0900,0000,4290,0020,5520,0021,453
4,000
Cig 91-13316.6.93coes (i)
56,850,0411,520,011,742,860,017,6712,200,047,700,03100,67
2,0010,0002,001
0,4780,0460,0000,0010,525
0,4020,0840,0000,4600,0010,5250,0011,475
4,000
Cig 91-13416.6.93coes (i)
56,570,0311,570,001,264,020,047,1111,880,017,680,03100,20
2,0060,0002,006
0,4830,0340,0000,0010,518
0,3760,1190,0010,4510,0000,5280,0011,477
4,000
Cig 91-13516.6.93cpx
56,330,0010,630,021,653,770,057,5812,770,047,240,02100,10
2,0050,0002,005
0,4460,0440,0010,0000,491
0,4020,1120,0020,4870,0010,5000,0011,504
4,000
Cig 91-1628.11.93phe
56,010,0411,020,012,152,900,077,1811,750,017,780,0398,96
2,0080,0002,008
0,4660,0580,0000,0010,525
0,3840,0870,0020,4510,0000,5410,0011,467
4,000
Cig 91-11128.11.93phe
56,080,0510,680,022,313,620,077,3812,700,097,290,03100,32
1,9960,0042,000
0,4440,0620,0010,0010,507
0,3920,1080,0020,4840,0020,5030,0011,493
4,000
Cig 91-11228.11.93phe
56,230,1010,680,071,574,340,067,2512,790,067,220,02100,39
2,0020,0002,002
0,4480,0420,0020,0020,494
0,3850,1290,0020,4880,0020,4980,0011,504
4,000
Cig 91-1316.6.93coes (i)
56,820,0411,860,001,473,260,037,1511,150,008,100,0399,91
2,0110,0002,011
0,4950,0390,0000,0010,535
0,3770,0960,0010,4230,0000,5560,0011,454
4,000
Cig 91-1416.6.93coes (i)
56,930,0111,240,010,584,290,007,4312,200,027,520,01100,24
2,0160,0002,016
0,4690,0150,0000,0000,485
0,3920,1270,0000,4630,0010,5160,0001,499
4,000
Cig 91-1816.6.93gnt
56,960,0412,030,011,972,720,047,0410,890,008,370,02100,10
2,0100,0002,010
0,5000,0520,0000,0010,554
0,3700,0800,0010,4120,0000,5730,0011,437
4,000
C-15Appendix C Table C4 garnet
normed to 24 oxygens, Fe3 over charge balance
normed to 24 oxygens, Fe3 over charge balance
position means analysis of: core is core position in a grt grain, mineral x, rim position in grt grain in contact withmineral x, mineral x(i), grt at an inclusion of mineral x in grt
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOtotal
SiAlt
AloFe3CrTi
MgFe2MnCa
sum
Bk 10B3319.10.93achl
37,650,0621,100,220,6328,290,803,827,3099,87
5,9510,049
3,8810,0750,0270,0053,995
0,9003,7400,1071,2365,983
15,978
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOtotal
SiAlt
AloFe3CrTi
MgFe2MnCa
sum
Bk 10B3419.10.93achl
37,340,0620,860,001,5627,970,334,227,2399,58
5,8970,103
3,7790,1860,0000,0053,985
0,9933,6940,0441,2235,955
15,940
Bk 10B3519.10.93achl
37,420,1220,710,001,3527,370,802,978,9499,69
5,9300,070
3,7980,1610,0000,0103,982
0,7023,6280,1071,5185,954
15,937
Bk 10B3619.10.93achl
37,790,1121,090,041,2128,140,943,138,45100,90
5,9230,077
3,8190,1430,0050,0093,987
0,7313,6880,1251,4195,963
15,951
Bk 10B119.10.93bcore
36,720,0220,520,002,1226,353,262,088,7699,83
5,8510,149
3,7050,2540,0000,0023,981
0,4943,5120,4401,4965,941
15,923
Bk 10B219.10.93bcore
36,830,1220,570,031,9224,963,882,009,5499,85
5,8610,139
3,7190,2300,0040,0103,981
0,4743,3220,5231,6275,946
15,927
Bk 10B319.10.93bcore
37,050,1120,450,001,5526,411,922,529,1199,11
5,9190,081
3,7700,1860,0000,0093,980
0,6003,5290,2601,5595,948
15,928
Bk 10B419.10.93bchl
37,350,1420,710,011,5125,990,803,499,3299,32
5,9120,088
3,7750,1800,0010,0123,982
0,8233,4410,1071,5815,952
15,933
Bk 10B127.11.93chl
37,500,0821,130,010,9927,280,644,217,6499,48
5,9230,077
3,8570,1170,0010,0073,991
0,9913,6040,0861,2935,973
15,965
Bk 10B3027.11.93chl
37,460,0620,990,061,1027,880,983,228,2199,96
5,9240,076
3,8360,1310,0080,0053,990
0,7593,6870,1311,3915,969
15,958
Bk 10B3127.11.93chl
37,640,0720,870,051,2728,040,892,958,59100,38
5,9320,068
3,8090,1510,0060,0063,985
0,6933,6960,1191,4515,959
15,943
Bk 10B3427.11.93chl
37,400,0820,910,001,0027,920,783,308,0899,47
5,9390,061
3,8530,1200,0000,0073,989
0,7813,7080,1051,3755,969
15,957
Bk 10B3527.11.93chl
37,780,0820,910,051,0327,850,853,537,99100,07
5,9550,045
3,8400,1230,0060,0073,985
0,8293,6710,1131,3495,963
15,949
Bk 10B3627.11.93core
37,570,1620,770,031,3025,832,312,689,48100,13
5,9330,067
3,7990,1540,0040,0143,982
0,6313,4120,3091,6045,956
15,937
Bk 10B3727.11.93chl
37,330,0620,990,001,4928,200,863,697,44100,06
5,8890,111
3,7910,1770,0000,0053,988
0,8683,7200,1151,2575,960
15,948
Bk 10B3827.11.93chl
37,780,0521,160,021,1427,780,684,047,67100,31
5,9260,074
3,8370,1340,0020,0043,989
0,9443,6430,0901,2895,967
15,956
Bk 10B4027.11.93chl
38,050,0221,430,010,7124,711,603,5310,23100,29
5,9510,049
3,9000,0840,0010,0023,993
0,8233,2320,2121,7145,981
15,973
BK 17493.7.94chl
37,670,0521,020,000,2729,120,333,357,4099,21
6,0050,000
3,9490,0330,0000,0043,991
0,7963,8810,0451,2645,986
15,981
Bk 1825.8.94chl
38,020,0721,410,010,8927,161,053,978,18100,76
5,9340,066
3,8730,1040,0010,0063,992
0,9243,5460,1391,3685,976
15,968
Bk 1835.8.94chl
37,580,1521,310,020,9927,111,423,029,01100,61
5,9060,094
3,8530,1170,0020,0133,993
0,7073,5630,1891,5175,977
15,970
Bk 1855.8.94core
37,750,1421,170,000,7921,425,072,4211,31100,07
5,9470,053
3,8770,0940,0000,0123,989
0,5682,8210,6761,9095,975
15,964
Bk 1865.8.94chl
37,800,0521,230,000,7826,193,153,837,18100,21
5,9500,050
3,8880,0920,0000,0043,991
0,8993,4480,4201,2115,977
15,968
C-16 Appendix C Table C4 garnet
normed to 24 oxygens, Fe3 over charge balance
normed to 24 oxygens, Fe3 over charge balance
position means analysis of: core is core position in a grt grain, mineral x, rim position in grt grain in contact withmineral x, mineral x(i), grt at an inclusion of mineral x in grt
Bk 1885.8.94chl
37,690,0921,320,040,7327,231,522,948,92100,48
5,9330,067
3,8890,0870,0050,0083,995
0,6903,5850,2031,5055,982
15,977
Bk 1896.8.94core
38,110,0920,980,060,0023,952,622,5910,8099,20
6,0550,000
3,9290,0000,0080,0083,969
0,6133,1830,3531,8385,987
16,011
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOtotal
SiAlt
AloFe3CrTi
MgFe2MnCa
sum
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOtotal
SiAlt
AloFe3CrTi
MgFe2MnCa
sum
Bk 397,213.3.93amph (i)
36,642,7520,780,120,0528,400,763,327,68100,51
5,8320,168
3,7310,0060,0150,2353,988
0,7883,7810,1021,3105,981
15,968
Bk 3911,213.3.93core
37,100,1020,750,001,5825,981,662,769,5899,51
5,8900,110
3,7720,1890,0000,0093,984
0,6533,4490,2231,6295,955
15,939
Bk 3912,213.3.93core
37,470,1021,130,081,1726,771,582,969,12100,38
5,9010,099
3,8240,1380,0100,0083,991
0,6953,5260,2111,5395,971
15,962
Bk 3913,213.3.93core
37,610,0521,010,061,2826,331,003,878,6599,87
5,9160,084
3,8110,1520,0070,0043,987
0,9073,4640,1331,4585,963
15,950
Bk 39123.3.92amph
37,040,0321,050,001,2426,350,523,718,9398,87
5,8870,113
3,8300,1490,0000,0033,993
0,8793,5020,0701,5215,972
15,964
Bk 39223.3.92amph
38,210,0121,610,040,5426,970,493,749,22100,83
5,9540,046
3,9230,0630,0050,0013,996
0,8693,5150,0651,5395,988
15,984
Bk 39323.3.92cpx (i)
36,930,0320,920,011,6727,080,723,688,2499,28
5,8590,141
3,7700,1990,0010,0033,989
0,8703,5920,0971,4015,960
15,949
Bk 39423.3.92cpx (i)
37,460,0421,260,001,0926,710,583,659,0199,80
5,9020,098
3,8510,1290,0000,0033,993
0,8573,5190,0771,5215,975
15,968
Bk 39523.3.92cpx (i)
37,080,0120,990,031,5125,450,483,949,4298,90
5,8740,126
3,7920,1790,0040,0013,989
0,9303,3710,0641,5995,964
15,954
Bk 391423.3.92cpx (i)
37,190,0521,350,031,2927,840,934,696,4299,79
5,8590,141
3,8230,1530,0040,0043,997
1,1013,6680,1241,0845,977
15,973
Bk 391523.3.92amph
36,740,0521,180,031,2626,810,563,608,6698,90
5,8510,149
3,8270,1510,0040,0043,998
0,8553,5720,0761,4785,979
15,977
Bk 391823.3.92cpx (i)
36,870,0321,260,031,6126,600,553,868,7199,52
5,8250,175
3,7830,1910,0040,0033,996
0,9093,5150,0741,4745,971
15,967
Bk 39224.6.92cpx (i)
37,370,0421,230,061,1725,240,324,818,7498,98
5,8900,110
3,8330,1390,0070,0033,993
1,1303,3260,0431,4765,975
15,968
Bk 39524.6.92amph
37,090,0121,040,001,3027,180,703,708,1899,20
5,8880,112
3,8240,1550,0000,0013,992
0,8753,6090,0941,3915,970
15,962
Bk 39724.6.92amph
36,820,0421,160,001,4329,500,693,286,9799,89
5,8470,153
3,8080,1710,0000,0033,997
0,7763,9180,0931,1865,973
15,970
Bk 39824.6.92cpx (i)
37,790,0521,560,030,8726,000,354,968,2699,87
5,9070,093
3,8790,1020,0040,0043,997
1,1563,3990,0461,3835,984
15,981
Bk 391224.6.92core
36,500,0620,730,021,3029,531,042,367,4498,98
5,8790,121
3,8140,1580,0030,0053,994
0,5673,9770,1421,2845,970
15,963
Bk 391324.6.92core
36,730,0321,190,081,1829,270,623,706,5599,36
5,8540,146
3,8340,1420,0100,0034,001
0,8793,9020,0841,1185,983
15,983
Bk 391424.6.92cpx (i)
36,640,0521,190,031,5429,280,753,526,7599,74
5,8220,178
3,7910,1840,0040,0043,999
0,8343,8900,1011,1495,974
15,973
Bk 395624.6.92cpx
37,690,0621,340,010,9125,240,464,938,6099,24
5,9200,080
3,8710,1080,0010,0053,993
1,1543,3150,0611,4475,978
15,971
C-17Appendix C Table C4 garnet
normed to 24 oxygens, Fe3 over charge balance
normed to 24 oxygens, Fe3 over charge balance
position means analysis of: core is core position in a grt grain, mineral x, rim position in grt grain in contact withmineral x, mineral x(i), grt at an inclusion of mineral x in grt
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOtotal
SiAlt
AloFe3CrTi
MgFe2MnCa
sum
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOtotal
SiAlt
AloFe3CrTi
MgFe2MnCa
sum
Bk 395724.6.92cpx
37,090,0320,990,031,3526,190,533,569,2999,06
5,8850,115
3,8110,1610,0040,0033,991
0,8423,4750,0711,5795,968
15,958
Bk 395824.6.92cpx (i)
37,220,0421,110,010,8724,970,364,449,1498,16
5,9200,080
3,8780,1040,0010,0033,994
1,0533,3210,0491,5585,980
15,974
Bk 39428.1.93cpx (i)
36,600,0520,880,030,7828,001,292,008,9398,56
5,9120,088
3,8870,0950,0040,0043,998
0,4823,7820,1761,5455,985
15,983
Bk 39528.1.93cpx (i)
37,220,1020,830,001,8726,731,422,789,37100,33
5,8660,134
3,7350,2220,0000,0083,983
0,6533,5230,1901,5825,948
15,931
Bk 39728.1.93cpx (i)
37,150,0321,100,061,4027,731,033,657,7199,86
5,8720,128
3,8030,1670,0070,0033,993
0,8603,6650,1381,3065,969
15,962
Bk 39828.1.93cpx (i)
36,730,0820,990,071,8627,510,963,937,4299,56
5,8180,182
3,7360,2220,0090,0073,992
0,9283,6450,1291,2595,961
15,952
Bk 391228.1.93cpx (i)
37,240,0020,990,001,5227,370,943,857,7599,65
5,8850,115
3,7940,1800,0000,0003,989
0,9073,6160,1261,3125,961
15,950
Bk 391828.1.93cpx (i)
36,990,1921,190,001,2727,000,724,597,1799,12
5,8600,140
3,8160,1510,0000,0163,995
1,0843,5770,0971,2175,974
15,969
Bk 391928.1.93cpx (i)
37,090,2121,400,031,6026,560,625,257,0299,78
5,8150,185
3,7700,1890,0040,0183,995
1,2273,4820,0821,1795,971
15,966
Bk 392028.1.93cpx (i)
37,120,2521,170,001,1527,500,743,518,3099,74
5,8750,125
3,8250,1370,0000,0213,994
0,8283,6400,0991,4085,974
15,968
Bk 392328.1.93cpx (i)
37,410,0521,350,051,7027,040,685,047,01100,33
5,8390,161
3,7660,2000,0060,0043,992
1,1733,5300,0901,1725,964
15,956
Bk 393228.1.93cpx (i)
36,890,1720,760,002,1426,151,842,459,84100,23
5,8290,171
3,6940,2540,0000,0143,983
0,5773,4550,2461,6665,944
15,927
Bk 395328.1.93ab
37,340,0621,190,021,8426,240,503,639,62100,44
5,8410,159
3,7470,2170,0020,0053,988
0,8463,4320,0661,6125,957
15,945
Bk 395428.1.93ab
37,100,0020,950,001,7525,740,553,479,8399,40
5,8620,138
3,7630,2080,0000,0003,987
0,8173,4020,0741,6645,957
15,943
Bk 395828.1.93cpx
37,570,0821,320,002,0425,960,455,377,73100,52
5,8270,173
3,7240,2380,0000,0073,986
1,2413,3680,0591,2845,952
15,939
Bk 395928.1.93cpx
37,650,2621,240,341,5425,060,395,058,96100,49
5,8460,154
3,7330,1800,0420,0223,990
1,1693,2550,0511,4915,965
15,955
Bk 396228.1.93amph
37,100,1321,010,021,1424,690,374,778,8798,10
5,8960,104
3,8310,1360,0030,0113,991
1,1303,2820,0501,5105,972
15,963
Bk 396528.1.93core
36,970,0420,830,051,5527,301,502,678,7999,69
5,8770,123
3,7790,1850,0060,0033,989
0,6333,6290,2021,4975,961
15,949
Bk 396828.1.93core
37,150,0120,840,001,6527,171,243,028,7199,80
5,8830,117
3,7720,1970,0000,0013,986
0,7133,5980,1661,4785,955
15,941
Bk 391.4928.8.92cpx
37,150,0221,440,021,4226,360,514,198,6899,78
5,8400,160
3,8130,1680,0020,0023,997
0,9823,4650,0681,4625,977
15,974
Bk 391.5028.8.92cpx
37,150,0621,250,001,6325,820,493,769,6499,80
5,8410,159
3,7790,1930,0000,0053,992
0,8813,3960,0651,6245,966
15,958
Bk 391.5128.8.92cpx
37,370,0421,440,040,8126,140,483,759,4199,48
5,8990,101
3,8870,0970,0050,0033,999
0,8823,4500,0641,5915,988
15,988
C-18 Appendix C Table C4 garnet
normed to 24 oxygens, Fe3 over charge balance
normed to 24 oxygens, Fe3 over charge balance
position means analysis of: core is core position in a grt grain, mineral x, rim position in grt grain in contact withmineral x, mineral x(i), grt at an inclusion of mineral x in grt
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOtotal
SiAlt
AloFe3CrTi
MgFe2MnCa
sum
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOtotal
SiAlt
AloFe3CrTi
MgFe2MnCa
sum
Bk 391.5228.8.92cpx
37,130,0421,190,001,2125,900,543,759,3599,11
5,8810,119
3,8360,1440,0000,0033,994
0,8853,4310,0721,5875,975
15,969
Bk 391,14.5.92cpx
37,190,0421,090,011,0625,760,494,068,9898,69
5,9050,095
3,8520,1270,0010,0033,993
0,9613,4210,0661,5285,975
15,968
Bk 391,24.5.92cpx
37,110,0321,310,061,2126,360,504,078,6999,34
5,8630,137
3,8320,1440,0070,0033,997
0,9593,4830,0671,4715,979
15,977
Bk 392,14.5.92cpx
37,460,0421,340,041,1925,150,264,709,1399,31
5,8840,116
3,8350,1400,0050,0033,994
1,1003,3040,0351,5375,975
15,969
Bk 394,14.5.92cpx
37,610,0321,190,011,2124,850,254,719,3199,17
5,9090,091
3,8320,1430,0010,0033,989
1,1033,2650,0331,5675,969
15,958
Bk 395,14.5.92cpx
37,720,0521,200,021,4124,420,315,079,2499,44
5,8970,103
3,8020,1660,0020,0043,987
1,1813,1930,0411,5485,963
15,949
Bk 396,14.5.92cpx
37,790,0721,030,021,4824,130,315,099,3899,30
5,9110,089
3,7870,1740,0020,0063,982
1,1873,1560,0411,5725,955
15,938
Bk 397,14.5.92cpx
37,480,0421,170,071,3024,360,325,418,6598,80
5,8910,109
3,8130,1540,0090,0033,990
1,2673,2020,0431,4575,969
15,959
Bk 398,14.5.92cpx
37,640,0421,120,021,1825,910,425,107,7799,20
5,9190,081
3,8330,1400,0020,0033,988
1,1953,4070,0561,3095,967
15,956
Bk 399,14.5.92cpx
37,480,0821,040,011,4724,550,324,979,0598,97
5,8930,107
3,7920,1740,0010,0073,986
1,1653,2280,0431,5255,960
15,946
Bk 3910,14.5.92cpx (i)
36,980,0620,820,090,9926,820,583,478,6298,43
5,9190,081
3,8460,1200,0110,0053,982
1,8283,5890,0791,4785,974
15,966
Bk 3911,14.5.92core
36,360,0820,600,001,6228,101,272,498,1298,64
5,8580,142
3,7700,1960,0000,0073,990
0,5983,7870,1731,4025,960
15,950
Bk 3913,14.5.92core
36,610,0220,720,031,3230,001,152,047,4899,36
5,8870,113
3,8140,1590,0040,0023,993
0,4894,0340,1571,2895,968
15,961
Bk 3914,14.5.92core
36,770,0720,420,001,4130,011,012,117,3799,16
5,9190,081
3,7940,1700,0000,0063,985
0,5064,0400,1381,2715,955
15,940
Bk 3915,14.5.92core
36,370,0620,780,001,5730,350,842,506,8199,29
5,8460,154
3,7820,1900,0000,0053,994
0,5994,0800,1141,1735,966
15,960
Bk 3915,24.5.92cpx
37,480,0521,190,011,1924,760,415,108,6598,84
5,9010,099
3,8340,1410,0010,0043,990
1,1973,2600,0551,4595,971
15,961
Bk 3916,14.5.92core
36,790,0520,870,001,2529,820,503,136,7999,21
5,8880,112
3,8250,1510,0000,0043,993
0,7473,9910,0681,1645,970
15,964
Bk 3916,24.5.92cpx
37,850,0121,320,001,2824,320,285,289,1499,49
5,9060,094
3,8260,1510,0000,0013,988
1,2283,1740,0371,5285,967
15,955
Bk 39616.7.92cpx
37,380,1321,340,041,4725,080,794,908,5799,70
5,8520,148
3,7900,1730,0050,0113,992
1,1433,2830,1051,4385,969
15,961
Bk 7625.6.92core
36,990,0921,200,001,0828,290,743,038,2499,66
5,8790,121
3,8490,1290,0000,0083,997
0,7183,7590,1001,4035,980
15,977
Bk 7725.6.92core
37,150,0021,300,040,8927,920,653,817,6099,36
5,8960,104
3,8800,1060,0050,0003,999
0,9013,7050,0871,2925,986
15,986
Bk 7825.6.92core
37,520,0521,380,040,9727,310,405,186,6699,51
5,9000,100
3,8630,1150,0050,0043,996
1,2143,5910,0531,1225,981
15,977
C-19Appendix C Table C4 garnet
normed to 24 oxygens, Fe3 over charge balance
normed to 24 oxygens, Fe3 over charge balance
position means analysis of: core is core position in a grt grain, mineral x, rim position in grt grain in contact withmineral x, mineral x(i), grt at an inclusion of mineral x in grt
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOtotal
SiAlt
AloFe3CrTi
MgFe2MnCa
sum
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOtotal
SiAlt
AloFe3CrTi
MgFe2MnCa
sum
Bk 7925.6.92core
37,240,0221,320,402,6226,580,565,836,73101,30
5,7400,260
3,6130,3040,0490,0023,991
1,3393,4270,0731,1115,951
15,942
Bk 71025.6.92core
37,650,0221,700,031,0027,360,565,835,89100,04
5,8760,124
3,8680,1180,0040,0024,000
1,3563,5710,0740,9855,986
15,986
Bk 71125.6.92amph
37,620,0221,820,010,9526,910,526,245,7599,85
5,8680,132
3,8790,1120,0010,0024,002
1,4513,5100,0690,9615,991
15,993
Bk 71225.6.92cpx
37,830,0121,370,000,9225,470,736,915,5398,77
5,9280,072
3,8750,1090,0000,0013,992
1,6143,3380,0970,9285,977
15,969
Bk 71325.6.92cpx
38,330,0422,120,130,8924,210,547,486,75100,49
5,8760,124
3,8730,1030,0160,0034,001
1,7093,1040,0701,1095,992
15,993
Bk 71425.6.92cpx
38,350,0321,800,020,4323,860,617,476,5499,11
5,9520,048
3,9390,0510,0020,0033,998
1,7283,0970,0801,0875,992
15,991
Bk 71525.6.92cpx
37,900,0121,630,010,5626,160,486,535,8399,12
5,9340,066
3,9260,0670,0010,0013,999
1,5243,4260,0640,9785,991
15,990
Bk 71625.6.92cpx
37,870,0221,400,000,6726,040,526,326,0398,88
5,9470,053
3,9070,0800,0000,0023,995
1,4793,4200,0691,0155,983
15,978
Bk 71725.6.92ap (i)
37,770,0521,680,021,2825,110,695,957,52100,07
5,8630,137
3,8290,1490,0020,0043,996
1,3773,2590,0911,2515,977
15,973
Bk 71925.6.92ap (i)
37,140,0521,100,011,0826,630,504,667,4598,62
5,8990,101
3,8490,1290,0010,0043,994
1,1033,5370,0671,2685,976
15,969
Bk 72025.6.92cpx (i)
37,570,0721,450,001,0426,660,565,217,0899,64
5,8920,108
3,8570,1230,0000,0063,996
1,2183,4970,0741,1905,979
15,975
Bk 72225.6.92amph (i)
37,600,0521,370,041,1727,520,574,527,38100,22
5,8900,110
3,8360,1380,0050,0043,994
1,0553,6050,0761,2395,975
15,969
Bk 72425.6.92amph
37,150,0321,250,020,7728,280,334,866,0398,73
5,9100,090
3,8940,0930,0030,0033,999
1,1523,7630,0441,0285,987
15,986
Bk 72525.6.92amph (i)
37,540,0821,460,011,1226,960,575,057,0999,88
5,8820,118
3,8450,1320,0010,0073,996
1,1793,5330,0761,1905,978
15,974
Bk 72625.6.92amph
37,800,0321,450,011,0328,720,434,596,55100,60
5,9080,092
3,8600,1210,0010,0033,994
1,0693,7540,0571,0975,977
15,971
Bk 72725.6.92cpx
37,190,0521,130,001,1629,480,383,626,8499,85
5,8930,107
3,8400,1380,0000,0043,994
0,8553,9060,0511,1615,974
15,968
Bk 72825.6.92cpx
37,090,0621,080,050,8928,880,573,507,1799,29
5,9100,090
3,8690,1070,0060,0053,996
0,8313,8490,0771,2245,981
15,977
Bk 72925.6.92amph
37,320,0621,150,011,0428,050,593,468,0699,73
5,9080,092
3,8540,1240,0010,0053,994
0,8163,7130,0791,3675,975
15,969
Bk 73025.6.92core
35,800,0621,020,001,9826,370,743,878,1297,96
5,7540,246
3,7360,2390,0000,0053,999
0,9273,5440,1011,3985,970
15,970
Bk 7126.4.93cpx
38,140,0521,990,050,6726,110,776,506,14100,42
5,9000,100
3,9090,0780,0060,0044,002
1,4993,3780,1011,0185,995
15,997
Bk 7426.4.93cpx
38,570,0021,990,010,5524,780,577,076,69100,22
5,9390,061
3,9300,0630,0010,0003,999
1,6233,1910,0741,1045,991
15,990
Bk 72526.4.93phe (i)
37,350,0521,330,020,9225,910,554,268,7699,15
5,9010,099
3,8720,1100,0020,0043,997
1,0033,4230,0741,4835,983
15,979
C-20 Appendix C Table C4 garnet
normed to 24 oxygens, Fe3 over charge balance
normed to 24 oxygens, Fe3 over charge balance
position means analysis of: core is core position in a grt grain, mineral x, rim position in grt grain in contact withmineral x, mineral x(i), grt at an inclusion of mineral x in grt
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOtotal
SiAlt
AloFe3CrTi
MgFe2MnCa
sum
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOtotal
SiAlt
AloFe3CrTi
MgFe2MnCa
sum
Bk 72726.4.93phe (i)
37,640,0621,250,001,1924,881,134,628,7899,55
5,9050,095
3,8340,1410,0000,0053,990
1,0803,2630,1501,4765,970
15,960
Bk 72826.4.93amph (i)
37,650,1121,410,000,8924,831,084,608,9299,49
5,9110,089
3,8730,1050,0000,0093,994
1,0763,2600,1441,5005,981
15,975
Bk 73926.4.93cpx (i)
37,780,2121,400,051,0224,560,704,859,2499,80
5,9010,099
3,8400,1190,0060,0183,992
1,1293,2080,0931,5465,976
15,968
Bk 74326.4.93cpx (i)
38,060,1421,390,030,7924,640,674,999,0399,74
5,9410,059
3,8770,0920,0040,0123,991
1,1613,2170,0891,5105,977
15,968
Bk 74426.4.93cpx (i)
38,250,0421,660,050,4824,820,766,267,2399,55
5,9540,046
3,9280,0560,0060,0033,997
1,4523,2310,1001,2065,990
15,987
Bk 76526.4.93phe (i)
37,410,0421,320,061,3125,930,714,478,5099,75
5,8720,128
3,8160,1550,0070,0033,994
1,0463,4030,0941,4295,973
15,967
Bk 7227.8.91amph
37,230,0621,710,041,0426,200,565,656,8799,35
5,8450,155
3,8620,1230,0050,0054,004
1,3223,4390,0741,1565,992
15,995
Bk 7327.8.91amph
37,360,0021,840,060,5226,100,856,106,0798,90
5,8830,117
3,9350,0610,0070,0004,009
1,4323,4370,1131,0246,006
16,015
Bk 7427.8.91core
37,710,0421,960,001,3225,580,726,107,10100,53
5,8300,170
3,8320,1540,0000,0034,000
1,4063,3080,0941,1765,984
15,984
Bk 7527.8.91amph
37,230,1021,110,031,7524,880,924,069,6299,70
5,8470,153
3,7540,2060,0040,0083,988
0,9503,2670,1221,6195,959
15,946
Bk 712,14.5.92core
36,590,0920,470,031,7728,681,102,148,3899,25
5,8710,129
3,7420,2130,0040,0083,985
0,5123,8480,1491,4415,950
15,935
Bk 7216.7.92core
37,330,0321,300,041,3428,450,394,706,4099,98
5,8690,131
3,8160,1580,0050,0033,995
1,1013,7410,0521,0785,973
15,967
Bk 7226.7.92cpx
38,210,0221,650,010,9124,920,727,655,3499,43
5,9220,078
3,8770,1060,0010,0023,994
1,7673,2310,0950,8875,979
15,973
k 7246.7.92amph
37,980,0821,420,030,9124,200,476,797,0498,92
5,9270,073
3,8660,1070,0040,0073,992
1,5793,1580,0621,1775,976
15,968
Bk 7266.7.92amph
37,280,0421,130,001,1727,860,543,987,5299,52
5,8990,101
3,8390,1390,0000,0033,993
0,9393,6860,0721,2755,972
15,965
Bk 7276.7.92core
36,900,0820,890,021,6326,960,732,789,5499,53
5,8600,140
3,7700,1950,0030,0073,989
0,6583,5810,0981,6235,960
15,949
Bk 7286.7.92core
36,670,0820,700,021,5328,130,802,438,7799,13
5,8730,127
3,7800,1850,0030,0073,989
0,5803,7670,1091,5055,961
15,950
Bk 7296.7.92ab
37,930,0821,120,000,7427,530,843,148,90100,27
5,9700,030
3,8880,0870,0000,0073,989
0,7373,6240,1121,5015,973
15,962
Bk 7316.7.92amph
36,510,0620,970,031,5127,580,852,858,6999,05
5,8380,162
3,7900,1820,0040,0053,995
0,6793,6880,1151,4895,971
15,966
Bk 7366.7.92amph
37,100,0421,040,031,0227,540,623,588,0799,04
5,9070,093
3,8550,1230,0040,0033,994
0,8503,6670,0841,3775,977
15,971
Bk 7386.7.92amph
37,160,1121,270,021,4026,240,754,637,8699,44
5,8550,145
3,8040,1650,0020,0093,994
1,0873,4580,1001,3275,972
15,966
Bk 7466.7.92cpx (i)
36,750,9920,400,001,4822,961,125,028,9997,71
5,8640,136
3,7010,1780,0000,0853,976
1,1943,0630,1511,5375,946
15,922
C-21Appendix C Table C4 garnet
normed to 24 oxygens, Fe3 over charge balance
normed to 24 oxygens, Fe3 over charge balance
position means analysis of: core is core position in a grt grain, mineral x, rim position in grt grain in contact withmineral x, mineral x(i), grt at an inclusion of mineral x in grt
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOtotal
SiAlt
AloFe3CrTi
MgFe2MnCa
sum
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOtotal
SiAlt
AloFe3CrTi
MgFe2MnCa
sum
Bk 7486.7.92cpx (i)
37,470,1021,210,131,0824,301,045,088,5899,00
5,8970,103
3,8310,1280,0160,0083,993
1,1923,1990,1391,4475,976
15,968
Bk 7496.7.92cpx (i)
37,700,0721,360,061,0024,940,954,828,6799,57
5,9090,091
3,8540,1170,0070,0063,993
1,1263,2690,1261,4565,977
15,971
Bk 7516.7.92amph
37,120,0321,340,020,9627,700,434,816,5999,00
5,8840,116
3,8710,1140,0030,0033,999
1,1363,6720,0581,1195,986
15,985
Bk 7526.7.92gl (i)
37,450,0421,400,050,8825,740,804,538,4299,31
5,9020,098
3,8760,1040,0060,0033,997
1,0643,3920,1071,4225,985
15,982
Bk 7536.7.92amph (i)
37,310,0521,290,041,1325,190,794,878,3198,98
5,8840,116
3,8420,1340,0050,0043,995
1,1453,3230,1061,4045,978
15,972
Bk 7576.7.92cpx
37,220,0221,320,060,8628,130,454,586,5899,22
5,8980,102
3,8800,1020,0080,0023,999
1,0823,7270,0601,1175,987
15,986
Bk 7586.7.92core
37,410,0921,110,031,2625,711,353,828,8999,68
5,8960,104
3,8170,1500,0040,0083,990
0,8973,3890,1801,5015,968
15,958
Bk 7596.7.92core
37,020,0921,100,021,6426,121,693,089,25100,00
5,8450,155
3,7710,1950,0020,0083,991
0,7253,4480,2261,5655,964
15,955
Bk 7606.7.92core
36,920,1021,120,001,4226,111,203,668,7299,25
5,8550,145
3,8020,1700,0000,0093,993
0,8653,4630,1611,4825,971
15,964
Bk 7626.7.92core
37,140,1221,170,001,4425,710,794,238,7299,32
5,8610,139
3,7980,1710,0000,0103,992
0,9953,3930,1061,4745,968
15,960
Bk 7636.7.92qtz
37,720,0321,520,020,8824,590,586,327,2198,87
5,9080,092
3,8810,1030,0020,0033,996
1,4753,2210,0771,2105,984
15,980
Bk 7656.7.92cpx (i)
38,170,0021,160,070,8927,350,694,567,40100,29
5,9670,033
3,8660,1050,0090,0003,987
1,0633,5760,0911,2395,969
15,956
Bk 7666.7.92cpx
37,610,0221,340,071,1026,240,805,836,3499,35
5,8990,101
3,8440,1300,0090,0023,994
1,3633,4410,1061,0655,976
15,970
Bk 7676.7.92cpx
37,560,0121,400,010,7525,760,536,266,2098,48
5,9220,078
3,8990,0890,0010,0013,997
1,4713,3960,0711,0475,986
15,983
Bk 787.7.92cpx
37,560,0321,600,001,0424,790,586,007,5299,12
5,8790,121
3,8640,1220,0000,0033,998
1,4003,2460,0771,2615,984
15,981
Bk 797.7.92amph
37,640,0321,610,040,9124,450,566,417,2698,91
5,8900,110
3,8760,1070,0050,0033,998
1,4953,2000,0741,2175,987
15,985
Bk 7197.7.92amph
37,680,0221,680,030,6625,260,596,037,1199,07
5,9070,093
3,9120,0780,0040,0024,001
1,4093,3120,0781,1945,994
15,995
Bk 7227.7.92cpx (i)
37,320,0221,550,070,9526,510,636,325,5498,90
5,8730,127
3,8700,1120,0090,0024,001
1,4823,4890,0840,9345,989
15,990
Bk 7237.7.92cpx (i)
37,180,0421,560,011,2626,700,525,756,2999,31
5,8420,158
3,8350,1490,0010,0034,000
1,3473,5080,0691,0595,983
15,983
Bk 7257.7.92cpx (i)
37,160,0521,220,141,0525,310,555,267,7698,51
5,8820,118
3,8400,1250,0180,0043,997
1,2413,3510,0741,3165,981
15,978
Bk 7267.7.92cpx (i)
37,100,0121,500,061,4225,300,725,197,9899,28
5,8290,171
3,8110,1680,0070,0013,999
1,2153,3250,0961,3435,980
15,978
Bk 7307.7.92cpx (i)
37,370,0121,390,000,9525,760,585,247,5398,84
5,8970,103
3,8750,1130,0000,0013,997
1,2323,4000,0781,2735,983
15,980
C-22 Appendix C Table C4 garnet
normed to 24 oxygens, Fe3 over charge balance
normed to 24 oxygens, Fe3 over charge balance
position means analysis of: core is core position in a grt grain, mineral x, rim position in grt grain in contact withmineral x, mineral x(i), grt at an inclusion of mineral x in grt
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOtotal
SiAlt
AloFe3CrTi
MgFe2MnCa
sum
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOtotal
SiAlt
AloFe3CrTi
MgFe2MnCa
sum
Bk 7317.7.92cpx (i)
37,200,0021,430,031,3125,540,635,357,5999,08
5,8530,147
3,8270,1550,0040,0003,997
1,2553,3600,0841,2795,979
15,976
Bk 7337.7.92amph
36,900,0621,260,081,2225,850,704,448,2998,80
5,8520,148
3,8260,1460,0100,0053,998
1,0503,4290,0941,4095,981
15,979
Bk 7347.7.92ab
36,980,1521,230,001,6324,780,924,169,4899,32
5,8290,171
3,7730,1930,0000,0133,992
0,9773,2660,1231,6015,967
15,960
Bk 7357.7.92core
37,490,0521,540,041,1323,410,804,919,9299,29
5,8700,130
3,8450,1340,0050,0043,997
1,1463,0650,1061,6645,981
15,978
Bk 7367.7.92core
37,500,0721,290,051,6124,070,875,258,8699,57
5,8560,144
3,7750,1890,0060,0063,989
1,2223,1440,1151,4825,964
15,953
Bk 7377.7.92amph
37,590,0421,440,030,8726,750,525,995,9199,15
5,9070,093
3,8790,1030,0040,0033,997
1,4033,5160,0690,9955,984
15,980
Bk 7477.7.92cpx (i)
37,560,0621,290,050,2724,171,852,8710,9099,03
5,9660,034
3,9520,0330,0060,0053,999
0,6803,2110,2491,8555,995
15,994
Bk 7487.7.92cpx (i)
37,420,1021,210,001,3824,340,994,0010,1099,54
5,8790,121
3,8070,1630,0000,0083,990
0,9373,1980,1321,7005,967
15,957
Bk 7517.7.92cpx (i)
37,380,0321,230,031,1826,841,364,756,7499,54
5,8920,108
3,8360,1400,0040,0033,993
1,1163,5380,1821,1385,974
15,967
Bk 7617.7.92core
37,010,1421,150,001,4224,520,993,6010,2999,12
5,8550,145
3,7990,1690,0000,0123,992
0,8493,2440,1331,7445,970
15,962
Bk 7737.7.92amph
37,330,0321,180,020,9526,670,634,208,0799,07
5,9130,087
3,8680,1130,0030,0033,994
0,9923,5330,0851,3705,979
15,973
Bk 83014.3.93amph
38,180,0021,700,001,5025,260,517,695,40100,24
5,8710,129
3,8040,1740,0000,0003,991
1,7633,2480,0660,8905,967
15,957
Bk 83114.3.93amph
37,840,0721,720,001,0527,200,786,534,99100,19
5,8810,119
3,8590,1230,0000,0063,998
1,5133,5360,1030,8315,982
15,980
Bk 83214.3.93cpx
37,840,3521,650,000,8526,000,646,196,47100,00
5,8890,111
3,8600,1000,0000,0293,996
1,4363,3840,0841,0795,983
15,979
Bk 83314.3.93cpx
37,770,0921,670,001,0125,340,506,566,5499,48
5,8840,116
3,8630,1180,0000,0083,997
1,5233,3020,0661,0925,983
15,980
Bk 83414.3.93cpx
37,910,0121,440,031,0524,610,516,547,0499,13
5,9140,086
3,8560,1230,0040,0013,992
1,5213,2100,0671,1775,975
15,967
Bk 83514.3.93cpx
38,110,0021,740,000,9925,070,576,477,0299,97
5,9030,097
3,8720,1150,0000,0003,995
1,4943,2470,0751,1655,981
15,976
Bk 85114.3.93amph
38,380,0221,710,001,1825,490,497,225,90100,39
5,9050,095
3,8430,1370,0000,0023,991
1,6563,2790,0640,9735,972
15,963
Bk 85214.3.93core
37,900,0721,640,021,1927,370,336,285,59100,40
5,8800,120
3,8360,1400,0020,0063,995
1,4523,5520,0430,9295,976
15,971
Bk 85314.3.93core
37,240,0121,490,031,3629,790,283,906,65100,75
5,8450,155
3,8210,1600,0040,0013,999
0,9123,9100,0371,1185,978
15,978
Bk 85414.3.93core
37,360,0320,950,011,1728,880,672,957,9699,99
5,9210,079
3,8340,1400,0010,0033,989
0,6973,8280,0901,3525,967
15,956
Bk 85514.3.93core
37,110,1020,550,011,8628,661,112,248,60100,24
5,8870,113
3,7300,2220,0010,0093,981
0,5303,8020,1491,4625,943
15,923
C-23Appendix C Table C4 garnet
normed to 24 oxygens, Fe3 over charge balance
normed to 24 oxygens, Fe3 over charge balance
position means analysis of: core is core position in a grt grain, mineral x, rim position in grt grain in contact withmineral x, mineral x(i), grt at an inclusion of mineral x in grt
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOtotal
SiAlt
AloFe3CrTi
MgFe2MnCa
sum
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOtotal
SiAlt
AloFe3CrTi
MgFe2MnCa
sum
Bk 81029.1.93ap
38,130,0122,020,001,1725,010,408,245,02100,00
5,8630,137
3,8530,1350,0000,0013,998
1,8883,2160,0520,8275,983
15,982
Bk 81129.1.93cpx
37,890,0022,030,001,2924,700,558,125,2399,81
5,8390,161
3,8400,1490,0000,0004,000
1,8653,1840,0720,8645,984
15,984
Bk 81529.1.93core
37,240,0721,130,041,6225,701,463,828,8699,94
5,8560,144
3,7720,1920,0050,0063,989
0,8953,3800,1941,4935,963
15,952
Bk 81729.1.93core
36,860,1920,780,031,1926,850,703,059,0698,71
5,8970,103
3,8160,1430,0040,0163,990
0,7273,5930,0951,5535,968
15,958
Bk 81829.1.93core
36,680,2820,970,191,7127,311,152,918,87100,07
5,8100,190
3,7250,2040,0240,0243,993
0,6873,6180,1541,5055,965
15,958
Bk 81929.1.93cpx (i)
37,230,0021,270,001,6125,041,523,719,5499,91
5,8490,151
3,7880,1900,0000,0003,992
0,8693,2900,2021,6065,967
15,958
Bk 82429.1.93cpx (i)
37,310,1321,180,001,3825,381,533,429,6099,93
5,8740,126
3,8040,1630,0000,0113,990
0,8033,3420,2041,6195,968
15,958
Bk 82529.1.93core
37,510,1221,240,001,4824,541,194,589,0999,75
5,8720,128
3,7920,1740,0000,0103,988
1,0693,2130,1581,5255,964
15,952
Bk 9162.7.94amph
37,580,0521,310,050,9827,810,684,047,62100,12
5,9090,091
3,8590,1160,0060,0043,995
0,9473,6570,0911,2845,978
15,973
Bk 9172.7.94chl
37,580,1020,890,021,2524,332,741,6911,75100,35
5,9290,071
3,8140,1480,0020,0083,984
0,3973,2100,3661,9865,960
15,944
Bk 9182.7.94core
37,750,1020,770,081,0320,466,012,5410,9599,69
5,9650,035
3,8330,1220,0100,0083,981
0,5982,7040,8041,8545,961
15,942
Bk 9192.7.94core
37,830,2420,940,071,0120,564,153,1811,6599,63
5,9470,053
3,8270,1190,0090,0203,983
0,7452,7030,5531,9625,963
15,946
Bk 9202.7.94chl
38,330,0321,650,020,4827,060,505,856,28100,20
5,9620,038
3,9300,0570,0020,0033,996
1,3563,5190,0661,0475,988
15,984
Cig 90/40461.6.91core
37,080,0920,940,011,5928,460,533,018,32100,03
5,8690,131
3,7760,1890,0010,0083,989
0,7103,7680,0711,4115,960
15,949
Cig 90/40471.6.91core
37,090,1220,980,001,7929,510,513,017,63100,64
5,8480,152
3,7470,2130,0000,0103,989
0,7073,8910,0681,2895,956
15,944
Cig 90/40481.6.91cpx
37,370,0521,330,021,4227,450,915,355,9399,83
5,8630,137
3,8060,1670,0020,0043,994
1,2513,6020,1210,9975,971
15,964
Cig 90/40491.6.91core
36,820,0720,910,001,6429,340,572,707,8999,93
5,8540,146
3,7720,1960,0000,0063,991
0,6403,9010,0771,3445,962
15,953
Cig 90/40501.6.91core
36,940,1120,970,021,1628,430,623,028,0899,35
5,8900,110
3,8310,1390,0030,0093,993
0,7183,7910,0841,3805,973
15,966
Cig 90/40561.6.91core
37,740,0321,450,031,2027,410,924,946,73100,45
5,8900,110
3,8360,1410,0040,0033,994
1,1493,5780,1221,1255,974
15,968
Cig 90/40571.6.91core
37,210,0821,040,001,6426,060,782,8510,37100,03
5,8640,136
3,7720,1950,0000,0073,988
0,6693,4350,1041,7515,959
15,947
Cig 90/4011.6.91acore
37,000,1120,850,051,2428,910,512,887,9799,52
5,8970,103
3,8130,1490,0060,0093,991
0,6843,8530,0691,3615,967
15,958
Cig 90/4021.6.91acore
37,240,0820,880,041,6129,190,522,937,93100,42
5,8810,119
3,7670,1920,0050,0073,987
0,6903,8550,0701,3425,956
15,943
C-24 Appendix C Table C4 garnet
normed to 24 oxygens, Fe3 over charge balance
normed to 24 oxygens, Fe3 over charge balance
position means analysis of: core is core position in a grt grain, mineral x, rim position in grt grain in contact withmineral x, mineral x(i), grt at an inclusion of mineral x in grt
Cig 90/4051.6.91acore
37,040,1020,840,001,5029,040,523,017,7599,80
5,8840,116
3,7850,1790,0000,0093,988
0,7133,8580,0701,3195,960
15,948
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOtotal
SiAlt
AloFe3CrTi
MgFe2MnCa
sum
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOtotal
SiAlt
AloFe3CrTi
MgFe2MnCa
sum
Cig 90/4011.6.91bcore
37,350,0921,020,021,0129,140,532,927,93100,01
5,9220,078
3,8500,1210,0030,0083,992
0,6903,8640,0711,3475,972
15,964
Cig 90/4041.6.91bcore
37,010,0920,920,001,4627,890,593,378,1299,46
5,8770,123
3,7930,1750,0000,0083,990
0,7983,7050,0791,3825,963
15,953
Cig 90/4081.6.91bcpx
37,490,0321,180,021,1627,250,745,425,9899,28
5,9060,094
3,8380,1380,0020,0033,992
1,2733,5910,0991,0095,971
15,963
Cig 91-11016.6.93cpx
38,540,0121,920,020,8226,250,357,704,87100,48
5,9220,078
3,8910,0950,0020,0013,996
1,7633,3730,0460,8025,984
15,980
Cig 91-11116.6.93cpx
38,580,0221,930,020,9026,020,297,834,97100,56
5,9170,083
3,8800,1030,0020,0023,995
1,7903,3380,0380,8175,982
15,977
Cig 91-11416.6.93cz
38,070,0521,600,021,1225,041,265,697,52100,37
5,9010,099
3,8460,1300,0020,0043,993
1,3153,2460,1651,2495,975
15,967
Cig 91-11716.6.93gl
38,570,0421,710,021,2126,630,367,125,37101,03
5,9120,088
3,8340,1400,0020,0033,990
1,6273,4140,0470,8825,969
15,958
Cig 91-11816.6.93gl
38,200,0521,530,001,4926,830,326,835,41100,66
5,8870,113
3,7980,1730,0000,0043,988
1,5693,4580,0420,8935,962
15,951
Cig 91-11916.6.93biot
38,340,0621,630,030,7827,860,445,945,68100,76
5,9380,062
3,8870,0910,0040,0053,994
1,3713,6080,0580,9435,980
15,974
Cig 91-12016.6.93biot
38,200,0121,730,011,3427,970,496,025,61101,37
5,8810,119
3,8240,1550,0010,0013,993
1,3813,6010,0640,9255,971
15,965
Cig 91-12116.6.93biot
38,220,0321,670,020,9328,070,465,895,57100,86
5,9180,082
3,8730,1080,0020,0023,995
1,3593,6350,0600,9245,979
15,974
Cig 91-12216.6.93biot
38,330,0021,760,001,1428,260,425,875,66101,44
5,9020,098
3,8510,1330,0000,0003,994
1,3473,6390,0550,9345,975
15,969
Cig 91-12416.6.93qtz (i)
38,240,0321,640,001,1426,640,776,106,20100,76
5,9070,093
3,8460,1330,0000,0023,992
1,4043,4420,1011,0265,973
15,965
Cig 91-12516.6.93qtz (i)
38,120,0221,500,000,7328,540,595,465,44100,40
5,9470,053
3,9000,0860,0000,0023,994
1,2703,7240,0780,9095,981
15,975
Cig 91-12616.6.93gl
38,770,0221,950,001,2325,260,288,285,16100,95
5,9010,099
3,8380,1410,0000,0023,991
1,8783,2160,0360,8415,971
15,962
Cig 91-12716.6.93gl
38,900,0522,090,020,9824,930,258,684,99100,89
5,9120,088
3,8680,1120,0020,0043,994
1,9663,1680,0320,8125,979
15,973
Cig 91-12816.6.93gl
38,840,0521,910,000,5926,590,507,594,71100,78
5,9570,043
3,9170,0680,0000,0043,994
1,7353,4100,0650,7745,984
15,979
Cig 91-12916.6.93gl
38,970,0122,100,051,0125,570,348,285,03101,36
5,9120,088
3,8640,1150,0060,0013,994
1,8723,2450,0440,8185,979
15,972
Cig 91-13816.6.93biot
39,420,0022,370,030,5724,270,249,484,73101,11
5,9470,053
3,9250,0640,0040,0003,997
2,1323,0620,0310,7655,989
15,986
Cig 91-13916.6.93cpx (i)
39,100,0422,510,000,5624,140,179,594,67100,78
5,9160,084
3,9310,0640,0000,0034,002
2,1633,0540,0220,7575,996
15,998
Cig 91-14016.6.93biot
39,310,0022,050,050,7625,960,258,434,64101,46
5,9560,044
3,8930,0870,0060,0003,992
1,9043,2900,0320,7535,979
15,970
C-25Appendix C Table C4 garnet
normed to 24 oxygens, Fe3 over charge balance
normed to 24 oxygens, Fe3 over charge balance
position means analysis of: core is core position in a grt grain, mineral x, rim position in grt grain in contact withmineral x, mineral x(i), grt at an inclusion of mineral x in grt
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOtotal
SiAlt
AloFe3CrTi
MgFe2MnCa
sum
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOtotal
SiAlt
AloFe3CrTi
MgFe2MnCa
sum
Cig 91-14116.6.93biot
38,830,0421,960,001,0225,570,248,414,74100,81
5,9190,081
3,8640,1170,0000,0033,992
1,9113,2600,0310,7745,976
15,968
Cig 91-14216.6.93biot
38,750,0422,200,030,9025,430,398,334,96101,03
5,8980,102
3,8810,1030,0040,0033,998
1,8903,2370,0500,8095,986
15,984
Cig 91-14316.6.93biot
38,600,0221,990,020,9926,570,637,075,42101,31
5,9050,095
3,8690,1140,0020,0023,996
1,6123,3990,0820,8885,981
15,976
Cig 91-14416.6.93cpx (i)
38,860,0222,230,021,0425,170,328,884,57101,10
5,8930,107
3,8660,1180,0020,0023,996
2,0073,1910,0410,7425,982
15,978
Cig 91-14516.6.93core
38,860,0721,890,021,0727,050,257,305,12101,64
5,9200,080
3,8500,1230,0020,0063,991
1,6583,4470,0320,8365,972
15,963
Cig 91-14616.6.93cpx (i)
39,050,2522,130,030,7024,830,228,894,87100,97
5,9270,073
3,8850,0800,0040,0203,994
2,0113,1520,0280,7925,983
15,978
Cig 91-14716.6.93biot
38,740,0121,880,011,3926,150,217,865,09101,34
5,8940,106
3,8170,1590,0010,0013,990
1,7823,3280,0270,8305,967
15,956
Cig 91-14816.6.93biot
38,590,0221,930,061,2626,280,227,745,10101,20
5,8860,114
3,8290,1450,0070,0023,993
1,7603,3520,0280,8345,974
15,967
Cig 91-14916.6.93biot
38,960,0121,940,000,5125,910,287,875,07100,55
5,9690,031
3,9310,0590,0000,0013,994
1,7973,3200,0360,8325,985
15,980
Cig 91-14817.6.93biot
38,930,0122,180,000,7424,420,248,915,06100,49
5,9260,074
3,9050,0850,0000,0013,997
2,0223,1090,0310,8255,986
15,983
Cig 91-14917.6.93biot
38,970,0322,140,001,0024,730,238,904,92100,92
5,9110,089
3,8690,1140,0000,0023,994
2,0123,1370,0300,8005,979
15,972
Cig 91-15017.6.93biot
39,180,1322,330,280,4525,220,268,804,89101,53
5,9240,076
3,9030,0510,0330,0114,002
1,9833,1890,0330,7925,997
15,999
Cig 91-15117.6.93biot
38,820,0021,870,000,9225,450,348,254,86100,51
5,9370,063
3,8780,1060,0000,0003,992
1,8813,2550,0440,7965,976
15,968
Cig 91-15217.6.93biot
38,620,1121,900,000,4926,990,606,815,27100,79
5,9500,050
3,9260,0570,0000,0093,997
1,5643,4770,0780,8705,989
15,986
Cig 91-15317.6.93core
38,240,0321,450,001,2427,240,446,275,65100,55
5,9180,082
3,8300,1440,0000,0023,988
1,4463,5250,0580,9375,966
15,954
Cig 91-15417.6.93core
38,830,0021,590,021,1326,140,307,645,08100,73
5,9470,053
3,8430,1300,0020,0003,986
1,7443,3480,0390,8345,964
15,950
Cig 91-15917.6.93core
37,940,1221,080,051,2026,031,414,487,92100,23
5,9320,068
3,8170,1410,0060,0103,985
1,0443,4040,1871,3275,961
15,946
Cig 91-16017.6.93core
38,130,0421,140,021,3825,791,145,047,71100,39
5,9290,071
3,8030,1620,0020,0033,983
1,1683,3530,1501,2855,956
15,939
Cig 91-16117.6.93core
38,250,0721,190,041,1625,111,205,287,90100,21
5,9450,055
3,8270,1360,0050,0063,984
1,2233,2640,1581,3165,961
15,945
Cig 91-16217.6.93core
38,330,0821,370,001,6025,540,955,997,08100,94
5,9000,100
3,7770,1850,0000,0073,983
1,3743,2880,1241,1685,954
15,937
Cig 91-16317.6.93core
38,500,0721,220,031,3425,060,885,787,70100,58
5,9430,057
3,8040,1560,0040,0063,981
1,3303,2360,1151,2745,954
15,935
Cig 91-16717.6.93phe(i)
38,290,0121,480,001,4827,090,835,276,97101,42
5,9000,100
3,8010,1710,0000,0013,987
1,2103,4910,1081,1515,960
15,947
C-26 Appendix C Table C4/C5 garnet/glaucophane
normed to 24 oxygens, Fe3 over charge balance
position means analysis of: core is core position in a grt grain, mineral x, rim position in grt grain in contact withmineral x, mineral x(i), grt at an inclusion of mineral x in grt
sampleanalysedateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2O
H2Ototal
SiAlt
AloFe3CrTiMgFe2MnZn
CaNa
NaK
sum
OH
Bk 392724.6.92core
56,290,0511,310,042,087,980,0710,361,33n.a6,850,02
2,1598,53
7,8330,1678,000
1,6880,2180,0040,0042,1490,9280,008 -5,000
0,1981,8022,000
0,0470,0040,050
15,050
2
Bk 392824.6.92core
55,930,0211,280,042,677,480,0310,421,22n.a6,880,03
2,1598,14
7,8110,1898,000
1,6680,2810,0040,0012,1690,8730,004 -5,000
0,1831,8172,000
0,0450,0050,051
15,051
2
Bk 393924.6.92core
56,100,0311,240,022,727,040,0710,501,04n.a6,870,02
2,1597,80
7,8400,1608,000
1,6910,2860,0020,0022,1870,8230,008 -5,000
0,1561,8442,000
0,0170,0040,021
15,021
2
Bk 394124.6.92core
56,720,0511,640,073,885,450,0710,931,00n.a6,600,02
2,1898,60
7,8150,1858,000
1,7060,4020,0080,0042,2450,6280,008 -5,000
0,1481,7632,000
0,0000,0040,004
15,004
2
Bk 394427.8.92rim
58,170,0311,580,001,846,870,0411,191,190,126,880,03
2,21100,15
7,8960,1048,000
1,7490,1880,0000,0022,2640,7800,0050,0125,000
0,1731,8112,000
0,0000,0050,005
15,005
2
Bk 39443.7.94core
57,580,0611,540,003,306,800,0010,981,240,106,920,03
2,21100,76
7,8120,1888,000
1,6570,3370,0000,0042,2200,7720,0000,0105,000
0,1801,8202,000
0,0000,0050,006
15,006
2
Bk 39453.7.94core
56,910,0411,410,001,947,720,0410,391,100,106,840,04
2,1798,69
7,8800,1208,000
1,7420,2020,0000,0032,1440,8940,0050,0105,000
0,1631,8362,000
0,0000,0070,007
15,007
2
Bk 3915.5.92core
55,490,0211,040,000,699,870,099,801,60n.a6,950,04
2,1297,71
7,8440,1568,000
1,6830,0740,0000,0022,0651,1660,011 -5,000
0,2421,7582,000
0,1470,0070,154
15,154
2
Bk 3925.5.92core
56,680,0411,410,021,398,750,0210,181,17n.a7,090,01
2,1698,92
7,8620,1388,000
1,7280,1450,0020,0032,1051,0150,002 -5,000
0,1741,8262,000
0,0810,0020,083
15,083
2
Bk 7432.7.94core
57,610,0211,710,071,356,250,0211,721,450,176,910,03
2,2099,50
7,8560,1448,000
1,7390,1380,0080,0012,3820,7120,0020,0175,000
0,2121,7882,000
0,0390,0050,044
15,044
2
Bk 7442.7.94core
57,370,0211,900,022,205,960,0011,381,290,296,840,03
2,2099,50
7,8310,1698,000
1,7450,2260,0020,0012,3150,6810,0000,0295,000
0,1891,8102,000
0,0000,0050,005
15,005
2
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOtotal
SiAlt
AloFe3CrTi
MgFe2MnCa
sum
Cig 91-18317.6.93biot
38,840,0122,010,000,9825,790,188,204,93100,94
5,9190,081
3,8730,1120,0000,0013,993
1,8633,2870,0230,8055,978
15,971
Cig 91-18417.6.93biot
38,680,0421,860,041,1625,790,277,985,06100,88
5,9070,093
3,8410,1330,0050,0033,991
1,8163,2940,0350,8285,973
15,964
Cig 91-18517.6.93core
38,410,0321,840,001,1228,570,346,155,19101,65
5,8990,101
3,8520,1290,0000,0023,994
1,4083,6700,0440,8545,976
15,971
Cig 91-18617.6.93core
38,290,0421,200,001,5426,141,135,257,32100,91
5,9210,079
3,7850,1800,0000,0033,981
1,2103,3810,1481,2135,952
15,933
Cig 91-18717.6.93core
38,220,1421,500,010,7128,071,274,966,05100,93
5,9470,053
3,8900,0830,0010,0123,993
1,1503,6530,1671,0095,979
15,972
Cig 91-1528.11.93core
38,820,3321,910,010,4726,010,337,914,88100,67
5,9500,050
3,9080,0540,0010,0273,994
1,8073,3340,0430,8015,985
15,980
position means analysis of: core is core position in a gln grain, rim is rim position in a gln grain
normed on 23 oxygen, Fe3 over Si+Ti+Al+Fe+Mn+Mg+Ca+Zn = 15
C-27Appendix C Table C5 glaucophane
sampleanalysedateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2O
H2Ototal
SiAlt
AloFe3CrTiMgFe2MnZn
CaNa
NaK
sum
OH
normed on 23 oxygen, Fe3 over Si+Ti+Al+Fe+Mn+Mg+Ca+Zn = 15
sampleanalysedateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2O
H2Ototal
SiAlt
AloFe3CrTiMgFe2MnZn
CaNa
NaK
sum
OH
normed on 23 oxygen, Fe3 over Si+Ti+Al+Fe+Mn+Mg+Ca+Zn = 15
Bk 7452.7.94core
56,680,0311,870,072,846,690,0010,801,240,266,970,03
2,1999,66
7,7760,2248,000
1,6950,2930,0080,0022,2080,7670,0000,0265,000
0,1821,8182,000
0,0360,0050,042
15,042
2
Bk 71426.4.93rim
57,150,0811,720,121,306,450,0611,491,540,196,810,04
2,1999,14
7,8380,1628,000
1,7320,1350,0130,0062,3490,7390,0070,0195,000
0,2261,7742,000
0,0370,0070,044
15,044
2
Bk 7197.8.92core
57,130,0011,820,011,965,930,0011,180,910,236,950,03
2,1898,33
7,8720,1288,000
1,7920,2040,0010,0002,2960,6840,0000,0235,000
0,1341,8572,000
0,0000,0050,005
15,005
2
Bk 7237.8.92rim
56,060,0311,700,002,027,220,0510,541,400,246,760,04
2,1598,22
7,8070,1938,000
1,7270,2120,0000,0022,1880,8410,0060,0255,000
0,2091,7912,000
0,0340,0070,041
15,041
2
Bk 7247.8.92core
56,840,0411,660,002,406,830,0510,781,370,236,690,04
2,1899,11
7,8270,1738,000
1,7200,2490,0000,0032,2130,7860,0060,0235,000
0,2021,7862,000
0,0000,0070,007
15,007
2
Bk 7257.8.92rim
55,950,0211,740,002,477,520,0310,391,570,286,730,05
2,1698,91
7,7660,2348,000
1,6860,2580,0000,0012,1490,8730,0040,0295,000
0,2331,7672,000
0,0450,0090,054
15,054
2
Bk 7297.8.92rim
55,260,0711,620,002,147,000,0711,082,390,176,310,05
2,1598,31
7,7110,2898,000
1,6220,2250,0000,0052,3050,8170,0080,0185,000
0,3571,6432,000
0,0650,0090,074
15,074
2
Bk 7317.8.92rim
56,570,0311,860,012,996,130,0810,731,280,236,550,03
2,1798,66
7,8090,1918,000
1,7380,3110,0010,0022,2080,7070,0090,0235,000
0,1891,7532,000
0,0000,0050,005
15,005
2
Bk 7447.8.92core
55,830,0211,860,033,556,660,0910,571,660,216,570,06
2,1799,29
7,7150,2858,000
1,6470,3690,0030,0012,1770,7700,0110,0215,000
0,2461,7542,000
0,0060,0110,017
15,017
2
Bk 7467.8.92core
56,900,0011,810,042,955,700,0311,191,240,206,700,04
2,1898,98
7,8120,1888,000
1,7230,3050,0040,0002,2900,6540,0030,0205,000
0,1821,7842,000
0,0000,0070,007
15,007
2
Bk 81429.1.93bcore
57,500,1511,720,002,694,320,0012,080,690,197,160,05
2,2098,74
7,8540,1468,000
1,7410,2770,0000,0112,4590,4930,0000,0195,000
0,1011,8962,000
0,0000,0090,009
15,009
2
Bk 81529.1.93brim
57,150,0311,810,002,405,750,0411,511,360,216,800,05
2,1999,30
7,8170,1838,000
1,7210,2470,0000,0022,3470,6570,0050,0215,000
0,1991,8012,000
0,0030,0090,012
15,012
2
Bk 81729.1.93brim
56,630,0311,590,032,617,020,0810,351,070,266,740,06
2,1698,63
7,8450,1558,000
1,7370,2720,0030,0022,1370,8130,0090,0275,000
0,1591,8102,000
0,0000,0110,011
15,011
2
Bk 81829.1.93bcore
56,860,0211,920,041,586,600,0110,910,870,307,170,06
2,1798,52
7,8500,1508,000
1,7900,1650,0040,0012,2450,7630,0010,0315,000
0,1291,8712,000
0,0480,0110,059
15,059
2
Bk 82029.1.93brim
57,050,0311,630,032,806,720,0110,560,890,226,890,04
2,1899,05
7,8540,1468,000
1,7400,2900,0030,0022,1670,7740,0010,0225,000
0,1311,8392,000
0,0000,0070,007
15,007
2
Bk 962.7.94core
57,700,0411,460,002,385,770,0511,571,400,076,520,04
2,2099,19
7,8800,1208,000
1,7240,2440,0000,0042,3550,6590,0060,0075,000
0,2051,7261,931
0,0000,0070,007
14,938
2
Bk 972.7.94core
57,660,0511,660,142,126,000,0611,401,300,156,700,02
2,2099,46
7,8640,1368,000
1,7380,2170,0150,0052,3170,6850,0070,0155,000
0,1901,7721,962
0,0000,0040,004
14,965
2
Bk 9102.7.94core
56,250,0510,820,022,316,710,0511,883,040,125,830,07
2,1799,33
7,7590,2418,000
1,5180,2400,0020,0052,4430,7740,0060,0125,000
0,4491,5512,000
0,0080,0130,021
15,021
2
Bk 9112.7.94core
57,350,0111,730,023,604,640,0011,851,140,066,780,05
2,2099,43
7,8070,1938,000
1,6890,3680,0020,0012,4040,5290,0000,0065,000
0,1661,7901,956
0,0000,0090,009
14,965
2
Bk 9423.2.94rim
57,780,0211,800,052,365,230,0211,481,060,176,570,04
2,1998,77
7,8950,1058,000
1,7950,2430,0050,0022,3380,5970,0020,0175,000
0,1551,7411,896
0,0000,0070,007
14,903
2
Bk 9123.2.94arim
58,200,0212,010,032,325,180,0511,551,040,166,620,03
2,2199,42
7,8940,1068,000
1,8130,2370,0030,0022,3350,5870,0060,0165,000
0,1511,7411,892
0,0000,0050,005
14,897
2
Bk 9223.2.94arim
58,010,0711,560,032,485,220,0111,591,090,176,540,03
2,2099,00
7,9090,0918,000
1,7670,2540,0030,0072,3550,5950,0010,0175,000
0,1591,7291,888
0,0000,0050,005
14,893
2
C-28 Appendix C Table C5/C6 glaucophane/clinozoisite
position means analysis of: i(x), inclusion of czo in mineral x, core is core position in a czox grain, mineral x, rimposition in czo grain in contact with mineral x, mineral x(i), czo at an inclusion of mineral x in czo
sampleanalysedateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2O
H2Ototal
SiAlt
AloFe3CrTiMgFe2MnZn
CaNa
NaK
sum
OH
normed on 23 oxygen, Fe3 over Si+Ti+Al+Fe+Mn+Mg+Ca+Zn = 15
Bk 9323.2.94arim
55,970,0311,200,025,463,890,0611,791,970,205,850,21
2,1898,84
7,7120,2888,000
1,5310,5660,0020,0032,4210,4490,0070,0205,000
0,2911,5631,854
0,0000,0380,038
14,891
2
Bk 9423.2.94arim
57,060,0211,350,012,735,560,0111,821,880,176,360,06
2,1999,22
7,8150,1858,000
1,6470,2820,0010,0022,4130,6370,0010,0175,000
0,2761,6891,965
0,0000,0110,011
14,975
2
Cig 91-17017.6.93rim
58,270,0111,650,001,396,940,0511,160,920,087,080,03
2,2099,78
7,9250,0758,000
1,7920,1420,0000,0012,2620,7900,0060,0085,000
0,1341,8662,000
0,0010,0050,006
15,006
2
Cig 91-17117.6.93rim
57,870,0111,660,001,278,100,0010,510,880,057,150,03
2,1999,73
7,9140,0868,000
1,7940,1310,0000,0012,1420,9270,0000,0055,000
0,1291,8712,000
0,0250,0050,030
15,030
2
Cig 91-17217.6.93core
58,470,0111,750,021,127,540,0410,790,640,077,270,03
2,2199,96
7,9460,0548,000
1,8280,1150,0020,0012,1860,8570,0050,0075,000
0,0931,9072,000
0,0090,0050,014
15,014
2
Cig 91-17917.6.93rim
57,400,0711,740,021,388,580,0010,201,050,057,060,04
2,1999,77
7,8760,1248,000
1,7750,1430,0020,0052,0860,9840,0000,0055,000
0,1541,8462,000
0,0330,0070,040
15,040
2
Cig 91-18117.6.93rim
58,350,0211,810,021,426,580,0311,310,770,017,160,05
2,2199,74
7,9210,0798,000
1,8110,1450,0020,0012,2890,7470,0030,0015,000
0,1121,8852,000
0,0000,0090,009
15,009
2
Cig 91-18817.6.93rim
58,860,1811,570,011,326,460,0211,590,640,017,320,02
2,22100,21
7,9470,0538,000
1,7880,1340,0010,0132,3320,7290,0020,0015,000
0,0931,9072,000
0,0090,0040,012
15,012
2
position means analysis of: core is core position in a gln grain, rim is rim position in a gln grain
sampleanalysisdateposition
SiO2Al2O3Fe2O3CaO
H2OTotal
Si
AlFe3
Ca
OH
XAl2Fe
Bk 10B2618.10.93sympl
38,6025,5210,9723,44
1,9198,53
3,026
2,3580,6473,005
1,969
1,000
0,644
Bk 10B2718.10.93core
39,1929,135,9824,07
1,9598,37
3,020
2,6460,3472,992
1,987
1,000
0,349
Bk 10B2818.10.93core
39,1529,215,7924,03
1,9498,18
3,021
2,6560,3362,993
1,987
1,000
0,339
Bk 10B1119.10.93asympl
37,8026,219,2523,03
1,8896,29
3,014
2,4630,5553,018
1,968
1,000
0,545
Bk 10B1219.10.93asympl
37,9128,465,6823,34
1,8995,39
3,011
2,6640,3393,003
1,986
1,000
0,338
Bk 10B1319.10.93acore
38,0828,096,6923,94
1,9196,80
2,990
2,6000,3952,995
2,014
1,000
0,397
Bk 10B1419.10.93asympl
37,6326,049,7423,72
1,8997,13
2,979
2,4290,5803,009
2,012
1,000
0,575
Bk 10B1519.10.93aclz
38,3429,485,4724,34
1,9497,63
2,970
2,6910,3193,010
2,020
1,000
0,316
Bk 10B2019.10.93asympl
38,0626,818,3523,69
1,9096,91
3,005
2,4950,4962,991
2,004
1,000
0,501
Bk 10B2119.10.93acore
38,2727,627,7123,95
1,9297,55
2,993
2,5460,4543,000
2,007
1,000
0,454
Bk 10B2219.10.93aclz
38,4028,177,0024,28
1,9397,85
2,986
2,5820,4102,991
2,023
1,000
0,413
normed on 8 kations, all iron assumed to be Fe3
C-29Appendix C Table C6 clinozoisite
position means analysis of: i(x), inclusion of czo in mineral x, core is core position in a czo grain, mineral x, rimposition in czo grain in contact with mineral x, mineral x(i), czo at an inclusion of mineral x in czo
sampleanalysisdateposition
SiO2Al2O3Fe2O3CaO
H2OTotal
Si
AlFe3
Ca
OH
XAl2Fe
normed on 8 kations, all iron assumed to be Fe3
sampleanalysisdateposition
SiO2Al2O3Fe2O3CaO
H2OTotal
Si
AlFe3
Ca
OH
XAl2Fe
normed on 8 kations, all iron assumed to be Fe3
sampleanalysisdateposition
SiO2Al2O3Fe2O3CaO
H2OTotal
Si
AlFe3
Ca
OH
XAl2Fe
normed on 8 kations, all iron assumed to be Fe3
Bk 171225.7.94sympl
38,1926,189,7123,53
1,9097,61
3,008
2,4300,5763,006
1,986
1,000
0,572
Bk 171325.7.94core
37,9427,307,8923,79
1,9096,92
2,989
2,5350,4683,003
2,008
1,000
0,467
Bk 18225.8.94amph
37,9227,188,7623,75
1,9197,61
2,974
2,5130,5173,030
1,996
1,000
0,502
Bk 18235.8.94core
38,2227,228,4623,77
1,9197,67
2,994
2,5130,4993,011
1,995
1,000
0,493
Bk 18245.8.94par
38,1427,088,6023,76
1,9197,58
2,992
2,5040,5083,011
1,997
1,000
0,502
Bk 18106.8.94rut
38,7127,698,3623,59
1,9398,35
3,009
2,5370,4893,026
1,965
1,000
0,477
Bk 39213.3.93clz
37,5226,209,2124,18
1,9097,11
2,965
2,4400,5482,988
2,047
1,000
0,555
Bk 39313.3.93sympl
37,9627,018,1724,00
1,9097,14
2,987
2,5050,4842,989
2,024
1,000
0,489
Bk 39413.3.93core
37,8726,898,4123,59
1,9096,76
2,995
2,5060,5013,007
1,999
1,000
0,49
Bk 39513.3.93clz
37,9426,558,8623,83
1,9097,18
2,992
2,4680,5262,994
2,014
1,000
0,529
Bk 39613.3.93clz
37,9826,429,0123,73
1,9097,14
2,999
2,4580,5352,994
2,007
1,000
0,539
Bk 39713.3.93clz
38,0927,268,4523,62
1,9197,42
2,991
2,5230,4993,022
1,987
1,000
0,488
Bk 39813.3.93clz
37,8328,895,7623,26
1,9095,74
2,993
2,6930,3433,036
1,971
1,000
0,331
Bk 10B2319.10.93acore
38,4428,925,4123,32
1,9096,09
3,027
2,6840,3213,005
1,968
1,000
0,319
Bk 10B2419.10.93aamph
38,8025,6211,1723,05
1,9198,64
3,040
2,3660,6593,025
1,935
1,000
0,643
Bk 10B2519.10.93aamph
38,2627,487,8024,09
1,9297,63
2,991
2,5320,4592,991
2,018
1,000
0,463
Bk 10B2619.10.93acore
38,5429,125,6223,99
1,9397,27
2,999
2,6710,3293,000
2,000
1,000
0,329
Bk 10B2719.10.93acore
38,2827,657,4824,11
1,9297,52
2,993
2,5480,4402,988
2,020
1,000
0,445
Bk 10B2819.10.93aclz
38,3428,865,4923,86
1,9196,55
3,006
2,6660,3242,990
2,004
1,000
0,327
Bk 10B2919.10.93asympl
38,4828,295,7624,15
1,9196,68
3,017
2,6140,3402,954
2,029
1,000
0,356
Bk 17925.7.94ab
37,7725,8310,2823,47
1,8997,35
2,989
2,4090,6123,021
1,990
1,000
0,599
Bk 171025.7.94clz
38,2727,598,0523,78
1,9297,69
2,992
2,5420,4733,016
1,992
1,000
0,466
Bk 171125.7.94core
38,1026,1810,0423,49
1,9197,81
2,998
2,4280,5943,022
1,980
1,000
0,581
Bk 17259.7.94clz
38,0925,6510,5523,69
1,9097,98
2,998
2,3790,6253,004
1,998
1,000
0,622
Bk 17269.7.94ab
37,5724,8411,3623,46
1,8897,23
2,990
2,3300,6803,010
2,000
1,000
0,673
Bk 17279.7.94sympl
37,7825,3610,9123,55
1,8997,60
2,989
2,3650,6503,015
1,996
1,000
0,640
Bk 17389.7.94ab
37,8925,4710,9523,33
1,9097,64
2,997
2,3740,6523,026
1,977
1,000
0,635
Bk 17399.7.94clz
38,8926,7510,0624,20
1,9599,90
2,994
2,4270,5833,010
1,996
1,000
0,577
Bk 17409.7.94sympl
38,4725,2511,4523,68
1,9298,85
3,011
2,3290,6743,003
1,986
1,000
0,672
Bk 17469.7.94core
38,1627,008,5723,79
1,9197,52
2,995
2,4980,5063,004
2,001
1,000
0,504
Bk 186125.7.94sympl
38,1629,355,3223,88
1,9296,71
2,983
2,7040,3133,017
2,000
1,000
0,308
Bk 186225.7.94core
37,9928,975,8723,64
1,9196,47
2,983
2,6810,3473,028
1,989
1,000
0,337
Bk 18195.8.94core
38,1727,508,1123,95
1,9297,73
2,984
2,5330,4773,011
2,006
1,000
0,472
C-30 Appendix C Table C6 clinozoisite
position means analysis of: i(x), inclusion of czo in mineral x, core is core position in a czo grain, mineral x, rimposition in czo grain in contact with mineral x, mineral x(i), czo at an inclusion of mineral x in czo
sampleanalysisdateposition
SiO2Al2O3Fe2O3CaO
H2OTotal
Si
AlFe3
Ca
OH
XAl2Fe
normed on 8 kations, all iron assumed to be Fe3
sampleanalysisdateposition
SiO2Al2O3Fe2O3CaO
H2OTotal
Si
AlFe3
Ca
OH
XAl2Fe
sampleanalysisdateposition
SiO2Al2O3Fe2O3CaO
H2OTotal
Si
AlFe3
Ca
OH
XAl2Fe
normed on 8 kations, all iron assumed to be Fe3
Bk 39913.3.93clz
38,3630,244,6924,05
1,9497,34
2,971
2,7600,2733,034
1,996
1,000
0,264
Bk 391013.3.93clz
37,9228,486,2923,73
1,9096,42
2,985
2,6420,3733,014
2,001
1,000
0,367
Bk 391213.3.93sympl
37,8227,158,2423,76
1,9096,97
2,982
2,5230,4893,011
2,007
1,000
0,483
Bk 391313.3.93core
38,2428,406,5123,63
1,9196,78
3,001
2,6270,3853,012
1,987
1,000
0,380
Bk 391513.3.93clz
37,8426,978,7623,64
1,9097,21
2,981
2,5040,5193,023
1,995
1,000
0,507
Bk 391613.3.93clz
38,2227,218,4224,04
1,9297,89
2,986
2,5060,4953,001
2,013
1,000
0,495
Bk 391713.3.93par
37,9127,557,7023,71
1,9096,87
2,986
2,5570,4563,014
2,001
1,000
0,450
Bk 391813.3.93par
38,0827,637,7923,93
1,9197,43
2,982
2,5500,4593,010
2,008
1,000
0,455
Bk 391913.3.93par
37,9427,358,4123,99
1,9297,69
2,970
2,5230,4963,019
2,012
1,000
0,486
Bk 392013.3.93par
37,9227,198,2723,74
1,9097,12
2,985
2,5230,4903,013
2,002
1,000
0,484
Bk 392113.3.93clz
38,2429,135,6823,81
1,9296,86
2,989
2,6830,3343,017
1,994
1,000
0,328
Bk 392213.3.93clz
38,2129,006,0323,95
1,9297,19
2,980
2,6650,3543,019
2,001
1,000
0,347
Bk 392313.3.93sympl
38,2828,157,6123,63
1,9297,67
2,988
2,5890,4473,036
1,976
1,000
0,431
Bk 392413.3.93sympl
38,0327,168,7623,47
1,9197,42
2,989
2,5160,5183,034
1,977
1,000
0,501
Bk 39924.6.92i (grt)
37,3128,946,3623,29
1,9095,90
2,951
2,6970,3783,076
1,973
1,000
0,352
Bk 391724.6.92i (grt)
37,9628,427,3323,49
1,9197,20
2,973
2,6230,4323,056
1,971
1,000
0,409
Bk 392024.6.92par
37,2526,479,1023,66
1,8996,48
2,961
2,4800,5443,024
2,015
1,000
0,532
Bk 392124.6.92clz
37,2827,777,4023,51
1,8995,96
2,960
2,5980,4423,041
2,000
1,000
0,425
Bk 392224.6.92core
37,5126,578,6823,90
1,8996,66
2,972
2,4810,5182,999
2,029
1,000
0,518
Bk 393524.6.92par
37,7527,427,4823,82
1,9096,47
2,984
2,5540,4452,999
2,017
1,000
0,445
Bk 393624.6.92clz
38,0228,835,7323,75
1,9196,33
2,989
2,6710,3393,011
2,000
1,000
0,336
Bk 394224.6.92sympl
37,1725,869,4823,77
1,8896,28
2,966
2,4320,5693,001
2,032
1,000
0,568
Bk 394424.6.92core
37,9129,395,4623,97
1,9296,73
2,964
2,7080,3213,029
2,008
1,000
0,312
Bk 394524.6.92cpx
37,5226,768,8123,75
1,9096,84
2,968
2,4950,5253,019
2,013
1,000
0,515
Bk 394624.6.92core
37,5626,878,6223,47
1,8996,52
2,979
2,5120,5153,026
1,994
1,000
0,501
Bk 394724.6.92clz
37,6427,916,9123,74
1,9096,20
2,976
2,6010,4113,012
2,011
1,000
0,406
Bk 394824.6.92par
37,5026,908,3923,57
1,8996,36
2,977
2,5170,5013,018
2,005
1,000
0,492
Bk 39128.1.93i (grt)
37,4327,407,8623,12
1,8895,81
2,982
2,5730,4713,044
1,974
1,000
0,451
Bk 39228.1.93i (grt)
38,3629,854,6323,46
1,9196,30
3,004
2,7550,2733,028
1,968
1,000
0,266
Bk 391728.8.92cpx
37,9228,736,8923,92
1,9297,46
2,957
2,6400,4043,045
1,998
1,000
0,387
Bk 391928.8.92cpx
37,6828,557,2224,21
1,9297,66
2,935
2,6210,4233,044
2,021
1,000
0,405
Bk 395,25.5.92cpx
37,7528,605,6923,90
1,9095,94
2,980
2,6610,3382,999
2,021
1,000
0,338
Bk 396,25.5.92core
37,6426,348,7523,79
1,8996,52
2,989
2,4650,5232,987
2,024
1,000
0,529
normed on 8 kations, all iron assumed to be Fe3
C-31Appendix C Table C6 clinozoisite
position means analysis of: i(x), inclusion of czo in mineral x, core is core position in a czo grain, mineral x, rimposition in czo grain in contact with mineral x, mineral x(i), czo at an inclusion of mineral x in czo
sampleanalysisdateposition
SiO2Al2O3Fe2O3CaO
H2OTotal
Si
AlFe3
Ca
OH
XAl2Fe
normed on 8 kations, all iron assumed to be Fe3
sampleanalysisdateposition
SiO2Al2O3Fe2O3CaO
H2OTotal
Si
AlFe3
Ca
OH
XAl2Fe
sampleanalysisdateposition
SiO2Al2O3Fe2O3CaO
H2OTotal
Si
AlFe3
Ca
OH
XAl2Fe
normed on 8 kations, all iron assumed to be Fe3
Bk 397,25.5.92sympl
37,6126,138,4823,94
1,8896,16
2,996
2,4530,5082,961
2,043
1,000
0,529
Bk 4549.7.94vein
38,3728,526,3323,87
1,9297,09
3,000
2,6280,3733,001
2,000
1,000
0,372
Bk 4559.7.94vein
38,5028,256,8124,10
1,9397,66
2,998
2,5920,3992,992
2,011
1,000
0,403
Bk 4569.7.94vein
38,4528,047,4523,83
1,9297,77
2,997
2,5760,4373,013
1,990
1,000
0,431
Bk 4589.7.94vein
38,5327,896,9924,01
1,9297,42
3,011
2,5680,4112,979
2,010
1,000
0,420
Bk 4599.7.94vein
38,8528,756,5023,80
1,9397,90
3,014
2,6290,3803,008
1,978
1,000
0,376
Bk 4609.7.94vein
38,3328,356,4823,62
1,9196,78
3,008
2,6230,3833,005
1,986
1,000
0,381
Bk 4619.7.94vein
38,1528,425,9323,76
1,9096,26
3,005
2,6380,3522,990
2,005
1,000
0,355
Bk 4629.7.94vein
38,4028,586,3523,65
1,9296,98
3,006
2,6370,3743,011
1,984
1,000
0,370
Bk 4639.7.94vein
38,5227,936,9823,85
1,9297,28
3,014
2,5760,4112,987
1,999
1,000
0,417
Bk 76726.4.93i (grt)
38,0228,516,9323,52
1,9196,98
2,981
2,6340,4093,044
1,976
1,000
0,392
Bk 76826.4.93i (grt)
37,9227,717,4523,23
1,8996,31
3,001
2,5850,4443,029
1,970
1,000
0,431
Bk 76926.4.93i (grt)
37,6027,388,2023,51
1,9096,69
2,971
2,5500,4883,038
1,991
1,000
0,470
Bk 77026.4.93i (grt)
37,6427,098,7623,35
1,9096,84
2,976
2,5250,5213,046
1,978
1,000
0,498
Bk 7927.8.92amph
37,6028,156,8123,99
1,9096,55
2,960
2,6120,4043,016
2,024
1,000
0,397
Bk 71027.8.92ap
37,7127,846,9923,47
1,8996,01
2,989
2,6010,4173,018
1,993
1,000
0,410
Bk 71127.8.92cpx
37,3727,927,1223,52
1,8995,93
2,965
2,6110,4253,036
1,999
1,000
0,411
Bk 71227.8.92core
37,4628,336,4823,81
1,9096,08
2,960
2,6390,3853,024
2,016
1,000
0,376
Bk 71327.8.92cpx
37,8328,656,0624,37
1,9296,91
2,959
2,6410,3572,998
2,043
1,000
0,357
Bk 71427.8.92par
37,5927,657,2823,59
1,8996,11
2,979
2,5830,4343,017
2,003
1,000
0,427
Bk 72027.8.92par
37,4728,226,6723,64
1,8996,00
2,966
2,6320,3973,030
2,005
1,000
0,386
Bk 72127.8.92par
37,6527,507,9124,07
1,9197,13
2,959
2,5470,4683,015
2,027
1,000
0,461
Bk 72227.8.92cpx
37,5028,127,1323,82
1,9096,57
2,955
2,6110,4233,034
2,011
1,000
0,409
Bk 7147.7.92ab
37,2827,567,3623,97
1,8996,17
2,953
2,5730,4393,012
2,035
1,000
0,433
Bk 7157.7.92ab
37,4627,317,9223,65
1,8996,34
2,969
2,5510,4733,023
2,008
1,000
0,462
Bk 7167.7.92clz
37,5127,826,9923,91
1,9096,23
2,966
2,5930,4163,008
2,026
1,000
0,412
Bk 7177.7.92par
37,0028,636,3223,56
1,8995,51
2,938
2,6790,3783,057
2,005
1,000
0,357
Bk 7527.7.92par
37,2326,797,9823,70
1,8895,70
2,972
2,5210,4793,000
2,027
1,000
0,479
Bk 7537.7.92par
37,3827,198,1123,82
1,8996,50
2,959
2,5370,4833,020
2,020
1,000
0,474
Bk 7547.7.92gnt
37,6627,337,8223,91
1,9096,72
2,972
2,5420,4653,006
2,022
1,000
0,462
Bk 8214.3.93core
38,4228,576,1623,71
1,9196,86
3,010
2,6380,3633,001
1,990
1,000
0,363
Bk 8314.3.93par
37,8727,987,0123,78
1,9096,64
2,982
2,5970,4163,012
2,006
1,000
0,411
Bk 8414.3.93core
38,1328,496,7123,23
1,9096,56
3,001
2,6430,3983,040
1,959
1,000
0,382
normed on 8 kations, all iron assumed to be Fe3
C-32 Appendix C Table C6 clinozoisite
position means analysis of: i(x), inclusion of czo in mineral x, core is core position in a czo grain, mineral x, rimposition in czo grain in contact with mineral x, mineral x(i), czo at an inclusion of mineral x in czo
Bk 8514.3.93clz
37,6727,487,4823,63
1,8996,26
2,984
2,5650,4463,011
2,005
1,000
0,441
sampleanalysisdateposition
SiO2Al2O3Fe2O3CaO
H2OTotal
Si
AlFe3
Ca
OH
XAl2Fe
normed on 8 kations, all iron assumed to be Fe3
sampleanalysisdateposition
SiO2Al2O3Fe2O3CaO
H2OTotal
Si
AlFe3
Ca
OH
XAl2Fe
normed on 8 kations, all iron assumed to be Fe3
sampleanalysisdateposition
SiO2Al2O3Fe2O3CaO
H2OTotal
Si
AlFe3
Ca
OH
XAl2Fe
normed on 8 kations, all iron assumed to be Fe3
Bk 8814.3.93clz
38,1027,657,7923,69
1,9197,23
2,990
2,5580,4603,018
1,992
1,000
0,452
Bk 8914.3.93par
37,8328,266,5623,55
1,9096,20
2,987
2,6300,3903,020
1,993
1,000
0,382
Bk 81014.3.93clz
38,0428,027,0523,65
1,9196,76
2,992
2,5980,4173,015
1,993
1,000
0,411
Bk 81114.3.93sympl
37,7527,077,8623,49
1,8996,17
2,998
2,5340,4703,003
1,999
1,000
0,468
Bk 82114.3.93par
38,1229,385,1523,81
1,9196,46
2,986
2,7120,3033,016
1,998
1,000
0,299
Bk 82214.3.93zoi
38,2529,414,9324,10
1,9296,69
2,987
2,7070,2902,997
2,016
1,000
0,291
Bk 912.7.94par
38,1427,607,3123,92
1,9196,97
2,997
2,5560,4322,989
2,014
1,000
0,437
Bk 922.7.94core
38,5029,255,1524,17
1,9397,07
2,998
2,6840,3012,986
2,016
1,000
0,306
Bk 932.7.94par
38,1627,667,3623,70
1,9196,88
3,002
2,5650,4363,000
1,998
1,000
0,435
Bk 9282.7.94zoi
38,1528,166,8323,72
1,9196,86
2,995
2,6060,4043,009
1,995
1,000
0,400
Bk 9292.7.94par
38,3226,668,9223,58
1,9197,48
3,014
2,4710,5282,999
1,987
1,000
0,529
Bk 9302.7.94clz
38,6729,675,2223,99
1,9497,55
2,996
2,7090,3043,013
1,991
1,000
0,300
Bk 9312.7.94sympl
37,6725,5710,3123,67
1,8997,22
2,986
2,3890,6153,004
2,010
1,000
0,613
Bk 91623.2.94par
38,0427,568,5823,72
1,9297,90
2,972
2,5380,5043,042
1,986
1,000
0,484
Bk 91723.2.94core
37,9627,598,9623,56
1,9298,06
2,964
2,5390,5263,065
1,971
1,000
0,494
Bk 91823.2.94core
38,3929,935,8223,90
1,9498,04
2,963
2,7230,3383,061
1,976
1,000
0,319
Bk 91923.2.94amph
38,4829,166,4623,96
1,9498,05
2,978
2,6600,3763,036
1,987
1,000
0,363
Bk 92123.2.94amph
38,2229,077,0923,99
1,9498,37
2,954
2,6480,4123,060
1,986
1,000
0,389
Bk 92223.2.94ab
38,2228,917,4323,78
1,9498,35
2,958
2,6370,4333,070
1,972
1,000
0,405
Bk 92323.2.94par
37,9627,298,5923,80
1,9197,64
2,974
2,5210,5073,027
1,998
1,000
0,493
Bk 92423.2.94par
38,1228,756,8123,85
1,9297,54
2,970
2,6400,3993,039
1,991
1,000
0,384
Bk 92523.2.94par
38,3228,457,3123,90
1,9397,98
2,977
2,6050,4283,033
1,990
1,000
0,414
Bk 92623.2.94core
38,0728,507,4023,98
1,9397,96
2,959
2,6110,4333,044
1,997
1,000
0,415
Bk 92823.2.94clz
38,3329,016,6324,11
1,9498,08
2,967
2,6470,3863,033
2,000
1,000
0,374
Bk 92923.2.94core
38,5830,325,3324,24
1,9598,48
2,959
2,7410,3083,049
1,992
1,000
0,294
Bk 93023.2.94par
37,7327,997,6023,75
1,9197,07
2,963
2,5900,4493,039
1,998
1,000
0,432
Bk 93323.2.94par
38,2829,196,3224,16
1,9497,95
2,964
2,6640,3683,032
2,004
1,000
0,357
Bk 93523.2.94clz
38,3828,457,3123,54
1,9297,68
2,991
2,6140,4293,043
1,966
1,000
0,411
Bk 93623.2.94par
38,3428,817,0024,03
1,9498,18
2,969
2,6290,4083,037
1,994
1,000
0,393
Bk 93723.2.94par
38,3829,296,4923,94
1,9498,10
2,968
2,6700,3783,048
1,984
1,000
0,361
Bk 93823.2.94par
38,2128,097,6323,97
1,9397,91
2,975
2,5780,4473,025
2,000
1,000
0,436
Bk 93923.2.94core
38,4329,496,4724,18
1,9598,56
2,957
2,6750,3753,049
1,994
1,000
0,357
C-33Appendix C Table C6/C7 clinozoisite/zoisite
position means analysis of: i(x), inclusion of czo/zoi in mineral x, core is core position in a czo/zoi grain, mineral x,rim position in czo/zoi grain in contact with mineral x, mineral x(i), czo/zoi at an inclusion of mineral x in czo/zoi
sampleanalysisdateposition
SiO2Al2O3Fe2O3CaO
H2OTotal
Si
AlFe3
Ca
OH
XAl2Fe
normed on 8 kations, all iron assumed to be Fe3
sampleanalysisdateposition
SiO2Al2O3Fe2O3CaO
H2OTotal
Si
AlFe3
Ca
OH
XAl2Fe
normed on 8 kations, all iron assumed to be Fe3
sampleanalysisdateposition
SiO2Al2O3Fe2O3CaO
H2OTotal
Si
AlFe3
Ca
OH
XAl2Fe
normed on 8 kations, all iron assumed to be Fe3
Bk 954.3.94zoi
39,2329,346,6324,23
1,9699,43
2,996
2,6410,3813,022
1,982
1,000
0,373
Bk 964.3.94chl
39,1829,566,4024,06
1,9699,20
2,996
2,6640,3683,033
1,971
1,000
0,357
Bk 974.3.94chl
38,9228,747,2723,98
1,9598,91
2,995
2,6070,4213,028
1,977
1,000
0,410
Bk 984.3.94core
38,8529,256,6524,00
1,9598,75
2,987
2,6510,3853,035
1,977
1,000
0,371
Cig 91-11316.6.93i (grt)
38,0626,639,3522,83
1,8996,87
3,016
2,4870,5573,045
1,939
1,000
0,533
Cig 91-15517.6.93i (grt)
38,4328,576,8724,14
1,9398,01
2,981
2,6120,4013,013
2,006
1,000
0,396
Cig 91-15617.6.93i (grt)
38,4928,487,0224,08
1,9398,07
2,985
2,6030,4103,013
2,001
1,000
0,405
Bk 9824.2.94chl
38,2129,605,9324,02
1,9497,77
2,959
2,7020,3463,048
1,993
1,000
0,330
Bk 9924.2.94chl
38,3029,426,0124,21
1,9497,94
2,962
2,6820,3503,032
2,006
1,000
0,339
Bk 91024.2.94chl
38,0928,867,0623,98
1,9397,99
2,956
2,6390,4123,051
1,993
1,000
0,392
Bk 91124.2.94chl
38,0328,457,4823,09
1,9197,05
2,985
2,6320,4423,073
1,942
1,000
0,412
Bk 91224.2.94chl
38,3229,586,0323,90
1,9497,83
2,967
2,6990,3523,051
1,983
1,000
0,335
Bk 91324.2.94chl
37,3725,4910,9723,57
1,8997,40
2,962
2,3820,6543,036
2,002
1,000
0,632
Bk 96924.2.94chl
38,2230,005,2524,26
1,9497,73
2,954
2,7320,3053,038
2,009
1,000
0,294
Bk 97424.2.94sympl
37,8526,729,3123,89
1,9197,77
2,970
2,4710,5503,021
2,009
1,000
0,539
Bk 97524.2.94core
38,2028,347,2923,81
1,9297,64
2,979
2,6040,4283,032
1,989
1,000
0,414
Bk 97624.2.94zoi
38,0729,246,1623,95
1,9397,42
2,962
2,6810,3603,042
1,996
1,000
0,346
Bk 944.3.94zoi
39,2729,316,6024,28
1,9699,46
2,998
2,6370,3793,016
1,986
1,000
0,373
Bk 8114.3.93par(i)
39,0531,861,7124,34
1,9596,96
3,005
2,8890,0992,988
2,007
1
0,10
Bk 8714.3.93core
38,3531,142,3424,95
1,9496,78
2,963
2,8350,1362,972
2,065
1
0,14
Bk 9272.7.94par
39,4631,532,5424,74
1,9798,27
3,005
2,8300,1462,976
2,019
1
0,15
Bk 91423.2.94par
39,4132,792,2624,14
1,9898,59
2,985
2,9270,1293,056
1,959
1
0,12
Bk 91523.2.94core
38,7431,943,0624,65
1,9798,39
2,949
2,8660,1753,041
2,010
1
0,17
Bk 92723.2.94core
39,3032,812,0124,41
1,9898,53
2,976
2,9280,1153,043
1,981
1
0,11
Bk 93123.2.94core
38,7732,331,8224,04
1,9596,96
2,982
2,9310,1053,036
1,981
1
0,10
Bk 93223.2.94par(i)
39,0232,891,6224,58
1,9798,12
2,964
2,9440,0933,036
2,000
1
0,09
Bk 9124.2.94qtz(i)
38,9732,482,1124,39
1,9797,95
2,970
2,9180,1213,039
1,992
1
0,12
Bk 97024.2.94core
38,7832,252,5124,63
1,9798,17
2,953
2,8940,1443,038
2,009
1
0,14
Bk 97124.2.94qtz(i)
39,2933,101,8024,45
1,9898,64
2,969
2,9480,1023,051
1,980
1
0,10
C-34 Appendix C Table C7/C8 zoisite/paragonite
position means analysis of: i(x), inclusion of zoi in mineral x, core is core position in a zoi grain, mineral x, rimposition in zoi grain in contact with mineral x, mineral x(i), zoi at an inclusion of mineral x in zoi
normed on 8 kations, all iron assumed to be Fe3
sampleanalysisdate
SiO2Al2O3Fe2O3MgOCaONa2OK2Ototal
H2O
Si
AloFe3
MgCa
NaK
sum
OH
Bk 10B2119.10.93
47,1237,841,070,670,136,841,4295,09
4,66
3,030
2,8680,0522,920
0,0640,0090,073
0,8530,1190,972
4,141
2
Bk 18156.8.94
47,3239,800,460,180,217,010,8395,81
4,73
3,003
2,9770,0222,998
0,0170,0140,031
0,8620,0690,931
4,036
2
Bk 18166.8.94
47,3738,760,570,250,176,671,3195,10
4,68
3,033
2,9250,0272,953
0,0240,0120,036
0,8280,1090,937
4,016
2
Bk 18176.8.94
46,5739,470,420,150,207,130,6794,61
4,67
2,993
2,9890,0203,010
0,0140,0140,028
0,8880,0560,944
4,051
2
Bk 391,213.3.93
46,3939,830,300,140,157,590,2794,67
4,67
2,977
3,0120,0143,027
0,0130,0100,024
0,9440,0230,967
4,070
2
Bk 392,213.3.93
46,9239,940,490,170,257,380,2895,43
4,71
2,986
2,9950,0233,019
0,0160,0170,033
0,9110,0230,934
4,066
2
Bk 394113.3.93
46,3538,970,480,220,157,680,5094,35
4,64
2,992
2,9650,0232,988
0,0210,0100,032
0,9610,0421,003
4,101
2
Bk 394213.3.93
46,2739,420,540,320,187,490,4094,62
4,66
2,976
2,9880,0263,014
0,0310,0120,043
0,9340,0340,968
4,121
2
Bk 394313.3.93
47,3239,080,420,470,317,580,2895,46
4,71
3,013
2,9330,0202,953
0,0450,0210,066
0,9360,0230,959
4,084
2
Bk 394513.3.93
46,9438,630,420,420,177,590,4494,61
4,66
3,018
2,9270,0202,947
0,0400,0120,052
0,9460,0370,983
4,075
2
Bk 394713.3.93
47,1637,680,480,240,197,670,4193,83
4,63
3,056
2,8780,0232,901
0,0230,0130,036
0,9640,0350,998
4,019
2
sampleanalysisdate
SiO2Al2O3Fe2O3MgOCaONa2OK2Ototal
H2O
Si
AloFe3
MgCa
NaK
sum
OH
Cig 90/40111.6.91bclz
39,1431,472,9024,02
1,9597,53
3,006
2,8490,1683,017
1,977
1
0,16
sampleanalysisdateposition
SiO2Al2O3Fe2O3CaO
H2OTotal
Si
AlFe3
Ca
OH
XAl2Fe
Bk 97224.2.94core
39,0632,931,9624,55
1,9898,50
2,958
2,9390,1113,050
1,992
1
0,11
Bk 97324.2.94core
38,9432,472,5824,43
1,9798,41
2,958
2,9070,1473,054
1,988
1
0,14
Bk 914.3.94clz
40,0832,732,4824,92
2,01100,21
2,990
2,8780,1393,017
1,992
1
0,14
Bk 924.3.94clz
39,8732,212,8524,70
1,9999,63
2,997
2,8530,1613,014
1,989
1
0,16
Cig 90/40101.6.91bcore
38,8931,442,1024,62
1,9597,05
2,994
2,8530,1222,975
2,031
1
0,12
Bk 394813.3.93
46,6240,010,360,130,187,080,3394,71
4,68
2,984
3,0190,0173,036
0,0120,0120,025
0,8790,0280,906
4,026
2
Bk 394913.3.93
46,4539,850,360,200,177,400,3594,78
4,68
2,977
3,0100,0173,027
0,0190,0120,031
0,9200,0290,949
4,072
2
Bk 395013.3.93
47,1139,660,470,140,206,960,5795,11
4,70
3,006
2,9820,0223,005
0,0130,0140,027
0,8610,0470,908
4,012
2
Bk 395113.3.93
46,4340,000,440,130,257,030,3394,61
4,68
2,977
3,0230,0213,044
0,0120,0170,030
0,8740,0280,901
4,048
2
Bk 395213.3.93
46,7539,330,380,220,237,380,5594,84
4,68
2,998
2,9720,0182,991
0,0210,0160,037
0,9180,0460,964
4,064
2
Bk 395313.3.93
46,8539,500,330,250,187,410,7495,26
4,69
2,994
2,9750,0162,991
0,0240,0120,036
0,9180,0620,980
4,075
2
Bk 395413.3.93
46,6639,900,320,140,237,080,5594,88
4,69
2,986
3,0090,0163,025
0,0130,0160,029
0,8780,0460,924
4,038
2
Bk 395513.3.93
46,6139,490,410,220,567,360,5995,24
4,69
2,982
2,9770,0202,997
0,0210,0380,059
0,9130,0490,962
4,118
2
Bk 395613.3.93
46,8039,150,400,270,217,200,7194,74
4,67
3,005
2,9620,0192,982
0,0260,0140,040
0,8960,0590,956
4,057
2
Bk 395713.3.93
46,9339,470,320,280,186,970,9095,05
4,69
3,002
2,9760,0162,991
0,0270,0120,039
0,8640,0750,940
4,040
2
Bk 395813.3.93
46,8039,600,340,220,207,400,6595,21
4,69
2,991
2,9820,0172,999
0,0210,0140,035
0,9170,0540,971
4,072
2
normed on 22 oxygen, all iron assumed to be Fe3
normed on 22 oxygen, all iron assumed to be Fe3
C-35Appendix C Table C8 paragonite
sampleanalysisdate
SiO2Al2O3Fe2O3MgOCaONa2OK2Ototal
H2O
Si
AloFe3
MgCa
NaK
sum
OH
sampleanalysisdate
SiO2Al2O3Fe2O3MgOCaONa2OK2Ototal
H2O
Si
AloFe3
MgCa
NaK
sum
OH
sampleanalysisdate
SiO2Al2O3Fe2O3MgOCaONa2OK2Ototal
H2O
Si
AloFe3
MgCa
NaK
sum
OH
Bk 391024.6.92
46,8937,071,300,830,096,851,2294,25
4,62
3,042
2,8340,0632,898
0,0800,0060,087
0,8620,1030,965
4,163
2
Bk 392324.6.92
46,0839,360,360,250,197,440,4094,08
4,64
2,978
2,9980,0173,016
0,0240,0130,037
0,9320,0340,966
4,091
2
Bk 392424.6.92
46,2339,430,330,260,176,690,8393,94
4,64
2,989
3,0050,0163,021
0,0250,0120,037
0,8390,0700,909
4,035
2
Bk 392524.6.92
46,0939,530,320,150,227,260,3993,96
4,64
2,979
3,0110,0163,027
0,0140,0150,030
0,9100,0330,943
4,061
2
Bk 393024.6.92
45,8239,770,300,080,217,210,3093,69
4,63
2,968
3,0360,0153,051
0,0080,0150,022
0,9060,0250,931
4,056
2
Bk 393124.6.92
45,8439,800,260,120,196,800,3293,33
4,62
2,975
3,0440,0123,056
0,0120,0130,025
0,8560,0270,883
4,014
2
Bk 393224.6.92
45,5439,290,320,150,187,440,5393,45
4,60
2,966
3,0160,0163,032
0,0150,0130,027
0,9400,0450,985
4,102
2
Bk 393324.6.92
45,8239,220,460,150,167,300,5993,70
4,62
2,976
3,0030,0223,025
0,0150,0110,026
0,9190,0500,969
4,090
2
Bk 394924.6.92
46,0339,350,320,220,177,220,6393,94
4,63
2,980
3,0020,0163,018
0,0210,0120,033
0,9060,0530,959
4,075
2
Bk 395024.6.92
46,2239,530,380,190,177,310,5894,38
4,65
2,979
3,0030,0183,021
0,0180,0120,030
0,9130,0490,962
4,080
2
Bk 395124.6.92
46,0039,070,470,240,137,070,8693,84
4,62
2,985
2,9880,0233,011
0,0230,0090,032
0,8900,0730,962
4,083
2
Bk 393528.1.93
47,2538,560,910,400,137,500,2695,01
4,68
3,024
2,9090,0442,952
0,0380,0090,047
0,9310,0220,952
4,087
2
Bk 393628.1.93
47,3838,100,900,610,107,460,1794,72
4,67
3,039
2,8800,0432,924
0,0580,0070,065
0,9280,0140,942
4,083
2
Bk 393828.1.93
46,5139,210,720,120,157,390,1894,28
4,66
2,996
2,9770,0353,012
0,0120,0100,022
0,9230,0150,938
4,063
2
Bk 393928.1.93
46,7038,580,710,400,137,320,2194,05
4,64
3,015
2,9360,0352,970
0,0380,0090,047
0,9160,0180,934
4,068
2
Bk 394028.1.93
47,4838,260,760,210,127,360,9495,13
4,68
3,043
2,8900,0362,926
0,0200,0080,028
0,9150,0790,993
4,049
2
Bk 394128.1.93
45,7439,330,690,180,127,430,9394,42
4,63
2,960
2,9990,0343,033
0,0170,0080,026
0,9320,0781,011
4,162
2
Bk 394228.1.93
45,9439,290,460,110,157,030,4993,47
4,62
2,985
3,0080,0223,031
0,0110,0100,021
0,8860,0410,927
4,045
2
Bk 394328.1.93
46,3838,730,580,340,297,390,1693,87
4,63
3,002
2,9540,0282,982
0,0330,0200,053
0,9270,0130,941
4,085
2
Bk 394428.1.93
46,3739,700,780,090,567,470,4195,38
4,69
2,965
2,9920,0373,029
0,0090,0380,047
0,9260,0340,960
4,158
2
Bk 394628.1.93
46,9538,250,910,240,497,440,1094,38
4,65
3,025
2,9050,0442,949
0,0230,0340,057
0,9300,0080,938
4,089
2
Bk 394728.1.93
46,6339,070,670,130,137,400,6094,63
4,66
3,000
2,9620,0322,995
0,0120,0090,021
0,9230,0500,973
4,075
2
Bk 394828.1.93
46,0039,790,530,090,197,230,3894,21
4,65
2,967
3,0250,0263,051
0,0090,0130,022
0,9040,0320,936
4,082
2
Bk 394928.1.93
45,8039,270,590,130,157,280,6093,82
4,62
2,972
3,0040,0293,033
0,0130,0100,023
0,9160,0510,967
4,103
2
Bk 395028.1.93
46,6939,220,920,120,257,460,4095,06
4,68
2,991
2,9610,0443,006
0,0110,0170,029
0,9270,0330,960
4,112
2
Bk 3934.5.92
46,2138,910,500,150,217,500,6494,12
4,63
2,992
2,9690,0242,993
0,0140,0150,029
0,9410,0540,995
4,096
2
Bk 395,25.5.92
46,4038,440,410,140,167,690,5393,77
4,62
3,013
2,9420,0202,962
0,0140,0110,025
0,9680,0451,013
4,064
2
Bk 397,25.5.92
45,7239,100,400,110,217,730,3893,65
4,61
2,973
2,9970,0203,016
0,0110,0150,025
0,9750,0321,007
4,113
2
Bk 39125.5.92
47,2637,720,530,120,387,720,4194,14
4,64
3,055
2,8740,0262,900
0,0120,0260,038
0,9680,0351,002
4,030
2
Bk 39135.5.92
46,4938,690,440,180,177,090,6893,74
4,62
3,014
2,9570,0222,978
0,0170,0120,029
0,8910,0570,949
4,029
2
Bk 39.12028.8.92
46,1740,080,560,060,167,650,4695,14
4,68
2,956
3,0250,0273,051
0,0060,0110,017
0,9500,0380,988
4,126
2
Bk 39.12228.8.92
46,6439,970,560,160,207,450,3995,37
4,70
2,974
3,0040,0273,031
0,0150,0140,029
0,9210,0320,954
4,095
2
Bk 39.12328.8.92
46,3040,490,310,080,277,340,3295,11
4,70
2,956
3,0470,0153,062
0,0080,0180,026
0,9090,0270,935
4,080
2
normed on 22 oxygen, all iron assumed to be Fe3
normed on 22 oxygen, all iron assumed to be Fe3
normed on 22 oxygen, all iron assumed to be Fe3
C-36 Appendix C Table C8 paragonite
sampleanalysisdate
SiO2Al2O3Fe2O3MgOCaONa2OK2Ototal
H2O
Si
AloFe3
MgCa
NaK
sum
OH
sampleanalysisdate
SiO2Al2O3Fe2O3MgOCaONa2OK2Ototal
H2O
Si
AloFe3
MgCa
NaK
sum
OH
sampleanalysisdate
SiO2Al2O3Fe2O3MgOCaONa2OK2Ototal
H2O
Si
AloFe3
MgCa
NaK
sum
OH
normed on 22 oxygen, all iron assumed to be Fe3
normed on 22 oxygen, all iron assumed to be Fe3
normed on 22 oxygen, all iron assumed to be Fe3
Bk 76027.8.92
46,3339,960,360,120,257,280,4894,78
4,68
2,971
3,0200,0173,038
0,0110,0170,029
0,9050,0400,945
4,074
2
Bk 76127.8.92
46,7039,970,420,190,146,640,8494,90
4,69
•
2,987
3,0130,0203,034
0,0180,0100,028
0,8240,0700,894
4,023
2
Bk 76227.8.92
46,6640,300,290,110,217,250,5595,37
4,71
2,973
3,0260,0143,040
0,0100,0140,025
0,8960,0460,941
4,058
2
Bk 76327.8.92
46,1839,540,410,260,196,801,1294,50
4,65
2,977
3,0040,0203,024
0,0250,0130,038
0,8500,0940,944
4,084
2
Bk 76427.8.92
46,9139,760,370,280,176,611,0395,13
4,69
2,997
2,9930,0183,011
0,0270,0120,038
0,8190,0860,904
4,027
2
Bk 76527.8.92
46,7240,010,310,170,196,920,6794,99
4,69
2,986
3,0140,0153,028
0,0160,0130,029
0,8570,0560,913
4,030
2
Bk 76627.8.92
46,3240,260,340,090,256,840,5194,61
4,68
2,970
3,0420,0173,059
0,0090,0170,026
0,8500,0430,893
4,037
2
Bk 76727.8.92
46,2940,190,420,120,156,490,6794,33
4,67
2,975
3,0440,0203,064
0,0110,0100,022
0,8090,0560,865
4,014
2
Bk 76827.8.92
46,5440,120,370,100,166,840,6094,73
4,68
2,980
3,0280,0183,046
0,0100,0110,021
0,8490,0500,899
4,022
2
Bk 76927.8.92
46,1239,770,320,110,216,750,4693,74
4,64
2,982
3,0300,0163,046
0,0110,0150,025
0,8460,0390,885
4,013
2
Bk 7707.8.92
46,4540,240,460,160,166,490,8294,78
4,68
2,974
3,0370,0223,059
0,0150,0110,026
0,8060,0680,874
4,029
2
Bk 7627.7.92
47,6640,390,910,510,236,900,2396,83
4,79
2,986
2,9820,0433,025
0,0480,0150,063
0,8380,0190,857
4,094
2
Bk 7687.7.92
47,6840,550,670,300,156,700,9697,01
4,78
2,988
2,9950,0313,026
0,0280,0100,038
0,8140,0780,892
4,058
2
Bk 82314.3.93
47,2140,890,570,130,206,460,5796,03
4,75
2,978
3,0400,0273,067
0,0120,0140,026
0,7900,0470,837
4,009
2
Bk 84614.3.93
46,5739,770,510,130,227,140,5594,89
4,68
2,983
3,0020,0253,027
0,0120,0150,028
0,8870,0460,933
4,064
2
Bk 84714.3.93
46,8139,600,440,250,186,910,8295,01
4,69
2,995
2,9860,0213,007
0,0240,0120,036
0,8570,0680,926
4,048
2
Bk 84814.3.93
47,3639,800,430,140,247,000,4395,40
4,72
3,010
2,9810,0213,002
0,0130,0160,030
0,8620,0360,898
4,000
2
Bk 84914.3.93
46,3539,170,300,120,346,440,7093,42
4,62
3,007
2,9950,0153,010
0,0120,0240,035
0,8100,0590,869
3,979
2
Bk 85014.3.93
46,7338,690,830,350,527,010,6894,81
4,66
3,004
2,9310,0402,972
0,0340,0360,069
0,8740,0570,931
4,122
2
Bk 9342.7.94
46,4439,320,480,130,257,450,3194,38
4,66
2,991
2,9840,0233,007
0,0120,0170,030
0,9300,0260,956
4,069
2
Bk 9352.7.94
46,8338,960,280,210,217,210,5894,28
4,65
3,017
2,9580,0132,971
0,0200,0140,035
0,9010,0490,949
4,017
2
Bk 94023.2.94
48,5141,660,410,160,276,540,7498,29
4,87
2,990
3,0260,0193,045
0,0150,0180,033
0,7810,0590,841
3,989
2
Bk 94123.2.94
47,8341,330,340,110,326,990,5297,44
4,82
2,977
3,0320,0163,048
0,0100,0210,032
0,8440,0420,886
4,029
2
Bk 94223.2.94
48,1441,860,440,200,566,510,9498,65
4,87
2,965
3,0380,0213,059
0,0180,0370,055
0,7770,0750,853
4,064
2
Bk 94323.2.94
47,2141,960,410,070,286,820,2797,02
4,80
2,946
3,0860,0193,106
0,0070,0190,025
0,8250,0220,847
4,042
2
Bk 94523.2.94
47,1241,360,500,110,276,860,2496,46
4,78
2,959
3,0610,0243,084
0,0100,0180,028
0,8350,0200,855
4,043
2
Bk 94623.2.94
47,3741,170,480,090,277,120,3296,82
4,79
2,967
3,0400,0233,062
0,0080,0180,027
0,8650,0260,891
4,051
2
Bk 94823.2.94
48,3341,380,530,210,236,280,9097,86
4,84
2,993
3,0200,0253,045
0,0190,0150,035
0,7540,0730,827
3,990
2
Bk 94923.2.94
47,4441,730,640,260,276,840,3497,52
4,82
2,950
3,0580,0303,088
0,0240,0180,042
0,8250,0280,852
4,085
2
Bk 95023.2.94
47,3841,330,440,080,256,980,4396,89
4,79
2,965
3,0490,0213,069
0,0070,0170,024
0,8470,0350,882
4,042
2
Bk 95123.2.94
47,8041,640,480,100,166,700,5197,39
4,82
2,972
3,0520,0223,074
0,0090,0110,020
0,8080,0410,849
4,008
2
Bk 94524.2.94
47,3840,730,340,190,247,150,3796,40
4,77
2,980
3,0200,0163,036
0,0180,0160,034
0,8720,0300,902
4,039
2
Bk 94624.2.94
47,6740,870,380,240,177,000,7397,06
4,79
2,982
3,0140,0183,031
0,0220,0110,034
0,8490,0600,909
4,043
2
C-37Appendix C Table C8/C9 paragonite/phengite
sampleanalysisdateposition
SiO2TiO2Al2O3Fe2O3FeOMgONa2OK2O
H2Ototal
SiAlt
AloTiFe3
Fe2Mg
NaK
sum
OH
Mg/(Mg+Fe)Na/(Na+K)
Bk 10B6318.10.93large core
51,720,1724,491,130,684,590,3810,57
4,4398,16
3,4920,508
1,4400,0090,0581,506
0,0380,4620,500
0,0500,9300,980
6,987
2
0,830,05
Bk 10B6418.10.93large core
52,230,1924,961,160,734,560,3210,71
4,4899,34
3,4850,515
1,4470,0100,0581,515
0,0410,4530,494
0,0410,9310,973
6,982
2
0,820,04
Bk 10B2719.10.93bsmall
50,120,3027,891,520,193,580,6710,15
4,4798,88
3,3520,648
1,5510,0150,0761,642
0,0100,3570,367
0,0870,8850,972
6,981
2
0,800,09
Bk 10B3119.10.93bsmall
49,210,1727,691,920,163,330,6910,21
4,4097,78
3,3370,663
1,5500,0090,0981,657
0,0090,3370,346
0,0910,9020,993
6,995
2
0,760,09
Bk 10B3219.10.93bsmall
49,270,2327,641,830,003,480,6310,29
4,4197,78
3,3390,661
1,5460,0120,0941,651
0,0000,3510,351
0,0830,9090,992
6,994
2
0,790,08
Bk 10B3319.10.93bsmall
49,350,2127,991,890,003,460,6610,16
4,4298,14
3,3280,672
1,5530,0110,0961,659
0,0000,3480,348
0,0860,8930,979
6,986
2
0,780,09
Bk 10B3419.10.93bsmall
49,180,3527,911,650,023,420,6210,36
4,4197,92
3,3280,672
1,5540,0180,0841,656
0,0010,3450,346
0,0810,9140,995
6,997
2
0,800,08
Bk 74526.4.93i (grt)
48,560,2027,862,620,003,260,899,95
4,3897,73
3,2970,703
1,5270,0100,1341,671
0,0000,3300,330
0,1170,8810,998
6,998
2
0,710,12
Bk 74626.4.93i (grt)
48,220,2027,363,410,003,720,909,77
4,3797,96
3,2640,736
1,4470,0100,1741,631
0,0000,3750,375
0,1180,8620,980
6,987
2
0,680,12
Bk 74826.4.93i (grt)
48,890,1727,841,880,522,990,9210,19
4,3997,79
3,3240,676
1,5550,0090,0961,659
0,0300,3030,333
0,1210,9031,024
7,016
2
0,710,12
Bk 75026.4.93i (grt)
49,210,1828,102,700,003,170,8710,16
4,4398,82
3,3090,691
1,5350,0090,1371,681
0,0000,3180,318
0,1130,8901,004
7,002
2
0,700,11
sampleanalysisdate
SiO2Al2O3Fe2O3MgOCaONa2OK2Ototal
H2O
Si
AloFe3
MgCa
NaK
sum
OH
normed on 22 oxygen, all iron assumed to be Fe3
Bk 94724.2.94
45,6540,480,570,070,217,340,3994,71
4,67
2,933
3,0650,0273,093
0,0070,0140,021
0,9140,0330,947
4,137
2
Bk 94824.2.94
47,1340,870,410,090,237,420,3696,51
4,76
2,966
3,0310,0193,051
0,0080,0160,024
0,9050,0300,935
4,073
2
Bk 95224.2.94
49,1038,670,480,130,247,130,5796,32
4,77
3,089
2,8670,0232,890
0,0120,0160,028
0,8700,0470,916
3,909
2
Bk 93230.6.94
46,6139,690,360,130,247,310,6294,96
4,68
2,986
2,9960,0173,013
0,0120,0160,029
0,9080,0520,960
4,065
2
Bk 93330.6.94
46,4939,200,360,170,217,300,7794,50
4,65
2,995
2,9760,0172,994
0,0160,0140,031
0,9120,0650,977
4,066
2
Bk 93430.6.94
46,4439,320,480,130,257,450,3194,38
4,66
2,991
2,9840,0233,007
0,0120,0170,030
0,9300,0260,956
4,069
2
Bk 93530.6.94
46,8338,960,280,210,217,210,5894,28
4,65
3,017
2,9580,0132,971
0,0200,0140,035
0,9010,0490,949
4,017
2
Cig 91-12717.6.93
47,3039,411,000,270,116,661,4896,23
4,73
3,002
2,9480,0482,995
0,0260,0070,033
0,8190,1220,942
4,099
2
Cig 91-13117.6.93
47,3439,451,070,340,167,091,4196,86
4,75
2,991
2,9380,0512,988
0,0320,0110,043
0,8690,1160,985
4,160
2
Cig 91-13517.6.93
48,0538,171,120,790,146,571,3696,20
4,73
3,048
2,8530,0542,907
0,0750,0100,084
0,8080,1120,920
4,103
2
Cig 91-13617.6.93
48,2137,901,070,880,136,341,6296,15
4,72
3,060
2,8360,0512,887
0,0830,0090,092
0,7800,1340,914
4,087
2
normed on 11 oxygen, Fe3 estimated over Fetot - (Si-Mg-3) iterativ
Position means analysis of: large core, core of large phengite; large rim, rim of large phengite: large c-r, undefinedposition in a large phengite; small, a small phengite; i(grt), phengite inclusion in garnet
C-38 Appendix C Table C9 phengite
Position means analysis of: large core, core of large phengite; large rim, rim of large phengite: large c-r, undefinedposition in a large phengite; small, a small phengite; i(grt), phengite inclusion in garnet
sampleanalysisdateposition
SiO2TiO2Al2O3Fe2O3FeOMgONa2OK2O
H2Ototal
SiAlt
AloTiFe3
Fe2Mg
NaK
sum
OH
Mg/(Mg+Fe)Na/(Na+K)
normed on 11 oxygen, Fe3 estimated over Fetot - (Si-Mg-3) iterativ
sampleanalysisdateposition
SiO2TiO2Al2O3Fe2O3FeOMgONa2OK2O
H2Ototal
SiAlt
AloTiFe3
Fe2Mg
NaK
sum
OH
Mg/(Mg+Fe)Na/(Na+K)
normed on 11 oxygen, Fe3 estimated over Fetot - (Si-Mg-3) iterativ
Bk 75426.4.93i (grt)
49,330,2228,292,200,353,020,9810,25
4,4599,09
3,3100,690
1,5480,0110,1111,670
0,0200,3020,322
0,1280,8971,024
7,016
2
0,700,12
Bk 75526.4.93i (grt)
49,740,2127,921,610,563,210,8110,30
4,4598,80
•
3,3420,658
1,5530,0110,0811,645
0,0310,3210,353
0,1060,9021,007
7,005
2
0,740,10
Bk 75626.4.93i (grt)
48,600,2128,822,040,002,950,8210,33
4,4198,19
3,2860,714
1,5820,0110,1041,697
0,0000,2970,297
0,1070,9101,018
7,012
2
0,740,11
Cig 91-17716.6.93small
49,890,3729,392,450,282,930,7710,22
4,53100,83
3,2850,715
1,5650,0180,1221,705
0,0160,2880,303
0,0980,8770,975
6,984
2
0,680,10
Cig 91-17816.6.93small
50,560,2428,762,130,373,210,7110,51
4,54101,03
3,3230,677
1,5510,0120,1051,668
0,0200,3140,335
0,0900,9000,991
6,994
2
0,710,09
Cig 91-1217.6.93small c
52,310,1824,670,960,764,630,3311,05
4,4899,37
3,4950,505
1,4370,0090,0481,495
0,0430,4610,504
0,0430,9621,005
7,003
2
0,840,04
Cig 91-1317.6.93small c
51,970,2024,841,170,604,560,3211,16
4,4799,29
3,4780,522
1,4380,0100,0591,507
0,0330,4550,488
0,0420,9731,015
7,010
2
0,830,04
Cig 91-1417.6.93small c
52,800,1624,800,631,254,500,3210,97
4,5199,94
3,5070,493
1,4480,0080,0321,488
0,0700,4460,515
0,0410,9500,991
6,994
2
0,820,04
Cig 91-1617.6.93small r
48,990,3528,342,860,412,840,8010,14
4,4499,17
3,2900,710
1,5330,0180,1451,695
0,0230,2840,308
0,1040,8870,992
6,994
2
0,630,11
Cig 91-1717.6.93small
49,580,2928,112,260,243,220,7010,36
4,4599,21
3,3200,680
1,5390,0150,1141,667
0,0130,3210,335
0,0910,9040,995
6,997
2
0,720,09
Cig 91-1817.6.93small
50,130,2027,612,420,103,500,6910,50
4,4799,62
3,3440,656
1,5140,0100,1211,646
0,0060,3480,354
0,0890,9131,002
7,001
2
0,730,09
Cig 91-1917.6.93small
48,690,3528,913,080,002,851,0110,35
4,4599,69
3,2550,745
1,5330,0180,1551,705
0,0000,2840,284
0,1310,9021,033
7,022
2
0,650,13
Cig 91-11017.6.93small
49,030,2628,523,000,003,140,8610,54
4,4699,81
•
3,2720,728
1,5150,0130,1511,678
0,0000,3120,312
0,1110,9171,028
7,019
2
0,670,11
Cig 91-11117.6.93small
50,300,2228,402,180,013,420,8510,41
4,51100,30
3,3270,673
1,5410,0110,1081,660
0,0010,3370,338
0,1090,8971,006
7,004
2
0,760,11
Cig 91-11217.6.93small
49,960,2127,812,480,003,590,8110,45
4,4899,78
3,3250,675
1,5060,0110,1241,640
0,0000,3560,356
0,1050,9061,011
7,007
2
0,740,10
Cig 91-11317.6.93small
50,150,2828,091,810,783,100,7010,66
4,49100,06
3,3370,663
1,5400,0140,0911,644
0,0430,3070,351
0,0900,9241,015
7,010
2
0,700,09
Cig 91-11417.6.93small
50,190,1927,652,290,263,430,7010,54
4,4799,72
3,3460,654
1,5180,0100,1151,643
0,0150,3410,355
0,0900,9161,006
7,004
2
0,720,09
Cig 91-11517.6.93small
49,810,1828,042,330,163,280,8410,44
4,4799,54
3,3260,674
1,5330,0090,1171,659
0,0090,3260,335
0,1090,9091,017
7,012
2
0,720,11
Cig 91-11917.6.93small
49,570,2627,792,400,343,190,7610,50
4,4599,26
3,3250,675
1,5220,0130,1211,656
0,0190,3190,338
0,0990,9181,017
7,011
2
0,690,10
Cig 91-12017.6.93small
49,930,2928,711,870,453,090,6310,49
4,4999,96
3,3170,683
1,5640,0140,0941,672
0,0250,3060,331
0,0810,9080,989
6,993
2
0,720,08
Cig 91-12117.6.93large core
52,460,2125,151,700,364,640,2711,31
4,52100,62
3,4670,533
1,4250,0100,0841,520
0,0200,4570,477
0,0350,9741,009
7,006
2
0,810,03
Cig 91-12217.6.93large core
52,240,2624,721,640,304,750,3211,26
4,4999,98
3,4740,526
1,4120,0130,0821,507
0,0160,4710,487
0,0410,9761,017
7,012
2
0,830,04
C-39Appendix C Table C9 phengite
Position means analysis of: large core, core of large phengite; large rim, rim of large phengite: large c-r, undefinedposition in a large phengite; small, a small phengite; i(grt), phengite inclusion in garnet
sampleanalysisdateposition
SiO2TiO2Al2O3Fe2O3FeOMgONa2OK2O
H2Ototal
SiAlt
AloTiFe3
Fe2Mg
NaK
sum
OH
Mg/(Mg+Fe)Na/(Na+K)
normed on 11 oxygen, Fe3 estimated over Fetot - (Si-Mg-3) iterativ
sampleanalysisdateposition
SiO2TiO2Al2O3Fe2O3FeOMgONa2OK2O
H2Ototal
SiAlt
AloTiFe3
Fe2Mg
NaK
sum
OH
Mg/(Mg+Fe)Na/(Na+K)
normed on 11 oxygen, Fe3 estimated over Fetot - (Si-Mg-3) iterativ
Cig 91-12317.6.93large core
52,520,2424,610,980,864,630,2911,29
4,5099,92
3,4950,505
1,4260,0120,0491,487
0,0480,4590,507
0,0370,9791,017
7,011
2
0,830,04
Cig 91-12417.6.93large core
52,350,2424,781,380,504,700,2611,19
4,4999,89
3,4820,518
1,4240,0120,0691,505
0,0280,4660,494
0,0340,9701,003
7,002
2
0,830,03
Cig 91-11728.11.93large core
51,760,1924,250,820,844,580,3211,14
4,4398,33
3,4990,501
1,4320,0100,0421,483
0,0480,4620,509
0,0420,9821,024
7,016
2
0,840,04
Cig 91-11828.11.93large core
51,130,1824,380,841,024,340,3210,63
4,3897,22
3,4900,510
1,4520,0090,0431,504
0,0580,4420,500
0,0420,9460,988
6,992
2
0,810,04
Cig 91-11928.11.93large c-r
50,660,2225,561,660,294,180,4310,75
4,4298,17
3,4270,573
1,4650,0110,0851,561
0,0170,4210,438
0,0560,9481,004
7,003
2
0,810,06
Cig 91-12028.11.93large c-r
50,920,3025,140,960,874,150,4210,82
4,4197,99
3,4540,546
1,4630,0150,0491,527
0,0490,4200,469
0,0550,9561,012
7,008
2
0,810,05
Cig 91-12228.11.93large c-r
50,770,2425,400,451,263,900,4510,76
4,4097,64
3,4550,545
1,4920,0120,0231,528
0,0720,3960,467
0,0590,9541,014
7,009
2
0,810,06
Cig 91-12328.11.93large c-r
50,660,1826,021,050,633,960,4010,84
4,4298,17
3,4260,574
1,5000,0090,0531,562
0,0360,3990,435
0,0520,9551,008
7,005
2
0,820,05
Cig 91-12428.11.93large core
51,380,1824,430,721,144,320,3910,71
4,4097,67
3,4930,507
1,4510,0090,0371,497
0,0650,4380,503
0,0510,9491,000
7,000
2
0,810,05
Cig 91-12528.11.93large core
51,630,2124,190,591,264,400,2510,91
4,4197,85
3,5060,494
1,4430,0110,0301,483
0,0720,4450,517
0,0330,9660,999
6,999
2
0,810,03
Cig 91-12628.11.93large rim
50,330,2026,732,450,103,701,3110,28
4,4699,57
3,3640,636
1,4700,0100,1231,604
0,0060,3690,374
0,1700,8961,065
7,044
2
0,740,16
Cig 91-12828.11.93large c-r
51,050,1925,890,641,283,790,6210,53
4,4498,43
3,4440,556
1,5020,0100,0331,544
0,0720,3810,453
0,0810,9261,007
7,005
2
0,780,08
Cig 91-13028.11.93large core
51,770,2124,290,841,014,500,2411,00
4,4398,29
3,5000,500
1,4360,0110,0431,489
0,0570,4530,511
0,0310,9691,001
7,000
2
0,820,03
Cig 91-12517.6.93large rim
49,960,2127,771,890,273,400,6110,76
4,4699,33
3,3440,656
1,5340,0110,0951,640
0,0150,3390,354
0,0790,9391,018
7,012
2
0,750,08
Cig 91-12617.6.93large core
52,330,2025,090,801,004,410,2911,28
4,5099,90
3,4830,517
1,4510,0100,0401,502
0,0560,4380,493
0,0370,9791,016
7,011
2
0,820,04
Cig 91-12917.6.93large rim
48,620,3628,672,690,072,890,7610,21
4,4298,69
3,2760,724
1,5530,0180,1361,707
0,0040,2900,294
0,0990,8970,996
6,997
2
0,670,10
Cig 91-13017.6.93large rim
49,480,3528,121,940,583,060,7810,26
4,4599,02
3,3210,679
1,5460,0180,0981,661
0,0330,3060,339
0,1020,8980,999
6,999
2
0,700,10
Cig 91-14217.6.93small
50,350,2227,431,760,463,491,0410,19
4,4799,41
3,3620,638
1,5210,0110,0881,620
0,0260,3470,373
0,1350,8871,021
7,014
2
0,750,13
Cig 91-11328.11.93large rim
50,580,2628,441,410,723,220,7010,53
4,52100,38
3,3440,656
1,5610,0130,0701,644
0,0400,3170,357
0,0900,9070,997
6,998
2
0,740,09
Cig 91-11428.11.93large rim
49,270,2927,591,190,933,070,6210,40
4,4097,76
3,3490,651
1,5590,0150,0611,635
0,0530,3110,364
0,0820,9211,003
7,002
2
0,730,08
Cig 91-11528.11.93large core
51,710,2124,510,661,264,320,2710,94
4,4398,31
3,4960,504
1,4490,0110,0341,494
0,0710,4350,507
0,0350,9640,999
7,000
2
0,810,04
Cig 91-11628.11.93large core
51,430,2224,150,780,944,500,2711,05
4,4097,74
3,4980,502
1,4340,0110,0401,486
0,0530,4560,509
0,0360,9801,015
7,010
2
0,830,04
C-40 Appendix C Table C9/C10 phengite/rutile
sampleanalysisdateposition
SiO2TiO2Al2O3Fe2O3FeOMgONa2OK2O
H2Ototal
SiAlt
AloTiFe3
Fe2Mg
NaK
sum
OH
Mg/(Mg+Fe)Na/(Na+K)
normed on 11 oxygen, Fe3 estimated over Fetot - (Si-Mg-3) iterativ
Position means analysis of: large core, core of large phengite; large rim, rim of large phengite: large c-r, undefinedposition in a large phengite; small, a small phengite; i(grt), phengite inclusion in garnet
Cig 91-1.2542.7.94large core
51,990,1824,840,900,814,520,3910,68
4,4698,77
3,4890,511
1,4530,0090,0451,507
0,0460,4520,498
0,0510,9340,985
6,990
2
0,830,05
SampleDateNr
TiO2Fe2O3
sum
TiFe3
Bk 10B19.10.935
97,000,59
97,59
0,9940,006
Bk 10B19.10.936
98,830,46
99,29
0,9950,005
Bk 186.8.941
99,700,57
100,27
0,9940,006
Bk 392.7.9420
97,870,77
98,64
0,9920,008
Bk 392.7.9421
98,090,77
98,86
0,9920,008
Bk 395.5.9212
98,090,58
98,67
0,9940,006
Bk 39.128.8.9215
99,020,66
99,68
0,9930,007
Bk 39a28.1.9327
98,621,04
99,66
0,9900,010
Bk 39a28.1.9330
98,570,73
99,30
0,9930,007
Bk 730.6.9453
98,230,42
98,65
0,9960,004
Bk 76.7.9242
98,50,63
99,13
0,9940,006
Bk 76.7.9270
98,170,47
98,64
0,9950,005
SampleDateNr
TiO2Fe2O3
sum
TiFe3
Bk 814.3.9345
97,120,71
97,83
0,9930,007
Bk 829.1.931
97,720,54
98,26
0,9950,005
Bk 829.1.932
98,050,62
98,67
0,9940,006
Bk 829.1.934,2
97,360,63
97,99
0,9940,006
Bk 829.1.936,2
96,60,60
97,20
0,9940,006
Bk 829.1.9316,2
98,420,81
99,23
0,9920,008
Bk 924.2.942
98,40,49
98,89
0,9950,005
Bk 924.2.943
96,60,62
97,22
0,9940,006
Bk 924.2.9477
97,410,40
97,81
0,9960,004
Bk 924.2.9478
990,44
99,44
0,9960,004
Bk 930.6.9423
98,240,47
98,71
0,9950,005
Cig 91-1.2552.7.94large rim
49,520,2627,331,710,453,380,6810,26
4,4198,00
3,3530,647
1,5350,0130,0871,635
0,0250,3410,367
0,0890,9060,995
6,997
2
0,750,09
Cig 91-1.213.7.94large rim
50,600,2227,321,310,843,490,5910,27
4,4799,11
3,3840,616
1,5370,0110,0661,614
0,0470,3480,395
0,0770,8950,972
6,981
2
0,750,08
Cig 91-1.223.7.94large c-r
51,890,2124,030,750,964,660,2910,68
4,4297,89
3,5140,486
1,4320,0110,0381,481
0,0550,4700,525
0,0380,9430,981
6,987
2
0,840,04
Cig 91-1.233.7.94large core
52,010,2124,460,690,744,700,3910,70
4,4498,34
3,5030,497
1,4440,0110,0351,490
0,0420,4720,513
0,0510,9390,990
6,993
2
0,860,05
Cig 91-1.243.7.94large core
52,240,1924,400,850,734,730,4310,78
4,4698,82
3,5050,495
1,4340,0100,0431,486
0,0410,4730,514
0,0560,9430,998
6,999
2
0,850,06
Cig 91-1.253.7.94large core
51,190,2025,041,240,784,260,3610,57
4,4298,05
3,4630,537
1,4600,0100,0631,533
0,0440,4300,474
0,0470,9320,979
6,986
2
0,800,05
Cig 91-1.263.7.94large core
52,020,1624,450,511,224,470,3110,65
4,4498,23
3,5100,490
1,4550,0080,0261,489
0,0690,4500,519
0,0410,9370,977
6,985
2
0,830,04
Cig 91-1.273.7.94large core
51,650,1524,230,761,084,460,3710,74
4,4197,85
3,5040,496
1,4420,0080,0391,488
0,0610,4510,512
0,0490,9500,998
6,999
2
0,820,05
SampleDateNr
TiO2Fe2O3
sum
TiFe3
Bk 930.6.9423
98,290,46
98,75
0,9950,005
Cig 91.1.22.7.9413
98,890,56
99,45
0,9940,006
normed on 1cation
normed on 1cation
normed on 1cation
C-41Appendix C Table C11/C12 dolomite/calcite
normed on 2 cations
normed on 1cation
Bk766.7.92
33,9017,408,340,5660,20
51,06111,26
1,042
0,7440,2000,0140,958
2
normed on 2 cations
sampleanalysisdateCL colour
CaMgFeMn
CO2total
Ca
MgFeMn
CO3
Bk 7726.4.93yellow
52,391,972,130,65
44,97102,11
0,914
0,0480,0290,009
1
Bk 7826.4.93brown
50,902,552,410,65
44,61101,12
0,895
0,0620,0330,009
1
Bk 72126.4.93yellow
51,102,392,190,56
44,40100,64
0,903
0,0590,0300,008
1
Bk 72226.4.93yellow
50,552,432,450,53
44,15100,11
0,898
0,0600,0340,007
1
Bk 76326.4.93yellow
53,281,311,470,63
44,53101,22
0,939
0,0320,0200,009
1
Bk 76426.4.93yellow
51,921,301,570,57
43,4898,84
0,937
0,0330,0220,008
1
Bk 726.7yellow
63,611,241,400,86
52,66119,77
0,948
0,0260,0160,010
1
Bk 746.7yellow
62,281,682,111,06
52,66119,79
0,928
0,0350,0250,012
1
Bk 7106.7orange
59,982,182,721,29
51,92118,09
0,907
0,0460,0320,015
1
Bk 7336.7yellow
62,601,011,871,07
52,04118,59
0,944
0,0210,0220,013
1
Bk 7Th311.6.94yellow
54,901,851,200,64
46,24104,83
0,932
0,0440,0160,009
1
Bk 7Th411.6.94yellow
54,281,771,540,68
45,90104,17
0,928
0,0420,0210,009
1
sampleanalysisdate
CaMgFeMnsum
CO2total
Ca
MgFeMn
CO3
Bk7526.4.93
29,6715,697,790,4053,55
45,4398,98
1,025
0,7540,2100,0110,975
2
Bk7626.4.93
29,9015,987,590,4153,88
45,8199,69
1,024
0,7620,2030,0110,976
2
Bk7926.4.93
29,3215,437,810,4753,03
44,9397,96
1,024
0,7500,2130,0130,976
2
Bk71026.4.93
33,3413,186,910,5653,99
45,1399,12
1,159
0,6380,1880,0150,841
2
Bk71126.4.93
29,9515,688,040,5454,21
45,88100,09
1,025
0,7460,2150,0150,975
2
Bk71226.4.93
30,3415,437,600,5153,88
45,6399,51
1,044
0,7380,2040,0140,956
2
Bk72326.4.93
29,6114,628,550,4053,18
44,6897,86
1,040
0,7140,2340,0110,960
2
Bk72426.4.93
29,5115,757,960,4153,63
45,4899,11
1,018
0,7560,2140,0110,982
2
Bk75926.4.93
29,4515,537,920,5453,44
45,2598,69
1,021
0,7490,2140,0150,979
2
Bk76026.4.93
29,4616,047,560,4353,49
45,5399,02
1,016
0,7690,2030,0120,984
2
Bk796.7.92
33,2616,818,820,6159,50
50,24109,74
1,039
0,7310,2150,0150,961
2
Bk7346.7.92
32,6117,528,840,6359,60
50,52110,12
1,013
0,7570,2140,0150,987
2
sampleanalysisdate
CaMgFeMnsum
CO2total
Ca
MgFeMn
CO3
sampleanalysisdateCL colour
CaMgFeMn
CO2total
Ca
MgFeMn
CO3
Bk 7Th711.6.94orange
53,651,971,850,73
45,84104,04
0,918
0,0470,0250,010
1
Bk 7Th1611.6.94yellow
51,421,751,430,50
43,4598,55
0,929
0,0440,0200,007
1
Bk 7Th1711.6.94orange
51,381,832,120,96
44,21100,50
0,912
0,0450,0290,013
1
Bk 7Th1811.6.94orange
52,791,962,520,82
45,62103,71
0,908
0,0470,0340,011
1
Bk 7Th1911.6.94yellow
51,541,301,770,72
43,4098,73
0,932
0,0330,0250,010
1
Bk 7Th2011.6.94yellow
52,911,261,730,71
44,40101,01
0,935
0,0310,0240,010
1
Bk 7Th2111.6.94orange
49,871,661,960,74
42,6196,84
0,919
0,0430,0280,011
1
Bk 7Th2211.6.94orange
50,591,621,900,68
43,0697,85
0,922
0,0410,0270,010
1
Bk 7Th2311.6.94orange
50,051,701,800,69
42,6696,90
0,921
0,0440,0260,010
1
Bk 7Th2411.6.94yellow
50,211,411,790,54
42,3796,32
0,930
0,0360,0260,008
1
normed on 1cation
C-42 Appendix C Table C12 calcite
sampleanalysisdateCL colour
CaMgFeMn
CO2total
Ca
MgFeMn
CO3
normed on 1cation
sampleanalysisdateCL colour
CaMgFeMn
CO2total
Ca
MgFeMn
CO3
normed on 1cation
sampleanalysisdateCL colour
CaMgFeMn
CO2total
Ca
MgFeMn
CO3
normed on 1cation
sampleanalysisdateCL colour
CaMgFeMn
CO2total
Ca
MgFeMn
CO3
normed on 1cation
Bk 7Th3611.6.94brown
50,981,601,940,70
43,3898,60
0,922
0,0400,0270,010
1
Bk 7Th3711.6.94brown
50,371,641,790,66
42,8397,29
0,923
0,0420,0260,010
1
Bk 7Th3811.6.94brown
50,521,601,930,60
42,9597,60
0,923
0,0410,0280,009
1
Bk 7Th4011.6.94brown
51,271,511,690,68
43,3498,49
0,928
0,0380,0240,010
1
Bk 7Th4111.6.94yellow
53,030,720,750,69
43,2998,48
0,961
0,0180,0110,010
1
Bk 7Th4211.6.94yellow
52,140,980,970,65
42,9997,73
0,952
0,0250,0140,009
1
Bk 7Th4311.6.94yellow
53,130,710,730,62
43,3098,49
0,963
0,0180,0100,009
1
Bk 7Th4411.6.94yellow
51,721,330,930,55
42,9597,48
0,945
0,0340,0130,008
1
Bk 7Th4511.6.94yellow
52,471,220,980,75
43,5899,00
0,945
0,0310,0140,011
1
Bk 7Th4611.6.94yellow
52,241,000,870,58
42,9897,67
0,954
0,0250,0120,008
1
Bk 7Th4711.6.94yellow
53,380,720,920,56
43,5999,17
0,961
0,0180,0130,008
1
Bk 7Th4811.6.94yellow
51,471,601,450,70
43,4698,68
0,929
0,0400,0200,010
1
Bk 7Th4911.6.94orange
51,191,521,290,71
43,0697,77
0,933
0,0390,0180,010
1
Bk 7Th5011.6.94orange
52,241,431,460,64
43,8599,62
0,935
0,0360,0200,009
1
Bk 7Th5111.6.94orange
51,581,411,190,52
43,0797,77
0,940
0,0360,0170,007
1
Bk 7Th5211.6.94orange
52,051,401,160,64
43,4898,73
0,939
0,0350,0160,009
1
Bk 95223.2.94
64,320,790,630,30
51,91117,95
0,972
0,0170,0070,004
1
Bk 93024.2.94
63,380,220,760,28
50,62115,26
0,983
0,0050,0090,003
1
Bk 93124.2.94
64,310,180,650,25
51,22116,61
0,985
0,0040,0080,003
1
Bk 93224.2.94
62,370,741,170,51
50,79115,58
0,964
0,0160,0140,006
1
Bk 9424.2.94
62,150,641,140,44
50,44114,81
0,967
0,0140,0140,005
1
Bk 93524.2.94
63,080,280,660,37
50,44114,83
0,981
0,0060,0080,005
1
Bk 93624.2.94
61,350,430,660,24
49,17111,85
0,979
0,0100,0080,003
1
Bk 9144.3.94
63,480,600,670,34
51,09116,18
0,975
0,0130,0080,004
1
Bk 9154.3.94
63,990,440,650,37
51,33116,78
0,978
0,0090,0080,004
1
Bk 9174.3.94
65,160,891,310,37
53,14120,87
0,962
0,0180,0150,004
1
Bk 9184.3.94
65,040,781,280,41
52,93120,44
0,964
0,0160,0150,005
1
Bk 97Th5411.6.94orange
57,010,380,430,41
45,67103,90
0,980
0,0090,0060,006
1
Bk 97Th5511.6.94orange
54,980,370,540,48
44,18100,55
0,977
0,0090,0070,007
1
Bk 97Th5611.6.94orange
54,810,290,390,43
43,8499,76
0,981
0,0070,0050,006
1
Bk 97Th5711.6.94brown
53,110,750,640,41
43,1498,05
0,966
0,0190,0090,006
1
Bk 97Th5811.6.94orange
54,260,190,450,41
43,3298,63
0,983
0,0050,0060,006
1
Bk 97Th5911.6.94yellow
53,710,240,380,41
42,9097,64
0,983
0,0060,0050,006
1
Bk 97Th6011.6.94yellow
54,350,280,400,33
43,4198,77
0,983
0,0070,0060,005
1
Bk 7Th2511.6.94orange
49,401,691,980,74
42,2996,10
0,917
0,0440,0290,011
1
Bk 7Th2611.6.94yellow
51,131,341,570,59
42,9297,55
0,935
0,0340,0220,009
1
Bk 7Th2811.6.94orange
49,921,762,270,62
42,8797,44
0,914
0,0450,0320,009
1
Bk 7Th2911.6.94orange
50,641,711,940,70
43,2398,22
0,919
0,0430,0270,010
1
Bk 7Th3011.6.94yellow
50,641,752,130,67
43,3798,56
0,916
0,0440,0300,010
1
Bk 7Th3111.6.94orange
50,921,381,970,60
43,0597,92
0,928
0,0350,0280,009
1
Bk 7Th3311.6.94yellow
50,631,502,020,46
42,8997,50
0,926
0,0380,0290,007
1
Bk 7Th3411.6.94yellow
52,621,051,600,55
43,7699,58
0,944
0,0260,0220,008
1
Bk 7Th3311.6.94yellow
50,631,502,020,46
42,8997,50
0,926
0,0380,0290,007
1
Bk 7Th3411.6.94yellow
52,621,051,600,55
43,7699,58
0,944
0,0260,0220,008
1
C-43Appendix C Table C12/C13 calcite/albite
normed on 1cation
sampleanalysisdateposition
SiO2Al2O3Fe2O3CaOBaONa2OK2OTotal
SiAlFe3
CaBaNaK
sum
An%
Bk 10B518.10.93sympl
69,3720,060,260,500,0311,270,07101,56
2,9791,0150,0204,014
0,0230,0010,9380,0040,966
4,980
2,382
Bk 10B1318.10.93sympl
70,3220,250,230,190,0010,660,08101,73
2,9991,0180,0184,036
0,0090,0000,8820,0040,895
4,930
0,970
Bk 10B4518.10.93sympl
67,4519,800,180,681,3110,830,10100,35
2,9631,0250,0134,002
0,0320,0230,9220,0060,983
4,984
3,257
Bk 10B3219.10.93asympl
68,7619,700,440,560,0111,060,05100,58
2,9781,0060,0344,018
0,0260,0000,9290,0030,958
4,976
2,713
Bk 173913.7.94sympl
67,6419,650,040,220,0310,980,0598,61
2,9891,0230,0034,016
0,0100,0010,9410,0030,955
4,970
1,091
Bk 174113.7.94sympl
67,9420,080,080,620,0011,060,0799,85
2,9701,0350,0064,011
0,0290,0000,9380,0040,971
4,981
2,992
Bk 174213.7.94grt ps
66,3121,200,101,930,0310,440,07100,08
2,9061,0950,0084,008
0,0910,0010,8870,0040,982
4,990
9,226
Bk 174313.7.94grt ps
66,3320,870,071,720,0010,350,0799,41
2,9221,0830,0054,010
0,0810,0000,8840,0040,969
4,979
8,376
Bk 174413.7.94grt ps
66,0121,140,031,970,0010,280,1099,53
2,9081,0980,0034,008
0,0930,0000,8780,0060,977
4,985
9,519
Bk 174613.7.94sympl
68,0919,790,120,670,0011,060,0699,79
2,9781,0200,0094,007
0,0310,0000,9380,0030,973
4,980
3,228
Bk 17563.7.94sympl
68,4019,980,210,500,1811,250,03100,55
2,9721,0230,0164,011
0,0230,0030,9480,0020,976
4,987
2,385
Bk 17573.7.94sympl
67,8919,720,080,470,0310,780,0599,02
2,9871,0230,0064,016
0,0220,0010,9200,0030,945
4,961
2,344
normed on 8 oxygen, all Fe assumed Fe3
sampleanalysisdateCL colour
CaMgFeMn
CO2total
Ca
MgFeMn
CO3
Bk 97Th6111.6.94brown
53,720,460,540,35
43,2198,28
0,976
0,0120,0080,005
1
Bk 97Th6211.6.94brown
53,400,340,550,35
42,8397,47
0,978
0,0090,0080,005
1
Bk 97Th6311.6.94brown
53,770,330,550,35
43,1198,11
0,979
0,0080,0080,005
1
Bk 97Th6411.6.94brown
53,340,620,850,57
43,4198,79
0,964
0,0160,0120,008
1
Bk 97Th6511.6.94brown
53,500,510,610,40
43,1698,18
0,973
0,0130,0090,006
1
Bk 97Th6611.6.94brown
53,590,320,790,48
43,1998,37
0,974
0,0080,0110,007
1
Bk 97Th6711.6.94brown
54,460,530,570,26
43,8399,65
0,975
0,0130,0080,004
1
Bk 97Th6811.6.94orange
53,350,260,500,38
42,6997,18
0,981
0,0070,0070,006
1
Bk 97Th6911.6.94orange
54,100,250,490,37
43,2698,47
0,981
0,0060,0070,005
1
Bk 97Th7011.6.94yellow
53,850,260,390,41
43,0497,95
0,982
0,0070,0060,006
1
sampleanalysisdateposition
SiO2Al2O3Fe2O3CaOBaONa2OK2OTotal
SiAlFe3
CaBaNaK
sum
An%
normed on 8 oxygen, all Fe assumed Fe3
Bk 17583.7.94sympl
67,6919,700,080,350,0611,320,0699,26
2,9791,0220,0064,006
0,0170,0010,9660,0030,987
4,993
1,672
Bk 17593.7.94sympl
66,3420,650,121,420,0010,200,0598,78
2,9341,0760,0094,019
0,0670,0000,8750,0030,945
4,964
7,122
Bk 17603.7.94sympl
68,1419,820,170,480,0311,170,0499,85
2,9781,0210,0134,011
0,0220,0010,9460,0020,972
4,983
2,313
Bk 17613.7.94sympl
66,1320,490,121,430,0910,460,0698,78
2,9311,0700,0094,010
0,0680,0020,8990,0030,972
4,982
6,988
Bk 17623.7.94sympl
68,1619,620,060,290,0011,190,0699,38
2,9911,0150,0044,009
0,0140,0000,9520,0030,969
4,978
1,407
Bk 17633.7.94sympl
68,2519,530,040,260,0511,360,0399,52
2,9921,0090,0034,005
0,0120,0010,9660,0020,981
4,986
1,246
Bk 17643.7.94sympl
68,2819,630,070,210,0111,150,0599,40
2,9931,0140,0054,013
0,0100,0000,9480,0030,961
4,973
1,027
Bk 1739.7.94sympl
66,9320,330,341,250,0210,790,0399,69
2,9351,0510,0264,013
0,0590,0000,9180,0020,978
4,991
6,004
Bk 17149.7.94sympl
68,7419,760,070,310,0011,380,05100,31
2,9891,0130,0054,007
0,0140,0000,9600,0030,977
4,984
1,479
Bk 17159.7.94sympl
68,3419,950,060,370,0011,280,02100,02
2,9811,0260,0044,010
0,0170,0000,9540,0010,972
4,983
1,778
position: sympl is albite in symplectite, grt ps is albite in chlorite albite epidoze aggregates after garnet,vein is albite in veins
C-44 Appendix C Table C13 albite
position: sympl is albite in symplectite, grt ps is albite in chlorite albite epidoze aggregates after garnet,vein is albite in veins
sampleanalysisdateposition
SiO2Al2O3Fe2O3CaOBaONa2OK2OTotal
SiAlFe3
CaBaNaK
sum
An%
normed on 8 oxygen, all Fe assumed Fe3
Bk 17169.7.94vein
66,4521,270,081,820,0010,460,06100,14
2,9081,0970,0064,011
0,0850,0000,8880,0030,976
4,987
8,741
Bk 17179.7.94vein
66,1920,970,081,820,0010,420,0399,51
2,9141,0880,0064,008
0,0860,0000,8900,0020,977
4,985
8,787
Bk 17189.7.94vein
66,6520,830,081,650,0010,550,0799,83
2,9241,0770,0064,007
0,0780,0000,8970,0040,979
4,986
7,923
Bk 17199.7.94vein
66,5320,920,111,670,0510,440,0499,76
2,9201,0820,0084,011
0,0790,0010,8890,0020,970
4,981
8,095
Bk 17209.7.94vein
67,4520,380,131,220,0110,890,04100,12
2,9471,0490,0104,006
0,0570,0000,9220,0020,982
4,988
5,815
Bk 17219.7.94vein
66,4720,700,141,670,0010,410,0699,45
2,9251,0740,0114,010
0,0790,0000,8880,0030,970
4,980
8,114
Bk 17229.7.94sympl
68,6319,610,210,110,0011,340,0399,93
2,9911,0070,0164,015
0,0050,0000,9580,0020,965
4,980
0,532
Bk 17239.7.94sympl
68,9419,580,090,050,0011,260,0299,94
3,0031,0050,0074,015
0,0020,0000,9510,0010,954
4,969
0,244
Bk 17529.7.94sympl
68,5219,390,100,090,0011,270,0299,39
3,0021,0010,0084,011
0,0040,0000,9570,0010,963
4,974
0,439
Bk 17539.7.94sympl
68,7719,530,200,130,0011,500,02100,15
2,9931,0020,0154,010
0,0060,0000,9700,0010,978
4,988
0,620
Bk 18175.8.94sympl
67,9720,290,130,840,0010,620,0399,88
2,9661,0440,0104,020
0,0390,0000,8990,0020,940
4,959
4,180
sampleanalysisdateposition
SiO2Al2O3Fe2O3CaOBaONa2OK2OTotal
SiAlFe3
CaBaNaK
sum
An%
normed on 8 oxygen, all Fe assumed Fe3
Bk 18185.8.94sympl
68,6820,080,330,280,0110,900,11100,39
2,9771,0260,0264,029
0,0130,0000,9160,0060,935
4,964
1,390
Bk 391113.3.93sympl
69,0220,100,000,360,0011,500,02101,00
2,9831,0240,0004,006
0,0170,0000,9640,0010,981
4,988
1,699
Bk 393313.3.93sympl
67,8219,440,290,440,1811,570,0399,77
2,9741,0050,0224,001
0,0210,0030,9840,0021,009
5,010
2,048
Bk 395424.6.92sympl
69,1320,080,210,170,0211,160,01100,78
2,9851,0220,0164,024
0,0080,0000,9340,0010,943
4,967
0,834
Bk 395524.6.92sympl
68,2219,850,520,510,1110,570,0299,80
2,9731,0200,0404,033
0,0240,0020,8930,0010,920
4,953
2,589
Bk 395924.6.92sympl
68,3820,230,290,290,0511,270,02100,53
2,9661,0340,0224,022
0,0130,0010,9480,0010,963
4,985
1,399
Bk 396024.6.92sympl
66,6920,610,260,930,0010,830,0299,34
2,9331,0680,0194,021
0,0440,0000,9230,0010,968
4,989
4,525
Bk 3965.5.92sympl
67,2419,350,400,540,0511,260,0298,86
2,9701,0070,0304,008
0,0260,0010,9640,0010,992
4,999
2,576
Bk 39.12128.8.92sympl
67,2819,880,080,610,1011,460,0099,41
2,9631,0320,0064,000
0,0290,0020,9780,0001,009
5,009
2,852
Bk 39.12528.8.92sympl
68,8019,750,120,310,0011,460,03100,47
2,9871,0110,0094,007
0,0140,0000,9650,0020,981
4,988
1,470
Bk 39.12628.8.92sympl
69,2120,760,060,360,0010,580,03101,00
2,9781,0530,0044,035
0,0170,0000,8830,0020,901
4,936
1,842
sampleanalysisdateposition
SiO2Al2O3Fe2O3CaOBaONa2OK2OTotal
SiAlFe3
CaBaNaK
sum
An%
normed on 8 oxygen, all Fe assumed Fe3
Bk 39.14528.8.92sympl
68,8019,480,930,840,0010,140,03100,22
2,9770,9930,0724,042
0,0390,0000,8510,0020,891
4,933
4,369
Bk 72727.8.92sympl
68,2020,940,220,440,0511,140,04101,03
2,9451,0660,0174,028
0,0200,0010,9330,0020,956
4,985
2,129
Bk 73627.8.92sympl
68,9020,960,090,540,0010,750,05101,29
2,9621,0620,0074,031
0,0250,0000,8960,0030,924
4,955
2,693
Bk 81314.3.93sympl
68,4820,340,580,870,0010,080,23100,58
2,9601,0360,0454,041
0,0400,0000,8450,0130,898
4,939
4,487
Bk 86014.3.93sympl
69,0818,750,780,740,039,870,0599,30
3,0120,9640,0604,035
0,0350,0010,8340,0030,872
4,908
3,963
Bk 9252.7.94sympl
67,4519,990,070,700,0010,890,0799,17
2,9691,0370,0054,011
0,0330,0000,9290,0040,966
4,978
3,416
Bk 9262.7.94sympl
67,5120,180,090,910,0010,980,0699,73
2,9581,0420,0074,007
0,0430,0000,9330,0030,979
4,987
4,364
Bk 91724.2.94sympl
68,5820,120,220,480,0111,010,04100,46
2,9741,0290,0174,020
0,0220,0000,9260,0020,951
4,971
2,346
Bk 91824.2.94sympl
68,6820,150,280,230,0911,090,09100,61
2,9751,0290,0214,025
0,0110,0020,9310,0050,949
4,973
1,125
Bk 91924.2.94sympl
68,6220,100,100,250,0511,310,05100,48
2,9791,0280,0084,015
0,0120,0010,9520,0030,967
4,982
1,202
Bk 92024.2.94sympl
68,7020,030,210,270,0011,230,04100,48
2,9791,0240,0164,019
0,0130,0000,9440,0020,959
4,978
1,308
C-45Appendix C Table C13/C14 albite/amphibolearound garnet
position: sympl is albite in symplectite, grt ps is albite in chlorite albite epidoze aggregates after garnet,vein is albite in veins
normed on 8 oxygen, all Fe assumed Fe3
sampleanalysisdate
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2O
H2Ototal
SiAlt
AloFe3CrTiMgFe2MnZn
CaNa
NaK
sum
OH
name
amphibole names after Leake (1978): ed-hbl is edenitic-hornblende, fer-act-hbl is ferro-actinolitic-hornblende, fer-par is ferroan-pargasite, fer-par-hbl is ferroan-pargasitic-hornblende, mag-has is magnesian-hastingite, mag-hst-hbl ismagnesian-hastingitic-hornblende, tscherm is tschermakite
Bk 10 B819.10.93b
41,310,1211,750,0010,3213,920,236,679,280,272,880,68
1,9699,39
6,3201,680
0,4391,1890,0000,0101,5211,7810,0300,031
1,5210,4792,000
0,3760,1360,511
15,511
2
mag-hst-hbl
sampleanalysisdateposition
SiO2Al2O3Fe2O3CaOBaONa2OK2OTotal
SiAlFe3
CaBaNaK
sum
An%
Bk 92124.2.94sympl
68,4820,120,260,410,0010,990,05100,30
2,9741,0300,0204,023
0,0190,0000,9250,0030,947
4,970
2,014
Bk 92224.2.94sympl
69,5320,100,190,150,0011,310,04101,32
2,9881,0180,0154,020
0,0070,0000,9420,0020,951
4,972
0,726
Bk 92324.2.94sympl
68,6920,030,170,240,1011,290,05100,57
2,9791,0240,0134,016
0,0110,0020,9490,0030,965
4,981
1,156
Cig91-13417.6.93sympl
64,2121,283,030,850,0010,030,1499,54
2,7981,0930,2324,123
0,0400,0000,8470,0080,895
5,017
4,434
Bk 10 B919.10.93b
40,900,0611,740,0210,1314,730,166,379,370,182,900,72
1,9599,22
6,2931,707
0,4231,1730,0020,0051,4611,8950,0210,020
1,5450,4552,000
0,4100,1440,554
15,554
2
mag-hst-hbl
Bk 10 B1019.10.93b
39,390,0813,990,0010,0513,850,276,089,700,332,740,88
1,9599,32
6,0521,948
0,5861,1620,0000,0071,3921,7800,0350,037
1,5970,4032,000
0,4130,1760,589
15,589
2
mag-has
Bk 10 B1519.10.93b
41,240,0212,210,0210,0213,760,236,799,370,042,790,70
1,9699,16
6,3031,697
0,5031,1530,0020,0021,5471,7590,0300,005
1,5340,4662,000
0,3610,1390,501
15,501
2
mag-hst-hbl
Bk 10 B326.11.93
38,380,1714,860,009,1215,240,215,309,740,252,821,04
1,9399,07
5,9502,050
0,6651,0640,0000,0141,2251,9760,0280,029
1,6180,3822,000
0,4650,2100,676
15,676
2
mag-has
Bk 10 B526.11.93
41,530,1712,850,018,3514,170,206,649,520,192,460,84
1,9698,89
6,3431,657
0,6570,9590,0010,0141,5121,8100,0260,021
1,5580,4422,000
0,2860,1670,454
15,454
2
fer-act-hbl
Bk 10 B926.11.93
41,470,0211,930,008,3615,100,226,599,570,172,790,70
1,9598,87
6,3731,627
0,5340,9670,0000,0021,5091,9400,0290,019
1,5760,4242,000
0,4070,1400,547
15,547
2
mag-hst-hbl
Bk 10 B1626.11.93
39,940,1113,830,007,6515,360,156,299,850,002,890,83
1,9598,84
6,1521,848
0,6620,8870,0000,0091,4441,9780,0200,000
1,6260,3742,000
0,4890,1670,655
15,655
2
mag-has
Bk 10 B1826.11.93
41,350,0614,210,027,7713,010,157,529,860,222,790,74
1,9999,69
6,2241,776
0,7450,8800,0020,0051,6871,6380,0190,024
1,5900,4102,000
0,4040,1450,549
15,549
2
mag-has
Bk 10 B1926.11.93
38,300,0515,920,017,4015,650,175,219,790,172,801,15
1,9398,54
5,9432,057
0,8540,8640,0010,0041,2052,0300,0220,019
1,6280,3722,000
0,4700,2330,702
15,702
2
mag-has
Bk 1895.8.94
41,160,2512,600,025,7915,820,287,4011,370,292,120,62
1,9799,69
6,2741,726
0,5380,6640,0020,0291,6812,0160,0360,033
1,8570,1432,000
0,4840,1230,607
15,607
2
mag-hst-hbl
normed on 23 oxygens, Fe3 over Si+Ti+Al+Fe+Mn+Mg+Ca+Zn = 13
C-46 Appendix C Table C14 amphibole aroundgarnet
sampleanalysisdate
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2O
H2Ototal
SiAlt
AloFe3CrTiMgFe2MnZn
CaNa
NaK
sum
OH
name
amphibole names after Leake (1978): ed-hbl is edenitic-hornblende, fer-act-hbl is ferro-actinolitic-hornblende, fer-par is ferroan-pargasite, fer-par-hbl is ferroan-pargasitic-hornblende, mag-has is magnesian-hastingite, mag-hst-hbl ismagnesian-hastingitic-hornblende, tscherm is tschermakite
normed on 23 oxygens, Fe3 over Si+Ti+Al+Fe+Mn+Mg+Ca+Zn = 13
sampleanalysisdate
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2O
H2Ototal
SiAlt
AloFe3CrTiMgFe2MnZn
CaNa
NaK
sum
OH
name
normed on 23 oxygens, Fe3 over Si+Ti+Al+Fe+Mn+Mg+Ca+Zn = 13
Bk 18125.8.94
40,230,2212,540,0013,208,650,228,6610,300,151,740,51
1,9798,40
6,1131,887
0,3591,5100,0000,0251,9611,0990,0280,017
1,6770,3232,000
0,1900,1010,291
15,291
2
tscherm
Bk 392123.3.92
40,200,0313,060,005,4913,630,218,589,65n.a4,290,34
1,9497,42
6,2141,786
0,5930,6380,0000,0021,9771,7620,027 -
1,5980,4022,000
0,8840,0680,952
15,952
2
mag-has
Bk 392223.3.92
39,600,0613,670,016,7812,920,218,459,68n.a4,200,40
1,9597,93
6,0971,903
0,5780,7860,0010,0051,9391,6640,027 -
1,5970,4032,000
0,8510,0800,931
15,931
2
mag-has
Bk 392423.3.92
41,440,2214,910,002,7412,760,129,049,04n.a4,490,47
1,9797,19
6,3061,694
0,9790,3130,0000,0182,0501,6230,015 -
1,4740,5262,000
0,7980,0930,892
15,892
2
fer-par-hbl
Bk 7256.7.92
40,970,0815,730,033,6911,850,219,3110,10n.a3,740,41
1,9998,11
6,1701,830
0,9630,4180,0040,0062,0901,4920,027 -
1,6300,3702,000
0,7220,0800,802
15,802
2
fer-par
Bk 7117.7.92
43,270,1013,960,003,0014,110,208,198,68n.a4,160,47
1,9998,13
6,5251,475
1,0060,3400,0000,0081,8411,7800,026 -
1,4020,5982,000
0,6190,0920,711
15,711
2
ed-hbl
Bk 7137.7.92
44,880,1012,350,004,1112,810,139,458,68n.a4,170,31
2,0299,01
6,6691,331
0,8310,4590,0000,0082,0931,5920,016 -
1,3820,6182,000
0,5830,0600,643
15,643
2
ed-hbl
Bk 777.8.92
40,720,0515,480,035,5810,900,219,5810,070,164,000,31
2,0099,09
6,0911,909
0,8210,6280,0040,0042,1361,3640,0270,018
1,6140,3862,000
0,7740,0600,835
15,835
2
fer-par
Bk 787.8.92
43,080,1014,670,004,1510,440,1610,149,430,313,890,44
2,0298,83
6,3821,618
0,9430,4630,0000,0082,2391,2930,0200,034
1,4970,5032,000
0,6140,0850,699
15,699
2
fer-par-hbl
Bk 82414.3.93
41,240,0715,320,004,6613,490,287,729,380,113,840,43
1,9898,52
6,2381,762
0,9690,5300,0000,0061,7411,7060,0360,012
1,5200,4802,000
0,6460,0850,731
15,731
2
fer-par
Bk 82514.3.93
42,540,0013,460,045,5413,620,287,799,080,193,810,23
1,9898,57
6,4311,569
0,8300,6300,0050,0001,7551,7230,0360,021
1,4710,5292,000
0,5880,0450,633
15,633
2
fer-par-hbl
Bk 82814.3.93
41,650,0814,580,006,5513,090,327,429,090,253,770,33
1,9999,12
6,2771,723
0,8660,7430,0000,0061,6671,6490,0410,028
1,4680,5322,000
0,5690,0650,634
15,634
2
fer-par-hbl
Bk 82914.3.93
42,280,0713,960,036,4312,860,227,948,790,124,070,30
1,9999,06
6,3551,645
0,8280,7270,0040,0061,7791,6160,0280,013
1,4160,5842,000
0,6020,0590,660
15,660
2
fer-par-hbl
Cig 91-16817.6.93
41,160,0818,380,001,9514,520,177,189,070,004,420,61
2,0199,55
6,1281,872
1,3530,2180,0000,0061,5931,8070,0210,000
1,4470,5532,000
0,7230,1180,841
15,841
2
fer-par
Cig 91-16917.6.93
42,560,0617,090,003,0313,480,137,858,760,014,360,55
2,0399,92
6,2801,720
1,2510,3370,0000,0051,7261,6630,0160,001
1,3850,6152,000
0,6320,1060,738
15,738
2
fer-par-hbl
C-47Appendix C Table C15 amphibole aroundglaucophane
sampleanalysisdate
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2O
H2Ototal
SiAlt
AloFe3CrTiMgFe2MnZn
CaNa
NaK
sum
OH
name
amphibole names after Leake (1978): ac-hbl is actinolitic-hornblende, act is actinolite, barr is barroisite, ed isedenite, ed-hbl is edenitic-hornblende, mag-hbl is magnesio-hornblende, mag-kat is magnesio-katophorite
normed on 23 oxygens, Fe3 over Si+Ti+Al+Fe+Mn+Mg+Ca+Zn = 13
sampleanalysisdate
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2O
H2Ototal
SiAlt
AloFe3CrTiMgFe2MnZn
CaNa
NaK
sum
OH
name
normed on 23 oxygens, Fe3 over Si+Ti+Al+Fe+Mn+Mg+Ca+Zn = 13
Bk 392924.6.92
49,330,1910,300,053,7911,340,089,625,35n.a.5,330,18
2,0497,60
7,2580,742
1,0440,4200,0060,0152,1101,3950,010-
0,8431,1572,000
0,3640,0350,398
15,398
2
barr
Bk 393724.6.92
50,480,1210,360,024,997,550,0711,334,81n.a.5,460,13
2,0797,39
7,3090,691
1,0770,5440,0020,0092,4450,9140,009-
0,7461,2542,000
0,2790,0250,303
15,303
2
barr
Bk 394024.6.92
46,850,109,660,023,359,470,1512,649,11n.a.3,810,23
2,0297,41
6,9441,056
0,6310,3740,0020,0082,7921,1730,019-
1,4470,5532,000
0,5420,0440,586
15,586
2
ed
Bk 7267.8.92
50,380,097,220,022,579,100,2013,789,260,223,150,17
2,0698,22
7,3290,671
0,5670,2810,0020,0072,9881,1070,0250,024
1,4430,5572,000
0,3320,0320,364
15,364
2
ac-hbl
Bk 7457.8.92
47,590,048,160,014,146,900,1715,0911,000,182,590,15
2,0598,06
6,9601,040
0,3670,4550,0010,0033,2900,8440,0210,019
1,7240,2762,000
0,4580,0290,487
15,487
2
mag-hbl
Bk 7527.8.92
52,270,043,860,062,286,820,1917,3411,790,251,520,09
2,0998,60
7,5090,491
0,1620,2470,0070,0033,7130,8190,0230,027
1,8150,1852,000
0,2380,0170,255
15,255
2
act
Bk 82329.1.93b
48,780,1611,610,011,4211,440,1111,078,230,164,030,29
2,0799,39
7,0530,947
1,0320,1540,0010,0122,3861,3840,0130,017
1,2750,7252,000
0,4050,0550,459
15,459
2
barr
Bk 82429.1.93b
48,090,149,260,014,288,880,0613,219,850,203,040,31
2,0799,40
6,9761,024
0,5590,4670,0010,0112,8561,0770,0070,021
1,5310,4692,000
0,3860,0590,444
15,444
2
mag-hbl
Bk 982.7.94
50,670,056,520,003,716,390,0716,1911,370,251,740,17
2,1099,23
7,2460,754
0,3450,4000,0000,0053,4510,7640,0080,026
1,7420,2582,000
0,2250,0320,256
15,256
2
mag-hbl
Bk 992.7.94
48,960,039,950,003,537,980,0913,409,590,132,890,19
2,0898,82
7,0570,943
0,7480,3830,0000,0032,8790,9620,0110,014
1,4810,5192,000
0,2890,0360,324
15,324
2
mag-hbl
Bk 9523.2.94
47,330,058,220,042,0610,580,1313,3511,760,161,690,23
2,0297,62
7,0230,977
0,4610,2300,0050,0062,9531,3120,0160,018
1,8700,1302,000
0,3560,0440,400
15,400
2
mag-hbl
Bk 10 B2018.10.93
49,600,058,460,004,799,350,1712,749,930,372,410,26
2,09100,22
7,1310,869
0,5640,5180,0000,0042,7301,1240,0210,039
1,5300,4702,000
0,2010,0490,250
15,250
2
mag-hbl
Bk 10 B2118.10.93
50,500,108,080,004,948,330,0913,189,580,162,180,22
2,0999,45
7,2460,754
0,6120,5340,0000,0082,8191,0000,0110,017
1,4730,5272,000
0,0790,0410,120
15,120
2
mag-hbl
Bk 10 B519.10.93b
46,960,547,940,018,6313,180,268,418,600,212,450,29
2,0199,49
7,0130,987
0,4110,9700,0010,0431,8721,6460,0330,023
1,3760,6242,000
0,0860,0560,142
15,142
2
mag-hbl
Bk 10 B719.10.93b
46,550,177,370,028,5213,270,268,809,190,272,280,30
1,9998,99
7,0050,995
0,3130,9640,0020,0141,9741,6700,0330,030
1,4820,5182,000
0,1470,0590,206
15,206
2
mag-hbl
Bk 18135.8.94
49,310,195,050,009,5610,410,5110,878,940,202,100,18
2,0399,35
7,2770,723
0,1561,0620,0000,0212,3911,2850,0640,022
1,4140,5862,000
0,0150,0350,049
15,049
2
ac-hbl
Bk 1826.8.94
52,000,198,530,002,759,000,1412,417,490,203,440,14
2,0998,37
7,4650,535
0,9090,2970,0000,0212,6561,0800,0170,021
1,1520,8482,000
0,1100,0260,136
15,136
2
barr
Bk 1856.8.94
49,180,135,060,017,8012,600,4110,569,850,151,780,16
2,0399,72
7,2770,723
0,1600,8680,0010,0142,3291,5600,0510,016
1,5620,4382,000
0,0720,0310,103
15,103
2
ac-hbl
Bk 1866.8.94
48,840,215,770,009,7211,430,369,978,300,182,670,20
2,0399,67
7,2180,782
0,2231,0800,0000,0232,1961,4120,0450,020
1,3140,6862,000
0,0790,0390,118
15,118
2
barr
Bk 1876.8.94
48,970,205,780,0310,0211,400,409,978,520,272,520,22
2,04100,34
7,1990,801
0,2001,1090,0030,0222,1851,4020,0500,029
1,3420,6582,000
0,0600,0420,102
15,102
2
mag-hbl
Bk 1886.8.94
51,250,158,460,034,359,050,1411,917,300,053,520,13
2,0898,42
7,3940,606
0,8320,4730,0030,0162,5611,0920,0170,005
1,1280,8722,000
0,1130,0240,137
15,137
2
barr
Bk 392624.6.92
45,400,2410,750,035,4011,640,1510,038,25n.a.4,170,32
2,0198,39
6,7761,224
0,6670,6070,0040,0192,2311,4530,019-
1,3190,6812,000
0,5260,0620,588
15,588
2
mag-kat
C-48 Appendix C Table C15/C16 amphibole aroundglaucophane/in symplectite
sampleanalysisdate
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2O
H2Ototal
SiAlt
AloFe3CrTiMgFe2MnZn
CaNa
NaK
sum
OH
name
amphibole names after Leake (1978): ac-hbl is actinolitic-hornblende, act is actinolite, barr is barroisite, ed isedenite, ed-hbl is edenitic-hornblende, mag-hbl is magnesio-hornblende, mag-kat is magnesio-katophorite
normed on 23 oxygens, Fe3 over Si+Ti+Al+Fe+Mn+Mg+Ca+Zn = 13
sampleanalysisdate
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2O
H2Ototal
SiAlt
AloFe3CrTiMgFe2MnZn
CaNa
NaK
sum
OH
name
normed on 23 oxygens, Fe3 over Si+Ti+Al+Fe+Mn+Mg+Ca+Zn = 13
Cig 91-17817.6.93
45,400,2611,950,002,0211,210,1311,9610,710,093,120,39
2,0499,28
6,6671,333
0,7350,2230,0000,0212,6181,3770,0160,010
1,6850,3152,000
0,5730,0750,648
15,648
2
ed-hbl
Cig 91-13116.6.93
48,180,1214,000,024,1211,100,078,895,850,005,190,35
2,0999,98
6,9241,076
1,2960,4460,0020,0091,9041,3340,0090,000
0,9011,0992,000
0,3470,0660,413
15,413
2
barr
Cig 91-17617.6.93
52,190,1410,820,011,808,990,0812,025,830,045,160,20
2,1299,40
7,3820,618
1,1850,1920,0010,0112,5341,0630,0100,004
0,8831,1172,000
0,2990,0370,335
15,335
2
barr
Cig 91-17717.6.93
54,360,0712,010,010,9910,410,059,842,940,006,460,09
2,1499,37
7,6220,378
1,6060,1040,0010,0052,0561,2210,0060,000
0,4421,5582,000
0,1980,0160,214
15,214
2
gln
Bk 10 B1619.10.93
51,550,086,840,051,758,690,0414,7110,610,151,770,17
2,0898,49
7,4180,582
0,5780,1890,0060,0063,1551,0450,0050,016
1,6360,3642,000
0,1300,0320,161
15,161
2
act-hbl
Bk 10 B1 q18.10.93
54,790,031,790,082,899,080,1416,4212,010,350,610,03
2,11100,33
7,7760,224
0,0750,3090,0090,0023,4731,0770,0170,037
1,8260,1681,994
0,0000,0060,006
15,006
2
act
Bk 10 B8 q18.10.93
55,510,031,620,000,899,840,1216,8312,060,190,750,07
2,11100,02
7,8730,127
0,1440,0950,0000,0023,5581,1670,0140,020
1,8330,1672,000
0,0390,0130,052
15,052
2
act
Bk 10 B9 q18.10.93
52,290,085,180,032,959,170,1614,7510,750,181,620,15
2,0999,39
7,5030,497
0,3790,3180,0030,0063,1551,1000,0190,019
1,6530,3472,000
0,1030,0280,131
15,131
2
act
Bk 10 B10 q18.10.93
55,600,041,670,201,609,220,1516,9412,010,160,720,06
2,13100,50
7,8430,157
0,1210,1690,0220,0033,5621,0880,0180,017
1,8150,1852,000
0,0120,0110,023
15,023
2
act
Bk 10 B11 q18.10.93
54,220,073,630,003,078,900,1315,5010,860,351,360,12
2,12100,32
7,6820,318
0,2880,3270,0000,0053,2731,0540,0160,037
1,6480,3522,000
0,0220,0220,044
15,044
2
act
Bk 10 B12 q18.10.93
53,640,104,170,002,678,770,2015,5111,020,001,170,13
2,1099,48
7,6430,357
0,3430,2860,0000,0083,2941,0450,0240,000
1,6820,3182,000
0,0060,0240,030
15,030
2
act
Bk 10 B1618.10.93
51,720,026,180,023,378,160,1215,3010,930,201,930,17
2,11100,23
7,3530,647
0,3880,3600,0020,0023,2420,9700,0140,021
1,6650,3352,000
0,1970,0310,228
15,228
2
act-hbl
Bk 10 B1718.10.93
53,180,025,120,004,997,261,1515,2211,010,261,530,15
2,14102,03
7,4420,558
0,2860,5260,0000,0023,1740,8490,1360,027
1,6510,3492,000
0,0660,0270,093
15,093
2
act-hbl
Bk 10 B31 q18.10.93
54,410,093,530,180,648,930,0716,7811,940,060,950,11
2,1299,81
7,7030,297
0,2920,0690,0200,0073,5411,0570,0080,006
1,8110,1892,000
0,0720,0200,092
15,092
2
act
Bk 10 B32 q18.10.93
54,560,113,530,110,869,850,1016,0311,440,311,380,12
2,12100,53
7,7130,287
0,3010,0920,0120,0083,3781,1650,0120,032
1,7330,2672,000
0,1110,0220,133
15,133
2
act
C-49Appendix C Table C16 amphiboleinsymplectite
sampleanalysisdate
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2O
H2Ototal
SiAlt
AloFe3CrTiMgFe2MnZn
CaNa
NaK
sum
OH
name
analysis q is in contact with quartz, amphibole names after Leake (1978): ac-hbl is actinolitic-hornblende, act isactinolite, barr is barroisite, ed is edenite, ed-hbl is edenitic-hornblende, mag-hbl is magnesio-hornblende
normed on 23 oxygens, Fe3 over Si+Ti+Al+Fe+Mn+Mg+Ca+Zn = 13
sampleanalysisdate
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2O
H2Ototal
SiAlt
AloFe3CrTiMgFe2MnZn
CaNa
NaK
sum
OH
name
normed on 23 oxygens, Fe3 over Si+Ti+Al+Fe+Mn+Mg+Ca+Zn = 13
Bk 10 B35 q18.10.93
55,660,093,110,200,109,470,1216,5411,240,021,270,10
2,13100,05
7,8400,160
0,3560,0110,0220,0073,4721,1150,0140,002
1,6960,3042,000
0,0430,0180,061
15,061
2
act
Bk 10 B39 q18.10.93
53,500,114,690,222,418,230,1416,0211,210,201,460,16
2,12100,48
7,5510,449
0,3320,2560,0250,0083,3700,9710,0170,021
1,6950,3052,000
0,0950,0290,124
15,124
2
act
Bk 10 B4218.10.93
51,840,096,040,063,507,070,0915,7510,860,101,680,19
2,1099,37
7,3870,613
0,4020,3750,0070,0073,3450,8430,0110,011
1,6580,3422,000
0,1220,0350,158
15,158
2
act-hbl
Bk 10 B10 q26.11.93
54,850,031,340,001,819,200,0816,9312,240,380,560,11
2,1099,63
7,8280,172
0,0540,1940,0000,0023,6021,0980,0100,040
1,8720,1282,000
0,0270,0200,047
15,047
2
act
Bk 10 B11 q26.11.93
54,290,051,880,062,428,990,1216,3811,740,300,770,08
2,0999,17
7,7850,215
0,1030,2620,0070,0043,5011,0780,0150,032
1,8040,1962,000
0,0180,0150,033
15,033
2
act
Bk 10 B1226.11.93
51,710,135,870,043,838,250,1014,7410,630,181,620,17
2,0999,36
7,4120,588
0,4040,4130,0050,0103,1490,9890,0120,019
1,6330,3672,000
0,0830,0320,115
15,115
2
act-hbl
Bk 10 B1326.11.93
49,990,146,830,024,488,560,2013,9310,650,161,730,21
2,0798,97
7,2440,756
0,4110,4880,0020,0113,0091,0370,0250,017
1,6540,3462,000
0,1400,0400,179
15,179
2
mag-hbl
Bk 1727 q25.7.94
51,720,114,230,043,1410,410,1814,2810,890,011,500,16
2,0698,74
7,5260,474
0,2520,3440,0050,0123,0971,2670,0220,001
1,6980,3022,000
0,1210,0300,151
15,151
2
act
Bk 1728 q25.7.94
52,210,093,780,023,6010,370,2014,3010,950,001,290,13
2,0799,01
7,5740,426
0,2200,3930,0020,0103,0921,2580,0250,000
1,7020,2982,000
0,0650,0250,089
15,089
2
act
Bk 172925.7.94
52,440,073,890,014,0410,350,2714,0810,630,021,500,13
2,0899,50
7,5740,426
0,2360,4390,0010,0083,0311,2500,0330,002
1,6450,3552,000
0,0650,0240,090
15,090
2
act
Bk 17523.7.94
47,420,2110,630,014,379,750,1311,559,030,063,140,30
2,0598,65
6,9321,068
0,7640,4800,0010,0232,5171,1920,0160,006
1,4140,5862,000
0,3040,0570,362
15,362
2
mag-hbl
Bk 17533.7.94
47,180,2010,350,014,369,610,1411,969,250,003,210,32
2,0598,63
6,9071,093
0,6930,4800,0010,0222,6101,1760,0170,000
1,4510,5492,000
0,3620,0610,423
15,423
2
mag-hbl
Bk 17543.7.94
48,700,167,680,035,949,770,3012,319,720,002,470,26
2,0699,40
7,1020,898
0,4220,6520,0030,0182,6761,1920,0370,000
1,5190,4812,000
0,2170,0490,267
15,267
2
mag-hbl
Bk 17553.7.94
46,870,259,160,046,0710,130,3211,019,170,122,750,33
2,0298,25
6,9481,052
0,5480,6770,0050,0282,4331,2560,0400,013
1,4560,5442,000
0,2470,0640,310
15,310
2
mag-hbl
Bk 1749.7.94
54,170,072,850,033,379,560,2415,0510,490,071,440,07
2,0999,50
7,7540,246
0,2350,3630,0030,0083,2111,1440,0290,007
1,6090,3912,000
0,0080,0130,021
15,021
2
act
Bk 1769.7.94
51,880,125,410,035,088,890,2913,629,560,122,080,14
2,0899,30
7,4720,528
0,3900,5510,0030,0132,9241,0710,0350,013
1,4750,5252,000
0,0560,0260,082
15,082
2
act-hbl
Bk 177 q9.7.94
53,510,062,500,032,3810,850,2614,6810,970,061,160,09
2,0798,61
7,7690,231
0,1970,2600,0030,0073,1771,3170,0320,006
1,7070,2932,000
0,0330,0170,050
15,050
2
act
Bk 178 q9.7.94
51,770,124,020,055,2711,100,2112,9510,000,081,790,17
2,0699,60
7,5250,475
0,2140,5770,0060,0132,8061,3500,0260,009
1,5570,4432,000
0,0620,0320,094
15,094
2
act
Bk 17109.7.94
50,820,156,730,155,299,050,2112,969,150,002,470,16
2,0899,22
7,3380,662
0,4840,5750,0170,0162,7891,0930,0260,000
1,4160,5842,000
0,1070,0300,137
15,137
2
act-hbl
Bk 17429.7.94
46,450,2510,090,056,1811,220,1510,429,300,032,850,39
2,0499,42
6,8401,160
0,5910,6850,0060,0282,2871,3820,0190,003
1,4670,5332,000
0,2810,0750,356
15,356
2
mag-hbl
Bk 17509.7.94
50,600,146,680,034,3110,420,4412,539,390,002,550,19
2,0799,35
7,3410,659
0,4830,4700,0030,0152,7091,2650,0540,000
1,4600,5402,000
0,1770,0360,213
15,213
2
act-hbl
Bk 17519.7.94
50,270,167,380,024,879,390,3212,899,460,032,560,20
2,0899,63
7,2510,749
0,5060,5290,0020,0172,7711,1320,0390,003
1,4620,5382,000
0,1780,0380,216
15,216
2
act-hbl
C-50 Appendix C Table C16 amphibole insymplectite
sampleanalysisdate
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2O
H2Ototal
SiAlt
AloFe3CrTiMgFe2MnZn
CaNa
NaK
sum
OH
name
analysis q is in contact with quartz, amphibole names after Leake (1978): ac-hbl is actinolitic-hornblende, act isactinolite, barr is barroisite, ed is edenite, ed-hbl is edenitic-hornblende, mag-hbl is magnesio-hornblende
normed on 23 oxygens, Fe3 over Si+Ti+Al+Fe+Mn+Mg+Ca+Zn = 13
sampleanalysisdate
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2O
H2Ototal
SiAlt
AloFe3CrTiMgFe2MnZn
CaNa
NaK
sum
OH
name
normed on 23 oxygens, Fe3 over Si+Ti+Al+Fe+Mn+Mg+Ca+Zn = 13
Bk 1850 q25.7.94
52,360,034,470,071,318,850,1616,1011,820,221,290,12
2,0898,89
7,5310,469
0,2880,1420,0080,0033,4511,0650,0190,023
1,8210,1792,000
0,1810,0220,204
15,204
2
act
Bk 185125.7.94
50,250,075,450,023,868,390,2314,8711,330,301,480,15
2,0698,46
7,3200,680
0,2560,4230,0020,0083,2291,0220,0280,032
1,7680,2322,000
0,1860,0280,215
15,215
2
act-hbl
Bk 185325.7.94
51,680,065,440,074,007,980,2014,8310,390,211,820,16
2,0898,92
7,4400,560
0,3630,4340,0080,0063,1820,9600,0240,022
1,6030,3972,000
0,1110,0300,141
15,141
2
act-hbl
Bk 18145.8.94
49,650,138,990,113,428,790,1312,778,970,212,940,20
2,0798,38
7,1990,801
0,7360,3730,0130,0142,7601,0660,0160,022
1,3940,6062,000
0,2200,0380,258
15,258
2
mag-hbl
Bk 18155.8.94
52,580,096,060,086,044,690,1015,859,510,232,190,13
2,1399,67
7,4140,586
0,4210,6410,0090,0103,3310,5530,0120,024
1,4370,5632,000
0,0350,0240,059
15,059
2
act-hbl
Bk 1816 q5.8.94
53,160,105,220,052,517,800,1615,4010,130,191,910,11
2,1098,84
7,5880,412
0,4670,2700,0060,0113,2770,9310,0190,020
1,5490,4512,000
0,0780,0200,098
15,098
2
act
Bk 392513.3.93
50,530,176,630,021,088,170,0815,8310,780,112,550,22
2,0798,24
7,3120,688
0,4430,1170,0020,0133,4140,9890,0100,012
1,6710,3292,000
0,3870,0410,428
15,428
2
act-hbl
Bk 392713.3.93
51,450,086,460,023,287,470,1115,5710,250,212,670,18
2,1199,86
7,3260,674
0,4100,3520,0020,0063,3040,8900,0130,022
1,5640,4362,000
0,3010,0330,334
15,334
2
act-hbl
Bk 395224.6.92
49,030,116,990,032,858,680,0914,7610,560,002,680,19
2,0598,01
7,1760,824
0,3810,3140,0030,0093,2201,0620,0110,000
1,6560,3442,000
0,4160,0360,453
15,453
2
mag-hbl
Bk 395324.6.92
49,010,107,840,002,889,060,0813,869,630,003,180,19
2,0597,89
7,1760,824
0,5290,3180,0000,0083,0251,1100,0100,000
1,5110,4892,000
0,4140,0360,450
15,450
2
mag-hbl
Bk 7557.7.92
46,900,1510,550,041,7210,490,1812,079,280,003,580,24
2,0297,22
6,9551,045
0,7990,1920,0050,0122,6681,3020,0230,000
1,4750,5252,000
0,5040,0460,550
15,550
2
edenite
Bk 7437.8.92
46,570,069,650,033,0510,180,1912,4410,010,203,220,21
2,0297,84
•
6,9061,094
0,5930,3410,0040,0052,7501,2630,0240,022
1,5900,4102,000
0,5160,0410,557
15,557
2
edenite
Bk 7477.8.92
47,260,049,510,003,379,640,2112,8610,100,153,100,20
2,0498,48
6,9391,061
0,5840,3720,0000,0032,8141,1840,0260,016
1,5890,4112,000
0,4710,0380,510
15,510
2
edenite
Bk 8514.3.93
49,980,158,950,083,048,070,1213,809,200,163,190,24
2,0999,07
7,1790,821
0,6950,3290,0090,0122,9550,9700,0150,017
1,4160,5842,000
0,3040,0450,349
15,349
2
mag-hbl
Bk 81714.3.93
51,230,036,460,000,628,830,1115,5310,700,192,520,16
2,0898,45
7,3930,607
0,4920,0670,0000,0023,3401,0650,0130,020
1,6540,3462,000
0,3590,0300,390
15,390
2
act-hbl
Bk 81814.3.93
48,240,0510,670,002,868,180,1013,269,370,233,380,26
2,0798,67
6,9801,020
0,7990,3110,0000,0042,8600,9890,0120,025
1,4530,5472,000
0,4010,0490,450
15,450
2
mag-hbl
Bk 856 q14.3.93
54,680,031,130,022,348,490,0617,0211,440,181,070,06
2,0998,61
7,8580,142
0,0490,2530,0020,0023,6461,0200,0070,019
1,7610,2392,000
0,0600,0110,071
15,071
2
act
Bk 857 q14.3.93
54,970,000,560,000,9310,240,0416,6311,870,230,780,03
2,0798,36
7,9500,050
0,0460,1010,0000,0003,5851,2390,0050,025
1,8390,1612,000
0,0580,0060,064
15,064
2
act
Bk 82 q29.1.93b
53,110,083,430,060,709,700,0615,5710,730,181,700,10
2,0697,48
7,7340,266
0,3230,0770,0070,0063,3791,1810,0070,019
1,6740,3262,000
0,1540,0190,173
15,173
2
act
Bk 834 q29.1.93b
54,380,041,500,043,228,400,0416,4911,100,261,180,05
2,0998,79
7,8150,185
0,0690,3480,0050,0033,5321,0100,0050,028
1,7090,2912,000
0,0380,0090,047
15,047
2
act
Bk 9212.7.94
50,130,047,850,070,498,260,1515,4811,650,141,680,24
2,0898,26
7,2370,763
0,5730,0540,0080,0043,3310,9970,0180,015
1,8020,1982,000
0,2720,0450,317
15,317
2
mag-hbl
Bk 9222.7.94
50,370,028,620,040,028,990,0914,7111,270,211,780,22
2,0898,41
7,2550,745
0,7180,0020,0050,0023,1581,0820,0110,022
1,7390,2612,000
0,2360,0410,278
15,278
2
act-hbl
C-51Appendix C Table C16/C17 amphiboleinsymplectite/titanite
sampleanalysisdate
SiO2TiO2Al2O3Fe2O3CaO
total
FH2O
Si
TiAlFe3
Casum
FOH
Bk 10B719.10.93a
30,7536,672,030,4728,90
98,82
0,510,32
1,002
0,8990,0780,011
1,0093,000
0,0530,037
Bk 10B819.10.93a
29,8938,481,380,3028,60
98,65
0,000,52
0,982
0,9510,0530,007
1,0073,000
0,0000,061
Bk 10B919.10.93a
30,0237,341,980,3129,09
98,74
0,010,72
0,981
0,9170,0760,008
1,0183,000
0,0010,083
Bk 10B1019.10.93a
30,4237,151,990,2728,80
98,63
0,000,72
0,995
0,9130,0770,007
1,0093,000
0,0000,083
Bk 17463.7.94
30,1937,791,420,4728,60
98,47
0,270,33
0,992
0,9340,0550,012
1,0073,000
0,0280,038
Bk 17449.7.94
30,5336,252,640,6628,83
98,91
0,330,72
0,992
0,8860,1010,016
1,0043,000
0,0340,083
Bk 396728.1.93
29,9837,411,760,5228,77
98,44
0,530,24
0,984
0,9230,0680,013
1,0123,000
0,0550,026
Bk 391628.7.92
29,7037,781,450,4328,75
98,11
0,370,26
0,980
0,9370,0560,011
1,0163,000
0,0390,029
Bk 392728.7.92
30,2037,032,050,2029,29
98,77
0,790,02
0,985
0,9080,0790,005
1,0233,000
0,0810,002
Bk 39143.7.94
30,3037,551,680,3128,64
98,48
0,120,52
0,994
0,9260,0650,008
1,0073,000
0,0120,060
Bk 39153.7.94
30,4037,081,560,2728,80
98,11
0,250,35
1,000
0,9170,0600,007
1,0153,000
0,0260,041
sampleanalysisdate
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2O
H2Ototal
SiAlt
AloFe3CrTiMgFe2MnZn
CaNa
NaK
sum
OH
name
analysis q is in contact with quartz, amphibole names after Leake (1978): ac-hbl is actinolitic-hornblende, act isactinolite, barr is barroisite, ed is edenite, ed-hbl is edenitic-hornblende, mag-hbl is magnesio-hornblende
normed on 23 oxygens, Fe3 over Si+Ti+Al+Fe+Mn+Mg+Ca+Zn = 13
Bk 96 q23.2.94
52,040,124,990,040,859,160,0515,6211,430,191,390,13
2,0798,09
7,5330,467
0,3840,0930,0050,0133,3701,1090,0060,020
1,7730,2272,000
0,1630,0250,187
15,187
2
act
Bk 9823.2.94
51,450,086,810,001,968,120,1114,7410,050,142,150,14
2,0797,82
7,4350,565
0,5940,2130,0000,0093,1750,9810,0130,015
1,5560,4442,000
0,1580,0260,185
15,185
2
act-hbl
Bk 912 q23.2.94
53,630,054,350,040,079,290,0816,2511,490,111,420,08
2,1098,95
7,6600,340
0,3920,0070,0050,0053,4601,1090,0100,012
1,7580,2422,000
0,1520,0150,167
15,167
2
act
Bk 91323.2.94
50,360,128,090,031,768,810,1213,9510,030,232,370,18
2,0798,13
7,2930,707
0,6740,1920,0030,0133,0111,0680,0150,025
1,5560,4442,000
0,2220,0340,256
15,256
2
act-hbl
Bk 92724.2.94
49,400,008,100,062,737,980,0514,5610,570,112,310,14
2,0798,07
7,1720,828
0,5580,2980,0070,0003,1510,9690,0060,012
1,6440,3562,000
0,2940,0260,321
15,321
2
mag-hbl
Bk 92924.2.94
49,440,148,460,001,699,600,0713,459,990,122,540,21
2,0597,76
7,2210,779
0,6770,1860,0000,0152,9281,1720,0090,013
1,5630,4372,000
0,2820,0400,322
15,322
2
mag-hbl
Bk 9224.3.94
48,770,149,260,053,6810,300,1512,309,960,202,600,25
2,0799,73
7,0590,941
0,6380,4010,0060,0152,6541,2470,0180,021
1,5450,4552,000
0,2740,0470,321
15,321
2
mag-hbl
Bk 9234.3.94
48,770,178,580,002,8310,590,1512,6710,270,162,450,25
2,0698,95
7,1130,887
0,5880,3110,0000,0192,7541,2920,0190,017
1,6050,3952,000
0,2980,0480,345
15,345
2
mag-hbl
Cig 91-17317.6.93
47,670,288,820,000,989,380,0915,0511,680,002,660,33
2,0699,00
6,9391,061
0,4530,1080,0000,0223,2651,1410,0110,000
1,8220,1782,000
0,5720,0630,635
15,635
2
edenite
Cig 91-17417.6.93
45,180,2612,610,021,6310,110,1212,4010,240,003,550,40
2,0498,55
6,6401,360
0,8240,1800,0020,0212,7161,2420,0150,000
1,6120,3882,000
0,6240,0770,701
15,701
2
ed-hbl
normed on 3 kations
C-52 Appendix C Table C17 titanite
sampleanalysisdate
SiO2TiO2Al2O3Fe2O3CaO
total
FH2O
Si
TiAlFe3
Casum
FOH
normed on 3 kations
sampleanalysisdate
SiO2TiO2Al2O3Fe2O3CaO
total
FH2O
Si
TiAlFe3
Casum
FOH
normed on 3 kations
sampleanalysisdate
SiO2TiO2Al2O3Fe2O3CaO
total
FH2O
Si
TiAlFe3
Casum
FOH
normed on 3 kations
Bk 39163.7.94
30,3938,441,180,3628,61
98,98
0,230,26
0,995
0,9470,0460,009
1,0043,000
0,0240,030
Bk 39173.7.94
30,3937,641,530,3228,80
98,68
0,270,34
0,995
0,9270,0590,008
1,0113,000
0,0280,039
Bk 39183.7.94
30,2637,831,130,3928,85
98,46
0,020,44
0,995
0,9350,0440,010
1,0163,000
0,0020,051
Bk 39193.7.94
30,2938,731,020,4028,50
98,94
0,010,42
0,994
0,9550,0390,010
1,0023,000
0,0010,048
Bk 39293.7.94
30,3838,161,300,3028,75
98,89
0,010,49
0,995
0,9390,0500,007
1,0083,000
0,0010,057
Bk 39303.7.94
30,4238,461,080,2828,82
99,06
0,000,42
0,995
0,9460,0420,007
1,0103,000
0,0000,048
Bk 39323.7.94
30,5138,511,010,3228,67
99,02
0,000,41
0,999
0,9480,0390,008
1,0063,000
0,0000,047
Bk 39333.7.94
30,4037,911,390,3928,55
98,64
0,000,55
0,997
0,9350,0540,010
1,0043,000
0,0000,063
Bk 39373.7.94
30,2737,161,870,5828,52
98,40
0,200,57
0,993
0,9170,0720,014
1,0033,000
0,0210,066
Bk 39383.7.94
30,4938,701,040,3828,40
99,01
0,140,30
0,999
0,9540,0400,009
0,9973,000
0,0150,035
Bk 39393.7.94
30,3237,811,400,3828,75
98,66
0,360,23
0,994
0,9320,0540,009
1,0103,000
0,0370,026
Bk 396628.1.93
29,1337,161,460,4828,57
96,80
0,000,62
0,974
0,9340,0580,012
1,0233,000
0,0000,070
Bk 39403.7.94
30,1438,041,160,3928,67
98,40
0,110,37
0,992
0,9420,0450,010
1,0113,000
0,0110,043
Bk 3910,25.5.92
29,4938,400,800,3228,56
97,57
0,020,34
0,981
0,9610,0310,008
1,0183,000
0,0020,037
Bk 3911,25.5.92
30,1636,751,630,5028,84
97,88
0,270,43
0,994
0,9110,0630,012
1,0193,000
0,0280,048
Bk 7462.7.94
29,8037,351,780,3628,78
98,07
0,260,44
0,981
0,9250,0690,009
1,0163,000
0,0270,051
Bk 7472.7.94
30,1436,352,430,2728,54
97,73
0,260,63
0,992
0,9000,0940,007
1,0073,000
0,0270,074
Bk 7482.7.94
30,2438,051,430,1828,99
98,89
0,210,33
0,989
0,9360,0550,004
1,0163,000
0,0220,038
Bk 7492.7.94
30,3438,301,050,3028,76
98,75
0,150,28
0,996
0,9450,0410,007
1,0113,000
0,0160,032
Bk 7512.7.94
30,2137,771,700,2228,71
98,61
0,290,35
0,990
0,9310,0660,005
1,0083,000
0,0300,041
Bk 7187.7.92
29,7535,942,510,2029,07
97,47
0,650,32
0,980
0,8910,0970,005
1,0263,000
0,0680,035
Bk 4127.6.94
30,2637,211,930,2229,02
98,64
0,180,53
0,989
0,9150,0740,005
1,0163,000
0,0190,061
Bk 4227.6.94
30,3637,221,950,2229,03
98,78
0,060,64
0,991
0,9140,0750,005
1,0153,000
0,0060,074
Bk 4327.6.94
30,4737,282,100,1728,92
98,94
0,170,58
0,993
0,9130,0810,004
1,0093,000
0,0180,067
Bk 4427.6.94
30,4837,422,000,2728,98
99,15
0,230,52
0,991
0,9150,0770,007
1,0103,000
0,0240,060
Bk 4527.6.94
30,0736,652,030,1828,95
97,88
0,090,67
0,989
0,9070,0790,004
1,0213,000
0,0090,074
Bk 4627.6.94
30,2937,281,980,2428,91
98,70
0,120,60
0,990
0,9160,0760,006
1,0123,000
0,0120,070
Bk 4727.6.94
30,4637,442,060,2029,06
99,22
0,060,72
0,990
0,9150,0790,005
1,0123,000
0,0060,078
Bk 4827.6.94
30,6437,361,930,2629,03
99,22
0,130,62
0,996
0,9130,0740,006
1,0113,000
0,0130,067
Bk 4927.6.94
30,2938,271,440,2128,97
99,18
0,270,30
0,988
0,9390,0550,005
1,0133,000
0,0280,033
Bk 41027.6.94
30,4937,282,120,1729,01
99,07
0,000,79
0,992
0,9120,0810,004
1,0113,000
0,0000,085
Bk 41127.6.94
30,3737,871,660,1728,90
98,97
0,340,30
0,991
0,9300,0640,004
1,0113,000
0,0350,033
Bk 4649.7.94
30,3339,910,180,4228,91
99,75
0,110,05
0,991
0,9800,0070,010
1,0123,000
0,0110,006
C-53Appendix C Table C17/C18/C19 titanite/ilmenite/dark mica
sampleanalysisdate
SiO2TiO2Al2O3Fe2O3CaO
total
FH2O
Si
TiAlFe3
Casum
FOH
normed on 3 kations
Bk 942.7.94
30,0637,671,690,2628,59
98,27
0,090,54
0,989
0,9320,0660,006
1,0083,000
0,0090,062
Bk 952.7.94
30,0736,902,000,2628,91
98,14
0,230,52
0,988
0,9110,0770,006
1,0173,000
0,0240,060
Bk 9122.7.94
30,1538,211,390,3428,42
98,51
0,160,39
0,991
0,9450,0540,009
1,0013,000
0,0170,046
Bk 9132.7.94
29,4136,851,580,2829,47
97,59
0,350,27
0,972
0,9160,0620,007
1,0443,000
0,0370,032
Bk 9142.7.94
30,3137,371,700,3128,83
98,52
0,410,27
0,993
0,9210,0660,008
1,0123,000
0,0420,031
Bk 9152.7.94
30,2438,111,480,2128,56
98,60
0,360,22
0,993
0,9410,0570,005
1,0043,000
0,0370,025
sampleanalysisdate
SiO2TiO2Al2O3FeOMnOMgONa2OK2O
FH2Ototal
SiAlt
AloTi
FeMgMn
NaK
sum
FOH
Mg/(Mg+Fe)
Cig 91-14117.6.93
34,560,4719,7216,850,0712,130,529,79
0,191,8794,11
2,6471,3383,985
0,4420,0190,461
1,0791,3850,0052,469
0,0770,9771,055
7,970
0,0921,908
0,562
Cig 91-18116.6.93
34,700,1720,7717,480,1311,020,679,05
0,001,9693,99
2,6511,3373,988
0,5330,0070,540
1,1171,2550,0082,380
0,0990,9011,000
7,908
0,0002,000
0,529
Cig 91-18016.6.93
33,690,5120,1018,520,1410,840,598,85
0,341,7793,24
2,6181,3463,963
0,4950,0210,516
1,2031,2550,0092,468
0,0890,8960,985
7,933
0,1671,833
0,511
Cig 91-17916.6.93
33,710,5019,4218,770,0710,920,498,40
0,271,7892,28
2,6441,3393,983
0,4560,0210,477
1,2311,2760,0052,512
0,0750,8590,933
7,904
0,1341,866
0,509
Cig 91-17616.6.93
35,780,3718,6419,100,109,910,409,33
0,001,9493,63
2,7681,3084,076
0,3910,0150,407
1,2361,1430,0072,385
0,0600,9411,001
7,868
0,0002,000
0,480
Cig 91-17516.6.93
34,060,0620,0519,500,169,480,389,70
0,001,9293,39
2,6591,3353,994
0,5100,0030,512
1,2731,1030,0112,387
0,0580,9871,045
7,938
0,0002,000
0,464
Cig 91-17416.6.93
34,300,4919,9319,440,159,920,399,69
0,001,9494,31
2,6531,3373,990
0,4800,0200,500
1,2571,1440,0102,411
0,0580,9771,035
7,936
0,0002,000
0,476
Cig 91-17316.6.93
34,450,3920,6119,720,0910,120,459,54
0,001,9695,37
2,6311,3423,973
0,5120,0160,528
1,2591,1520,0062,417
0,0670,9491,016
7,934
0,0002,000
0,478
Cig 91-15816.6.93
36,180,0920,2315,750,1312,380,259,62
0,002,0094,63
2,7171,3214,038
0,4700,0040,474
0,9891,3860,0082,383
0,0360,9420,978
7,873
0,0002,000
0,583
Cig 91-15716.6.93
35,610,1319,2018,360,0911,350,289,65
0,061,9494,67
2,7161,3214,037
0,4050,0050,410
1,1711,2900,0062,467
0,0410,9591,001
7,916
0,0291,971
0,524
Cig 91-15116.6.93
34,910,0420,1619,120,1210,270,299,50
0,001,9594,41
2,6781,3304,009
0,4930,0020,494
1,2271,1740,0082,409
0,0430,9500,993
7,905
0,0002,000
0,489
sampledateanalysisposition
TiO2FeOMn
total
Ti
FeMn
Bk 730.6.9452rt
52,0643,881,19
97,13
1,019
0,9550,026
Bk 392.7.9423rt
50,3244,152,04
96,51
0,989
0,9650,045
Bk 392.7.9424grt
50,0244,343,06
97,42
0,973
0,9600,067
Bk 392.7.9426grt
55,2638,375,48
99,11
1,062
0,8200,119
Bk 392.7.9427grt
50,5442,665,06
98,26
0,975
0,9150,110
Bk 392.7.9434rt
53,1144,431,4
98,94
1,020
0,9490,030
Bk 392.7.9436rt
51,5545,21,92
98,67
0,992
0,9670,042
Bk 392.7.9441rt
56,7337,911,79
96,43
1,124
0,8360,040
Bk 392.7.9442rt
51,1444,542,08
97,76
0,993
0,9620,045
normed on 22 oxygens, all Fe assumed Fe2
normed on 2 kations
position: grt is ilmenite in garnet, rt is ilmenite in contact with rutile
C-54 Appendix C Table C20 coarse amphibole
sampleanalysisdate
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2O
H2Ototal
SiAlt
AloFe3CrTiMgFe2MnZn
CaNa
NaK
sum
OH
name
analysis vein is amphibole from a vein, amphibole names after Leake (1978): ac-hbl is actinolitic-hornblende, act isactinolite, barr is barroisite, mag-hbl is magnesio-hornblende
normed on 23 oxygens, Fe3 over Si+Ti+Al+Fe+Mn+Mg+Ca+Zn = 13
sampleanalysisdate
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2O
H2Ototal
SiAlt
AloFe3CrTiMgFe2MnZn
CaNa
NaK
sum
OH
name
normed on 23 oxygens, Fe3 over Si+Ti+Al+Fe+Mn+Mg+Ca+Zn = 13
Bk 92023.2.94
45,270,1511,040,054,4310,620,1711,0410,020,122,770,28
2,0197,97
6,7391,261
0,6760,4960,0060,0172,4491,3220,0210,013
1,5980,4022,000
0,3970,0540,452
15,452
2
mag-hbl
Bk 91424.2.94
47,260,3010,260,013,2210,050,0912,039,720,072,810,26
2,0498,13
6,9441,056
0,7210,3570,0010,0332,6351,2350,0110,008
1,5300,4702,000
0,3310,0500,380
15,380
2
mag-hbl
Bk 91524.2.94
48,160,289,900,043,229,990,1411,799,040,173,030,23
2,0498,03
7,0610,939
0,7720,3560,0050,0312,5771,2250,0170,018
1,4200,5802,000
0,2820,0440,325
15,325
2
mag-hbl
Bk 91624.2.94
48,380,408,340,103,259,750,1212,9010,250,182,270,23
2,0498,21
7,0950,905
0,5360,3590,0120,0442,8201,1950,0150,019
1,6100,3902,000
0,2560,0440,300
15,300
2
mag-hbl
Bk 92524.2.94
45,990,2210,270,003,4111,110,1411,4610,160,162,780,29
2,0298,01
6,8381,162
0,6370,3810,0000,0252,5401,3820,0180,018
1,6190,3812,000
0,4200,0560,476
15,476
2
mag-hbl
Bk 92624.2.94
46,740,049,890,023,3010,470,1112,0410,180,102,680,28
2,0297,88
6,9211,079
0,6470,3670,0020,0042,6571,2970,0140,011
1,6150,3852,000
0,3840,0540,438
15,438
2
mag-hbl
Bk 10 B3318.10.93
52,090,075,490,003,326,710,0016,1210,820,701,930,17
2,1099,52
7,4200,580
0,3420,3560,0000,0073,4230,7990,0000,074
1,6510,3492,000
0,1840,0320,216
15,216
2
act-hbl
Bk 10 B3418.10.93
53,010,115,000,010,918,830,0015,9711,180,071,530,14
2,1098,86
7,5800,420
0,4220,0980,0010,0123,4041,0560,0000,007
1,7130,2872,000
0,1370,0260,163
15,163
2
act
Bk 10 B4918.10.93
49,790,106,990,003,308,730,0014,5311,060,001,660,30
2,0798,53
7,2280,772
0,4240,3610,0000,0113,1441,0600,0000,000
1,7200,2802,000
0,1880,0570,244
15,244
2
mag-hbl
Bk 10 B5018.10.93
52,180,105,460,004,377,090,1115,7210,970,251,510,22
2,11100,10
7,4040,596
0,3170,4670,0000,0113,3250,8420,0130,026
1,6680,3322,000
0,0830,0410,124
15,124
2
act-hbl
Bk 10 B5218.10.93
50,370,086,490,004,618,980,1014,1811,080,251,580,30
2,09100,11
7,2380,762
0,3370,4990,0000,0093,0371,0790,0120,027
1,7060,2942,000
0,1460,0560,202
15,202
2
mag-hbl
Bk 10 B5418.10.93
50,520,036,700,044,807,470,1314,6510,820,501,710,25
2,0999,71
7,2450,755
0,3780,5180,0050,0033,1320,8960,0160,053
1,6630,3372,000
0,1380,0470,185
15,185
2
mag-hbl
Bk 10 B5518.10.93
50,260,057,060,092,729,240,0814,5511,180,351,970,29
2,0999,92
7,2220,778
0,4180,2940,0100,0053,1161,1100,0100,037
1,7210,2792,000
0,2700,0540,324
15,324
2
mag-hbl
Bk 10 B219.10.93a
47,240,029,240,006,937,110,0013,5710,780,001,830,37
2,0799,16
6,8591,141
0,4400,7580,0000,0022,9370,8640,0000,000
1,6770,3232,000
0,1920,0700,262
15,262
2
mag-hbl
Bk 10 B319.10.93a
50,200,055,580,004,178,030,1515,0611,260,251,500,27
2,0698,58
7,2980,702
0,2540,4560,0000,0053,2630,9760,0180,027
1,7540,2462,000
0,1770,0510,228
15,228
2
act-hbl
Bk 10 B419.10.93a
50,940,065,320,025,706,790,2415,4311,310,301,240,23
2,0999,67
7,3040,696
0,2030,6150,0020,0063,2980,8150,0290,032
1,7380,2622,000
0,0820,0430,125
15,125
2
act-hbl
Bk 185225.7.94
49,570,048,160,064,408,680,2413,159,690,322,580,25
2,0799,21
7,1700,830
0,5610,4790,0070,0042,8351,0500,0290,034
1,5020,4982,000
0,2250,0470,272
15,272
2
mag-hbl
Bk 185525.7.94
52,850,054,970,044,057,930,2314,749,920,241,830,13
2,0999,07
7,5670,433
0,4060,4360,0050,0053,1460,9490,0280,025
1,5220,4782,000
0,0300,0240,054
15,054
2
act
Bk 185625.7.94
51,720,076,720,045,357,710,2913,388,710,262,560,15
2,0999,05
7,4230,577
0,5600,5780,0050,0082,8620,9250,0350,028
1,3390,6612,000
0,0520,0280,080
15,080
2
act-hbl
Bk 185725.7.94
52,960,055,660,032,416,720,1115,839,870,132,090,12
2,1098,08
7,5730,427
0,5270,2590,0030,0053,3740,8040,0130,014
1,5120,4882,000
0,0920,0220,114
15,114
2
act
Bk 185825.7.94
48,730,067,140,063,918,970,2213,7510,880,281,940,18
2,0498,16
7,1520,848
0,3870,4310,0070,0073,0081,1020,0270,030
1,7110,2892,000
0,2630,0340,297
15,297
2
mag-hbl
Bk 1826.8.94
52,000,198,530,002,759,000,1412,417,490,203,440,14
2,0998,37
7,4650,535
0,9090,2970,0000,0212,6561,0800,0170,021
1,1520,8482,000
0,1100,0260,136
15,136
2
barr
C-55Appendix C Table C20/C21 coarseamphibole/chlorite
analysis vein is amphibole from a vein, amphibole names after Leake (1978): ac-hbl is actinolitic-hornblende, act isactinolite, barr is barroisite, mag-hbl is magnesio-hornblende
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgO
H2Ototal
SiAl t
AloCrTiFe3+Fe2MgMn
OH
Mg/(Mg+Fe2)
Bk 10B1427.11.93grt
24,910,0419,880,016,1620,650,1815,25
11,3298,40
5,2782,7228,000
2,2430,0020,0060,9823,6594,8160,03211,741
19,741
16
0,568
Bk 10B1527.11.93grt
25,250,0119,900,006,0720,370,2315,51
11,3898,72
5,3202,6808,000
2,2620,0000,0020,9623,5894,8710,04111,727
19,727
16
0,576
Bk 10B1919.10.93bgrt
25,470,0218,950,045,6921,730,2114,74
11,2498,10
5,4332,5678,000
2,1970,0070,0030,9143,8764,6860,03811,721
19,721
16
0,547
Bk 10B2419.10.93bgrt
24,920,0319,310,046,0021,160,2514,90
11,2297,83
5,3282,6728,000
2,1940,0070,0050,9663,7834,7480,04511,748
19,748
16
0,557
Bk 10B2527.11.93grt
25,220,0820,130,005,6821,390,1814,15
11,2898,11
5,3622,6388,000
2,4070,0000,0130,9093,8034,4840,03211,648
19,648
16
0,541
Bk 10B2627.11.93grt
24,640,0720,250,016,0621,590,2414,06
11,2498,16
5,2572,7438,000
2,3480,0020,0110,9733,8524,4710,04311,699
19,699
16
0,537
Bk 10B2727.11.93grt
24,770,1119,500,025,7622,190,2213,70
11,1397,39
5,3412,6598,000
2,2960,0030,0180,9354,0004,4030,04011,695
19,695
16
0,524
Bk 10B3227.11.93grt
24,790,0520,280,035,8021,590,2213,70
11,2097,66
5,3092,6918,000
2,4270,0050,0080,9353,8664,3730,04011,654
19,654
16
0,531
Bk 10B3327.11.93grt
25,300,1020,040,035,5521,060,1914,21
11,2697,75
5,3902,6108,000
2,4210,0050,0160,8903,7534,5120,03411,631
19,631
16
0,546
Bk 171425.7.94?
26,730,0619,910,015,5518,130,1917,32
11,6699,56
5,4972,5038,000
2,3220,0020,0090,8583,1185,3090,03311,651
19,651
16
0,630
Bk 171525.7.94?
25,840,0519,840,045,9618,010,3717,20
11,5398,85
5,3742,6268,000
2,2380,0070,0080,9343,1335,3320,06511,716
19,716
16
0,630
sampleanalysisdate
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgOCaOZnONa2OK2O
H2Ototal
SiAlt
AloFe3CrTiMgFe2MnZn
CaNa
NaK
sum
OH
name
normed on 23 oxygens, Fe3 over Si+Ti+Al+Fe+Mn+Mg+Ca+Zn = 13
Bk 1836.8.94
47,390,069,770,004,309,730,1212,069,710,182,770,31
2,0498,44
6,9591,041
0,6490,4760,0000,0072,6391,1940,0150,020
1,5280,4722,000
0,3160,0590,376
15,376
2
mag-hbl
Bk 1846.8.94
52,950,054,970,000,1110,580,1514,259,910,182,090,11
2,0697,41
7,7100,290
0,5630,0120,0000,0053,0931,2880,0190,019
1,5460,4542,000
0,1360,0210,157
15,157
2
barr
Bk 1886.8.94
51,250,158,460,034,359,050,1411,917,300,053,520,13
2,0898,42
7,3940,606
0,8320,4730,0030,0162,5611,0920,0170,005
1,1280,8722,000
0,1130,0240,137
15,137
2
act
Bk 1712 vein9.7.94
50,790,113,340,002,1815,280,5011,9311,830,070,880,17
2,0299,11
7,5470,453
0,1320,2440,0000,0122,6421,8990,0630,008
1,8830,1172,000
0,1370,0330,170
15,170
2
act
Bk 1713 vein9.7.94
51,960,082,200,001,7815,520,4912,1311,840,040,540,12
2,0298,72
7,7240,276
0,1090,1990,0000,0092,6881,9290,0620,004
1,8860,1142,000
0,0410,0230,065
15,065
2
act
Bk 1711 vein9.7.94
52,260,082,150,061,2415,820,5312,1911,950,100,560,12
2,0299,08
7,7420,258
0,1170,1380,0070,0092,6921,9590,0670,011
1,8970,1032,000
0,0580,0230,081
15,081
2
act
Bk 1838 vein25.7.94
51,850,163,020,052,6111,300,2414,1711,270,001,070,10
2,0497,88
7,6330,367
0,1570,2890,0060,0183,1091,3910,0300,000
1,7780,2222,000
0,0830,0190,102
15,102
2
act
Bk 1837 vein25.7.94
53,100,062,340,022,039,730,2115,4511,310,050,880,09
2,0597,31
7,7720,228
0,1750,2230,0020,0073,3701,1910,0260,005
1,7740,2262,000
0,0230,0170,040
15,040
2
act
Bk 1836 vein25.7.94
52,080,154,400,002,1512,420,2513,1410,450,001,750,17
2,0699,01
7,5920,408
0,3480,2360,0000,0162,8551,5140,0310,000
1,6320,3682,000
0,1270,0320,159
15,159
2
act
normed on 28 oxygens, Fe3=Al(t)-Al(o)-Cr-2*Ti
position: grt is chlorite at garnet, pg is chlorite at paragonite, v is chlorite in vein, ? is chlorite at undeterminedtextural position
C-56 Appendix C Table C21 chlorite
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgO
H2Ototal
SiAl t
AloCrTiFe3+Fe2MgMn
OH
Mg/(Mg+Fe2)
normed on 28 oxygens, Fe3=Al(t)-Al(o)-Cr-2*Ti
position: grt is chlorite at garnet, pg is chlorite at paragonite, v is chlorite in vein, ? is chlorite at undeterminedtextural position
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgO
H2Ototal
SiAl t
AloCrTiFe3+Fe2MgMn
OH
Mg/(Mg+Fe2)
normed on 28 oxygens, Fe3=Al(t)-Al(o)-Cr-2*Ti
Bk 171625.7.94?
25,600,0619,960,075,7718,050,4116,49
11,4197,83
5,3812,6198,000
2,3260,0120,0090,9133,1745,1670,07311,674
19,674
16
0,619
Bk 171725.7.94?
25,360,0720,400,046,0518,060,3016,63
11,4798,38
5,3032,6978,000
2,3300,0070,0110,9523,1585,1830,05311,693
19,693
16
0,621
Bk 171825.7.94?
25,030,0819,770,035,9819,290,4615,70
11,2997,63
5,3162,6848,000
2,2650,0050,0130,9553,4264,9700,08311,717
19,717
16
0,592
Bk 171925.7.94?
25,390,0920,640,106,1317,810,3216,82
11,5498,84
5,2782,7228,000
2,3360,0160,0140,9593,0975,2120,05611,691
19,691
16
0,627
Bk 172025.7.94?
25,750,1020,000,065,9618,320,4116,86
11,5398,99
5,3572,6438,000
2,2600,0100,0160,9333,1865,2280,07211,705
19,705
16
0,621
Bk 172125.7.94?
25,680,0720,440,035,8017,780,3716,59
11,4998,25
5,3622,6388,000
2,3920,0050,0110,9123,1045,1630,06511,653
19,653
16
0,625
Bk 172225.7.94?
25,900,0519,720,075,7718,170,2816,91
11,4898,36
5,4132,5878,000
2,2700,0120,0080,9083,1765,2670,05011,691
19,691
16
0,624
Bk 172325.7.94?
25,630,0620,330,076,1318,610,3116,75
11,5799,46
5,3132,6878,000
2,2790,0110,0090,9563,2265,1750,05411,711
19,711
16
0,616
Bk 172425.7.94?
25,480,0720,030,056,0118,520,4516,51
11,4698,58
5,3322,6688,000
2,2720,0080,0110,9463,2425,1500,08011,709
19,709
16
0,614
Bk 172525.7.94v
26,510,0519,130,145,5117,190,3217,83
11,5298,21
5,5182,4828,000
2,2100,0230,0080,8642,9925,5310,05611,685
19,685
16
0,649
Bk 172625.7.94v
26,330,1219,250,135,5717,880,3517,34
11,5198,48
5,4852,5158,000
2,2120,0210,0190,8733,1155,3840,06211,686
19,686
16
0,633
Bk 17309.7.94?
25,870,0619,700,005,7518,000,3216,95
11,4698,10
5,4162,5848,000
2,2780,0000,0090,9063,1515,2900,05711,691
19,691
16
0,627
Bk 17319.7.94?
25,890,0819,680,005,7917,710,3617,22
11,4898,21
5,4092,5918,000
2,2560,0000,0130,9113,0945,3630,06411,699
19,699
16
0,634
Bk 17339.7.94?
25,760,0719,930,005,8418,180,3016,82
11,4898,38
5,3832,6178,000
2,2920,0000,0110,9193,1785,2390,05311,692
19,692
16
0,622
Bk 17349.7.94?
26,320,0219,910,005,5817,420,3317,26
11,5498,38
5,4702,5308,000
2,3460,0000,0030,8723,0285,3460,05811,653
19,653
16
0,638
Bk 17359.7.94?
26,070,0919,670,005,7117,060,3017,66
11,5198,07
5,4342,5668,000
2,2650,0000,0140,8962,9735,4860,05311,688
19,688
16
0,649
Bk 17369.7.94?
26,130,0520,060,005,9417,040,3317,92
11,6399,10
5,3902,6108,000
2,2660,0000,0080,9222,9405,5090,05811,703
19,703
16
0,652
Bk 17379.7.94?
26,310,0419,720,005,7416,960,2517,97
11,5898,57
5,4492,5518,000
2,2620,0000,0060,8942,9375,5470,04411,691
19,691
16
0,654
Bk 17704.7.94v
25,910,1119,130,155,9317,260,3218,02
11,5098,33
5,4042,5968,000
2,1070,0250,0170,9313,0115,6020,05711,749
19,749
16
0,650
Bk 17714.7.94v
25,960,0118,980,115,6716,190,2918,21
11,3996,81
5,4672,5338,000
2,1790,0180,0020,8992,8515,7160,05211,717
19,717
16
0,667
Bk 18206.8.94?
25,150,0021,360,005,9915,410,0917,40
11,4696,86
5,2662,7348,000
2,5370,0000,0000,9442,6985,4310,01611,626
19,626
16
0,668
Bk 18216.8.94?
25,580,0220,520,005,7716,470,1017,25
11,4497,15
5,3632,6378,000
2,4340,0000,0030,9112,8875,3910,01811,643
19,643
16
0,651
C-57Appendix C Table C21 chlorite
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgO
H2Ototal
SiAl t
AloCrTiFe3+Fe2MgMn
OH
Mg/(Mg+Fe2)
normed on 28 oxygens, Fe3=Al(t)-Al(o)-Cr-2*Ti
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgO
H2Ototal
SiAl t
AloCrTiFe3+Fe2MgMn
OH
Mg/(Mg+Fe2)
normed on 28 oxygens, Fe3=Al(t)-Al(o)-Cr-2*Ti
position: grt is chlorite at garnet, pg is chlorite at paragonite, v is chlorite in vein, ? is chlorite at undeterminedtextural position
Bk 18226.8.94?
25,130,0121,120,005,9816,360,1316,93
11,4397,09
5,2752,7258,000
2,5000,0000,0020,9452,8725,2970,02311,638
19,638
16
0,648
Bk 9114.3.94?
27,630,0719,480,035,4915,770,1519,69
11,88100,19
5,5782,4228,000
2,2130,0050,0110,8342,6625,9250,02611,675
19,675
16
0,690
Bk 9134.3.94?
26,590,0419,180,005,3716,170,1818,31
11,4997,33
5,5492,4518,000
2,2660,0000,0060,8442,8215,6950,03211,664
19,664
16
0,669
Bk 9164.3.94?
25,310,0420,620,005,8314,370,1418,21
11,3995,92
5,3292,6718,000
2,4450,0000,0060,9242,5305,7140,02511,645
19,645
16
0,693
Bk 9194.3.94?
27,260,0420,240,045,3816,860,1818,06
11,7999,85
5,5452,4558,000
2,3970,0060,0060,8232,8695,4760,03111,608
19,608
16
0,656
Bk 9204.3.94grt
24,610,0721,000,055,9017,970,1715,41
11,2596,43
5,2482,7528,000
2,5250,0080,0110,9463,2054,8980,03111,625
19,625
16
0,604
Bk 9214.3.94grt
25,590,0321,140,045,8917,510,1916,54
11,5498,47
5,3172,6838,000
2,4940,0070,0050,9213,0425,1230,03311,625
19,625
16
0,627
Bk 93724.2.94?
26,100,0319,750,055,5318,220,1916,66
11,4597,99
5,4662,5348,000
2,3410,0080,0050,8723,1915,2010,03411,651
19,651
16
0,620
Bk 93824.2.94?
26,130,0919,580,095,2518,440,2316,12
11,3797,30
5,5142,4868,000
2,3830,0150,0140,8343,2555,0700,04111,613
19,613
16
0,609
Bk 93924.2.94?
25,600,0419,550,105,5917,870,1816,55
11,3196,79
5,4302,5708,000
2,3170,0170,0060,8923,1705,2320,03211,666
19,666
16
0,623
Bk 94024.2.94?
25,820,0519,970,025,8015,160,1418,54
11,4896,98
5,3942,6068,000
2,3120,0030,0080,9122,6495,7730,02511,682
19,682
16
0,685
Bk 94124.2.94?
25,310,0419,930,035,8414,100,1118,73
11,3495,43
5,3552,6458,000
2,3240,0050,0060,9302,4955,9060,02011,687
19,687
16
0,703
Bk 18255.8.94grt
25,490,0720,600,035,7321,670,3414,01
11,4299,36
5,3542,6468,000
2,4540,0050,0110,9063,8074,3860,06011,630
19,630
16
0,535
Bk 18265.8.94grt
25,440,0720,040,015,6221,000,3814,39
11,3298,27
5,3922,6088,000
2,3980,0020,0110,8973,7234,5460,06811,645
19,645
16
0,550
Bk 18275.8.94grt
25,480,0619,880,015,8121,620,3314,55
11,3899,12
5,3722,6288,000
2,3110,0020,0100,9223,8114,5720,05911,687
19,687
16
0,545
Bk 18295.8.94pg
26,250,0021,450,036,0512,340,2520,20
11,8298,39
5,3292,6718,000
2,4610,0050,0000,9252,0956,1120,04311,641
19,641
16
0,745
Bk 18305.8.94pg
26,210,0021,270,095,9812,070,2220,27
11,7797,88
5,3422,6588,000
2,4520,0150,0000,9182,0576,1580,03811,637
19,637
16
0,750
Bk 186325.7.94?
26,150,0320,170,015,8015,710,2218,41
11,5998,09
5,4112,5898,000
2,3290,0020,0050,9032,7185,6780,03911,673
19,673
16
0,676
Bk 186425.7.94?
25,180,0921,240,015,8715,770,2117,06
11,4396,86
5,2822,7188,000
2,5330,0020,0140,9272,7665,3340,03711,614
19,614
16
0,659
Bk 186525.7.94?
25,890,1021,170,045,8816,210,2517,54
11,6598,73
5,3322,6688,000
2,4710,0070,0150,9112,7935,3840,04411,624
19,624
16
0,658
Bk 994.3.94?
26,200,0620,150,005,7816,280,0918,21
11,6198,37
5,4152,5858,000
2,3240,0000,0090,8992,8145,6100,01611,672
19,672
16
0,666
Bk 9104.3.94?
27,480,1620,220,004,9615,970,1418,14
11,7498,82
5,6142,3868,000
2,4820,0000,0250,7632,7295,5230,02411,546
19,546
16
0,669
C-58 Appendix C Table C21 chlorite
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgO
H2Ototal
SiAl t
AloCrTiFe3+Fe2MgMn
OH
Mg/(Mg+Fe2)
normed on 28 oxygens, Fe3=Al(t)-Al(o)-Cr-2*Ti
sampleanalysisdateposition
SiO2TiO2Al2O3Cr2O3Fe2O3FeOMnOMgO
H2Ototal
SiAl t
AloCrTiFe3+Fe2MgMn
OH
Mg/(Mg+Fe2)
normed on 28 oxygens, Fe3=Al(t)-Al(o)-Cr-2*Ti
position: grt is chlorite at garnet, pg is chlorite at paragonite, v is chlorite in vein, ? is chlorite at undeterminedtextural position
Bk 94224.2.94?
25,970,0420,350,015,8014,390,1118,95
11,5697,18
5,3902,6108,000
2,3680,0020,0060,9062,4985,8620,01911,661
19,661
16
0,701
Bk 94324.2.94?
25,390,0520,010,015,8417,420,1916,87
11,3797,15
5,3572,6438,000
2,3330,0020,0080,9273,0745,3050,03411,683
19,683
16
0,633
Bk 94424.2.94?
25,710,0619,180,035,4318,310,2016,32
11,2696,49
5,4792,5218,000
2,2970,0050,0100,8703,2635,1840,03611,665
19,665
16
0,614
Bk 94924.2.94pg
26,040,0421,240,035,9112,420,2219,82
11,6997,41
5,3412,6598,000
2,4760,0050,0060,9122,1306,0600,03811,627
19,627
16
0,740
Bk 95024.2.94pg
26,240,0520,980,065,5712,470,1419,53
11,6296,66
5,4162,5848,000
2,5190,0100,0080,8652,1526,0080,02411,587
19,587
16
0,736
Bk 95324.2.94pg
26,210,0320,520,085,8212,110,1220,39
11,6596,94
5,3952,6058,000
2,3730,0130,0050,9022,0856,2560,02111,654
19,654
16
0,750
Bk 95323.2.94pg
26,210,0020,800,045,7811,270,1320,63
11,6596,51
5,3942,6068,000
2,4400,0070,0000,8951,9406,3290,02311,632
19,632
16
0,765
Bk 95423.2.94pg
26,150,0321,240,026,0910,640,1121,34
11,7997,41
5,3212,6798,000
2,4160,0030,0050,9331,8106,4730,01911,659
19,659
16
0,781
Bk 95424.2.94pg
25,760,0521,500,046,0412,180,1719,82
11,6897,23
5,2902,7108,000
2,4950,0060,0080,9332,0926,0670,03011,630
19,630
16
0,744
Bk 95724.2.94pg
25,780,0121,270,005,9811,480,1520,23
11,6396,53
5,3152,6858,000
2,4840,0000,0020,9271,9806,2170,02611,635
19,635
16
0,758
Bk 95824.2.94pg
25,220,0420,900,116,0011,300,1519,98
11,4595,16
5,2812,7198,000
2,4390,0180,0060,9461,9796,2360,02711,651
19,651
16
0,759
Bk 95924.2.94pg
25,760,0721,660,055,9811,120,1520,26
11,6896,73
5,2902,7108,000
2,5320,0080,0110,9241,9096,2010,02611,612
19,612
16
0,765
Bk 96024.2.94pg
26,310,1121,270,106,0510,890,1021,30
11,8597,97
5,3282,6728,000
2,4040,0160,0170,9221,8446,4290,01711,648
19,648
16
0,777
Bk 96124.2.94pg
26,180,0220,770,065,7611,660,1320,37
11,6496,60
5,3932,6078,000
2,4370,0100,0030,8932,0106,2550,02311,630
19,630
16
0,757
Bk 96224.2.94pg
25,770,0621,450,035,9610,870,0820,50
11,6596,37
5,3052,6958,000
2,5090,0050,0090,9231,8716,2900,01411,620
19,620
16
0,771
Bk 96324.2.94pg
27,010,0919,670,125,2711,310,0921,06
11,6596,26
5,5632,4378,000
2,3380,0200,0140,8161,9496,4650,01611,617
19,617
16
0,768
Bk 96424.2.94pg
26,620,0519,970,135,5311,080,1121,10
11,6496,22
5,4882,5128,000
2,3400,0210,0080,8571,9106,4840,01911,639
19,639
16
0,772
Bk 96524.2.94pg
26,080,0420,950,086,0410,760,1221,23
11,7397,03
5,3332,6678,000
2,3830,0130,0060,9301,8416,4710,02111,664
19,664
16
0,779
Bk 96624.2.94pg
26,120,0922,040,076,1210,230,0821,25
11,8897,88
5,2762,7248,000
2,5220,0110,0140,9311,7286,3970,01411,616
19,616
16
0,787
C-59Appendix C Table C22 epidote
position: grt is epidote in a chlorite, albite, epidote aggregate after garnet, vein is epidote in a vein
sampleanalysisdateposition
SiO2Al2O3Fe2O3CaO
H2Ototal
Si
AlFe3
Ca
OH
X Al2Fe
Bk 17482.7.94grt
37,4024,6311,1523,48
1,8796,66
2,993
2,3230,6712,994
2,013
1
0,68
Bk 17502.7.94grt
37,8525,2910,3123,40
1,8896,85
3,013
2,3730,6182,991
1,996
1
0,62
Bk 17125.7.94grt
37,1423,8113,2023,18
1,8797,33
2,972
2,2460,7953,041
1,987
1
0,76
Bk 17225.7.94grt
37,7524,9611,6023,31
1,8997,62
2,994
2,3330,6923,025
1,981
1
0,68
Bk 17325.7.94grt
37,6724,7811,9223,40
1,8997,77
2,986
2,3150,7113,026
1,987
1
0,69
Bk 17425.7.94grt
37,4224,7611,5523,56
1,8897,29
2,978
2,3220,6913,014
2,009
1
0,68
Bk 17525.7.94grt
37,6724,3412,3123,49
1,8997,81
2,990
2,2770,7353,012
1,998
1
0,73
Bk 17625.7.94grt
37,8325,2711,2823,30
1,8997,68
2,994
2,3580,6723,029
1,976
1
0,65
Bk 17725.7.94grt
37,8126,1710,1823,70
1,9197,86
2,974
2,4260,6033,029
1,997
1
0,59
Bk 17825.7.94grt
37,5624,7011,8923,32
1,8997,47
2,987
2,3150,7123,026
1,987
1
0,69
Bk 17289.7.94grt
36,8624,1211,6923,09
1,8595,76
2,984
2,3010,7123,013
2,003
1
0,70
Bk 17299.7.94grt
37,4823,3413,0822,99
1,8696,89
3,015
2,2130,7923,004
1,981
1
0,79
normed on 8 cations,all Fe assumed Fe3
sampleanalysisdateposition
SiO2Al2O3Fe2O3CaO
H2Ototal
Si
AlFe3
Ca
OH
X Al2Fe
normed on 8 cations,all Fe assumed Fe3
Bk 183125.7.94vein
38,0426,489,1523,16
1,8996,83
3,015
2,4730,5453,019
1,967
1
0,54
Bk 183225.7.94vein
38,0426,509,0123,25
1,8996,80
3,014
2,4750,5373,012
1,974
1
0,53
Bk 183425.7.94vein
37,4826,819,0623,04
1,8896,39
2,981
2,5130,5423,055
1,963
1
0,51
Bk 183525.7.94vein
36,9025,449,7822,77
1,8594,89
2,993
2,4320,5973,029
1,979
1
0,58
Bk 184725.7.94vein
37,6225,8210,0123,17
1,8896,62
2,997
2,4250,6003,025
1,978
1
0,59
Bk 184825.7.94vein
38,0225,939,5723,36
1,8996,88
3,017
2,4250,5712,997
1,986
1
0,57
Bk 184925.7.94vein
37,7425,799,7123,22
1,8896,46
3,009
2,4240,5833,007
1,984
1
0,58
Bk 18205.8.94grt
37,3524,4012,2023,38
1,8897,33
2,978
2,2930,7323,025
1,997
1
0,71
Bk 18215.8.94grt
37,5623,6813,0723,34
1,8897,65
2,995
2,2260,7843,010
1,994
1
0,78