Primitiv
eCaO-rich
,silica-undersaturate
dmelt
sin
islan
d
arcs
:Evidenc
efortheinvolvemen
tof
clinopyroxene-ric
hlithologie
sinthe
petrogenesi
sofarcmagmas
P.Schiano
Departmen
tde sScience
sdelaTerre(UMR6524),Universit
eÂBlaise-Pascal
,5rue Kessle
r,63038Clermont-Ferrand
cedex, France (schiano@opgc.univ-bpclermont.fr)
Divisio
nofGeologica
landPlanetar
yScience
s(170-25)
,Californi
aInstituteofTechnolog
y,Pasadena
,California
91125
J.M.Eiler
Divisio
nofGeologica
landPlanetar
yScience
s
(
170-25)
,Californi
aInstituteofTechnolog
y,Pasadena
,California
91125 (eiler@gps.caltech.edu)
I.D.Hutcheon
Analytica
landNuclearChemistr
yDivision
,Lawrenc
eLivermor
eNationa
lLaborator
y,P.O.Box808,Livermore,
California 94551 (hutcheon@llnl.gov)
E.M.Stolper
Divisio
nofGeologica
landPlanetar
yScience
s
(
170-25)
,Californi
aInstituteofTechnolog
y,Pasadena
,California
91125 (ems@gps.caltech.edu)
[1]
Abstract
:
Onthebasisofth estudyofolivine-hoste
dmeltinclusion
sinacalc-alka
linebasaltfrom
Bata nIsland
(
Philippines)wedefin eadistinctiv
etyp eofprimitive
,nepheline-no
rmativeislan darc
magmacharacterizedbyunusuall
yhighCaOcontent
s
(
upto19.0wt%)tha tcannotbesimplyexplained
bymeltingofth emetasomatize
dperidotiti
cmantl ewedgeabovesubductin
goceaniclithosphere
.CaO-
richmeltinclusion
swit hthesecharacteristicsar epreserve
dinFo
85±90
olivine ,andcompositional
variation
samongtheinclusion
sareinterpre
tedtoreflec tmixingbetweenmelt ssuchasthosefoundinthe
mostCaO-ric
hinclusion
s
(
presentinFo
90
olivine )andmeltssimilartoprimitiv
e``normal
''islandarc
magma
s
(
trappedinFo
85
olivine)
.Compilatio
nofprimi tiveislan darcmagma
sfromtheliteratureshows
thatwholerock sandolivine-hoste
dmeltinclusion
swit hCaOcontent
s>13wt%arefoundinmanyarc
volcanoe
sfromallovertheworldinadditiontoBatan .Thes einclusion
soccurinlavasrangin gfrom
CaO-ric
hankaramitestobasalticandesite
swit hlow-CaOcontent
s
(
i.e.,<13wt%) .Theglobally
occurrin
gCaO-ric
hinclusion
sandwholerock scompris
eagroupthatalthoug
hdefine donth ebasisof
theirCaOcontent
siscompositiona
llydistinctiv
ewhencompare
dtoislandarclavasthathavelowerCaO
contents
;forexample
,the yhavelowerFeOatagivenSiO
2
contenttha nmostarclavas ,andtheyareall
nephelin
enormative
,wit hnormativ
enephelin
econtent
spositivel
ycorrelate
dwithCaOcontents.
Variation
sinCaOcontentandnormativ
ecomposition
sofexperimenta
lpartialmeltsoflherzolit
erelated
tochange sofpressure
,temperature
,andsourcecompositio
nsuggesttha ttherearenocondition
sunder
whic hpartialmeltingofperidotit
ecangenerat
emelt shavingCaOcontent
sandotherproperties
comparabl
etothos eobserve
dfo rtheprimitive
,CaO-ric
harc-derivedmelt sidentifie
dhere.Although
meltin gofperidotit
eathig hpressur einthepresenc
eofCO
2
canproduceCaO-rich
,silica-poorliquids,
Copyright 200
0
bytheAmerica
nGeophysica
lUnion
G
3
G
3
Ge
ochemistry
Geophysics
Geosystems
Published by
AGU and the Geochemical Society
AN ELECT
RONIC JOUR
NAL OF
THE EA
RTH SCIENCES
Article
V
olume 1
May 30, 2000
P
a
per
n
umber
1999GC0000
32
ISSN:
1525-2027
Geochemistry
Geophysics
Geosystems
weconsid
eritu
nlikel ytha tthi sis
r
espo
nsiblefo rproducin
gtheCaO-rich
,silica-undersaturate
dmelts
considere
dinthisstudybecausetherearesignifican
tdifference
sinnearlyallothe rcompositional
characteristic
sbetwee ntheCaO-ric
har cmagma
sandmeltsknownorthough ttobeproduce
dbymelting
ofcarbonate
dperidotite
.Modelmajorelementcomposition
sofpartialmeltsofclinopyroxene-rich
lithologies
(
mantl epyroxenites
,lowercrusta lpyroxenites
,andeclogite
s)calculatedusingtheME LTS
algorith
msuggesttha tthemostCaO-rich
,nepheline-norm
ativemeltinclusion
sandwholerocks
identifie
dherecouldrepres entintermediat
etohig hdegree
(
10±40wt%)partialmeltsofpyroxenites
atlowercrusta ltouppermantlepressures
.Suchahypothesi
sissupporte
dbythecompariso
nbetweenthe
traceelemen tcomposition
sofmodelpyroxenit
esourcesofth eBatanCaO-ric
hmeltinclusion
sand
naturall
yoccurrin
gpyroxenites
.Themostlikel ysourceoftheprimi tiveCaO-rich
,silica-undersatura
ted
arcmelt sidentifiedhereislowe rcrusta landshallowuppermantlepyroxene-ric
hcumulate
sfromarc
environment
sbecausethesecumulate
shaveCaOconcentration
sattheupperendoftherang eobserved
formantl epyroxenites
.Theyar etherefor
emorelikel ytoyiel dpartialmelt swiththerestricte
drang eof
remarkabl
yhig hCaOcontent
softhemostCaO-ric
hinclusion
sandwholerock sidentifiedhere.
Moreove
r,thes ecumulate
softencontainamphibole
,whichwouldlowe rtheirsolidu stempera
tures
relativetoth eanhydrou
spyroxenit
eequivalent
stovaluesmoreconsisten
twiththoseexpecte
dindeep
crusta lorshallowsubarcenvironments.
Keywords
:
Meltinclusions
;ar clavas.
Inde
xterms
:
Chemica
levolution
;geochemica
lcycles;majorelementcomposition.
Receive
d
Novembe
r16,1999;
Revise
d
March9,2000;
Accepte
d
March15,2000;
Published
May 30, 2000.
Schiano, P., J. M. Eiler, I. D. Hutcheon, and E. M. Stolper, 2000. Primitive CaO-rich, silica-undersaturated melts
in island arcs: Evidence for the involvement of clinopyroxene-rich lithologies in the petrogenesis of arc magmas,
Geochem.
Geophys.
Geosyst
., vol. 1, Paper
number
1999GC000032
[15,276
words,
11 figures,
2 tables].
1. Int
roduction
[2] K
Mostislandarclava sarebelievedtobe
derivedfrommagma
sformedbypartialmelt-
ingofth emantleoverlyin
gsubductin
gocea-
niclithosphere
,wheremeltingisfluxedby
metasomati
cenrichmen
tinwater
(
andother
elements
)carriedbyaqueou
sfluid sand/or
silicatemelt sreleasedfromth esubducted
oceaniccrust[e.g.,
Nicholl
sandRingwoo
d
,
1973].Themantlesourcesonwhichthis
coupledenrichment-meltin
gproces soperates
arethough ttobeper idotitessimi lartoor
somewha
tmoredepletedthanthesourcesof
mid-ocea
nridgebasalts
(
MORBs
)[
Tatsum
iet
al
.,1986;
Davidso
n
,1987;
Nohd
aandWas-
serbu
rg
,1981;
Ryerso
nandWatso
n
,1987].
Thetraceelementcharacteristic
sofar clavas
e.g. ,thei rhi ghconcentrati onsoflarge- ion
lithophil
eelement
s
(
LILE)andthei rrelatively
lowconcentration
sofhigh-fiel
dstrengthele-
ments
(
HFSE))an dtheirmajorelementcom-
position
sareinfluence
dbythemetasomatism,
andhighthermodynami
cactivitie
sofH
2
O
stronglyaffectthecomposition
sofprimary
magma
sandtheirsubsequen
tdifferentiation
sequence
s[see
Stolpe
randNewma
n
,1994,
andreference
stherein].
[3]K
Althoug
hcouple
dmetasomatis
mand
fluxedmeltin gofperidotite
sinth emantle
wedgeisbelievedtobethedominan
tprocess
bywhichprimaryar cmagma
sform,somearc
magma
shavealsobeenpropose
dtoformby
May 30, 2000.
G
3
SCHIANO
E
T
A
L.:
CaO-RICH MELTS IN ISLAND ARC
S
1999GC000032
Geochemist
r
y
Geophysics
Geosystems
G
3
me
l
t
i
n
g
o
f
n
onperidotitic sources: for example,
partial melting of subducted crust [
Defant and
Drummond
, 1990;
Drummond and Defant
,
1990;
Kay
,1978],meltingatdeepcrustal
levels [
Pichler and Zeil
, 1972], and melting
of an ocean island basalt-type source [
Ito and
Stern
, 1985] have all been proposed. In this
article, we document a distinctive type of
primitive, nepheline-normative island arc mag-
ma characterized by unusually high CaO con-
tents
(
up to 19 wt %) that cannot be simply
reconciled with the standard model of arc
petrogenesis described above. Although arc-
derived samples with these characteristics
have been previously reported [
Metrich et
al
., 1999;
Sisson and Bronto
, 1998;
Della-
Pasqua and Varne
, 1997;
Gioncada et al
.,
1998;
Metrich and Clocchiatti
, 1996;
Foden
and Varne
, 1980;
Foden
, 1983;
Kennedy et
al
., 1990;
Carr and Rose
, 1984;
Thirwall and
Graham
, 1984;
Shimizu and Arculus
, 1975;
Arculus
, 1976], they have not been recognized
as a coherent, globally occurring magma type
or as distinct from CaO-rich magmas found in
oceanic island [
Tronnes
, 1990], mid-ocean
ridge [
Kamenetsky et al
., 1998;
Sours-Page
et al
., 1999], and back arc [
Kamenetsky et al
.,
1997] settings. After documenting the exis-
tence of this distinctive magma type, empha-
sizing in particular a well-defined group from
Batan Island
(
northernmost Philippines, Lu-
zon-Taiwan arc), but also showing that such
magmas occur in arcs from around the world,
we examine the compositions of CaO-rich,
silica-undersaturated magmas in subduction
zone settings with the following objectives in
mind:
(
1) to provide a compilation of the
occurrences and compositions of such mag-
mas;
(
2) to examine their relationship to more
typical magmas in subduction zone settings;
(
3) to estimate plausible chemical and miner-
alogical characteristics of their sources; and
(
4) to evaluate the implications of their ex-
istence for models of melt generation in sub-
duction zones.
2. Definition of a Distinctive
CaO-Rich, Silica-Undersaturated
Magma Type From Subduction
Zone Settings
2.1. CaO-Rich, Silica-Undersaturated
Melt Inclusions in Olivine Phenocrysts in
Lavas From Batan Island
(
Northernmost
Philippines, Luzon-Taiwan Arc)
2.1.1. Sample description, analytical
techniques, and results
[4]
The geologic setting of Batan Island and the
petrography of its principal rock types
(
basalts,
basaltic andesites, and andesites) are described
by
Richard et al
. [1986]. Plagioclase, olivine,
and clinopyroxene dominate the phenocryst
assemblages of the basalts, while basic and
acid andesites contain phenocrysts of clinopyr-
oxene, hornblende, plagioclase, and titanomag-
netite. Sample B45 from Mount Iraya, the
youngest
(
2.32 to <0.1 myr) volcano on Batan
Island [
Richard et al
., 1986], is a high-MgO
(
10.8 wt %) calc-alkaline basalt [
Metrich et al
.,
1999;
Richard et al
., 1986]. Compositions of
primary melt inclusions in olivine phenocrysts
(
Fo
90±75
) from this sample were determined on
glasses produced after heating each inclusion
up to its homogenization temperature
(
i.e., the
temperature at which the inclusion contents
(
gas, glass, and crystals) homogenized visually
to a uniform melt phase). Heating experiments
were performed with a high-temperature, opti-
cal heating-stage apparatus [
Sobolev et al
.,
1980] that allowed visual monitoring of indi-
vidual melt inclusions during heating. Homo-
genization temperatures were 1220 20
8
C, and
effective times of quenching were <1 s. Com-
parison between the compositions of homoge-
nized and unheated glass inclusions trapped in
olivine phenocrysts with similar forsterite con-
tent shows that the amount of host olivine
needed to be added to the unheated glass
inclusions to get the heated ones is relatively
G
3
SCHIANO
ET AL.:
CaO-RICH MELTS IN ISLAND ARCS
1999GC000032
Geochemistry
Geophysics
Geosystems
G
3
s
mall
(
15
%in
w
e
ight). Consequently, the
effect of the heating procedure on the concen-
trations of elements other than MgO
(
and to a
lesser extent FeO and SiO
2
) is relatively small,
and therefore the main conclusions of the paper
would be unchanged if unheated inclusions
were considered. It should be noted that this
statement applies not only to the Batan samples
but also to those in the compilation that will be
presented later in this article.
Table 1.
Representative Major and Trace Element Compositions of Homogenized Melt Inclusions in
Olivine in a Calc-Alkaline Basalt
(
B45) From Batan Island
(
20
8
25
0
N±121
8
54
0
E, Luzon-Taiwan Arc)
a
Sample Identification
B7-1 B7-2 B2-1
B4
B1-2 B1-1 B5-1 B8-1 B6-1
SiO
2
, wt %
44.02 45.05 44.00 45.61 44.10 44.04 45.89 49.42 54.73
TiO
2
, wt %
0.70
0.64
0.79
0.67
0.94
0.76
0.74
0.91
0.98
Al
2
O
3
, wt % 16.01 16.87 14.92 16.58 16.13 16.02 16.43 15.39 14.44
FeO*, wt %
7.31
6.80
8.86
8.02
8.82
8.85 12.27 11.11
8.84
MnO, wt %
0.12
0.10
0.15
0.14
0.14
0.15
0.20
0.18
0.19
MgO, wt %
8.30
8.27
8.96
8.36
7.67
7.72
6.71
7.17
5.63
CaO, wt %
18.54 17.08 17.20 16.27 17.20 17.06 11.57 10.22
7.48
Na
2
O, wt %
2.58
2.56
2.43
2.53
2.29
2.60
2.75
3.05
3.29
K
2
O, wt %
0.93
1.01
0.86
1.01
0.90
1.01
1.40
1.43
2.17
Cr
2
O
3
, wt %
0.05
0.04
0.05
0.08
0.04
0.03
0.08
0.08
0.03
SUM
98.57 98.42 98.20 99.26 98.23 98.24 98.02 98.95 97.77
HOST
Fo
89
Fo
89
Fo
89
Fo
87
Fo
86
Fo
86
Fo
78
Fo
79
Fo
78
Ba, ppm
219
214
185
237
136
245
215
323
423
Th, ppm
2.12
2.18
1.57
2.32
1.04
2.87
2.06
3.74
6.75
U, ppm
0.63
0.57
0.38
0.49
0.31
0.67
0.39
0.91
1.37
Nb, ppm
2.20
2.26
4.40
2.35
2.09
2.83
2.68
4.00
6.17
Sr, ppm
537
539
498
490
398
571
536
663
561
Zr, ppm
56.1
60.7
52.6
58.6
47.0
66.9
62.7
90.2 124.7
Y, ppm
17.3
17.0
19.9
14.1
13.4
17.1
17.9
26.7
25.2
Sc, ppm
53
44
62
43
56
48
N.D. N.D. 26
La, ppm
9.21
9.39
8.31
9.10
7.45 10.52
9.11 13.13 18.40
Ce, ppm
21.4
20.9
18.4
21.2
15.7
24.9
19.8
31.5
43.3
Nd, ppm
14.3
14.2
12.3
13.6
10.7
19.3
13.2
22.4
26.2
Sm, ppm
3.15
2.99
2.61
3.00
1.95
3.49
2.86
4.33
4.99
Eu, ppm
0.95
0.92
0.67
0.85
0.57
0.99
0.83
1.30
1.26
Dy, ppm
2.81
2.95
2.47
2.58
1.94
3.01
2.46
4.56
4.56
Er, ppm
2.09
2.01
1.85
1.82
1.21
2.07
1.93
3.42
3.32
Yb, ppm
2.34
2.26
2.26
2.09
1.39
2.31
2.25
3.77
3.37
a
Major element compositions were measured with the Caltech 5-spectrometer JEOL 733 microprobe using an accelerating voltage of
15Kv, a sample current of 10nA anda defocused beam
(
size
20
m
m). Data were reduced using a modified ZAF procedure
(
CITZAF
[
Armstrong
, 1988]). The reproducibility and accuracy of the Na measurements were tested on glass standards. The abundances of Sr, Y,
Zr, Nb, Ba, rare earth elements, Th, and U were determined with the Lawrence Livermore National Laboratory
(
LLNL) ion microprobe, a
modified Cameca IMS-3f instrument, using a 17 keV,
16
O
primary ion beam, focused into a
20-
m
m-diameter spot. Positive secondary
ions were extracted and accelerated, nominally to 4500 V. A field aperture inserted in the sample image plane allowed only ions from the
central 30-
m
m-diameter area of the imaged field to enter the mass spectrometer. Isobaric molecular interferences were minimized by
energy filtering, using a 40-eV window and offsetting the accelerating voltage by 100 V from the voltage at which the energy distribution
of
16
O
+
dropped to 10% of its maximum value. Trace element concentrations were determined from
42
Ca-normalized ion intensities
using sensitivity factors established from analyses of a suite of silicate glass and mineral standards. Each analysis consisted of 8±10
cycles over the masses of interest. On the basis of analyses of NIST glass standards
(
NBS-610, -612, and -614, using the concentrations
given by
Pearce et al
. [1997], the accuracy varies between 3 and 10% for Sr, Y, Zr, Ba, La, Ce, Nd, Er, and Yb, between 10 and
15% for Nb, Th, Sm, and Dy, and between 15 and 25% for U and Eu. Sc analyses were carried out at a mass resolving power of 4000
and zero energy offset, using a 2-nA
16
O
primary ion beam. The
42
Ca-normalized ion intensities were converted to concentrations using
sensitivity factors established from analyses of NIST standard glass SRM 612.
G
3
SCHIANO
ET AL.:
CaO-RICH MELTS IN ISLAND ARCS
1999GC000032
Geochemistry
Geophysics
Geosystems
G
3
100
30
20
10
0
10
20
0.0
0.4
0.8
1.2
1.6
200
300
400
10
20
30
40
50
60
40
Normative
nepheline(%)
Normative
hypersthene(%)
e
U
(ppm)
h
CaO (wt%)
20
16
12
8
4
g
Ba (ppm)
f
Sc (ppm)
trend B
CaO (wt%)
20
16
12
8
4
2
4
6
8
10
12
FeO* (wt%)
d
2
4
6
8
10
0
MgO (wt%)
c
80
85
90
Host forsterite (%)
a
75
45
50
55
60
SiO
2
(wt%)
b
trend A
LEGEND
Batan samples
< 13 % CaO melt inclusions (i.e., trend A)
> 13 % CaO melt inclusions (i.e., trend B)
< 13 % CaO whole rocks (i.e., trend A)
G
3
SCHIANO
ET AL.:
CaO-RICH MELTS IN ISLAND ARCS
1999GC000032
Geochemistry
Geophysics
Geosystems
G
3
[
5
]
H
o
m
o
g
enize
d inclusions were analyzed for
major and minor elements using the electron
microprobe at Caltech and for trace elements
(
Sc, Sr, Y, Zr, Nb, Ba, rare earth elements
(REE), Th, and U) using the ion microprobe
at the Lawrence Livermore National Labora-
tory
(
Table 1; see footnote for analytical pro-
cedures). The inclusions range in composition
from nepheline-normative basalt to quartz-nor-
mative dacite; major element variations in these
glasses are illustrated in Figure 1. The CaO and
MgO contents decrease from 18.5 to 5.0 wt %
and 9.5 to 1.3 wt %, respectively, as SiO
2
increases from 44.3 to 63.7 wt %. Variations
in the compositions of melt inclusions are well
correlated with the Mg# of their host olivines,
with the most SiO
2
-poor and CaO- and MgO-
rich inclusions trapped in the most magnesian
olivines
(
Fo
90
) and the most SiO
2
-rich and
CaO- and MgO-poor inclusions trapped in the
least magnesian olivines
(
Fo
75
).
[6]
Trace element compositions of olivine-
hosted melt inclusions are also well correlated
with major element composition: for example,
Sc content decreases from 65 to 20 ppm and
incompatible trace elements increase regularly
as CaO decreases
(
Figures 1f±1h). The mid-
ocean ridge basalt
(
MORB)-normalized trace
element patterns of the inclusions
(
Figure 2a)
aretypicalofarcmagmas
(
i.e.,enrichedinLILE
and depleted in HFSE and in high REE
(
HREE)
relative to MORB; enriched in low REE
(
LREE) relative to HREE); these trace element
features are thought to reflect melting of mantle
sources depleted with respect to the sources of
MORBthathavebeenmetasomatizedbyaslab-
derived, H
2
O-rich component [
Stolper and
Newman
, 1994]. Note that although the incom-
patible element concentration variations are
correlated with major element composition,
the La/Yb ratio does not increase as the CaO
content decreases
(
Figure 2a).
[7]
Although in most variation diagrams the
melt inclusions and previously analyzed whole
rocks from Batan [
Richard et al
., 1986;
Maury
et al
., 1998;
McDermott et al
., 1993] define a
single trend, with the CaO-rich inclusions fall-
ing on a continuous extension of the trend
defined by the inclusions with lower CaO con-
tents, Figure 1d shows that this is not the case
for FeO: that is, the CaO-rich inclusions define
a population offset toward lower FeO contents
from the trend of whole rocks and lower-CaO
inclusions. For the purposes of later discussion,
we refer to the trend defined by the Batan whole
rocks and lower-CaO inclusions as trend A and
the higher CaO, lower FeO trend as trend B.
Note that inclusions from trends A and B do not
occur in the same olivine phenocrysts. The
distinction between trends A and B is also
illustrated in Figure 3, in which the composi-
tions of the melt inclusions and Batan whole
rocks were first recalculated to equivalent CaO-
MgO-Al
2
O
3
-SiO
2
(
C-M-A-S) [
O'Hara
, 1968;
Basaltic Volcanism Study Project
, 1981] and
then projected from alumina onto the S-C-M
plane. Also shown on this diagram are experi-
mentally determined trends for olivine + clin-
Figure 1.
CaO variation diagrams comparing melt inclusions
(
circles) in olivine phenocrysts from B45
basalt from Batan Island
(
Luzon-Taiwan arc)
(
this study and
Metrich et al
. [1999]) with Batan whole rocks
(
triangles) [
Richard et al
., 1986;
Maury et al
., 1998;
McDermott et al
., 1993]. Trend A
(
open symbols)
comprises low-CaO melt inclusions and all Batan whole rocks and is interpreted as due to progressive
fractionation of olivine + clinopyroxene + amphibole
(
see Figure 3); trend B
(
dotted circles) comprises the
CaO-rich inclusions and is interpreted as due to magma mixing between liquids similar to the most CaO-rich
inclusions in trend B
(
i.e., in the Fo
90
olivines) and melts near the most primitive end of trend A. Normative
compositions are calculated assuming Fe
3+
=0.15
P
Fe. Half-solid circles and triangles in Figure 1e are
quartz normative samples.
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L
a (p
pm)
C
/
C
N
-
M
O
R
B
L
a
/
Y
b
C
a
O = 17.2 wt%
CaO = 17.1 wt%
CaO = 16.3 wt%
CaO = 11.6 wt%
CaO = 10.2 wt%
CaO = 7.5 wt%
Batan melt inclusions
}
}
trend A
trend B
Er
10000
1000
100
10
1
1
10
100
1000
b
Ti
Ce
K
U
Ba
Yb
Dy
Nd
Sr
La
Nb
Th
Zr Eu
Y
0.1
1
10
100
Sm
a
< 13 % CaO melt inclusions (i.e., trend A)
> 13 % CaO melt inclusions (i.e., trend B)
Oceanic and continental nephelinites
Oceanic and continental melilitites
Carbonatites
Nephelinites from SW Japan
Figure 2.
(a) Normal mid-ocean ridge basalt (NMORB)-normalized diagram showing trace element data
for melt inclusions in olivine phenocrysts in B45 basalt from Batan Island. The order of elements is based on
the incompatibility sequence during MORB petrogenesis [
Hofmann
, 1988]. Compositions are normalized to
the average NMORB composition of
Hofmann
[1988]. (b) Plot of La/Yb ratio versus La concentration
comparing data for Batan melt inclusions with data for primitive melilitites [
Wilson et al
., 1995], nephelinites
from oceanic and continental regions [
Wedephol et al
., 1994;
Hoernle and Schmincke
, 1993], nephelinites
from SW Japan [
Tatsumi et al
., 1999], and carbonatites from Africa, Australia, Europe, and North and South
America [
Nelson et al
., 1988]. Symbols are given in the accompanying legend, and the distinction between
trend A and trend B for the Batan samples is the same as in Figure 1.
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o
p
y
roxe
n
e+p
lagioclase-saturated liquids at 1
atm and olivine + clinopyroxene + amphibole-
saturated liquids at 2 kbar
(
H
2
O saturated)
[
Tormey et al
., 1987;
Grove and Bryan
, 1983;
Walker et al
., 1979;
Grove et al
., 1982;
Caw-
thorn and O'Hara
, 1976;
Sisson and Grove
,
1993] and the trend of whole rocks from the
Tonga arc
(
SW Pacific), a typical tholeiitic arc
series [
Ewart et al
., 1973, 1977;
Gill
, 1981].
2.1.2. Compositional evolution of Batan melt
inclusions
[8]
The observation that the most CaO-rich and
SiO
2
-poor melts are trapped in the most for-
LEGEND
Batan samples
> 13 % CaO melt inclusions (i.e., trend B)
<13 % CaO melt inclusions (i.e., trend A)
<13 % CaO whole rocks (i.e., trend A)
Tonga arc
<13 % CaO tholeiites
Ol-CPx-Pl
cotectic trend
Ol-Cpx-Amp
cotectic trend
S
CM
80
30
80
30
olivine
diopside
amphibole
plagioclase
trend A
trend B
Projection from Al
2
O
3
wt.%
Tonga
wollastonite
enstatite
Figure 3.
Compositions of Batan melt inclusions
(
circles) and whole rocks
(
triangles) recalculated to
equivalent CaO-MgO-Al
2
O
3
-SiO
2
(
C-M-A-S) and then projected from alumina onto the S-C-M plane. The
distinction between trend A
(
open symbols) and trend B
(
dotted circles) for the Batan samples is the same as
in Figure 1. Also shown on this diagram are experimentally determined trends for olivine-clinopyroxene-
plagioclase-saturated melts at 1 atm and olivine-clinopyroxene-amphibole-saturated liquids at 2 kbar
(
H
2
O-
saturated) [
Tormey et al
., 1987;
Grove and Bryan
, 1983;
Walker et al
., 1979;
Grove et al
., 1982;
Cawthorn
and O'Hara
, 1976;
Sisson and Grove
, 1993] and the trend of whole rocks
(
shaded triangles) from the Tonga
arc
(
SW Pacific), a typical tholeiitic arc series [
Ewart et al
., 1973, 1977;
Gill
, 1981]. Plagioclase and
amphibole compositions are from [
Tormey et al
., 1987;
Grove and Bryan
, 1983;
Walker et al
., 1979;
Grove et
al
., 1982;
Cawthorn and O'Hara
, 1976;
Sisson and Grove
, 1993]. Analyses have been recalculated as
CMAS components by following a modified version [
Basaltic Volcanism Study Project
, 1981] of the
procedure used by
O'Hara
[1968]. The procedure is as follows: C =
(
CaO
P
2
O
5
/3 + K
2
O + 2Na
2
O)56.08;
A=
(
Al
2
O
3
+Cr
2
O
3
+Fe
2
O
3
+Na
2
O)101.96; M =
(
MgO + FeO + MnO)40.30; S =
(
SiO
2
2Na
2
O
4K
2
O)60.08. All oxides are in molecular proportions.
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s
t
e
ritic oliv
i
ne crystals
(
F
i
g
u
r
e
1
a
)
s
u
g
g
e
s
t
s
t
h
a
t
t
h
e
C
a
O
-
r
i
c
h
,
s
i
l
i
ca-undersaturated melts are
relatively primitive. In this section, we evaluate
the origin of the compositional variation from
this primitive end of the array of melt inclusion
compositions to the CaO-poor, SiO
2
-rich com-
positions contained in the least forsteritic oli-
vines.
[9]
One possible explanation for the relation-
ship between melt inclusion composition and
the Mg# of the host olivine is that composi-
tional variations in melt inclusions represent a
trend of fractional crystallization. However,
although the correlated decreases in the Mg# of
thehostolivinesandtheMgOandCaOcontents
of the inclusions would be consistent with frac-
tional crystallization of a clinopyroxene oli-
vine-bearing assemblage, such a fractionating
assemblage
(
assuming the clinopyroxene to be
compositionally similar to the diopside, augite,
or salite phenocrysts in Batan lavas [
Richard et
al
., 1986]) could not readily account for the
decreaseinnormativenephelinewithdecreasing
CaO content shown in Figure 1e
(
i.e., crystal-
lization of such an assemblage from nepheline-
normative liquids typically results in increasing
rather than decreasing normative nepheline
[
Sack et al
., 1987]). Likewise, although frac-
tional crystallization of assemblages dominated
by nepheline-normative minerals such as am-
phibole, jadeite, or acmite could, in principle,
decrease the normative nepheline contents of
residual liquids, it would not decrease their
CaO contents.
[10]
Figures 1b±1d show that trend A
(
defined
by melt inclusions) is typical of the composi-
tional trend of whole rock analyses of lavas
from Batan
(
shown as triangles in Figure 1).
As indicated above, Figure 1d also demon-
strates the important point that trend B, de-
fined by the CaO-rich inclusions, is not
simply an extension or continuation of the
compositional trends of arc lavas from Batan;
this point is also made in Figure 3, where the
CaO-poor melt inclusions and whole rocks
defining trend A follow the olivine-clinopyr-
oxene-amphibole cotectic but the trend B melt
inclusions fall off this cotectic. The correspon-
dence of trend A to the olivine-clinopyroxene-
amphibole cotectic suggests that the composi-
tional variations of Batan whole rocks could
primarily reflect relatively low pressure crys-
tallization of an amphibole-bearing assem-
blage from low-CaO, high-FeO parental
melts comparable to those with
12 wt %
CaO trapped in Fo
85
olivine. This consistency
of major element variations in Batan lavas
with fractional crystallization of an amphi-
bole-bearing assemblage agrees with the con-
clusions of several previous studies [
Richard
et al., 1986; Maury et al., 1988; McDermott et
al
., 1993]. Notethatthetholeiitictrendofwhole
rocklavasfromtheTongaarcshowninFigure3
contrasts with the Batan trend and suggests the
Tonga trend is produced by low-pressure frac-
tionation of an olivine-clinopyroxene-plagio-
clase assemblage. This hypothesis is supported
by mass balance calculations [see
Gill
, 1981,
page 272] that indicate that fractionation of an
olivine-clinopyroxene-plagioclase assemblage
can account quantitatively for major element
variation within the Tonga volcanic suite.
[11]
We thus conclude that trend A, comprising
the low-CaO Batan melt inclusions and the
Batan whole rock lavas, can be interpreted
relatively simply in terms of progressive ex-
traction of olivine + clinopyroxene + amphi-
bole from a parental basaltic liquid with
12
wt % CaO and 8±10 wt % MgO, but that
trend B cannot be explained as readily by
crystallization differentiation. Likewise, pro-
gressive partial melting of a peridotitic source
is unlikely to account for trend B, since this
would produce a positive correlation between
CaO and FeO if the source contains residual
clinopyroxene [e.g.,
Kinzler and Grove,
1992a,
b;
Baker and Stolper
, 1994;
Hirose and Kush-
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Table 2.
Representative Major Element Compositions of the CaO-Rich, Silica-Undersaturated Melt Inclusions and Whole Rocks in Island Arcs
Identified in This Study
a
Host Arc
Volcano Sample SiO
2
TiO
2
Al
2
O
3
FeO* MnO MgO CaO Na
2
OK
2
OP
2
O
5
Cr
2
O
3
Sum Reference
Inclusion Fo
89
Java Galunggung J-1 45.00 1.20 19.20 6.04 0.09 4.39 18.70 3.07 0.53 0.14 N.D. 98.45 S&B
(
98)
Inclusion Fo
88
F-1 43.90 1.28 18.40 7.53 0.09 4.99 18.40 3.49 0.66 0.18 N.D. 99.03 S&B
(
98)
Inclusion Fo
84
I-E 44.20 1.30 19.20 8.60 0.10 4.10 17.70 2.70 0.42 0.12 N.D. 98.57 S&B
(
98)
Inclusion Fo
94
Vanuatu Merelava 31551 46.20 0.49 13.68 8.87 0.09 12.47 15.53 1.55 0.56 0.41 N.D. 99.98 D&V
(
97)
Inclusion Fo
91
31551 45.88 0.46 14.07 8.87 0.02 12.18 15.89 1.59 0.52 0.37 N.D. 99.98 D&V
(
97)
Inclusion Fo
91
E. Sunda Rindjani 48002 43.39 1.13 15.35 9.36 0.05 11.77 15.24 2.43 0.98 0.16 N.D. 100.00 D&V
(
97)
Inclusion Fo
90
48001 45.49 0.93 14.23 8.57 0.14 9.54 17.76 1.85 1.33 0.16 N.D. 100.13 D&V
(
97)
Lava
48001 48.32 0.69 10.53 9.05 0.17 14.02 14.38 1.50 0.90 0.15 N.D. 99.85 F
(
83)
Inclusion Fo
90
Eolian Stromboli ol5/b118 48.88 0.75 12.97 6.51 N.D. 8.16 13.78 1.85 1.59 0.32 N.D. 94.91 M&C
(
96)
Inclusion Fo
90
Vulcano IV88.1 44.46 0.55 11.69 7.82 0.15 8.50 15.58 2.63 3.67 0.43 0.05 95.65 G
(
98)
Inclusion Fo
90
IV88.3.1 45.34 0.80 9.99 7.92 0.11 8.94 15.30 2.34 3.04 0.44 0.06 94.40 G
(
98)
Lava
N. Guinea Lihir
L3 47.35 0.76 12.46 10.36 0.21 9.12 14.73 2.90 0.44 0.36 N.D. 98.85 K
(
90)
Lava
L6 47.24 0.90 12.69 10.37 0.21 7.47 13.12 2.15 2.23 0.49 N.D. 97.03 K
(
90)
Lava
Nicaragua N.D.
CR-T 43.74 1.75 13.81 9.39 0.15 8.87 15.26 2.66 1.03 0.90 N.D. 97.70 C&R
(
84)
Lava
Lesser Grenada 6155 46.93 0.97 16.16 9.39 0.17 7.57 14.53 1.82 1.01 0.20 N.D. 98.88 T&G
(
84)
Lava
Antilles
450 47.17 0.96 15.58 10.01 0.18 7.06 14.43 2.12 0.52 0.12 N.D. 98.31 T&G
(
84)
Lava
503 45.60 0.95 15.91 8.53 0.18 10.95 13.50 1.88 1.01 0.40 N.D. 99.04 S&A
(
75)
Inclusion Fo
89
Luzon
Batan B45/53 44.33 0.73 16.74 7.19 0.12 8.18 18.07 2.72 0.91 0.37 N.D. 99.91 M
(
98)
Inclusion Fo
89
B45/43a 46.98 0.64 14.03 7.82 0.14 8.95 17.50 2.51 0.96 0.17 N.D. 100.14 M
(
98)
Inclusion Fo
89
B45/43b 44.92 0.77 15.68 8.93 0.15 8.79 17.36 2.44 0.83 0.64 N.D. 101.05 M
(
98)
a
FeO* is total iron reported as FeO. N.D., not determined. References: S&B
(
98),
Sisson and Bronto
[1998]; D&V
(
97),
Della-Pasqua and Varne
[1997]; F
(
83),
Foden
[1983]; M&C
(
96),
Metrich and Clocchiatti
[1996]; G
(
98),
Gioncada et al
.[1996];K
(
90),
Kennedy et al
. [1990]; C&R
(
84),
Carr and Rose
[1984]; T&G
(
84),
Thirwall and Graham
[1984]; S&A
(
75),
Shimizu and Arculus
[1975]; M
(
98),
Metrich et al
. [1998].
SCHIANO
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CaO-RICH MELTS IN ISLAND ARCS
1999GC000032
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Geophysics
Geosystems
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iro
, 1993], contrary to what is observed for
trend B
(
Figure 1d). Moreover, as discussed
below
(
see section 4.1), trend B probably
cannot be explained by progressive melting of
a pyroxene-rich lithology at a constant pressure,
because current estimates suggest that progres-
sive melting of pyroxenite results in liquids
with increasing CaO and decreasing normative
nepheline, contrary to the observed trend.
[12]
Our preferred explanation for the composi-
tional variation among the CaO-rich inclusions
(
i.e., those defining trend B) is that it represents
a mixing trend between the most CaO-rich
inclusions
(
i.e., those in the Fo
90
olivines) and
melts near the most primitive end of the ``nor-
mal'' Batan trend that we have defined as trend
A. Figures 1 and 3 demonstrate that this can
indeed explain the trend B. Although it is
difficult to test this explanation for trend B
using only the chemical compositions of melt
inclusions, in principle, isotopic differences
between inclusions along the compositional
array or detailed petrographic investigation of
whole rocks on this trend could be used to
evaluate this hypothesis.
2.2. Compilation of the Occurrences and
Compositions of CaO-Rich,
Silica-Undersaturated Melts in
Subduction Zone Settings
[13]
We compiled from the literature the com-
positions of arc-related whole rock samples
Galunggung
Batan
Stromboli
Lihir
Nicaragua
Grenada
Lombok
Rindjani
Epi
Merelava
Vulcano
LEGEND
> 13% CaO arc lavas
> 13% CaO melt inclusions
> 13% CaO arc lavas and melt inclusions
Figure 4.
Map showing the locations of the CaO-rich, silica-undersaturated whole rocks and melt
inclusions mentioned in the text. Solid circles indicate locations where CaO-rich inclusions have been found,
open squares indicate locations where CaO-rich whole rocks have been found, and solid squares indicate
locations where both have been found.
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a
nd
oli
v
i
n
e-hosted melt inclusions having
CaO contents >13 wt %
(
Table 2). In addi-
tion to the Batan inclusions (this study and
Metrich et al
. [1999]), whole rocks and melt
inclusions with CaO contents >13 wt % are
found in volcanoes from many convergent
margins
(
Figure 4), including Galunggung
(
Sunda arc), Stromboli and Vulcano (Aeolian
arc), Lihir
(
New Guinea), Nicaragua
(
Central
America), Grenada
(
Lesser Antilles), Lombok
(
Sunda arc), Rindjani
(
Sunda arc), and Epi and
Merelava
(
Vanuatu arc) [
Sisson and Bronto
,
1998;
Della-Pasqua and Varne
,1997;
Gioncada
et al
., 1998;
Metrich and Clocchiatti
, 1996;
Foden and Varne
, 1980;
Foden
, 1983;
Kennedy
et al
., 1990;
Carr and Rose
, 1984;
Thirwall and
Graham
, 1984;
Shimizu and Arculus
, 1975;
Ar-
culus
, 1976].
[14]
All the inclusions reported in Table 2 are
hosted by Mg-rich olivine
(
Fo
84±94
) in basalts,
basaltic andesites, or ankaramites. As was
done for the Batan samples reported here, they
were homogenized by high-T experiments to
reverse postentrapment crystallization of the
host crystal [
Roedder
, 1984;
Schiano and
Bourdon
, 1999], with the exception of inclu-
sions from Galunggung [
Sisson and Bronto
,
1998], which were instead corrected by oli-
Figure 5.
Variation diagrams comparing Batan
CaO-rich melt inclusions
(
i.e., trend B) and CaO-
rich melt inclusions and whole rocks from other arc
environments
(
all of which have CaO > 13 wt %)
with ``normal'' melt inclusions and whole rocks
from Batan and other arcs
(
all of which have CaO
contents < 13 wt %)
(
shaded triangles without dot,
1350 basalts with MgO > 4.5 wt % from 30 arcs,
compiled by
Plank and Langmuir
[1988]. Shaded
circles without dot, melt inclusions in olivine
phenocrysts from
Gioncada et al
. [1998] and
Sisson
and Layne
[1993]). Symbols are given in the
accompanying legend. FeO* is total iron reported
as FeO. Major element concentrations have been
normalized to 100%.
FeO* (wt%)
CaO (wt%)
SiO
2
(wt%)
6
10
14
18
0
5
10
15
Al
2
O
3
(wt%)
25
20
15
10
2
40
45
50
55
60
65
LEGEND
Batan samples
> 13 % CaO melt inclusions (i.e., trend B)
< 13 % CaO melt inclusions (i.e., trend A)
< 13 % CaO whole rocks (i.e., trend A)
other arcs
> 13 % CaO melt inclusions
< 13 % CaO melt inclusions
> 13 % CaO whole rocks
< 13 % CaO whole rocks
CaO (wt%)
0
5
10
15
20
SiO
2
(wt%)
40
45
50
55
60
65
a
b
c
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