Tectonophwm,
411
187 (1991) 411-419
Elsevier Science Publishers
B.V., Amsterdam
High Ni in Archean Nicholas Max-Planck-Institut (Received
tholeiites
T. Arndt
ftir Chemte, Postfach 3060. D-6500 Matn:, FRG *
June 1, 1989; revised version accepted
July 5. 1989)
ABSTRACT Amdt. N.T.. 1991. High Ni in Archean 411-419.
tholeiltes.
In: J.L. Le Mou?l (Editor).
Beyond
Plate Tectonics.
Tectonoph,vsm.
187:
Archean tholeiites generally have h&her Ni, Co. Cr and Fe than most younger tholentes with similar MgO contents. These characteristics cannot be attributed to high T or P batch melting in the Archean mantle. because, although such melts are enriched in siderophile elements, they have higher MgO than normal tholeiites. As primary melts fractionate to lower MgO. they lose Ni, Co and Cr. Nor can the differences between Archean and younger tholeiites be attributed to secular variation in mantle compositions because Archean komatiites have Ni. Co, Cr contents similar to modern (Gorgona) komatiites. It is auggesied that the high siderophile element content of Archean tholeiltes results from mixing of either komatiitic with basaltic magmas. as might occur in an ascending, melting mantle plume or column, or of komatilte and more evolved rocks. as may take place when komatiite encounters and assimilates crustal rocks
Introduction Archean tholeiitic basalts are reported to have higher Ni, Co, Cr and Fe contents than younger tholeiites. Glickson (1971) observed that Ni contents in tholeiitic basalts in the Archean Yilgarn Block of Australia are higher than in modern oceanic basalts. and similar claims have been made by Gill and Bridgwater (1976) for the Ameralik dykes in Greenland; by Jolly (1975) for basalts in the Abitibi belt in Canada; by Jahn et al. (1980) for Finnish volcanics; and by Nesbitt and Sun Fig.
(1976), Gill (1979) and Condie (1984) in broader surveys. There is also general agreement that the Cr, Co and probably Fe contents of Archean volcanics are higher than in their younger equivalents (e.g. Glickson, 1971; Condie, 1984). In this paper I reconsider the differences in siderophile elements abundances in Archean and modern basalts, review some of the theories that have been
1. Histogram
elements
from Condie.
island
continental
propose
basalts
concentrations
basalts;
flood basalta:
to account
= mid-ocean
RI/? = rift
for these
a new explanation
address:
35042 Rennes
0040.1951/91/$03.50
lnstltut
de Geologie,
UniversltC
Rennes
Elsevier Science Publishers
ridge basalt;
basalts;
CFB =
differences,
and
for the enrichment. in Archean rocks:
Figure 1 illustrates some data that have been used to support the concept that Archean basalts
1,
Cedex, France.
0; 1991
basalts (data
IAB = island arc basalts.
Siderophile element enrichment the evidence * Present
of siderophlle
with those in modem
1984, table 1). MORB
OIB = oceanic
proposed
comparing
in Archean
B.V.
NT
412
have higher concentrations than
modern
has&s.
of siderophile
Shown
the average Ni, Co, Cr. and Fe contents normalized Condie
the
show conspicuous
from
five different
illustrated tents
compared
a similar
of Archean
enrichment
with modern
in
ferences
between
The modern
regimes.
Gill (1979)
obvious.
between
the Ni con-
Ni contents
ridge basalts (MORB)
Ascension
mid-ocean
modern
come
basafts
with relatively
oceanic (Weaver
from
(OlB)-White Naldretr Arndr Archean
and Vetter (1984):
et al. (1979). Feigenson
and Turner and Jenner
(1977). Arndt
(I?%),
age and Corgona
2a. but
plotted
at :t smaller
agram shows that komatiites are no
arc basalts
(lABI--Thorpe
et al. (1983). Weaver et al. (1987); Archean (unpublished
Arndt
and Nesbitt
data):
(;orgona data are from Briigmann
(1982).
(1982). Barnes (1985). Smith and Erlank et al. (1987):
scale
so that
Archean
Morris
(1982). Arndt
picrite
data
in
et al. (1984). tux
and
et al. (1982). Rautenschlein
et al. (1983): oceanic
hasalts-Hallberg
data from Neshitt (1986). Arndt
from
Weaver et al. (1987).
BVSP (1981).
the
komatiIsland, The di-
with concentrations
(1972). Nesbltt
(1982), Jahn Ed al. (1980. 1982). Redman
data). (b) MgU versus Ni plot &wing picritrs.
basalt
the Ni contents of Archean higher than in the Gorgona
et al. (1977). Sun et al. (1979). Schilling
and some modern
flood
compositions of Archenn and “modern” ites (the Tertiary Iavas from Gorgona Echeverria, 19X0) can also be plotted,
and Nesbitt {19X2). Smith and Erlank
and Arndt Island
island
(MORB)-Langmuir
et al., 1987). the
continentai
Fig. 2. iaf Xi contents uf Archean &oieiitts icirclesj plotted as a function of MgU content, and compared modern basal& Sources of data include: ail suites-BVSP (1981); continental flood hasaits (fFB)-Duncan ridge basalts
high
such as
sarily to the composition of the Archean mantle. Figure 2b shows data similar to those in Fig.
island basalts (OIB) and to a lesser extent, continental flood hasalts (CFB). These characteristics are in general accord with the observations of Gill (1979) and Condie (1954), in that when the predominant basalt types in each age group are com-
(1985). Fodor
islands
less
tents of Archean basalts might owe their origin to peculiarities of the environment of melting beneath Archean greenstone belts. and not neces-
generally higher than in modern MORB and IAB. but overlaps concentrations in modern oceanic
mid-ocean
basalis
sequences such as the Karoo (Duncan et al., 1984). These observations suggest that the high Ni con-
plotted against MgO content, and compared with Ni abundances in modern basalts. It can be seen that at any given MgO content, Ni contents of Archean basalts vary widely. The total range is
Hawkesworth
not considered
et al., 1979) and Hawaii (Feigensen
et al., 1983) and
in another greenstone
belts (data sources are given in the figure caption),
(1985);
Archean in Ni con-
in Fig. 2 are due
and Archean
from
and Gough
Azores (White
and island arc basalts (IAB).
Figure 2a shows the Ni abundances set of tholeiitic basalts from Archean
with
from sources
basalts
tectonic
and modern
IAB
a differertce
by Gill (1979) and Condie (1984) have been taken into account. which make the systematic dif-
contrast basalts
and
The differences
to the fact that data
from
hasalts
MORB
belt tholeiites).
tent is apparent.
of basahs.
of 60, taken
all four elements
(modern
greenstone
are
(1984, table 2). In this representation,
Archean
to a Mg number
pared
elements
in the diagram
AKNDT
compositions and Jenner Clarke
and Sun (1976),
and Keays {1985),
of knmatiites
and Sun {1976), Jahn Duncan
and basaits
of
et al. 11980. 1982),
(1986) and Arndt
(1970).
et al.
island basalts
(unpublished
er al. (1984) and
HIGH
‘J, IN AKCHF-ZN
komatiites.
Data
413
THOLEIITES
from both komatiite
on a single array, essentially
suites
a fractional
plot
crystalli-
zation trend that projects
to Ni contents
those of modern
basalts,
and lower than those in
most
basalts.
Archean
picrites,
such as those
and the Karoo province, the Archean
Modern from
Baffin
similar
to
indistinguishable.
but
and
Not only are the modern
they plot
noncumulate
majority
of Archean
Bay, Hawaii
of some OIB and CFB also argues against variation.
Although
phile elements
komatiites.
for high Ni, Co, Cr and Fe
out.
lustrated
lower
komatiites
on a trend
to Ni contents
ruled Previous explanations
these arguments.
of Archean
extends
plot on the same trend as
and modern
Fig. 2 reinforce Ni contents
basalts. minor
that
those
of a
The high Ni content enrichment
in the Archean
the more
than
pronounced
mantle
secular
of siderocannot
be
differences
il-
in Figs. 1 and 2 must have another
cause.
in Archean tholeiites Explanations for elevated siderophile abundance in Archean tholeiites fall groups:(a)
The high concentrations
ment of siderophile the basalts in the
elements Archean
elements into two
reflect emich-
in the source(s) of upper mantle (e.g.
Glickson, 1971; Gill, 1979). (b) The high concentrations result from different conditions of partial melting in the Archean mantle (e.g. Nesbitt and Sun, 1976; Condie, 1984). Siderophile
element enrichment
in the Archean man-
tle Support for the idea that the Archean mantle was enriched in siderophile elements comes not only from the compositions of Archean tholeiites, but also from apparently high Fe in the lunar mantle (Jagoutz and Wgnke, 1982), and from the “ Pb paradox”; the anomalously high ‘O’Pb/ lo4Pb in modern oceanic basalts. It is argued that the Moon and the Earth were derived from material enriched in siderophile elements, and that since the Archean the Earth’s mantle has become depleted in siderophile elements, as well as in Fe and Pb. as a result of core growth (e.g. Vollmer, 1977; Vidal and Dosso, 1978; Jagoutz and Wgnke, 1982). These ideas were questioned by Newsom et al. (1986) who cited a lack of correlation between Pb isotopic compositions and ratios of siderophile to lithophile elements (e.g. Pb/Ce, Mo/Pr, W/Ba) as evidence against the loss of siderophile elements to the core, and by Briigmann et al. (1987) who cited similar noble element abundances of Archean and modern komatiites as evidence for an essentially constant upper mantle composition throughout geological time. The data plotted in
Unusual melting conditions in the Archean
mantle
There are a number of variants of this explanation. In its simplest form, high temperatures in the Archean mantle degrees of partial magmas enriched
are supported to lead to high melting and to the formation of in siderophile elements. Melting
at high pressures can have the same result (Nesbitt and Sun, 1976). The enrichment is further enhanced by a decrease in partition coefficients with increasing temperature and pressure. Experimental studies by Hart and Davis (1978). Arndt (1977) and Bickle et al. (1977) show that 0;;‘;“” (the olivine-silicate liquid partition creases markedly with increasing
coefficient) temperature,
deand
the same is probably true for Co and Cr. Melts produced at high temperatures will therefore contain higher concentrations of these elements than melts produced
at lower temperatures.
The problem with such arguments is that an increase in T, P or percentage melting results in enrichment not only in siderophile elements, but also in MgO content or Mg number. The relationship between the Ni and MgO contents of mantle melts and the conditions of melting are shown in Fig. 3: a 75% partial melt has indeed four times the Ni content of a 5% partial melt, but it also has a high MgO content; a melt produced at 3 GPa has high Ni, hut also high MgO. The comparisons between the Ni contents of Archean and modern basalts discussed in the previous section were made at specific, relatively low MgO contents. Gill (1979) pointed out that as a highly magnesian primary melt evolves to lower MgO. olivine crystallization extracts Ni so efficiently that when the high temperature-high pres-
N.T. ARNDT
414
MgO (wt%)
(a) Fig. 3. (a) Calculated
compositions
crystallization
of melts
produced
by batch
of such melts. Sources of data and method
melting
in the mantle.
of calculation
(b) The paths
followed
by fractional
are given in the text and Appendix.
sure melt reaches a reference MgO value (e.g. 6% MgO; Fig. 3) it has a lower Ni content than
curvature and a steep slope at the high-MgO end. Because of this curvature, magmas formed by the
typical low temperature-low pressure conclusion applies for all reasonable
mixing of melts have higher Ni contents than batch melts with similar MgO contents (Fig. 6).
melts. This and inter-
nally consistent choices of melting conditions and partition coefficients. (The calculation presented
This observation provides an explanation high Ni of Archean tholeiites; namely
by Condie (1984, table 3) is questionable because the relatively high Ni content of his fractionated high temperature melt stems from the use of an unrealistically low Ni partition coefficient (2.62.8). Calculation using an incremental method in which the partition coefficient is redetermined after each small increment of olivine is subtracted (Appendix) yields lower Ni in evolved liquids, as
parental products
contents. But is the Ni content of mixed magmas sufficiently enhanced to account for the Ni enrichment
illustrated
in Archean
in Fig. 3.)
Similar arguments can also be made for Co, and for Cr, which would be stripped from the melt by fractional crystallization of chrome spinel. Another explanation for the high concentrations of these elements in Archean tholeiites is therefore needed.
for the that the
magmas of the Archean basalts are the of mixing between komatiite and basalt
or less magnesian melts or rocks, whereas the parental magmas of most modern tholeiites are mixtures of magmas with lower MgO and Ni
tholeiites,
and
are there
geologically
reasonable situations in which such mixing could take place? To test the model two types of mixed magmas Mixing
are considered. between mantle melts
Archean tholeiites as the products of mixing between komatiite and other magma or rock types
The eruption temperature of picrites and komatiites greatly exceed those of common basaltic magmas. Modern picrites probably reach the
The foundation of this explanation is given in Fig. 3 which shows the compositions of liquids produced by batch melting in the mantle. The manner in which these compositions were calculated is described in the Appendix. The compositions of batch melts fall on a line with a marked
surface at temperatures close to 1500°C and the most magnesian Archean komatiites probably erupted at temperatures exceeding 1600 o C. Typical eruption temperatures of MORB rarely exceed 1200 o C. This contrast has led to the suggestions in recent papers that the anomalously high magnesium contents of picrites and komatiites reflect
Hl(;H
N, IN ARC Ht.AN
anomalously sources. Bickle
THOLEIITFS
high
temperatures
McKenzie (1988)
komatiites
415
(1984)
propose
in their
and
that
modern
form in “hot jets”
in regions of lithospheric
Campbell
et al. (1989) have developed
the formation
of komatiites
mantle.
According
basalt
and
material
extension
while
a model for
plumes
ascend-
layer deeper
to this model, komatiite
forms by melting and
within
boundary
and
picrites
of mantle
ascending
ing from a thermal
mantle
McKenzie
in the magma
in the hot axial jet of the plume
by melting
in the cooler
5
head of the
10
IS
20
MgO (wt%)
plume. Both
situations
provide
an
environment
in
which highly magnesian magmas penetrate regions in which basaltic magmas are being produced, and under these conditions mixing between the two types of magma is inevitable. The Ni contents of the mixed magmas can be determined by considering two extreme situations: (a) simple mixing between komatiite and basalt end-members: and (b) mixing or pooling of the entire range of magmas produced within the melting region. The former situation might apply when komatiite mixes with basalt in a starting mantle plume; the latter corresponds to the “integrated melts” (Klein and Langmuir, 1987) that form by pooling of melts within a rising, melting mantle column beneath a spreading centre. Figure 4 shows the Ni contents of simple mixed melts and Fig. 5 the Ni contents of integrated melts. The Ni contents of both lie well above the batch-melt curve.
Fig. 5. Composition duced
by pooling
column The
and crystallization of melts
(squares).
paths
equilibrium
paths
in an ascending.
PO = the pressure
followed
by fractional
crystallization
(EC)
of magmas melting
at whxh crystallization
of the 5GPa
pro-
mantle
melting (FC)
starts. and
melt are also
shown.
However, it must be questioned whether this difference in Ni contents is sufficient to account for the high Ni of Archean
tholeiites.
The paths
followed by the two mixed melts as they evolve to lower MgO contents via olivine crystallization are also shown in Figs. 4 and 5. A simple mixed melt with 15% MgO evolves to a basalt with only about 70 ppm at the 6% MgO reference value (Fig. 4 and Table 1); another with 20% MgO evolves to a basalt with about 60 ppm Ni. Similar Ni contents are calculated for the magmas that evolve from the integrated melts shown in Fig. 5. Thus. if the melts evolve solely through fractional crystallization. the enhanced
Ni content
of the mixed melts
are insufficient to account for high Ni in Archean tholeiites. If, however, the melt evolved by equilibrium rather than fractional crystallization, the Ni content of the final liquid is higher. The product of equilibrium
crystallization
of the 15% MgO
simple mixed melt has about 150 ppm Ni: the product from an integrated melt with similar MgO has about 140 ppm. These values are comparable
MgO (wt%) Fig. 4. Composition magma and
produced
basalt
(square) by simple
(7% MgO)
path;
and mixing
melts.
EC = equilibrium
crystallization of komatiite
FC = fractional crystallization
paths
of a
(30% MgO) crystallization path.
to concentrations in Archean tholeiites (Figs. 1 and 2). The presence in komatiite lavas of olivine phenocrysts with unzoned cores and compositions in equilibrium with the host komatiite (e.g. Amdt, 1986) may be taken as evidence that during the ascent and emplacement of these magmas equilibrium crystallization was common. However,
K T ARNDT
416
TABLE
librium
1
Calculated
MgO (wt%) crystallization
5% meltmg at
F(g)
Ni (ppm)
*
from batch melt;
9.5
300
Evolved melt
6.0
80
crystallization
ment
Evolved melt Fractional
6.0
45
crystallization
Parent Evolved melt Equilibrium
Fractional
1140
6.0
50
crystallization
from integrated
19.0
984
6.0
41
Equilibrium
crystallization
Evolved melt Assimilation
from integrated
6.0
Evolved melt Assimilation
32
80
6.0 of granite
Assimilation
into
tholeiites
will increase
the evolved
magmas.
These
quantitatively,
however,
magma
abundances
processes
in
melts in
the parental
of Archean
cannot
because
in be
Co par-
at high P are poorly known
and
of komatiite
A second mechanism komatiite with basaltic
70
rocks,
of granite
205
55
magma
103
63
364
compositions
an increment
(see Appendix).
50
from Figs. 3-5.
and AFC
happen
parent which process cooling accompanying
by komatiite,
crystallization
may
during
the
passage
of
positions ranging from basaltic to granitoid. Crystallization will accompany contamination. and the liquid evolves via fractional or equilibrium crystallization. Again it is not immediately ap-
crystallization: 6.0
as
involves contamination of or more evolved crustal
komatiite through the basement or lower sections of greenstone belts. The contaminant has com-
by komatiite.
6.0
Evolved melt
paths
calculated
of 1%; equilibrium Ratio of fractionation
paths
numeriby mass
to assimilation
is 0.5. * F-percent
enriched
in high pressure
and admixture
Contamination
crystallization:
using
Cr are strongly
argu-
melt, 5 GPa:
crystallization:
Evolved melt
balance
43
of basalt by komatiite,
Assimilation
Fractional
which
in similar
pressure melt component. As explained by Langmuir and Hanson (1980) high-pressure melts are relatively enriched in Fe and are not depleted in Fe during crystallization.
melt, 5 GPa:
2300
6.0
Evolved melt
Parental
29
150
31
equilibrium
elements
siderophile
Cr contents of fractionated basalts are dominated by largely unpredictable chromite fractionation. The high Fe contents of Archean tholeiites are entirely consistent with the presence of a high-
43
crystallization:
fractional
tholei-
of basalt by komatiite,
Parent
equilibrium
which range
in Archean
are enriched
Co and
tition coefficients
from simple mixed melt: 173
Evolved melt
fractional
19.0
6.0
Parent
Ni contents
and probably
modelled
54
from simple mixed melt:
crystallization
Evolved me1 t
cally
1130
other
tholeiites
hold.
general.
from batch melt:
22.0
the
komatiite.
10
5’S melting at 3 GPa: Parent
ites. For Archean
1 GPa:
Parent
Fractional
to produce
up to the high levels observed
melt compositions
Fractional
paths,
crystallized.
strong zoning in other phenocrysts and the presence of xenocrysts in these and other lavas (Nisbet et al., 1987) indicate that re-equilibration between olivine and the evolving magma was imperfect. Likely crystallization paths for the high pressure magmas fall between the fractional and equi-
is the more likely, but slow contamination in a middle
to lower crust magma chamber probably involves some measure of equilibrium crystallization. As in the previous case, the model involving fractional crystallization produces basaltic melts with relatively low Ni contents, whereas equilibrium crystallization results in basalts with enhanced Ni contents. Examples of four basaltic melts produced by assimilation accompanied by fractional crystallization (AFC) and by equilibrium crystallization (AEC), with a basaltic and a granitoid contaminant, are listed in Table 1. At this stage it might be asked whether mixing is really necessary: could not the Archean tholeiites have evolved simply by equilibrium crystalli-
H,<;H
i-4, IN ARCHFAN
zation
of more magnesian
Fig. 4, shows batch
417
7HOLEIlTF.S
melts
250/O MgO Equilibrium
that
may
produce
Reference
crystallization
with MgO contents
high Ni contents. dance,
equilibrium
do not produce crystallization
komatiite geological
parents?
less than
nature
can it account differences
an evolved
of
/
,
/
I
,
/
,
I
Batch
_,
about
liquid
but such a mechanism
of most Archean
for the trace element
between
I
1
the required result. of more magnesian
grounds: it cannot explain the uniform composition
porphyritic
1500
to
komatiites
and
with
fails on the abunand non-
tholeiites,
nor
and isotopic tholeiites.
MgO (wt%)
In
comparison to komatiites, Archean basalts are usually enriched in incompatible elements (e.g. Nesbitt and Sun, 1976; Jahn et al., 1980; Gill, 1979; Redman and Keays. 1985) and have more evolved isotopic compositions (e.g. lower c:Nd f. These characteristics, which can be attributed to a component of low-degree melt in the parental mixed magmas. and/or to interaction with crustal
Fig. 6. Compositions
of mixed.
may be the Ni-enriched and
continental
flood
low MgO content
parents basalts
melts
mid-ocean
that
hi&P.
high MgO melts that
of oceanic (CFB).
and
island basalt (OIB) the mixed.
are the parents
low-P.
of Ni-depleted
ridge basalts (MORB).
rocks, are inconsistent with the concept that the basalts are simply crystallization products of
the base of the oceanic crust. Magmas that form in this environment are mixtures are melts that plot on the flat, low-MgO end of the batch melt
komatiite
curve and have relatively
parental
magmas.
low Ni contents.
High Ni contents of modem OIB and CFB
Conclusion
The mixing mechanisms advocated for the Archean basalts might also explain the relatively high Ni contents in many modern oceanic island
The relatively high concentrations of Ni and other siderophile elements in Archean tholeiites can be explained if the parental magmas result from mixing between komatiite and basaltic or
and continental flood basalts (Fig. 2). There is general agreement that OIB forms in plumes ascending from deeper levels in the mantle (BVSP. 1981),
and,
recently,
a similar
origin
has
been
proposed for CFB (Courtillot et al., 1986). In both situations, the magmas separate from their source peridotites at relatively great depths; in the case of OIB at or near the base of the oceanic lithosphere, and in the case of CFB somewhere between the base of continental crust and continental lithosphere. In both situations mixing between magmas produced by different extents of melting is likely. and in both cases the melts involved have relatively high MgO contents. These mixed melts therefore have compositions that lie above the central portion of the batch melt curve as illustrated in Fig. 6, and as such have elevated Ni contents. In contrast, MORB magmas form by melting within a mantle column that extends to
more evolved melts or rocks. Such mixing have taken place in two plausible geological
could situa-
tions: in an ascending mantle columns or plumes, or during interaction between komatiite and crustal rocks. In both cases the evolution of the parental magmas must have involved some measure of equilibrium crystallization; pure fractional crystallization tents similar
produces basalts to those in modern
with nickel tholeiites.
con-
Acknowledgements The ideas in this paper were clarified during discussions with W. McDonough, A. Rocholl, S. Goldstein and U. Christensen. and helpful reviews were provided by I.H. Campbell, A. Cattell, E.G. Nisbet. M.J. Bickle, K. Condie and anonymous reviewer.
NT
418
Appendix: Calculation of the compositions
of batch
taken
from
assuming
Arndt,
compositions
of the mantle
the experimental
(1980) and Takahashi
studies
ing equation
relating
MgO content
of the melt (MgO, ).
IX;“”
batch
the partition
= (12R,‘MgO,)
and
Green
and adopting
the follow-
(D:;“‘! ) to the
coefficient
(1)
was derived
lower
than
GPa
the calculated
from experimental
those
data
experiments
0;;‘;“”
under-
end but does not materially At a pressure
degrees
of melting
majorite
(Takahashi.
residual
assemblage
is less than
relationships
alter
of 5 GPa, a komatiite and
the residual
1. assuming
between
reported
phases
are olivine coefficient
D~~~“q=O.15
and a steep slope at the high-MgO method
similar
(from
of melting,
described and
calculated
by integrating
Ohtani
by
Klein
numerical
curve:
between
e.g. between
a
method.
trends
The composition distribution
were
two posior
which
MgO contents
yields
slightly
from higher
amount
Arndt
(1986).
O$;““
values (usually
was normalized
new olivine composition
was calculated,
repeated
MgO value was reached.
until the target
crystallization
paths
were calculated of olitine
needed
to reduce
content
of the liquid
to several
reference
values
and from these the Ni contents
was
Equilibrium
by determining.
partition
at
1%) was
and the procedure
the amount
initial and final values. Appropriate
This
at high
to 100%. the
balance,
determined.
a
for crystallization
of olivine
the liquid composition
using
of 0.30 and the equa-
than eqn. 1. is appropriate
levels. A small
subtracted,
calculated
of olivine was calculated
coefficient
D;;‘,“” = (MgO,/124)-2.2
equation,
were
by mass the MgO
between
coefficients
London.
and geochemistry
of komati-
komatiites: Earth
G.E., Arndt,
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