Tectonoph.vsics, 99
Convergence
271
( 1983) 21 l-211
Elsevier Science Publishers
B.V.. Amsterdam
- Printed
in The Netherlands
Tectonics and Sediment Subduction
SUBDUCTION
AND THE GEOCHEMICAL
CYCLE
W.S. FYFE Department of Geology. University of Western Ontario, London, N6A 587 (Canada) (Revised
September
7, 1981; received by Publisher
May 19, 1983)
ABSTRACT
Fyfe,
W.S..
1983. Subduction
and
the geochemical
cycle.
In: T.W.C.
Convergence
and Subduction.
Tectonophysics, 99: 21 l-217.
The present
balance
of crust
creation
to crust removal
processes
similar
been influenced surface
by surface
components
continents
hydrosphere,
are subducted,
and hydrosphere
at ocean
at subduction
ridges
atmosphere
and
subduction
S. Uyeda
(Editors).
zones appears
10% of the mass of the upper mantle
and crustal
then in a slowly cooling
can increase
and above
zones. Almost
Hilde
component
planet
contamination.
it is difficult
to be has
As long as
to see how the mass of
with time.
INTRODUCTION
One of the most fundamental problems of geological science is the understanding of the chemistry of the inaccessible portions of the earth. There are constraints imposed by the physical properties of the interior largely determined by seismic parameters but these are clearly ambiguous as shown by Anderson’s (1980) recent postulates that there is a great deal of eclogite in the lower mantle, a return to the older views of Goldschmidt (see Rankama and Sahama, 1950). The only definitive major constraint on bulk composition is that the material which rises near ocean ridges must be capable of producing a basaltic extract and a peridotite residue but the volume of mantle which is involved in the extraction process is still unknown (Turcotte, 1981) and depends on models of melt separation. Most model compositions of the petrologists involve a certain degree of circular argument or depend on analogies with a few tons of meteorite debris which may or may not be representative of our planet. Today we have a rather good idea of what materials come from the interior to form the new ocean floor crust with its ophiolite structure, the common model of such crust. We know the rate of crust production required by ocean-floor spreading and we know that this new crust is cooled partly by convective circulation of seawater deep into this crust. This process substantially modifies the primary 0040-1951/83/$03.00
0 1983 Elsevier Science Publishers
B.V.
272
mantle-derived chemistry but the exact chemistry of old ocean floor crust is not yet well quantified. We know that the ocean solute reservoir is fed by continental runoff. We know that ocean-floor crust created at ridges is almost quantitatively subducted; there is very little old ocean-floor crust in existence. We are beginning to think (Windley, 1979) that the modern type of convective structure of the planet commenced at the Archaean-Proterozoic boundary 2.5 Ga (billion years) ago, and has been going on, presumably with slowly diminishing intensity since that time. Given that new crust is formed at a rate of a little more than 10 km3 a- ‘, the total mass of crust that has circulated through the upper mantle is at a minimum of the order of 1O26g over 2.5 Ga. As the mass of the entire mantle is 4 * 102’ g this means that 2+% of the mass of the entire mantle has been through the crust cycle or about 10% of the upper mantle if convection is restricted to this region. The conclusion from such a simple consideration is that the mantle must contain a significant fraction of rock that has been modified and could hardly be expected to be a perfectly homogeneous body (Davies, 1981). Recent estimates of Karig and Kay (1981) indicate that andesite magma generation, the most obvious return flow process above subduction zones produces new crust at a rate of about 1.8. 10” g (0.5 km3) per year. These figures indicate that only a small percentage of subduction spilitic ophiolite returns; this remelting process may not be very efficient. But one must be cautious about such numbers until we really understand the root structure of continental regions like the Andes. An equally intriguing problem involves the possible subduction of sediments or direct tectonic erosion of continental edges in the subduction process. And related to this problem is the entire question of mechanisms of continental growth or decay. There is no doubt that in regions such as the Himalayas or Andes continental crust is thickened but this is a transient phenomena and is rapidly relaxed by erosion. Related to the process of ophiolite and sediment subduction, is the question of volatile recycling through the mantle and the resultant ambiguities in models of outgassing (or ingassing) of a planet which is vigorously mixing. ARE SEDIMENTS
SUBDUCTED?
I think that one of the most important aspects of the Texas conference was the evidence presented that sediment subduction is common if not ubiquitous (T. Wilde, 1983, this volume). It appears that accretionary sedimentary prisms of offscraped sediments are common only where the sediment load carried to the subduction site is very massive. Further, the mechanisms for locking initially light materials into the descending slab appear to be rdated to the roughness of the surface of the descending slab-a roughness first created by the ubiquitous block fat& patterns created at spreading centres and secondly by massive cr&tig of the bending slab. Thus, ideas concerning sediment subduction so elegantly expressed by Gifluly (197 1) and supported by workers such as Garrels and Lerman (1977) and Uyeda
(1978, p. 187) appear who proposed
the “indestructibility
tively low density”
inescapable. explain
criticism
the “irreversible
is clearly not valid. Thus the possibility
shown to be possible The mantle
becomes
by Molnar sediments
kyanite-bearing
(1978)
of its rela-
differentiation
of subduction
and Gray (1978) appears
even more muddy!
for these should produce
by Moorebath
sialic crust because
with this concept
the great lack of meta-pelagic
California
Typical
of continental
and associated
of the upper mantle” light material
to be substantiated.
of some now to be
These new observations
in regions
also
like the Franciscan
schists (Fyfe,
of
1980) and kyanite
blue schists are rare. THE GEOCHEMICAL
CYCLE
The major geochemical
cycle of the elements
involves:
(a) new crust production at ridges; (b) modification of new ocean floor crust by hydrosphere-atmosphere (c) (d) (e) (f) Of
subduction of modified ocean floor crust: return flow above subduction zones; erosion off the continents; return tectonic flow of sediments to the mantle. all these processes (a), (c) and (e) are reasonably
well known
exchange;
but there are
great gaps in our knowledge of (b), (d), and (f). Until these gaps are quantified any final arguments about detailed upper mantle chemistry and the past and future mass history
of continents
will be unsatisfactory.
NEW CRUST ALTERATION
It is now generally agreed that almost half of the energy focussed at ocean ridge systems is removed by deep convective circulation of sea water through the cracks and pores of the cooling crust. Anderson et al (1979) suggest that this process may continue in crust that is over 50 Ma old and that more than one third of the modern ocean floor crust is involved in such circulation at the present time. It is now clear that massive
exchange
processes
occur during
this process.
As recently
summarized
by Fyfe and Lonsdale (198 1) O,, CO,, S, H,O are volatiles added in significant quantities while Na, K, Mg, Rb, U are added and displace Ca and transition metals which may be removed Bischoff (1979) propose
and contribute to metal-enriched sediments. Bloch and that as much as half the K delivered to the oceans may
become fixed in spilites while Aumento (1979) has shown that uranium is substantially enriched. For species such as strontium, it has been clearly demonstrated that the 87Sr/86Sr ratio increases towards sea-water values as alteration proceeds (Spooner, 1976). Present sea-water strontium isotopes appear to show a balance between typical runoff and hydrothermal discharge values. But there are few elements for which the data are sufficient to allow realistic balance to be established.
214
it is unlikely “ typical”
RETURN
that this situation
ocean-floor
will improve
until there is sufficient
deep drilling
o!
crust.
FLOW
It is clear that for some species
there must be moderately
efficient
return
flow
processes. I shall here assume that most pelagic sediments are subducted. The present pelagic sedimentation rate is in the range 0.3- 1.O km3 a- ’ (Sibley and Vogel, 1976). First, consider water as an example. Water is fixed in hydrated upper altered layers of sea-floor basal& and in serpentized ultramafic
phases of the rocks, There is
clear evidence that such alteration proceeds to depths of several kilometers (Fyfe and Lonsdale, 1981) or even to 8- 10 km (Lewis and Snydsman, 1977). Assuming that average ocean-floor crust contains 5% H,O and the pelagic sediments 10% bound water in clays and chlorites, the present bound-water subduction rate is of the order of 1.5 . lOi g a-‘. At this rate the entire ocean mass (1.4 - 1O24 g) will be subducted in a billion years. Clearly there must be a return flow. First, as materials are compressed
and
metamorphosed
during
descent
and glaucophane
schist-eclogite
facies rocks are formed, there must be massive outflow of water. There is clear evidence for such flow in the metasomatic changes observed in some glaucophane schist terrains (Fyfe and Zardini, 1967) and there is even evidence for very high fluid pressures. Thus Essene and Fyfe (1967) have described glaucophane schist fluidbreccias with major gas cavities and even minerals such as omphacite, the characteristic eclogite pyroxene, growing into apparent free space. There is no doubt that explosive expulsion of water could be related to seismic activity (see Ruff and Kanamori, 1983, this volume). Water locked in amphiboles and in particular in phlogopite McBirney,
may not be released till very great 1975). Mixing of ultramafic materials
depths are attained (Fyfe and and potassic clays or feldspars
must generate phlogopite, e.g., KAISi,Os + 3Mg,SiO, + H,O + KMg,(AlSi,O,,)(OH), + 3MgSi0, (or talc). Fluids in such phases can persist to depths of 100 km or so (Wyllie, 1971). At the same time carbonates can be stable to even greater depths. Fluids
released from amphiboles
and micas carried
to great depth may either lead to
partial melting of the subducted material itself or extremely high pressure fluids which must be very rich in soluble components (K,O, Na,O, SiO,, etc.) may trigger melting in the overlying hotter mantle and cause strong enrichment in typical crustal elements. Uranium nicely illustrates the balance problem. Uranium moves to the crust from ocean ridge magmatism and subduction zone magmatism. It is quite difficult to decide on the uranium content of mantle magmas as they may be contaminated by crustal sources during ascent (Fyfe, 1979). Data from Aumento et al. (1976) might indicate a primary uranium content in ridge magmas of the order of 0.1-0.2 ppm.
275
This gives an annual and
Kay’s
subduction (0.2-0.4
figure
addition
of 1.8 * lOI
of 1S-3.0.
IO9 g of uranium
g a- ’ for the rate of andesite
zones and data from Carmichael ppm) in oceanic
per year. If we use Karig
regions then about
melt production
et al (1974) on U contents 1 . lo9 g of U returns
at
of andesites
above subduction
zones annually. Present uranium
water flux off the continents at about
is 3.6. lOI g a-’
the 0.1 ppb level. Thus
oceans
annually.
contain exactly
2-3 ppm U. Thus such sediments balancing the river input. Aumento
enriched sediment
Pelagic
in uranium, subduction
sediments
forming
about
and surface
waters carry
3.6. lo9 g is transported
at the rate of l-3.
lOI
to the
g per year
fix 2-6. lo9 g of U annually, almost (1979) has shown that spilites are also
even up to 4 ppm. If we use such figures and allow for pelagic we have:
U to surface = 2-4.
lo9 g a- ’
U subducted
lo9 g a-’
= 3-9.
All one can conclude is that the system is about that uranium is being purged from the mantle--if
balanced! There is little indication sediments are subducted!
CONCLUSION
At recent conferences I have listened to a number of workers indicate that convective motions may link ridges and subduction zones as shown in Fig. 1. Such models are attractive in explaining the almost steady state chemistry of the present earth. The mantle
is recharged
as fast as it is depleted
and models of heterogeneous
mantle are logical (Davies, 1981). Such models might also suggest that hot spot magmas simply represent small amounts of leakage off the deep conveyor belt and
Fig. 1. A possible taking
scenario
some sediments
for present-day
with it. Convective
trench-subduction.
Volcanic-plutonic
the deeper material
leads to hot-spot
convection.
New lithosphere
created
at ridges is subducted
flow goes from ridge to ridge at depths
mountain volcanism,
belts are built above
the subduction
and rain moves continental
materials
of 600-700
km via
zones, leakage to the oceans.
off
216
even features like high CO, magma types could fit with subducted materials. But a cooling planet cannot be in a perfect steady state. The present mass balance of crust and mantle is not stable in a cooling and mixing planet. Typical surface components such as K,O-SiO,-H,O-CO, would be more stable in phases such as phlogopite, pyroxene, carbonate in a cooler mantle and lithosphere: they are returned to the surface by energetic igneous processes. We need to pay attention to evidence for reduction in the volume of the hydrosphere and crust through time and keep very open minds on the old dogmas of continuous irreversible degassing and continental growth. Will we end up looking like Mars? REFERENCES
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