Yd. Jang et al., The differentiation trend of the Skaergaard intrusion and the timing of magnetite crystallization: iron enrichment revisited, EARTH PLAN, 189(3-4), 2001, pp. 189-196
Initial studies of the Skaergaard intrusion [L.R. Wager, J. Petrol. 1 (1960
) 364-398] and much of the subsequent work [R.J. Williams, Am. J. Sci. 271
(1971) 132-146: S.A. Morse et al.. Am. J. Sci. 280A (1980) 159-170: A.R. Mc
Birney, H.R. Naslund. Contrib. Mineral. Petrol. 104 (1990) 235-247, C. Tegn
er. Contrib. Mineral. Petrol. 128 (1997) 45-51, A.R. McBirney, Contrib. Min
eral. Petrol. 132 (1998) 103-105] concluded that the Skaergaard magma follo
wed an iron-enrichment trend with little or no silica enrichment until the
final stages of crystallization. Several recent reports [R.H. Hunter, R.S.J
. Sparks, Contrib. Mineral. Petrol. 95 (1987) 451-461. R.H. Hunter, R.S.J.
Sparks, Contrib. Mineral. Petrol. 104(1990) 248-254], however, have suggest
ed that the Skaergaard magma began to follow a silica-enrichment trend in L
ower Zone c (LZc) of the Layered Series where magnetite first became an abu
ndant mineral. Magnetite in LZc, however. generally occurs in aggregates of
magnetite-ulvospinel and ilmenite-hematite that have undergone extensive s
ubsolidus reequilibration and exsolution [E.A. Vincent. Neues Jahrb. Minera
l. Abh. 94 (1960) 993-1016; E.A. Vincent, Geochim. Cosmochim. Acta 6 (1954)
1-26; A.F. Buddington, D.H. Lindsley, J. Petrol. 5 (1964) 310C357, H.R. Na
slund, J. Petrol. 25 (1984) 185-212, A.R. McBirney, J. Petrol. 30 (1989) 36
3-397; Y.D. Jang, Petrological. Geochemical, and Mineralogical Variations i
n the Skaergaard Intrusion, East Greenland (Ph.D. Dissertation). State Univ
ersity of New York, Binghamton, NY, 1999, 219 pp.]. As a result, it is not
clear if magnetite in these samples was an equilibrium, liquidus mineral fr
actionated from the main magma reservoir, or if magnetite crystallized as a
later, interstitial mineral and did not directly affect the differentiatio
n trend of the main Skaergaard magma. The timing of the initial crystalliza
tion of abundant magnetite and ilmenite is a key factor in understanding th
e trend of Skaergaard differentiation. Because V is a strongly included ele
ment in oxides, and is not strongly included in silicate minerals, the V co
ntent of an evolving magma is generally controlled by the fractionation of
oxide minerals, in particular magnetite. The initial crystallization of mag
netite should, therefore, be accompanied by a sudden decrease in the V cont
ent of the evolving magma, and in all of the coexisting mafic phases in equ
ilibrium with that magma as well. The V content in Skaergaard pyroxene does
not decrease significantly until the upper part of the Middle Zone (MZ), s
uggesting that the onset of extensive magnetite fractionation is much later
than has previously been thought, and that the magnetite in LZc and the lo
wer part of the MZ might not have been a liquidus phase at that level. The
observed V trend in Skaergaard pyroxene can be modeled almost perfectly usi
ng published partition coefficients for the coexisting minerals in the Skae
rgaard intrusion, assuming that no magnetite fractionation occurred until t
he upper part of the MZ. Independently calculated trends for fO(2) in the S
kaergaard magma [R.J. Williams, Am. J. Sci. 271 (1971) 132-146; S.A. Morse
et al.. Am. J. Sci. 280A (1980) 159-170: A.R. McBirney, H.R. Naslund, Contr
ib. Mineral. Petrol. 104 (1990) 235-247] change in the upper part of the MZ
to more reducing conditions. The onset of magnetite fractionation would re
move Fe2O3 from the magma and could initiate such a change. The timing of m
agnetite fractionation will have a strong effect on whether magma evolves t
owards iron enrichment or silica enrichment. (C) 2001 Elsevier Science B.V.
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