Gw. Fowler et al., DIOGENITES AS ASTEROIDAL CUMULATES - INSIGHTS FROM ORTHO-PYROXENE MAJOR AND MINOR ELEMENT CHEMISTRY, Geochimica et cosmochimica acta, 58(18), 1994, pp. 3921-3929
Diogenites appear to be cumulates formed from one or more igneous rese
rvoirs in the interior of asteroid 4 Vesta. Magmatism in this parent b
ody gave rise to a series of related lithologies designated howardites
, eucrites, and diogenites or ''HED.'' Eucrites are pigeonite/plagiocl
ase basalts, and diogenites are orthopyroxenites. Howardites are brecc
iated mixtures of eucrites and diogenites. The major objective of this
paper is to characterize the major and minor element chemistry of ort
hopyroxene in diogenites and to interpret these data in terms of a pet
rogenetic model. This study, which involves interpretation of similar
to 1,200 high-quality electron microprobe analyses, demonstrates that
the systematics of Ca, Fe, and Mg in orthopyroxene were largely reset
by reaction with melt and by subsolidus exchange. However, the systema
tics of the minor elements Al, Cr, and Ti still effectively record the
ir igneous history. Aluminum and Ti are highly correlated with the inc
ompatible trace elements (e.g. Yb, Y) and thus are useful fractionatio
n indicators. As many as twenty of the twenty-three diogenites studied
may have formed from one igneous system based on Al, Cr, and Ti syste
matics in orthopyroxene. The Al content of the orthopyroxene in the tw
enty diogenites forms the basis for a fractionation sequence with Peck
elsheim the least fractionated and LEW 88008 the most fractionated. Ro
da and Manegaon, and possibly ALHA77256, fall off the main composition
al trends and may belong to different melt systems. The coupled substi
tutions that incorporate Al, Cr, and Ti into the orthopyroxene crystal
structure are Cr-VI(3+)-Al-IV(3+), Al-VI(3+)-Al-IV(3+), and Ti-VI(4+)
-2(IV)Al(3+). The dominant substitutional couple in the early stages o
f crystallization is Cr-VI(3+)-Al-IV(3+) while Al-VI(3+)-Al-IV(3+) is,
dominant in the late stages. These findings demonstrate the importanc
e of understanding the coupled substitutions for minor elements when a
ssessing the appropriate mineral/melt partition coefficients (D values
) or when discussing whether an element is compatible or incompatible.
For example, in diogenitic orthopyroxene, Al has three different comp
atibilities (D values) with Cr-VI(3+)-Al-IV(3+) more compatible than A
l-VI(3+)-Al-IV(3+) which is more compatible than (TI4+)-T-VI-2(IV)Al(3
+). Based on the assumption that D-Al increases during crystallization
from 0.05 to 0.1 corresponding to the crystallization interval repres
ented by Peckelsheim to LEW 88008, 60% crystallization is required. Th
e melt parental to LEW 88008 is estimated to contain similar to 12 wt%
Al2O3, very near plagioclase saturation.