Nature © Macmillan Publishers Ltd 1997
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NATURE | VOL 388 | 28 AUGUST 1997 857
This would involve very dense Fe-rich melts
15
, particularly before
the completion of core formation, and some of these melts may
have partially sunk with core-forming metal towards the martian
interior. Cumulate and residue flotation depends on the density
crossover between solid and liquid phases
27
, which is poorly con-
strained for Mars. However, if the outer portions of the planet were
rich in depleted residual solids during the magma ocean stage, the
W and Nd isotope compositions would be expected to be radiogenic
and to survive homogenization.
The sizes of inner Solar System planetary bodies seem to increase
with accretion and differentiation intervals, from the most primitive
and undifferentiated materials such as equilibrated chondrites
(6 Myr) to the eucrite parent body (10 Myr) to Mars (10–
30 Myr) and to the Earth–Moon system (50 Myr) (refs 2, 3). The
data are consistent with early termination of accretion of asteroids
and Mars, and longer-lived accretion of larger bodies resulting from
late planet-scale impacts. The trend corresponds to a transition in
the dominant mechanisms of heating from decay of short-lived
nuclides to the release of accretional energy. Whereas a late giant
impact on Earth may have been sufficiently energetic to effectively
homogenize the W isotope composition and destroy any proto-
core
2,3
, the W and Nd isotope data are inconsistent with an impact
sufficiently energetic to melt and homogenize Mars later than
4.53 Gyr (ref. 22).
Methods. All samples were powdered in an aluminum oxide mortar after
surface saw marks and fusion crusts had been removed through mild acid
leaching (1M HCl) and hand-picking. The samples were digested sequentially
with concentrated HF, 8M HNO
3
and 6M HCl. Roughly 10% of the solution
was separated and spiked with
178
Hf and
186
W, whereas the remaining solution
was dried and redissolved in 8ml of 4M HF. The method of chemical
separation of W was adapted from the first column of the Hf chemistry
developed by Salters and Hart
29
but on a reduced scale, with 3.5 ml of Bio-Rad
AG1 8 (200–400 mesh) anion resin. The Hf and W were eluted and collected
sequentially using a mixed solution of 6M HCl + 1M HF. The same chemical
procedure was used for the spiked solutions, but the column volume was
further reduced (1ml), and Hf and W were collected together. The total W
procedural blank was 0.4ng. Tungsten isotopic measurement by multiple
collector inductively coupled-plasma mass spectrometry (MC-ICPMS) has
been previously described by Lee and Halliday
30
. The NIST-3163 W standard
was run between every sample to monitor the performance of MC-ICPMS and
to check for memory effects, which were negligible. The W isotopic measure-
ments were normalized to
186
W=
184
W ¼ 0:927633 (ref. 30). The quoted 2j
standard errors all refer to the least significant figures. The concentrations of Hf
and W were determined by isotope dilution, and the uncertainty is typically
0.2% or better. All the W data are blank-corrected, which is negligible for all
analyses except for Juvinas which has been corrected by 1.5 e unit.
Received 3 April; accepted 15 July 1997.
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Acknowledgements. We thank M. Lindstrom, L. Nyquist, G. MacPherson, C. Perron and M. Wadhwa for
access to their meteorite collections at NASA, Smithsonian Institution of Washington, Museum National
d’Histoire Naturelle at Paris, and Field Museum in Chicago. We also thank J. Christensen,E. Essene, H.
Pollack, M. Rehka ¨mper, P. van Keken and Y. Zhang for their comments, M. Johnson and C. Hall for their
assistance, and K. Righter and M. Drake for access to unpublished papers. This work was supported by
NSF, DOE, NASA and the University of Michigan.
Correspondence and requests for materials should be addressed to D.-C.L. (e-mail: dclee@umich.edu)
Effect of microgravity on the
crystallization of a self-
assembling layered material
Homayoun Ahari*, Robert L. Bedard†, Carol L. Bowes*,
Neil Coombs‡,O
¨
mer Dag*, Tong Jiang*,
Geoffrey A. Ozin*, Srebri Petrov*, Igor Sokolov*,
Atul Verma*, Gregory Vovk* & David Young*
* Materials Chemistry Research Group, Lash Miller Chemical Laboratories,
University of Toronto, Toronto, Ontario M5S 3H6, Canada
† UOP, Research Division, 25 E. Algonquin Road, Des Plaines, Illinois 60017, USA
‡ Imagetek Analytical Imaging, 32 Manning Avenue, Toronto, Ontario M6J 2K4,
Canada
.........................................................................................................................
In microgravity, crystals of semiconductors and proteins can be
grown with improved crystallinity, offering the prospect of
improved structural analyses (for proteins) and better electronic
properties (for semiconductors)
1–3
. Here we study the effect of a
microgravity environment on the crystallization of a class of
materials—layered microporous tin(IV) sulphides
4–11
—whose
crystal structure is determined by weak interlayer interactions
(electrostatic, hydrogen-bonding and van der Waals) as well as
strong intralayer covalent bonds. We find that the crystals grown
in microgravity (on board the Space Shuttle Endeavour) show
improved crystal habits, smoother faces, greater crystallinity,
better optical quality and larger void volumes than the materials
grown on Earth. These differences are due at least in part to the