Published online on December 13, 2002, 10.1073/pnas.262514499
PNAS | December 24, 2002 | vol. 99 | no. 26 | 16556-16561
Previous Article |
Table of Contents
| Next Article
Geology
Direct imaging of nanoscale magnetic interactions in minerals
Richard J. Harrison *,
Rafal E. Dunin-Borkowski
, and
Andrew Putnis
*Department of Earth Sciences, University of Cambridge, Downing
Street, Cambridge CB2 3EQ, United Kingdom;
Department of
Materials Science and Metallurgy, University of Cambridge, Pembroke
Street, Cambridge CB2 3QZ, United Kingdom; and
Institut
für Mineralogie, Corrensstrasse 24, D-48149 Münster,
Germany
Edited by W. G. Ernst, Stanford University, Stanford, CA,
and approved November 4, 2002
(received for review August 26, 2002)
 |
Abstract
|
|---|
The magnetic microstructure of a natural, finely exsolved
intergrowth of submicron magnetite blocks in an ulvöspinel matrix
is characterized by using off-axis electron holography in the
transmission electron microscope. Single-domain and vortex states in
individual blocks, as well as magnetostatic interaction fields between
them, are imaged at a spatial resolution approaching the nanometer
scale. The images reveal an extremely complicated magnetic structure
dominated by the shapes of the blocks and magnetostatic interactions.
Magnetic superstates, in which clusters of magnetite blocks act
collectively to form vortex and multidomain states that have zero net
magnetization, are observed directly.
Abbreviations: SD, single domain; MD, multidomain; NRM, natural
remanent magnetization; TEM, transmission electron microscopy
Magnetite is the most
strongly magnetic mineral in nature. Small particles of magnetite in
single-domain (SD) or pseudo-SD magnetization states (with sizes
in the range of 3070 nm and 70 nm to 20 µm, respectively) are the
dominant carriers of remanent magnetization in rocks. Larger,
multidomain (MD) particles that contain magnetic domain walls would
have significantly lower coercivities and thermal stabilities than SD
and pseudo-SD particles (1). In most igneous rocks, the grain size of
primary magnetic minerals exceeds the MD threshold. Such rocks are less
likely to maintain strong and stable natural remanent magnetization
(NRM) over geological times than those containing SD particles. It has
long been proposed that solid-state processes such as subsolvus
exsolution can generate SD magnetite particles from MD grains, thus
increasing the stability of the NRM (2). Such processes are thought to
be responsible for the strong and stable remanent magnetization
exhibited by many rocks and have been proposed as a possible source of
magnetic anomalies on Mars. However, the magnetic microstructure of
finely exsolved minerals has never been observed directly at the
nanometer scale.
The magnetite-ulvöspinel
(Fe3O4-Fe2TiO4)
system forms a complete solid solution at temperatures above
450°C, but has a miscibility gap at lower temperatures (35).
Intermediate bulk compositions (termed titanomagnetites) exsolve during
slow cooling, at low or buffered oxygen fugacity, to yield an
intergrowth of SD or pseudo-SD magnetite-rich blocks separated by
nonmagnetic ulvöspinel-rich lamellae. In this article, off-axis
electron holography, a transmission electron microscopy (TEM) technique
that yields a vector map of the magnetic field in a sample with
nanometer resolution (68), is used to image the magnetic
microstructure of a natural titanomagnetite intergrowth. The high
spatial resolution of the technique makes it ideal for the study of
nanoscale particles at the boundary between SD and pseudo-SD behavior.
 |
Experimental Details
|
|---|
A finely exsolved titanomagnetite from Mount Yamaska, Quebec, one
of the Monterigian Hills of Cretacious age (Cambridge University Harker
Collection no. 92966) (8), was extracted from a petrographic thin
section and prepared for TEM examination by using ion-beam milling.
Some bulk magnetic properties of this material had been studied (2,
9), and its microstructure had been examined by using TEM (10).
Electron microprobe analysis indicates a bulk composition of 42%
Fe3O4, 39%
Fe2TiO4, 11%
MgAl2O4, and 8%
MgFe2O4. TEM observations
were carried out at 300 kV by using a Philips Electron Optics
(Eindhoven, The Netherlands) CM300-ST equipped with a field-emission
gun electron source, a Lorentz lens, an electrostatic biprism, and a
Gatan (Pleasanton, CA) imaging filter.
Fig. 1a shows a chemical map
of a representative area of the sample. Ulvöspinel-rich
exsolution lamellae (red) subdivide the original titanomagnetite grain
into a fairly regular array of magnetite-rich blocks (blue). The
profiles in Fig. 1 b and c, which were obtained
from the line marked C in Fig. 1a, confirm that little Ti is
present in the blocks, i.e., that they are essentially pure magnetite.
Similar maps reveal that Mg and Al are not present in this area in
significant quantities. Chosen magnetite blocks, whose linear
dimensions vary between 5 and 175 nm, are numbered in Fig. 1 so that
they can be referred to below. The width of the ulvöspinel
lamellae varies between 8 and 100 nm, whereas the aspect ratio of the
blocks in the plane of the sample varies between 1 and 10.
High-resolution images indicate that the interfaces between magnetite
and ulvöspinel are either coherent or semicoherent. The thickness
of the sample increases from 70 nm at the top to 195 nm at the bottom
of region B in Fig. 1, which will be examined in detail below. The
blocks in this region are therefore roughly equidimensional.

View larger version (119K):
[in this window]
[in a new window]
|
Fig 1. (a) Chemical map of titanomagnetite sample examined in
this study, acquired by using three-window, background-subtracted
elemental mapping at the Fe L2,3 and Ti L2,3
edges in a Gatan imaging filter (GIF). The GIF separates electrons that
have lost energy in the sample due to inelastic scattering from
elastically scattered electrons and refocuses them to form an image of
the sample. After suitable background correction, the image corresponds
to a chemical map, whose intensity is proportional to the concentration
of the appropriate element projected through the thickness of the
sample. Blue and red correspond to Fe and Ti concentrations,
respectively. The blue regions are magnetic and are rich in magnetite
(Fe3O4), whereas the red regions are
nonmagnetic and rich in ulvöspinel
(Fe2TiO4). The numbers refer to individual
magnetite-rich blocks, which are discussed in the text. The boxes
marked A and B correspond to regions referred to in subsequent figures.
(b and c) Line profiles obtained from the
Fe and Ti chemical maps, respectively, along the line marked C in
a. The short arrows mark the same point in the three
pictures.
|
|
The microscope geometry for off-axis electron holography is shown
schematically in Fig. 2a. The
sample is examined by using coherent illumination from a field-emission
gun, with the region of interest positioned so that it covers
approximately half the field of view. A positive voltage applied to an
electrostatic biprism causes an electron wave that has passed through
the sample to overlap with a reference wave that has passed through
vacuum. Holographic fringes form in the overlap region due to
interference between the sample and reference waves. Fig. 2b
shows a hologram obtained from the region marked A in Fig.
1a. The amplitude and phase of the electron wave leaving the
sample are recorded in the intensity and the position of the
holographic fringes, respectively (11). The phase shift is sensitive
both to the thickness and composition of the sample and to the in-plane
component of the magnetic induction integrated in the incident beam
direction. Once the magnetic contribution to the phase has been
extracted, a picture of the magnetic field lines in the sample is
obtained simply by adding contours to the phase image. Since both
thickness and composition vary in magnetite-ulvöspinel
intergrowths, these effects must be subtracted from the raw phase image
to yield the magnetic contribution to the phase. Fortunately, as the
mean inner potentials of magnetite and ulvöspinel are exactly
equal, only a thickness correction is required. The thickness was
determined from t/
i maps
obtained by using electron energy-loss spectroscopy (where
i is the inelastic mean-free-path of
electrons in the sample and is estimated to be
170 nm for the
present sample at 300 kV). The constant of proportionality between
t/
i and the mean inner
potential contribution to the phase was determined by least-squares
fitting to data collected near the edge of the wedge-shaped sample
(where the magnetic contribution is negligible), on the assumption that
the mean inner potential of magnetite is 17 V. (The ratio of the
magnetic contribution to the phase shift across a magnetite block to
the mean inner potential contribution was typically between 0.15 and
0.30.)

View larger version (42K):
[in this window]
[in a new window]
|
Fig 2. (a) Schematic illustration of set-up used for generating
off-axis electron holograms. The sample occupies approximately half the
field of view. Essential components are the field emission electron gun
(FEG) electron source, which provides coherent illumination, and the
positively charged electrostatic biprism (a thin gold-coated quartz
fiber, 0.6 µm in diameter), which causes overlap of the object and
(vacuum) reference waves. The resulting holographic interference
pattern is recorded digitally. The Lorentz lens allows imaging of
magnetic materials in close-to-field-free conditions.
(b) Off-axis electron hologram obtained from region A in
Fig. 1a. The edge of the sample is close to the top of
the picture, while the dark area results from diffraction contrast from
one of the magnetite-rich regions. The biprism voltage is 200 V, and
the holographic interference fringe spacing is 3.5 nm.
|
|
In a conventional electron microscope, the objective lens creates a
large vertical magnetic field at the position of the sample. For
holography of magnetic materials, the objective lens is switched off
and a Lorentz lens is used to examine the sample in field-free
conditions. By partially exciting the objective lens and tilting the
sample, different in-plane components of magnetic field can be applied
to the sample in situ, allowing reversal mechanisms,
hysteresis loops, and remanent states to be studied. In the present
work, remanent states were studied by initially tilting the sample to
the maximum available angle of 41° in zero field and turning the
objective lens on fully to saturate the sample in one direction. This
process provided a known starting point from which further fields could
be applied. The objective lens was then turned off, the sample was
tilted to 41° in zero field in the opposite direction, and the
objective lens was partially excited to apply a known in-plane
component of magnetic field to the sample in the opposite direction.
The objective lens was switched off and the sample was tilted back to
0° in zero field to record the hologram. This procedure was repeated
for a number of different applied fields.
 |
Results
|
|---|
Fig. 3 shows the magnetic
microstructure of region B marked in Fig. 1a for eight
different remanent states. The results were obtained after applying the
in-plane fields indicated in Fig. 3. (For in-plane applied fields of
1,340, 628, and 225 Oe, with the sample tilted by 41°, the
out-of-plane component of the applied field is 1,520, 713, and 255 Oe,
respectively.) The direction and the spacing of the black contour lines
provide the direction and the magnitude of the magnetic induction in
the plane of the sample, which can be correlated with the positions of
the magnetite blocks (outlined in white). The direction of the local
induction is also indicated by colors, according to the color wheel
shown at the bottom of Fig. 3, and arrows. The spacings of the contours
in the blocks decrease slightly from the top to the bottom, reflecting
the increase in the thickness of the sample. The recorded phase images
have been smoothed very slightly to remove noise, so that the spatial
resolution of the magnetic information is estimated to be between 10
and 20 nm.

View larger version (101K):
[in this window]
[in a new window]
|
Fig 3. Magnetic microstructure of region B in Fig. 1a measured
by using electron holography. Each image corresponds to a different
magnetic remanent state, acquired with the sample in field-free
conditions. The outlines of the magnetite-rich regions are marked in
white, while the direction of the measured magnetic induction is
indicated both using arrows and according to the color wheel shown at
the bottom (red = right, yellow = down, green = left,
blue = up). The spacing of the black contours is inversely
proportional to the in-plane component of the magnetic induction
projected in the incident electron beam direction, and thus provides a
measure of the strength of the magnetic field in the plane of the
sample. Images a, c, e,
and g were obtained after applying a large (>10,000 Oe)
field toward the top left of each picture, then the indicated field
toward the bottom right, after which the external magnetic field was
removed for hologram acquisition. Images b,
d, f, and h were obtained
after applying identical fields in the opposite directions.
|
|
General Observations.
Fig. 3 shows that the magnetic domain structure in this sample is
extremely complex. Although the magnetization is never saturated in the
direction of the applied field, analysis shows that the average
magnetization direction is parallel (or antiparallel) to this
direction. The contours outside the blocks are associated with stray
interaction fields and are, on average, more widely spaced than the
internal contours.
The ability to differentiate between internal and external
contributions to the magnetic field allows two fundamental issues
related to the magnetic behavior of fine-scale intergrowths to be
addressed: the magnetization states of individual blocks and the
collective behavior of the grain as a whole. The first point has been
the subject of intense study with micromagnetic simulations (12), which
predict the existence of "flower" and "vortex" states in
isolated magnetite cubes of equivalent size to those described here. If
the blocks can adopt vortex rather than SD states, then the magnetic
properties of the mineral (e.g., its remanent magnetization and
coercive force) are changed fundamentally. It is known from macroscopic
measurements that magnetostatic interactions between blocks play a
crucial role in determining the remanent properties of rocks.
Interactions result in a pronounced shearing of the hysteresis loop and
a reduction in remanent magnetization. They also provide a potential
mechanism for the acquisition of self-reversed thermoremanent
magnetization, i.e., the acquisition of a remanent magnetization
antiparallel to the direction of the applied field.
The details of the magnetic microstructure do not reverse exactly when
the same in-plane component of magnetic field is applied in opposite
directions. Some blocks (e.g., block 5) point in almost the same
direction irrespective of the magnitude and direction of the applied
field. This asymmetry may result from the presence of an out-of-plane
component of the applied magnetic field, which has been observed to
affect vortex helicity in lithographically patterned magnetic elements
(13). Alternative explanations include the region of interest not being
precisely flat at zero tilt and the effect of the shape of the ion-beam
thinned TEM sample. Although these effects should be taken into
consideration, they do not affect most of the conclusions presented
below.
Magnetization States of Individual Blocks.
The magnetite blocks are primarily in nonuniform SD states (e.g., block
5 in all of Fig. 3) or single vortex states (e.g., block 6 in Fig. 3
a and h). Some blocks are reminiscent of a flower
state, with the contour lines fringing out at their surface (e.g.,
block 9 in Fig. 3e). Others have a large component of their
magnetization perpendicular to the plane of the sample, and therefore
show few contours (e.g., blocks 7 and 12 in Fig. 3g).
The smallest block observed to form a vortex (number 14) has dimensions
of 115 x 90 x 145 nm. These dimensions are larger
than the predicted minimum size of 70 nm for vortices to form in
isolated cubes of magnetite11. Nonuniform SD
states are observed in blocks as large as 165 x 160 x 100
nm, which is smaller than the maximum size of 200 nm predicted for the
breakdown of SD to vortex states in isolated magnetite cubes. No blocks
significantly larger than 200 nm were present in the areas studied, so
the presence of larger SD blocks cannot be ruled out.
The SD and vortex states represent alternative local energy minima for
blocks of this size, which can adopt either state depending on the
direction and the magnitude of the applied magnetic field, as well as
on the magnetization states of their neighbors. (Compare, for example,
the magnetization state of block 6 in Fig. 3 a and
b.) The abundance of SD states implies that they have a
lower energy than vortex states in the presence of strong interactions.
For isolated cubes of magnetite, micromagnetic simulations predict the
opposite, with the vortex state having a lower energy than the SD state
over the size range 70 to 200 nm. The demagnetizing energy, which
normally destabilizes the SD state with respect to the vortex state in
isolated particles, is greatly reduced in an array of strongly
interacting particles. Hence, care must be taken when using simulations
of isolated particles to predict the domain states of interacting
particles in a fine-scale intergrowth.
Differences between the magnetic moments of individual SD blocks can be
seen in Fig. 3. For example, block 8 in Fig. 3e is
magnetized roughly north-northwest (blue), whereas in Fig.
3f it is magnetized roughly south-southeast (yellow).
It contains an off-centered vortex in Fig. 3b, suggesting
that magnetization reversal in this block could occur via the
formation, displacement, and subsequent annihalation of a vortex state
(14), rather than by coherent rotation of the SD moment.
The preferred magnetization direction of a SD particle is
determined by a number of factors, including magnetocrystalline
anisotropy, shape anisotropy, and magnetostatic interactions with
neighboring particles. The influence of magnetocrystalline anisotropy,
which results in preferred magnetization directions parallel to <111>
in magnetite, is relatively small. In the present study, it is apparent
from Fig. 3 that the magnetization directions of the blocks are
determined primarily by shape anisotropy and interactions. Shape
anisotropy dominates when the magnetization lies parallel to the long
axis of a block (e.g., in blocks 911 and 1618 in Fig. 3
e and g). In other cases, magnetostatic
interactions force the magnetization to point perpendicular to the long
axis (e.g., blocks 15 and 19 in Fig. 3h). The magnetization
can also lie parallel to the body diagonal (e.g., blocks 5 and 8 in
Fig. 3 e and g).
Collective Behavior.
In Fig. 3, several blocks are observed to act collectively to form
magnetic "superstates" that would normally be observed in single,
much larger magnetized regions. A common example is where two or more
blocks interact to form a vortex superstate. Two-, three-, and
five-block vortex superstates are visible in Fig. 3 (e.g., blocks 1 and
2 in Fig. 3g and blocks 13, 5, and 6 in Fig.
3e). A similar superstate involving three elongated blocks
is shown in Fig. 4b and
schematically in Fig. 5a. The
absence of closely spaced contours between the superstate and the
adjacent single vortex in Fig. 4b shows the efficiency with
which stray interaction fields are eliminated in the
intervening ulvöspinel. Flux closure is achieved with
considerably less curvature of magnetization within the three-component
blocks than in the adjacent conventional vortex, reducing the exchange
energy penalty associated with the nonuniform magnetization.

View larger version (93K):
[in this window]
[in a new window]
|
Fig 4. (a and c) Chemical maps (blue = Fe,
red = Ti) from two regions not shown in Figs. 1 and 3.
(b and d) The corresponding magnetic
microstructures, in the same format as Fig. 3. (b) Three
adjacent magnetite-rich regions combining to form a single vortex;
(d) a small region that is magnetically antiparallel to
its larger neighbors.
|
|

View larger version (43K):
[in this window]
[in a new window]
|
Fig 5. Schematic diagrams showing some of the possible magnetization states of
three closely spaced regions of magnetic material.
|
|
A second example of collective behavior involves the interaction of a
chain of blocks to form a SD superstate magnetized parallel to the
chain axis but perpendicular to the easy axes of the individual blocks.
This behavior is illustrated schematically in Fig. 5b and
can be found in several places in Fig. 3 (e.g., blocks 1618 in Fig. 3
a, b, d, f, and
h). If the three blocks are instead magnetized perpendicular
to the chain axis, then a third superstate equivalent to a three-domain
particle is generated (Fig. 5c). The central block is now
magnetized antiparallel to the blocks on either side of it. Several
examples of this behavior can be found (e.g., blocks 1618 and blocks
911 in Fig. 3 c, e, and g).
A similar phenomenon occurs when a small block is sandwiched between
larger ones, as shown in Fig. 4 c and d. In Fig.
4d, the two largest blocks are colored green, indicating
that they are both magnetized in the same direction. The small block in
between them is colored red, indicating that it is magnetized in the
opposite direction. The magnetization in the small block follows the
flux return paths of its larger neighbors, and the resulting
dipole-like magnetic field is clearly resolved. Fig. 4 provides a
direct observation of one of the fundamental causes of self-reversed
thermoremanent magnetization. The blocking temperature of a particle,
below which the magnetization direction of a particle becomes
"locked in" during cooling in the presence of an applied magnetic
field, is determined by its size. The present geomagnetic field
(0.30.6 Oe) is much lower than the switching fields of the magnetite
particles examined here. Larger blocks have a higher blocking
temperature than smaller blocks and will be first to acquire a
thermoremanent magnetization parallel to the applied field on cooling.
The magnetization directions of smaller blocks become locked in at a
lower temperature and may point antiparallel to the applied field
direction due to strong magnetostatic interactions with their
neighbors, as in the partially self-reversed configuration shown in
Fig. 4d. Similar interactions are likely to constrain the
magnetization directions of blocks that are small enough to be
superparamagnetic at room temperature if they were isolated, as
observed with electron holography for 20-nm magnetite crystals arranged
in chains in magnetotactic bacteria (15). Full self-reversal could be
achieved if the volumetric proportion of smaller blocks was greater
than that of larger blocks and the demagnetizing field of the larger
blocks was sufficient to overcome the applied field.
Macroscopic Behavior.
As well as providing detailed images of magnetic domain states at
the nanometer scale, the measurements yield semiquantitative
information about the net magnetic behavior of the sample at
mesoscopic-length scales. Fig. 6 shows a
"remanent hysteresis loop" determined from images such as those
shown in Fig. 3. The circles indicate the fraction of the magnetization
in the blocks that points in the direction of the applied field. The
open and closed circles correspond to opposite directions of the
applied field. The fitted curve tends to a value well below unity
because the magnetization is never saturated in the remanent state.
This graph provides an upper limit for the ratio of saturation remanent
magnetization to saturation magnetization
(Mrs/Ms)
of
0.5. A lower limit for
Mrs/Ms
of
0.2 is obtained from the slope of the recorded magnetic
contribution to the holographic phase shift. Values of
Mrs/Ms
of
0.20.5 are characteristic of SD behavior.

View larger version (17K):
[in this window]
[in a new window]
|
Fig 6. Remanent hysteresis loop obtained from the images shown in Fig. 3 by
plotting the average fraction of the measured magnetic induction in the
magnetite-rich blocks in the direction of the applied field. The graph
tends to a value below unity because the magnetic microstructure is
never saturated in the applied field direction in the remanent state.
|
|
An alternative test of SD vs. MD behavior is provided by the
ratio of the coercivity of remanence to the coercivity
(Hcr/Hc).
Fig. 6 yields an estimate for Hcr of
700 ± 200 Oe for this region of the sample. Typical estimates
(12) for the maximum coercivities Hc
of isolated magnetite blocks of this size are
100 Oe, yielding a
lower bound of
Hcr/Hc
7. This is above the limit of
Hcr/Hc
4 normally associated with MD behavior (16). (Isolated SD grains
would have 1 <
Hcr/Hc
< 2.) Similar MD-like behavior has been observed by using conventional
hysteresis measurements of synthetic intergrowths of magnetite and
spinel (MgAl2O4) (17).
 |
Discussion
|
|---|
The unusual combination of MD- and SD-like macroscopic properties
means that the ability of fine-scale intergrowths to carry strong and
stable NRM is not clear-cut. Strong magnetostatic interactions between
neighboring blocks create a large demagnetizing field in the grain as a
whole. These interactions cause a reduction in magnetization due
to the spontaneous formation of vortex or MD superstates when the
applied field is removed. Coarsening would reduce the number of
magnetite blocks per unit volume, resulting in weaker interactions and
more SD-like behavior. Coarsening would, however, increase the average
block size and the likelihood of vortex states. The low
magnetocrystalline anisotropy of magnetite and the roughly
equidimensional morphology of the blocks results in low intrinsic
coercivities. As a result, a block is able to respond readily to the
demagnetizing field created by its neighbors. Microstructures with a
more lamellar microstructure would have increased shape anisotropy and
a greater potential for maintaining stable NRM. Nevertheless, it is
clear from Fig. 6 that many blocks are sufficiently below their
blocking temperature to prevent reorientation of their magnetic moments
in response to interactions with their neighbors, leading to SD-like
values of
Mrs/Ms.
Understanding the behavior at higher temperatures, in smaller fields,
and over longer time scales is now of primary importance.
The recent discovery of large crustal magnetic anomalies in the
southern hemisphere of Mars (18, 19) has reignited the debate over
which minerals are capable of maintaining strong remanent
magnetizations over the
4 billion years since there was last a
magnetic field on Mars. Proper identification of the minerals and/or
microstructures responsible for the anomalies is a prerequisite for
developing a realistic geophysical model for the creation of the
Martian crust. The generation of SD magnetite by exsolution and/or
oxidation processes in titanomagnetite has been suggested as a possible
source of stable remanent magnetization on Mars (20). In both cases,
the microstructures would be similar to those observed here. It is
assumed that the cooling rate would be slow enough to allow phase
separation but fast enough to ensure that the resulting magnetite
blocks are of SD, rather than MD, size. The required cooling rate is
determined by analogy with terrestrial rocks and is used to constrain
the geophysical model. Slower cooling rates in terrestrial rocks result
in more coarsely exsolved titanomagnetites with a more lamellar
morphology and a greater ability to store stable NRM (10). Such
considerations have implications for the cooling-rate constraints used
in geophysical models of the Martian crust.
 |
Acknowledgements
|
|---|
We are grateful to the Royal Society, the Engineering and Physical
Sciences Research Council, and the Deutsche
Forschungsgemeinschaft for support.
 |
Footnotes
|
|---|
To whom correspondence should be addressed. E-mail:
rafal.db{at}msm.cam.ac.uk. 
This paper was submitted
directly (Track II) to the
PNAS office.
 |
References
|
|---|
- Dunlop, D. J. & Özdemir, Ö., (1997) Rock Magnetism, Fundamentals, and Frontiers (Cambridge Univ. Press, Cambridge, U.K.).
- Davis, P. M. & Evans, M. E. (1976) J. Geophys. Res. 81, 989-994.
- Vincent, E. A., Wright, J. B., Chevallier, R. & Mathieu, S. (1957) Miner. Mag. 31, 624-655.
- Price, G. D. (1981) Am. Mineral. 66, 751-758.[Abstract]
- Lindsley, D. H. (1981) Am. Mineral. 66, 759-762.[Abstract]
- Tonomura, A. (1992) Adv. Phys. 41, 59-103.[CrossRef]
- Midgley, P. A. (2001) Micron 32, 167-184.[Medline]
- Feininger, T. & Goodacre, A. K. (1995) Can. J. Earth Sci. 32, 1350-1364.
- Evans, M. E. & Wayman, M. L. (1974) Geophys. J. R. Astron. Soc. 36, 1-10.
- Price, G. D. (1980) Phys. Earth Planet. Inter. 23, 2-12.
- Dunin-Borkowski, R. E., McCartney, M. R., Kardynal, B., Parkin, S. S. P., Scheinfein, M. R. & Smith, D. J. (2000) J. Microsc. 200, 187-204.[Medline]
- Williams, W. & Wright, T. M. (1998) J. Geophys. Res. 103, 30537-30550.[CrossRef]
- Dunin-Borkowski, R. E., McCartney, M. R., Kardynal, B., Smith, D. J. & Scheinfein, M. R. (1999) Appl. Phys. Lett. 75, 2641-2643.[CrossRef]
- Dunin-Borkowski, R. E., McCartney, M. R., Kardynal, B. & Smith, D. J. (1998) J. Appl. Phys. 84, 374-378.[CrossRef][ISI]
- Dunin-Borkowski, R. E., McCartney, M. R., Frankel, R. B., Bazylinski, D. A., Pósfai, M. & Buseck, P. R. (1998) Science 282, 1868-1870.[Abstract/Free Full Text]
- Day, R., Fuller, M. D. & Schmidt, V. A. (1977) Phys. Earth Planet. Inter. 13, 260-267.
- Harrison, R. J. & Putnis, A. (1996) Am. Mineral. 82, 131-142.
- Acuña, M. H., Connerney, J. E. P., Ness, N. F., Lin, R. P., Mitchell, D., Carlson, C. W., McFadden, J., Anderson, K. A., Reme, H., Mazelle, C., et al. (1999) Science 284, 790-793.[Abstract/Free Full Text]
- Connerney, J. E. P., Acuña, M. H., Wasilewski, P. J., Ness, N. F., Reme, H., Mazelle, C., Vignes, D., Lin, R. P., Mitchell, D. L. & Cloutier, P. A. (1999) Science 284, 794-798.[Abstract/Free Full Text]
- Nimmo, F. (2000) Geology 28, 391-394.[Abstract/Free Full Text]
www.pnas.org/cgi/doi/10.1073/pnas.262514499

CiteULike
Complore
Connotea
Del.icio.us
Digg What's this?
This article has been cited by other articles in HighWire Press-hosted journals: