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Bulletin of the Czech Geological Survey, Vol. 77, No. 4, 243–252, 2002<br />
© Czech Geological Survey, ISSN 1210-3527<br />
Asteroids: Their composition and impact threat<br />
THOMAS H. BURBINE<br />
Department of Mineral Sciences, National Museum of Natural History, Smithsonian Institution, Washington, DC 20560-0119, USA; e-mail:<br />
burbine.tom@nmnh.si.edu<br />
Abstract. Impacts by near-Earth asteroids are serious threats to life as we know it. The energy of the impact will be a function of the mass of<br />
the asteroid and its impact velocity. The mass of an asteroid is very difficult to determine from Earth. One way to derive a near-Earth object’s mass is<br />
by estimating the object’s density from its surface composition. Reflectance spectra are the best way to determine an object’s composition since many<br />
minerals (e.g. olivine, pyroxene, hydrated silicates) have characteristic absorption features. However, metallic iron does not have characteristic absorption<br />
bands and is very hard to identify from Earth. For a particular size, asteroids with compositions similar to iron meteorites pose the biggest<br />
impact threat since they have the highest densities, but they are expected to be only a few percent of the impacting population. Knowing an asteroid’s<br />
composition is also vital for understanding how best to divert an incoming asteroid.<br />
Key words: Earth, asteroids, impact features, meteorites, mineral composition, geologic hazards<br />
Introduction<br />
As we enter a new millennium, we are constantly being<br />
bombarded with news of close encounters with near-Earth<br />
objects (NEOs). Observers have discovered over 2,000 near-<br />
Earth asteroids (NEAs); luckily none are known to be on a<br />
collision course with the Earth. Comets are also serious impact<br />
threats as shown by the collision of Shoemaker-Levy-9<br />
with Jupiter in 1994. Since the discovery of the iridium<br />
anomaly at the Cretaceous-Tertiary (K-T) boundary layer by<br />
Alvarez et al. (1980), there has been a considerable discussion<br />
of the possibility and consequences of such an impact<br />
(e.g. Chapman and Morrison 1994, Adushkin and Nemchinov<br />
1994, Toon et al. 1997, Garshnek et al. 2000).<br />
As we discover more Earth-approaching asteroids, we<br />
are also learning more about their compositions and structure.<br />
Charge-coupled devices (CCDs) now allow us to obtain<br />
visible and near-infrared telescopic spectra of<br />
near-Earth asteroids that are a few hundred meters or<br />
smaller in diameter (e.g. Binzel et al. 2001a). Technological<br />
improvements to the radio telescope at the Arecibo Observatory<br />
have allowed similarly sized objects to be<br />
characterized by radar (e.g. Ostro et al. 2002). Spacecraft<br />
missions now show asteroids to be geologic bodies with a<br />
variety of morphologic features. More meteorites are discovered<br />
every year and are being extensively studied in the<br />
laboratory with more precise analytical techniques.<br />
However as we continue our research on asteroids, a<br />
number of questions should be asked. “How do asteroid<br />
compositions affect the impact threat?” “How well can we<br />
determine asteroid compositions from Earth?” This paper<br />
will review what we currently know about asteroid compositions<br />
and how it affects the impact threat. Since we<br />
have not yet returned any samples from any asteroids, our<br />
knowledge of asteroid compositions is derived from analyses<br />
of meteorites, remote sensing observations from Earth,<br />
and spacecraft missions.<br />
Impact threat<br />
I will first briefly review what we know about the number<br />
of near-Earth objects and the energy and effects of impacts.<br />
The near-Earth object population is defined as small<br />
bodies with perihelion distance less than 1.3 AU (astronomical<br />
units) and aphelion distance greater than 0.983<br />
AU (Morbidelli et al. 2002). These objects are primarily<br />
thought to be asteroids ejected from the main belt; however,<br />
a few extinct comets probably exist in the population.<br />
Recent estimates of the numbers of NEAs larger than one<br />
kilometer in diameter vary from 855 (±110) (Morbidelli et<br />
al. 2002) to 1227 (uncertainties of +170 and –90) (Stuart<br />
2001).<br />
The kinetic energy (E) of an incoming asteroid is<br />
(1/2)mv 2 where m is the mass and v is the velocity. Mass is<br />
a function of the density (ρ) and volume (V) of the object.<br />
Since the energy of an impact is usually given as megatons<br />
of TNT, the kinetic energy equation can be written (Morbidelli<br />
et al. 2002) as<br />
E = 62.5 ρd 3 v 2<br />
where E is in megatons, ρ is in g/cm 3 , d is the diameter of<br />
the impactor in kilometers, and v is in km/s. The average<br />
impact velocity for asteroids with Earth are ~ 20 km/s (e.g.<br />
Hughes, 1998). Comets have lower densities (estimated to<br />
be around ~ 1 g/cm 3 ), but some long-period comets have<br />
much higher average impact velocities (~ 55 km/s) (Marsden<br />
and Steel 1994). Since water covers approximately<br />
three-fourths of the Earth’s surface, “large” impacts are<br />
likely to cause tsunamis (e.g. Paine 1999), giant tidal<br />
waves created by sudden disturbances.<br />
The best-characterized localized catastrophe is the impact<br />
at Tunguska where an object exploded 5–10 km in the<br />
air over an uninhabited region of Siberia (e.g. Chyba et al.<br />
1993, Vasilyev 1998). The energy was estimated to be<br />
~ 10–20 megatons and devastated an area of ~ 2000 km 2<br />
of forest area. In comparison, the energy is ~ 1,000 times<br />
243
Thomas H. Burbine<br />
larger than the bomb dropped on Hiroshima and the area is<br />
~ 4 times larger than New York City.<br />
The best-characterized “large” impact is the Chicxulub<br />
crater found in the Yucatan peninsula (e.g. Hildebrand et<br />
al. 1998). Hildebrand et al. (1998) argues that the crater is<br />
180 km in diameter, but other researchers (e.g. Morgan et<br />
al. 1998) argue that the actual crater size could be as large<br />
as 270 km. The energy of the impactor for producing the<br />
Chicxulub crater is estimated to be ~ 10 8 megatons (e.g.<br />
Toon et al. 1997). This impact occurred ~ 65 million years<br />
ago, which is the same age as the K-T extinction. The K-<br />
T boundary marks the demise of the dinosaurs as the dominant<br />
animal species on Earth (e.g. Milner 1998).<br />
We currently have evidence for over 160 impact craters<br />
on Earth over the last ~ 2 billion years that range from 15<br />
meters to 300 kilometers in diameter (Earth Impact<br />
Database 2002). Many more impacts have occurred over<br />
this time with evidence for these impacts wiped out due to<br />
erosion by water and wind. Cratering rates for the Earth<br />
(e.g. Neukum and Ivanov, 1994) can be estimated from determinations<br />
of the NEO population, the lunar cratering<br />
rate (where the effects of the Earth’s atmosphere needed to<br />
be added), and crater counts on terrestrial cratons.<br />
Neukum and Ivanov (1994) estimate that craters one kilometer<br />
in size or greater form on the Earth every ~ 1600<br />
years and craters 100 kilometers in size or greater form<br />
every 27 million years.<br />
Morbidelli et al. (2002) have done a recent study of<br />
collision probabilities of NEOs with the Earth. They estimate<br />
that a 1000 megaton impact, which would produce<br />
large-scale regional damage and a crater ~ 5 km in size<br />
(e.g. Hughes 1998), should occur every 63,000 ± 8,000<br />
years. They estimate that known NEOs carry only ~ 18%<br />
of the overall collision probability.<br />
The consequences of any impact on Earth will be a<br />
function of the mass (density times volume) and impact<br />
velocity plus the location, date, and time of the impact on<br />
Earth. Astrometric observations, which determine the<br />
location of an object in the sky, can help determine an asteroid’s<br />
orbit with a high degree of certainty. These observations<br />
can be used to predict the probability that an object<br />
will strike the Earth. If an object is on a collision course<br />
these astrometric observations can be used to predict the<br />
impact velocity and the location of the impact. Radar observations<br />
(e.g. Ostro et al. 2002) can image an asteroid (if<br />
it is large enough and close enough to Earth) and then determine<br />
its diameter, which can be used to calculate its<br />
volume.<br />
However, the determination of an asteroid’s mass is<br />
much more difficult from Earth. For the largest asteroids,<br />
masses can be determined by asteroid-asteroid interactions<br />
or their perturbations on Mars (Britt et al. 2002). To determine<br />
a near-Earth asteroid’s mass, the object needs to have<br />
a natural body revolving around it (e.g. Margot et al. 2002)<br />
or a spacecraft encounter (e.g. Veverka et al. 1999, Yeomans<br />
et al. 2000).<br />
However in the absence of such a mass determination,<br />
the best way to estimate a near-Earth asteroid’s mass<br />
would be to determine its surface composition, which<br />
would give insight into the object’s density. (Since near-<br />
Earth asteroids are fragments of much larger asteroids, we<br />
assume that the surface composition is representative of<br />
the object as a whole.) The mass could then be estimated<br />
by multiplying the inferred density by the object’s volume.<br />
Such an estimate would only give an upper limit on an object’s<br />
mass, since many asteroids are thought to be rubble<br />
piles with significant amounts of macroporosity (e.g. Britt<br />
and Consolmagno 2001, Britt et al. 2002). The estimated<br />
macroporosities for ~ 20 asteroids range from 0 to ~ 80%<br />
(Britt et al. 2002).<br />
Meteorites<br />
Except for ~ 50 samples from the Moon and Mars, meteorites<br />
appear to be fragments of sub-planetary sized bodies<br />
(asteroids) that formed ~ 4.56 billion years ago.<br />
Meteorites can basically be broken into two types: those that<br />
experienced heating but not melting (chondrites) (e.g.<br />
Brearley and Jones 1998) and those that experienced melting<br />
and differentiation (achondrites, stony-irons, irons) (e.g.<br />
Mittlefehldt et al. 1998). Silicate-rich meteorites are often<br />
referred to as stony and would include all chondrites and<br />
achondrites. Meteorites that are similar in terms of petrologic,<br />
mineralogical, bulk chemical, and isotopic properties<br />
are separated into groups (Table 1). In general, groups contain<br />
five or more members to allow for the compositional<br />
characteristics of the group to be adequately characterized.<br />
Currently, 13 groups (Table 1) of chondritic meteorites<br />
have been defined. Chondritic groups are subdivided according<br />
to petrologic type (1–6) with 1 being the most<br />
aqueously altered, 3.0 being the least altered, and 6 being<br />
heated to the highest temperatures. Mineralogically, meteorites<br />
of petrologic type 1 and 2 (CI, CM, CR) have compositions<br />
dominated by phyllosilicates. Visually, these<br />
meteorites are extremely dark. The other types of carbonaceous<br />
chondrites (CH, CV, CO, CK) tend to have<br />
mineralogies dominated by mafic silicates. The R chondrites<br />
are dominated by olivine. Ordinary chondrites (H,<br />
L, LL) are mixtures of mafic silicates and metallic iron,<br />
while enstatite chondrites are composed of enstatite (virtually<br />
FeO-free pyroxene) and metallic iron. In addition to<br />
these 13 well-defined groups, ~ 14 chondritic grouplets or<br />
unique meteorites (Meibom and Clark 1999, Weisberg et<br />
al. 2001, Mittlefehldt, 2002) have been recognized.<br />
The differentiated meteorites range from those that experienced<br />
only limited differentiation (primitive achondrites)<br />
to those (differentiated achondrites, stony-irons,<br />
irons) that were produced by extensive melting, melt migration,<br />
and fractional crystallization. These processes<br />
produce a wide variety of lithologies.<br />
Many of the differentiated meteorites are thought to<br />
sample the crusts (howardites, eucrites, and diogenites or<br />
HEDs; angrites), core-mantle boundaries (pallasites), and<br />
cores (irons) of differentiated bodies. Eucrites contain primarily<br />
plagioclase and both low-Ca and high-Ca pyrox-<br />
244
Asteroids: Their composition and impact threat<br />
enes, while diogenites are predominantly magnesian orthopyroxene.<br />
Howardites are breccias of eucritic and diogenitic<br />
material. Pallasites are mixtures of metallic iron<br />
and olivine. We do not appear to be sampling the mantles<br />
of these differentiated bodies (e.g. Burbine et al. 1996);<br />
however, we do appear to be sampling the mantles of veryreduced<br />
differentiated bodies in the form of aubrites.<br />
Iron meteorites are composed of metallic iron with<br />
5–20% Ni plus accessory phases such as sulfides,<br />
schreibersite, and silicate inclusions. Iron meteorites are<br />
classified according to siderophile (“iron-loving”) element<br />
(Ga, Ge, Ir, Ni) concentrations. Of the thirteen groups of<br />
iron meteorites, ten (IC, IIAB, IIC, IID, IIF, IIIAB, IIIE,<br />
IIIF, IVA, IVB) have fractional crystallization trends suggestive<br />
of prolonged cooling as expected from the cores of<br />
differentiated bodies. Three of the groups (IAB, IIE, and<br />
IIICD) do not display well-developed fractional crystallization<br />
trends and contain abundant silicate inclusions,<br />
which argues that they are not core fragments. Approximately<br />
90 irons (Grady 2000) are not classified as members<br />
of the 13 groups and are labeled anomalous. These<br />
ungrouped irons are believed to require 50-70 distinct parent<br />
bodies (Wasson 1995, Burbine et al. 2002b).<br />
Other types of differentiated meteorites have undergone<br />
varying amounts of melting. These include a number<br />
of primitive achondritic meteorites (acapulcoite-lodranites,<br />
winonaites), which are samples of partially differentiated<br />
asteroids. These meteorites are mixtures of olivine,<br />
pyroxene, and metallic iron. Mesosiderites are breccias<br />
composed of HED-like clasts of basaltic material mixed<br />
with metallic clasts. One possible scenario for the formation<br />
of the mesosiderites is the disruption of an asteroid<br />
with a molten core (Scott et al. 2001). Rounding out the<br />
differentiated meteorites are the olivine-dominated brachinites<br />
and the carbon-rich ureilites, whose origins are<br />
still being debated (e.g. Mittlefehldt et al. 1998).<br />
Meteorite densities and strengths<br />
Consolmagno and Britt (1998), Flynn et al. (1999), and<br />
Wilkinson and Robinson (2000) have recently done studies<br />
of meteorite bulk densities. The only CI chondrite<br />
measured had a bulk density of 1.58 g/cm 3 while the bulk<br />
densities of CM chondrites were 2.08–2.37 g/cm 3 . CO<br />
chondrites (2.36–2.98 g/cm 3 ) and CV chondrites<br />
(2.60–3.18 g/cm 3 ) tended to have slightly higher bulk densities.<br />
The only enstatite chondrite measured had a bulk<br />
density of 3.36 g/cm 3 . On average, ordinary chondrites<br />
(3.05–3.75 g/cm 3 for the most reliable measurements)<br />
have the highest bulk densities of the chondrites.<br />
HEDs have bulk densities of 2.99–3.29 g/cm 3 . Stonyirons<br />
such as mesosiderites (4.16–4.22 g/cm 3 ) and pallasites<br />
(4.82–4.97 g/cm 3 ) have higher bulk densities due to<br />
the presence of significant amounts of metallic iron. As expected,<br />
iron meteorites tend to have the highest bulk densities<br />
of all meteorite types (6.99–7.59 g/cm 3 for relatively<br />
unweathered specimens).<br />
Table 1. Meteorite groups<br />
Groups Composition* Fall percentages # (%)<br />
Carbonaceous chondrites<br />
CI phy, mag 0.5<br />
CM phy, toch, ol, 1.7<br />
CR phy, px, ol, met 0.3<br />
CO ol, px, CAIs, met 0.5<br />
CH px, met, ol, Only finds<br />
CV ol, px, CAIs 0.6<br />
CK ol, CAIs 0.3<br />
Enstatite chondrites<br />
EH enst, met, sul, plag, ± ol 0.8<br />
EL enst, met, sul, plag 0.7<br />
Ordinary chondrites<br />
H ol, px, met, plag, sul 34.1<br />
L ol, px, plag, met, sul 38.0<br />
LL ol, px, plag, met, sul 7.9<br />
R chondrites ol, px, plag, sul 0.1<br />
Primitive achondrites<br />
Acapulcoites a px, ol, plag, met, sul 0.1<br />
Lodranites a px, ol, met, ± plag, ± sul 0.1<br />
Winonaites ol, px, plag, met 0.1<br />
Differentiated achondrites<br />
Angrites TiO 2-rich aug, ol, plag 0.1<br />
Aubrites enst, sul 0.1<br />
Brachinites ol, cpx, ± plag Only finds<br />
Diogenites b opx 1.2<br />
Eucrites b pig, plag 2.7<br />
Howardites b eucritic-diogenitic breccia 2.1<br />
Ureilites ol, px, graph 0.5<br />
Stony-irons<br />
Mesosiderites basalt-met breccia 0.7<br />
Pallasites ol, met ol, met 0.5<br />
Irons c met, sul, schreib 4.2<br />
Table is revised from tables found in Burbine et al. (2002b).<br />
* Minerals or components are listed in decreasing order of average abundance.<br />
Abbreviations: ol – olivine, px – pyroxene, opx – orthopyroxene,<br />
pig – pigeonite, enst –enstatite, aug – augite, cpx – clinopyroxene, plag<br />
– plagioclase, mag – magnetite, met – metallic iron, sul – sulfides, phy –<br />
phyllosilicates, toch – tochilinite, graph – graphite, CAIs – Ca-Al-rich<br />
refractory inclusions, schreib – schreibersite, ± – may be present<br />
# Fall percentages are calculated from the 942 classified falls that are listed<br />
in Grady (2000), Grossman (2000), and Grossman and Zipfel (2001).<br />
a Acapulcoites and lodranites appear to come from the same parent body<br />
(e.g. Mittlefehldt et al. 1998).<br />
b Howardites, eucrites, and diogenites (HEDs) appear to come from the<br />
same parent body (e.g. Mittlefehldt et al. 1998).<br />
c There are 13 iron meteorite groups plus ~100 ungrouped irons.<br />
In terms of physical strength, most chondritic meteorites<br />
can be easily crushed into powders with a mortar<br />
and pestle. Meteorites containing phyllosilicates tend to be<br />
the most fragile with the CI chondrites being the weakest<br />
of these objects with laboratory crushing strengths of 1–10<br />
bars (e.g. Lewis 2000). What cannot be easily pulverized<br />
is metallic iron. Metallic iron is ductile and tends to flatten<br />
and elongate while being crushed at room temperatures. It<br />
is unclear how ductile metallic iron is at the colder temperatures<br />
found in the asteroid belt.<br />
Iron meteorites are extremely strong with strengths of<br />
approximately 3.5 kbars (e.g. Lewis, 2000). The much<br />
stronger physical strength of irons allows them to survive<br />
in space much longer than stony bodies as seen by their<br />
longer cosmic ray exposure ages. Cosmic ray exposure<br />
ages record the time an object has spent as a meter-sized<br />
245
Thomas H. Burbine<br />
Normalized Reflectance<br />
6<br />
5<br />
4<br />
3<br />
2<br />
1<br />
0<br />
0.2 0.6 1 1.4 1.8 2.2 2.6<br />
Wavelength (µm)<br />
or less body in space or within a few meters of the surface.<br />
Irons have cosmic ray exposure ages ranging from hundreds<br />
of millions to a few billion years (e.g. Voshage and<br />
Feldman 1979) while stony meteorites tend to have much<br />
shorter exposure ages (
Asteroids: Their composition and impact threat<br />
Asteroid observations<br />
This section will detail what we currently think we understand<br />
about asteroid compositions. Asteroid spectral<br />
surveys (e.g. Zellner et al. 1985, Bus and Binzel 2002a)<br />
have primarily been done in the visible due to the peaking<br />
of the illuminating solar flux and the relative transparency<br />
of the atmosphere at these wavelengths. Near-infrared observations<br />
(1-3.5 µm) have now become easier to obtain<br />
due to the advent of SpeX (an infrared spectrograph at the<br />
Infrared Telescope Facility on Mauna Kea) (e.g. Binzel et<br />
al. 2001b).<br />
Asteroids are generally grouped into classes (Table 2)<br />
based on their visible spectra (~ 0.4 to ~ 0.9–1.1 µm) and<br />
visual albedo (when available). The most widely used taxonomy<br />
(Tholen 1984) classifies objects observed in the<br />
eight-color asteroid survey (ECAS) (Zellner et al. 1985).<br />
Bus and Binzel (2002a) did a CCD spectral survey of over<br />
1300 objects and developed an expanded taxonomy (Bus<br />
and Binzel 2002b) with many more classes and subclasses<br />
to represent the diversity of spectral properties seen in<br />
higher-resolution spectra. Representative spectra of a<br />
number of Bus and Binzel (2002a, 2002b) asteroid classes<br />
are shown in Figure 2.<br />
As stated earlier, to accurately determine an asteroid’s<br />
mineralogy, observations are needed in the near-infrared<br />
since many minerals have diagnostic features in this wavelength<br />
region. Near-infrared asteroid spectra (Gaffey et al.<br />
1993, Rivkin et al. 2000, Burbine and Binzel 2002) at a variety<br />
of wavelengths have shown that each class tends to<br />
contain a wide variety of mineralogies. Only qualitative<br />
mineralogical descriptions will be given for asteroid classes<br />
discussed in this paper; quantitative analyses of asteroid<br />
compositions (determining the proportion and composition<br />
of different mineral species) are very difficult (e.g.<br />
Clark, 1995) since an asteroid’s reflectance spectrum is a<br />
function of a number of factors such as mineralogy, mineral<br />
chemistry, particle size, and temperature.<br />
Asteroid taxonomy is based on astronomically observed<br />
parameters without regard to composition. However, many<br />
asteroid classes have been given letter designations that<br />
“imply” specific compositions. This includes the letter “M”<br />
for metallic, “S” for siliceous (or stony or stony-iron), and<br />
“C” for carbonaceous. (Bus and Binzel (2002b) do not differentiate<br />
between E, M, and P asteroids and call them all X<br />
objects since there spectra are similar and albedo is not used<br />
in their taxonomy.) Since each asteroid class only groups asteroids<br />
with specific spectral characteristics, not all objects<br />
in a class have to have similar surface mineralogies. For example,<br />
it is unknown how many M-class asteroids actually<br />
have surfaces similar to iron meteorites. For example, enstatite<br />
chondrites (primarily mixtures of metallic iron and<br />
enstatite) also have relatively featureless spectra (Gaffey<br />
1976) and similar albedos to metallic iron. Also, a subgroup<br />
of M-class asteroids (called the W class) have distinctive 3<br />
µm features (e.g. Rivkin et al. 2000), which apparently indicate<br />
hydrated minerals and surface compositions inconsistent<br />
with metallic iron.<br />
Radar observations have been used to estimate the metal<br />
contents of asteroids (Ostro et al., 2002). Radar experiments<br />
of asteroids usually measure the distribution of echo<br />
power reflected from an object in time delay and Doppler<br />
Table 2. Asteroid Classes<br />
Class characteristics<br />
A Distinctive olivine absorption features<br />
B Weak UV feature, blue past 0.4 µm, subclass of C types; low albedo (generally less than 0.1)<br />
C a Weak UV feature, flat to reddish past 0.4 µm; low albedo (generally less than 0.10)<br />
D Very red spectrum; low albedo (usually around 0.05 or less)<br />
E Flat to slightly red, featureless spectrum; high albedo (> 0.30); usually associated with aubrites<br />
F Very weak UV feature, flat to bluish past 0.4 µm, subclass of C types; low albedo (< 0.10)<br />
G Strong UV feature, flat past 0.4 µm, subclass of C class; usually have strong 3 µm features; low albedo (< 0.10)<br />
J Stronger 1 µm feature than V types; appear to have compositions similar to the HEDs<br />
K Spectrum intermediate between S and C asteroids; usually associated with CO3/CV3 chondrites<br />
L b Very strong UV feature and then becoming approximately flat<br />
M Flat to slightly red, featureless spectrum; moderate albedo (0.10-0.30)<br />
O Weak UV feature out to 0.44 µm, very strong 1 µm feature; type spectrum is 3628 Božněmcová<br />
P Flat to slightly red, featureless spectrum; low albedo (usually around 0.05 or less)<br />
Q Strong UV and 1 µm feature; spectrum similar to ordinary chondrites<br />
R Strong UV and 1 µm feature; type spectrum is 349 Dembowska<br />
S c Strong UV feature; usually has 1 µm feature, indicating olivine and/or pyroxene; moderate albedo (0.10–0.30)<br />
T Weak UV feature, reddish past 0.4 µm; low albedo (< 0.10)<br />
V Distinctive 1 and 2 µm features due to pyroxene; appear to have compositions similar to the HEDs<br />
W M-class visible spectrum with a 3 µm absorption feature<br />
Spectrum similar to E, M, or P types, but no albedo information<br />
X d<br />
This table is revised from tables in Wetherill and Chapman (1988), Pieters and McFadden (1994), and Bus and Binzel (2002b). The term “red” refers<br />
to reflectances increasing with increasing wavelength and the term “blue” refers to reflectances decreasing with increasing wavelength.<br />
a Bus and Binzel (2001b) subdivided the C-class objects into the C, Cb, Cg, Ch, and Cgh subclasses based on CCD spectra. Bus and Binzel (2001b)<br />
do not define the F and G classes.<br />
b Bus and Binzel (2001b) subdivided the L-class objects into the L and Ld classes based on CCD spectra.<br />
c Gaffey et al. (1993) subdivided the S-class objects into the S(I) to S(VII) subclasses on the basis of both visible and near-infrared spectra. Bus and<br />
Binzel (2002b) have subdivided the S class into the S, Sa, Sk, Sl, Sq, and Sr subclasses based on CCD spectra.<br />
d Bus and Binzel (2002b) subdivided the X-class class objects into the X, Xc, Xe, and Xk subclasses based on CCD spectra.<br />
247
Thomas H. Burbine<br />
Normalized Reflectance<br />
2.8<br />
2.3<br />
1.8<br />
1.3<br />
1929 Kollaa (V)<br />
1542 Schalen (D)<br />
6 Hebe (S)<br />
221 Eos (K)<br />
64 Angelina (Xe)<br />
19 Fortuna (Ch)<br />
16 Psyche (X)<br />
0.8<br />
0.4 0.5 0.6 0.7 0.8 0.9 1<br />
Wavelength (µm)<br />
Fig. 2. Reflectance spectra of a number of Bus and Binzel (2002a,<br />
2002b) asteroid classes. All spectra are normalized to unity at 0.55 µm<br />
and offset in reflectance from each other. Error bars are one sigma. All<br />
spectra are available at the website http://smass.mit.edu.<br />
frequency in the opposite sense (OC) of circular polarization<br />
and the same sense. OC radar albedos are equal to the<br />
OC radar cross section divided by the target’s projected<br />
area. For homogeneous and particulate surfaces, radar<br />
albedos are functions of the near-surface bulk density,<br />
which is related to both the solid-rock density and the surface<br />
porosity of the object. Increasing the solid-rock density<br />
or decreasing the surface porosity would increase the<br />
radar albedo of an object. Without knowing the porosity of<br />
the surface, it is impossible to conclusively determine the<br />
surface assemblage of an object. M-asteroids with the<br />
highest radar albedos (0.6–0.7) could have surfaces of<br />
metallic iron with “lunar-like” porosities (35-55%) or solid<br />
enstatite-chondritic material with little to no porosity. It<br />
is unclear if such solid surfaces of enstatite chondrite material<br />
could exist on the surface of an asteroid. M asteroids<br />
tend to have higher radar albedos than C or S asteroids<br />
(Magri et al. 1999), apparently implying that they are richer<br />
in metallic iron.<br />
S asteroids tend to have 1 µm absorption features,<br />
which indicates assemblages containing Fe 2+ -bearing silicates<br />
such as olivine and/or pyroxene. On the basis of<br />
high-resolution CCD spectra, Bus and Binzel (2002b) subdivide<br />
the S asteroids into a number of subtypes (S, Sa, Sk,<br />
Sl, Sq, and Sr). The subscript represents that the objects is<br />
intermediate in spectral properties between that class (A,<br />
K, L, Q, and R) and the S class; however, it is currently<br />
unclear if each of these subclasses is grouping objects with<br />
similar compositions. From near-infrared spectra, Gaffey<br />
et al. (1993) finds that S asteroids tended to have compositions<br />
that ranged from olivine-rich (which he defined as<br />
S(I)) to pyroxene-rich (S(VII)). To classify these objects,<br />
they use the band area ratio (ratio of the area of Band I to<br />
the area of Band II) and the Band I minimum, which are<br />
both function of the olivine/pyroxene abundance (Cloutis<br />
et al., 1986). The band parameters of S(IV)-objects appear<br />
consistent with ordinary chondrites, but also consistent<br />
with other types of meteorites such as ureilites or acapulcoites/lodranites.<br />
S asteroids are the most abundant type of classified asteroid<br />
since they tend to be found in the inner main belt<br />
(closer to the Sun) and have higher albedos than C-types,<br />
making them brighter and easier to discover and observe.<br />
The biggest question concerning S asteroids is what fraction<br />
is compositionally similar to ordinary chondrites. S<br />
asteroids are spectrally redder than ordinary chondrites<br />
and tend to have weaker absorption bands (Figure 3). It<br />
has long been argued (e.g. Wetherill and Chapman 1988)<br />
whether these spectral differences are due to inherent compositional<br />
differences or simply due to an alteration<br />
process that can redden ordinary chondrite material. Analyses<br />
of lunar regolith (e.g. Pieters et al. 2000) and alteration<br />
experiments (e.g. Sasaki et al. 2001) appear to show<br />
that this reddening on asteroidal surfaces could be due to<br />
surface alteration processes (e.g. micrometeorite impacts,<br />
solar wind sputtering) that produce vapor-deposited coatings<br />
of nanophase iron.<br />
C-type asteroids (including the B, C, F, G, and P classes)<br />
tend to have relatively featureless spectra in low-resolution<br />
(photometric) surveys, which was consistent with<br />
carbonaceous meteorites. Higher-resolution spectral surveys<br />
(e.g. Bus and Binzel 2002b) have shown that almost<br />
half of observed C-type asteroids have a 0.7 µm feature.<br />
Observations (Jones et al. 1990) indicate that approximately<br />
two-thirds of all observed C-type asteroids have<br />
3 µm features.<br />
A-class asteroids tend to have strong UV and 1 µm features<br />
that appear similar to those of olivine. Near-infrared<br />
spectra (Figure 3) of these objects (Bell et al. 1988) confirm<br />
that these surfaces contain significant amounts of<br />
olivine as seen by the three distinctive olivine bands that<br />
make up the 1 µm feature. Two types of meteorites (brachinites<br />
and pallasites) have silicate mineralogies dominated<br />
by olivine and have been postulated to have<br />
compositions similar to the A asteroids.<br />
V- and J-type asteroids are the asteroids whose mineralogies<br />
appear to be the best-determined by remote sensing.<br />
These objects (including the 500-km diameter 4 Vesta<br />
and much smaller objects with diameters of 10 km or less)<br />
have visible and near-infrared spectra (Figure 3) (e.g.<br />
McCord et al. 1970, Binzel and Xu 1993, Burbine et al.<br />
2001b) similar to the HEDs, which have very distinctive<br />
spectral features due to pyroxene. The smaller V- and J-objects<br />
(called Vestoids) have been found in the Vesta family<br />
and between Vesta and the 3:1 and the ν 6 resonances. The<br />
presence of only one “large” body (4 Vesta) in the main<br />
belt with a spectrum similar to HEDs argues that Vesta is<br />
248
Asteroids: Their composition and impact threat<br />
the parent body of the HEDs (e.g. Consolmagno and<br />
Drake, 1977).<br />
E asteroids, due to their relatively featureless spectra and<br />
high albedos (greater than 0.3), have been interpreted as<br />
having surfaces composed predominately of an essentially<br />
iron-free silicate (e.g. Zellner et al. 1977). The most obvious<br />
meteoritic analog is the aubrites (enstatite achondrites),<br />
which are igneous meteorites composed primarily of essentially<br />
iron-free enstatite (Watters and Prinz 1979). However,<br />
the identification of an absorption feature in the 3 µm wavelength<br />
region of a number of main-belt E-asteroid spectra<br />
(Rivkin et al., 1995) has been interpreted as indicating hydrated<br />
minerals on the surfaces of some of these objects,<br />
which is inconsistent with an igneous origin. A feature centered<br />
at ~ 0.5 µm has also been identified in a number of E-<br />
class asteroids (Bus 1999, Fornasier and Lazzarin 2001) and<br />
these objects have been classified as Xe by Bus and Binzel<br />
(2002b) (Figure 2). This feature is believed to be due to a<br />
sulfide (Burbine et al. 2002a), which is commonly found in<br />
aubrites (Watters and Prinz 1979).<br />
The surface mineralogies of many other asteroid classes<br />
are thought to be somewhat understood. The K-class asteroids<br />
tend to have visible and near-infrared spectral<br />
properties similar to CO3/CV3 chondrites (Bell 1988,<br />
Burbine et al. 2001a, Burbine and Binzel 2002). Q asteroids<br />
(most notably 1862 Apollo) tend to have spectral<br />
properties similar to ordinary chondrites. D and P objects,<br />
which tend to be found in the outer main belt, are thought<br />
to have very primitive, organic-rich surfaces due to their<br />
relatively featureless and red spectra (e.g. Vilas and Gaffey,<br />
1989). R asteroids (most notably 349 Dembowska)<br />
appear to be mixtures of olivine and pyroxene (Gaffey et<br />
al., 1989). T asteroids tend to be very dark and featureless<br />
and Hiroi and Hasegawa (2002) have noted the spectral<br />
similarity of unusual carbonaceous chondrite Tagish Lake<br />
to T asteroids.<br />
The surface compositions of a few asteroid classes are<br />
unclear, but do appear to contain silicates. O-asteroid 3628<br />
Božněmcová has a 1 µm feature unlike any known meteorite<br />
(Burbine and Binzel 2002). L class objects have been<br />
newly defined by Bus and Binzel (2002b) and appear intermediate<br />
in spectral properties in the visible between the<br />
K and some S asteroids.<br />
Spacecraft missions<br />
The first dedicated asteroidal mission was the NEAR-<br />
Shoemaker spacecraft rendezvous with S-asteroid 433<br />
Eros (e.g. McCoy et al. 2002) and its flyby of C-asteroid<br />
253 Mathilde (e.g. Veverka et al. 1999). NEAR-Shoemaker<br />
Spacecraft obtained high-resolution images, reflectance<br />
spectra of different lithologic units, bulk density, magnetic<br />
field measurements, and bulk elemental compositions of<br />
433 Eros. Eros had a density of ~ 2.7 g/cm 3 , consistent<br />
with a silicate-rich assemblage while Mathilde had an extremely<br />
low density of 1.3 g/cm 3 .<br />
Eros was classified as an S(IV) object (Murchie and<br />
Normalized Reflectance<br />
3.5<br />
3<br />
2.5<br />
2<br />
1.5<br />
1<br />
Bouvante (eucrite)<br />
1929 Kollaa (V)<br />
Ehole (H5)<br />
6 Hebe (S)<br />
289 Neneta (A)<br />
0.5<br />
0.4 0.8 1.2 1.6 2 2.4<br />
Wavelength (µm)<br />
Fig. 3. Reflectance spectra of S-asteroid 6 Hebe versus H5 chondrite<br />
Ehole, A-asteroid 289 Nenetta, and 1929 Kollaa versus eucrite Bouvante.<br />
The 6 Hebe and 289 Nenetaa spectra are a combination of data from<br />
Binzel and Bus (2002a) and Bell et al. (1988) while the 1929 Kollaa<br />
spectrum is a combination of data from Binzel and Bus (2002a) and Burbine<br />
and Binzel (2002). All spectra are normalized to unity at 0.55 µm<br />
and offset in reflectance from each other. Error bars are one sigma. All<br />
the Binzel and Bus (2002a) and the Burbine and Binzel (2002) spectra<br />
are available at the website http://smass.mit.edu. The Bouvante spectrum<br />
is from Burbine et al. (2001b) and was taken at Brown University’s<br />
RELAB facility.<br />
Pieters 1996) and it was hoped that the NEAR-Shoemaker<br />
data would help “solve” the S-asteroid/ordinary chondrite<br />
question. The average olivine to pyroxene<br />
composition derived from band area ratios (McFadden et<br />
al. 2001) and elemental ratios (Mg/Si, Fe/Si, Al/Si, and<br />
Ca/Si) derived from X-ray data (Nittler et al. 2001) of Eros<br />
are consistent (McCoy et al. 2001) with ordinary chondrite<br />
compositions. However, the S/Si ratio derived from X-ray<br />
data (Nittler et al. 2001) and the Fe/O and Fe/Si ratios derived<br />
from gamma-ray data (Evans et al. 2001) are significantly<br />
depleted relative to ordinary chondrites. McCoy et<br />
al. (2001) believe that the best meteoritic analogs to Eros<br />
are an ordinary chondrite, whose surface mineralogy has<br />
been altered by the depletion of metallic iron and sulfides,<br />
or a primitive achondrite, derived from a precursor assemblage<br />
of the same mineralogy as one of the ordinary chondrite<br />
groups.<br />
What is the percentage of near-Earth asteroids<br />
with iron meteorite compositions?<br />
What is extremely difficult from Earth to determine is<br />
if an object has a composition similar to iron meteorites.<br />
This is a problem since for a particular size, the biggest<br />
249
Thomas H. Burbine<br />
devastation among asteroid impacts will occur for these<br />
objects. Metallic iron has no distinctive absorption features<br />
and radar observations are often inconclusive since<br />
we do not know the surface porosity. There is some evidence<br />
that these objects do exist in the near-Earth asteroid<br />
population. M-type near-Earth asteroid (6178 1986 DA)<br />
(Tedesco and Gradie 1987), has one of the highest radar<br />
albedos (~ 0.6) of any observed asteroid, strongly implying<br />
a metallic iron surface (Ostro et al. 1991).<br />
Fall percentages give a probability of 4% of an iron<br />
meteorite being seen to land on the Earth and a 94% probability<br />
of seeing a stony or stony-iron meteorite fall. It is<br />
unclear if these fall statistics can be extrapolated to hundreds<br />
of meters to tens of kilometer-sized bodies in the<br />
near-earth population; however, compositions interpreted<br />
from the classifications derived from NEA spectral surveys<br />
roughly correspond to these percentages. Binzel et al.<br />
(2001a) have published the spectra and classifications of<br />
48 near-Earth asteroids. Approximately 90% of the objects<br />
(S, B, C, L, Q, V, O, K) had compositions consistent with<br />
silicate-dominated mineralogies if our compositional interpretations<br />
of these asteroid classes are correct. Approximately<br />
10% of the objects were classified as X types. As<br />
stated before, only some percentage of the X types are<br />
probably similar in composition to iron meteorites.<br />
This estimated percentage of iron projectiles is roughly<br />
consistent with numbers derived from impact craters.<br />
Koerbel (1998) lists 41 impact craters with diameters<br />
greater than 100 meters where the compositional characteristics<br />
of the impactor have been tentatively identified.<br />
He listed 14 (34%) as being due to iron meteorite projectiles<br />
with 3 impacts (7%) being due to either chondritic or<br />
iron-meteorite assemblages. The rest of the impacts appeared<br />
to be due either to chondritic, achondritic, stone, or<br />
stony-iron objects. However, the impacts due to iron meteorite<br />
assemblages are predominately associated with the<br />
smallest craters. Ten of the eleven craters smaller than 1.2<br />
kilometers in diameter are all thought to be due to iron meteorite<br />
projectiles. This preponderance of iron meteorite<br />
impacts among small craters is due to the atmospheric selection<br />
effect (e.g. Melosh 1989) that allows smaller iron<br />
meteorite projectiles (since they are denser compared to<br />
chondritic ones) to reach the ground and produce hypervelocity<br />
impacts. For the 30 craters larger than 2 km in diameter,<br />
~ 25% could be due to iron (or stony-iron)<br />
projectiles. However, only one of the eleven craters greater<br />
than 24 kilometers in diameter listed by Koeberl (1998) is<br />
believed to be due to an asteroid with a composition similar<br />
to iron meteorites.<br />
The meteorite fall statistics, classification of NEAs,<br />
and the characterization of the impactors that produced<br />
large craters all tend to argue that iron meteorite projectiles<br />
are a small percentage of the impacting population.<br />
All these lines of evidence argue that iron meteorite projectiles<br />
are a few percent and certainly less than 10% of<br />
near-Earth asteroids. Silicate-dominated assemblages are<br />
much more likely to strike the Earth.<br />
Is it important to know the composition<br />
of an impacting asteroid?<br />
To estimate the effects of an impact, the mass needs to<br />
be known. Since most meteorites that land on the Earth<br />
have bulk densities between 2 and 4 g/cm 3 , we can estimate<br />
pretty well an upper limit on an incoming object’s<br />
mass by using a density of 4 g/cm 3 and multiplying it by<br />
the object’s volume computed from its diameter. Also<br />
making this mass estimate an upper limit is the fact that asteroids<br />
may have significant macroporosity.<br />
But in a real-world situation where a sizable asteroid<br />
(e.g. a kilometer in diameter) that will be extremely destructive<br />
(~ 5,000 MT) is known to be a collision course<br />
with Earth, we will care more about diverting the object<br />
than knowing exactly how destructive it will be. Compositional<br />
information will be vital for determining how best to<br />
divert an object (e.g. Ahrens and Harris 1994). Deflection<br />
techniques such as impacting an asteroid with a spacecraft<br />
or a nuclear explosion will work best with knowledge of<br />
the surface composition. We need to know how the surface<br />
will be affected by an impact or blast and this information<br />
can only be derived from compositional studies. For example,<br />
an asteroid with a composition similar to a carbonaceous<br />
chondrite would be expected to fracture much<br />
more easily than an object with a composition similar to<br />
iron meteorites.<br />
Conclusions<br />
It is certain that the Earth will be hit in the future by an<br />
asteroid. The only question is “When?” For this impacting<br />
object, compositional studies will be vital for trying to determine<br />
how destructive the impact will be and for diverting<br />
the object.<br />
Acknowledgments. The author would like to thank Clark Chapman<br />
and Guy Consolmagno for very thoughtful reviews and the editorial work<br />
of Roman Skála. Almost all of the meteorite spectra in this paper were<br />
measured at Brown University’s Keck/NASA Reflectance Experiment<br />
Laboratory (RELAB), which is a multi-user facility supported by NASA<br />
grant NAG5-3871.<br />
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Bulletin of the Czech Geological Survey, Vol. 77, No. 4, 253–263, 2002<br />
© Czech Geological Survey, ISSN 1210-3527<br />
The recognition of terrestrial impact structures<br />
ANN M. THERRIAULT – RICHARD A. F. GRIEVE – MARK PILKINGTON<br />
Natural Resources Canada, Booth Street, Ottawa, Ontario, KIA 0ES Canada; e-mail: ATherria@NRCan.gc.ca<br />
Abstract. The Earth is the most endogenically active of the terrestrial planets and, thus, has retained the poorest sample of impacts that have<br />
occurred throughout geological time. The current known sample consists of approximately 160 impact structures or crater fields. Approximately 30%<br />
of known impact structures are buried and were initially detected as geophysical anomalies and subsequently drilled to provide geologic samples. The<br />
recognition of terrestrial impact structures may, or may not, come from the discovery of an anomalous quasi-circular topographic, geologic or geophysical<br />
feature. In the geologically active terrestrial environment, anomalous quasi-circular features, however, do not automatically equate with an<br />
impact origin. Specific samples must be acquired and the occurrence of shock metamorphism, or, in the case of small craters, meteoritic fragments,<br />
must be demonstrated before an impact origin can be confirmed. Shock metamorphism is defined by a progressive destruction of the original rock and<br />
mineral structure with increasing shock pressure. Peak shock pressures and temperatures produced by an impact event may reach several hundreds of<br />
gigaPascals and several thousand degrees Kelvin, which are far outside the range of endogenic metamorphism. In addition, the application of shockwave<br />
pressures is both sudden and brief. Shock metamorphic effects result from high strain rates, well above the rates of normal tectonic processes.<br />
The well-characterized and documented shock effects in quartz are unequivocal indicators and are the most frequently used indicator for terrestrial impact<br />
structures and lithologies.<br />
Key words: Earth, impact structures, shock metamorphism, melting, glasses, shatter cones, geophysical anomaly<br />
Introduction<br />
On Earth, compared to the other terrestrial planets, the<br />
very active geologic environment tends to modify and destroy<br />
the impact crater record. Approximately 160 impact<br />
structures or crater fields are currently known on Earth.<br />
Impact involves the transfer of massive amounts of energy<br />
to a spatially limited area of the Earth’s surface, in an extremely<br />
short time interval. As a consequence, local geology<br />
of the target area is of secondary importance. The<br />
effects of impact are, however, scale-dependent and show<br />
progressive changes with increasing energy of the impact<br />
event. The net result is that, impacts of similar scale produce<br />
similar first-order geological and geophysical effects.<br />
Thus, general observations can be derived with respect to<br />
the appearance and geological and geophysical signatures<br />
of terrestrial impact structures, in specific size ranges.<br />
Terrestrial impact structures were first recognized by<br />
their bowl-like shape and meteorite fragments found in their<br />
vicinity or within them (the classic example being Meteor<br />
or Barringer Crater, Arizona). In the 1960’s, petrographic<br />
studies of rocks from impact structures defined a series of<br />
unique characteristics produced by a style of deformation<br />
called shock metamorphism (e.g. French and Short 1968).<br />
Shock metamorphic effects include shatter cones (e.g. Dietz<br />
1947, Milton 1977), the only macroscopic diagnostic shock<br />
effect observed at terrestrial impact structures, a number of<br />
microscopic effects in minerals, some of which are diagnostic<br />
of shock, and impact melting.<br />
The aim of this paper is to summarize the morphology<br />
and geoscientific aspects of terrestrial impact structures<br />
and provide a general description of shock-metamorphic<br />
effects.<br />
Morphology<br />
On most planetary bodies, well-preserved impact<br />
structures are recognized by their characteristic morphology<br />
and morphometry. The basic shape of an impact structure<br />
is a depression with an upraised rim. Detailed<br />
appearance, however, varies with crater diameter. With increasing<br />
diameter, impact structures become proportionately<br />
shallower and develop more complicated rims and<br />
floors, including the appearance of central peaks and interior<br />
rings. Impact craters are divided into three basic morphologic<br />
subdivisions: simple craters, complex craters,<br />
and basins (Dence 1972, Wood and Head 1976).<br />
Small impact structures have the form of a bowl-shaped<br />
depression with an upraised rim and are known as simple<br />
craters (Fig. 1). The exposed rim, walls, and floor define the<br />
so-called apparent crater. At the rim, there is an overturned<br />
flap of ejected target materials, which displays inverted<br />
stratigraphy, with respect to the original target materials.<br />
Beneath the floor is a lens of brecciated target material that<br />
is roughly parabolic in cross-section (Fig. 2). This breccia<br />
lens is allochthonous and polymict, with fractured blocks of<br />
various target materials. In places, near the top and the base,<br />
the breccia lens may contain highly shocked, and possibly<br />
melted, target materials. Beneath the breccia lens, parautochthonous,<br />
fractured rocks define the walls and floor<br />
of what is known as the true crater. In the case of terrestrial<br />
simple craters, the depth to the base of the breccia lens (i.e.,<br />
the base of the true crater) is roughly twice that of the depth<br />
to the top of the breccia lens (i.e., the base of the apparent<br />
crater, Fig. 2). Shocked rocks in the parautochthonous materials<br />
of the true crater floor are confined to a small central<br />
volume at the base of the true crater.<br />
253
Ann M. Therriault – Richard A. F. Grieve – Mark Pilkington<br />
a<br />
Figure 1. (a) Oblique aerial view of 1.2 km diameter, 50,000 years old simple crater, Meteor or Barringer Crater, Arizona, U.S.A. (b) Vertical aerial<br />
view of 3.8 km diameter, 450 ± 30 million years old, Brent Crater, Ontario, Canada. Note how this ancient crater has no rim, has been filled by sediments<br />
and lakes and is a generally subtle topographic feature.<br />
b<br />
With increasing diameter, simple craters show increasing<br />
evidence of wall and rim collapse and evolve into complex<br />
craters (Fig. 3). The transition diameter varies<br />
between planetary bodies and is, to a first approximation,<br />
an inverse function of planetary gravity (Pike 1980).<br />
Other variables, such as target material and possibly projectile<br />
type and velocity, play a lesser role, so that the transition<br />
diameter varies over a small range. The most<br />
obvious effect of secondary variables appears on Earth,<br />
where there are major areas of both sedimentary and crystalline<br />
rocks at the surface. Complex craters on Earth first<br />
occur at diameters greater than 2 km in layered sedimentary<br />
target rocks but not until diameters of 4 km or greater<br />
in stronger, more coherent, igneous or metamorphic, crystalline<br />
target rocks (Dence 1972).<br />
With a central topographic peak or peaks, a broad, flat<br />
floor, and terraced, inwardly slumped rim areas (Fig. 4),<br />
complex craters are a highly modified craterform compared<br />
to simple craters. The rim of a typical complex<br />
D<br />
<br />
yyyyyyyyy<br />
a D t<br />
<br />
yyyyyyyyy<br />
<br />
yyyyyyyyy Slump<br />
Autochthonous<br />
target rocks<br />
Simple crater – final form<br />
D<br />
Basal melt pool<br />
(minor fall back)<br />
breccia fill<br />
Figure 2. Schematic cross-section of a simple crater. D is the diameter<br />
and d a and d t are the depths of the apparent and true crater, respectively.<br />
See text for details.<br />
crater is a structural feature corresponding to a series of<br />
fault terraces. Interior to the rim lays an annular trough,<br />
which is partially filled by a sheet of impact-melt rock<br />
and/or polymict allochthonous breccia (Fig. 4). Only in<br />
the central area of the crater is there evidence of substantial<br />
excavation of target materials. This region is structurally<br />
complex and, in large part, occupied by a central<br />
peak, which is the topographic manifestation of a much<br />
broader and extensive area of uplifted rocks that occurs<br />
beneath the center of complex craters. Readers interested<br />
in the details of cratering mechanics at simple and complex<br />
structures are referred to Melosh (1989) and references<br />
therein.<br />
With increasing diameter, a fragmentary ring of interior<br />
peaks appears, marking the transition from craters to<br />
basins. While a single interior ring is required to define a<br />
basin, basins have been subdivided, with increasing diameter,<br />
on other planetary bodies, into central-peak basins,<br />
with both a peak and ring; peak ring basins, with only a<br />
ring; and multi-ring basins, with two or more interior rings<br />
(Wood and Head 1976). There have been claims that the<br />
largest known terrestrial impact structures have multi-ring<br />
forms, e.g. Chicxulub, Mexico (Sharpton et al. 1993),<br />
Sudbury, Canada (Stöffler et al. 1994, Spray and Thompson<br />
1995) and Vredefort, South Africa (Therriault et al.<br />
1997). Although certain of their geological and geophysical<br />
attributes form annuli, it is not clear that these correspond,<br />
or are related in origin, to the obvious<br />
topographical rings observed, for example, in lunar multiring<br />
basins (Spudis 1993, Grieve and Therriault 2000).<br />
Most terrestrial impact structures are affected by erosion.<br />
In extreme cases, the craterform has been completely<br />
removed. In such cases, recognition of structural and<br />
254
The recognition of terrestrial impact structures<br />
a<br />
Figure 3. (a) Oblique aerial photograph of the Gosses Bluff impact structure, Australia.<br />
Note that all that is visible of this originally 22 km, 142.5 ± 0.8 million<br />
years old structure is a 5 km annulus of hills, representing the eroded remains of<br />
a central uplift. See text for details. (b) Shuttle photograph of the Manicouagan<br />
impact structure, Canada, 100 km in diameter and 214 ± 1 million years old. Note<br />
that the annular trough (with a diameter of ~ 65 km) is filled by water.<br />
b<br />
geological effects of impact in the target rocks is essential<br />
to the identification of an impact structure rather than the<br />
presence of a characteristic craterform. For example,<br />
Gosses Bluff, Australia has a positive topographical form<br />
consisting of an annular ring of hills, approximately 5 km<br />
in diameter (Fig. 3). The ring consists of erosionally resistant<br />
beds from within the original central uplifted area<br />
of a complex impact structure. The original craterform,<br />
which has an estimated diameter of approximately 22 km<br />
(Milton et al. 1996), has been removed by erosion. There<br />
are several other impact structures, which have some form<br />
of rings, e.g. Manicouagan, Canada (Floran and Dence<br />
1976), Haughton, Canada (Robertson and Sweeney 1983),<br />
but it is not clear whether these are primary forms or secondary<br />
features, with some relation to primary structural<br />
features (Grieve and Head 1983).<br />
There are also other subtleties to the character of<br />
craterforms in the terrestrial record that do not appear on<br />
the other terrestrial planets. A number of relatively young,<br />
and, therefore, only slightly eroded, complex impact structures<br />
(e.g. Haughton, Canada; Ries Germany; Zhamanshin,<br />
Kazakhstan) do not have an emergent central peak or<br />
other interior topographical expression of a central uplift<br />
(Garvin and Schnetzler 1994). These structures are in<br />
mixed targets of platform sediments overlying crystalline<br />
basement. Although there are no known comparably<br />
young complex structures entirely in crystalline targets,<br />
the buried and well-preserved Boltysh structure, Ukraine,<br />
which is of comparable size, has a central peak (emergent<br />
from the crater-fill), similar to the appearance of lunar central<br />
peak craters. This difference in form is probably a target<br />
rock effect but it has not been studied in detail.<br />
The morphology of impact craters formed in marine<br />
environment is also quite distinct. These impact structures<br />
are characterized by a broad and shallow brim at the periphery<br />
of the crater, extensive infilling, and prominent<br />
fault blocks floored by apparent low-angle décollement<br />
surfaces at the periphery of the crater (e.g. Tsikalas et al.<br />
1999, Ormö and Lindström 2000). The extensive infilling<br />
is most likely due to large amounts of ejecta and crater<br />
wall material transported into the excavated crater by the<br />
collapse of the impact-induced water cavity and the subsequent<br />
rapid surge of sea water (Tsikalas et al. 1999, Ormö<br />
and Lindström 2000). The 40-km-diameter Mjølnir submarine<br />
impact structure in the Barents Sea, for example,<br />
consists of a central region of deep excavation surrounded<br />
by a shallow excavated shelf, without a raised crater rim<br />
(Tsikalas et al. 1998, 1999). This morphology is also observed<br />
at the 13.5-km-diameter Lockne impact structure,<br />
Sweden (Lindström et al. 1996).<br />
Attempts to define morphometric relations, particularly<br />
depth-diameter relations, for terrestrial impact structures<br />
have had limited success, because of the effects of<br />
erosion and, to a lesser degree, post-impact sedimentation.<br />
Unlike depth, the variation of stratigraphic uplift (SU, Fig.<br />
4) with diameter at complex impact structures is fairly<br />
d t<br />
d a<br />
Complex structure – final form<br />
Central Uplift Area<br />
Dcp<br />
D<br />
Melt/allochthonous<br />
breccia sheet<br />
"Autochthonous"<br />
crater floor<br />
SU<br />
Figure 4. Schematic cross-section of complex impact structure. Notation<br />
as in Figure 2, with SU corresponding to structural uplift and D cp to the<br />
diameter of the central uplift. Note preservation of beds in outer annular<br />
trough of the structure, with excavation limited to the central area. See<br />
text for details.<br />
255
Ann M. Therriault – Richard A. F. Grieve – Mark Pilkington<br />
well constrained with SU = 0.86D 1.03 (n = 24), where n is<br />
the number of data points (Grieve and Pilkington 1996).<br />
Similarly, the diameter of the central uplift area (D cp , Fig.<br />
4), at its maximum radial expression, is constrained by D cp<br />
= 0.31 D 1.02 (n = 44) (Therriault et al. 1997).<br />
Geophysics of impact structures<br />
Geophysical anomalies over terrestrial impact structures<br />
vary in their character and, in isolation, do not provide<br />
definitive evidence for an impact origin. About 30 per<br />
cent of known terrestrial impact structures are buried by<br />
post-impact sediments. Geophysical methods resulted in<br />
their initial discovery and subsequent drilling provided<br />
geologic samples, which confirmed their impact origin.<br />
Interpretation of a single geophysical data set over a suspected<br />
impact structure can be ambiguous (for example,<br />
Hildebrand et al. 1998, Sharpton et al. 1993). When combined,<br />
however, with complementary geophysical methods<br />
and the existing database over other known impact structures,<br />
a more definite assessment can be made (e.g. Ormö<br />
et al. 1999).<br />
Since potential-field data are available over large areas,<br />
with almost continuous coverage, gravity and magnetic<br />
observations have been the primary geophysical indicators<br />
used for evaluating the occurrence of possible terrestrial<br />
impact structures. Seismic data, although providing much<br />
better spatial resolution of subsurface structure, is used<br />
less, because it is less generally available. Electrical methods<br />
have been used even less (e.g. Henkel 1992). Given<br />
space limitations and some lack of specificity of the geophysical<br />
attributes of terrestrial impact craters, they are<br />
generally discussed here and the reader is referred to the<br />
most recent synthesis in Grieve and Pilkington (1996).<br />
Gravity signature<br />
The most notable geophysical signature associated<br />
with terrestrial impact structures is a negative gravity<br />
anomaly. These gravity lows are generally circular, extending<br />
to, or slightly beyond, the crater rim, and are due<br />
to lithological and physical changes associated with the<br />
impact process. In well-preserved impact structures, lowdensity<br />
sedimentary infill of the topographic depression of<br />
the crater contributes to the gravity low. In complex impact<br />
structures, relatively lower density impact-melt sheets<br />
also contribute to the negative gravity effect. However,<br />
such lithological effects are minor compared to density<br />
contrasts induced by fracturing and brecciation of the target<br />
rocks.<br />
In general, the amplitude of the maximum negative<br />
gravity anomaly associated with impact structures increases<br />
with the final crater diameter (Dabizha and Fedynsky<br />
1975, Dabizha and Feldman 1982). Over simple craters, a<br />
circular bowl-shaped negative anomaly is observed;<br />
whereas most of larger complex impact structures, greater<br />
than 30 km in diameter, tend to exhibit a central gravity<br />
high. Based on data from 58 terrestrial impact structures,<br />
Pilkington and Grieve (1992) showed that erosional level<br />
has only a secondary effect on gravity anomaly size.<br />
It is important to note that due to differences in target<br />
lithologies, large variations in gravity signature are observed<br />
between structures of similar sizes. In general,<br />
structures formed in sedimentary lithologies produce<br />
smaller anomalies than similar sized ones formed in crystalline<br />
rocks. Structures formed in unconsolidated sediments<br />
in continental shelf areas may not produce<br />
detectable negative gravity anomalies but are marked only<br />
by a central gravity high.<br />
Magnetic signature<br />
In general, magnetic anomalies associated with terrestrial<br />
impact structures are more complex than gravity<br />
anomalies. This observation reflects the greater variation<br />
possible in the magnetic properties of rocks. The dominant<br />
effect over impact structures is a magnetic low or subdued<br />
zone ranging in amplitude from tens to a few hundred nanotesla<br />
that is commonly manifested as a truncation of the<br />
regional magnetic fabric (Dabizha and Fedynsky 1975,<br />
Clark 1983). Magnetic lows are best defined over simple<br />
and some small complex craters, where the anomaly is<br />
smooth and simple; whereas at larger impact structures,<br />
the magnetic low can be modified by the presence of<br />
shorter-wavelength, large-amplitude, localized anomalies<br />
that usually occur at or near the centre of the structure.<br />
No correspondence exists between the magnetic anomaly<br />
character and crater morphology of impact structures.<br />
Moreover, the presence of a central gravity high does not<br />
imply the existence of a central magnetic anomaly. There<br />
are several structures with no obvious magnetic signature.<br />
Shock effects, thermal effects or chemical effects may<br />
cause magnetic anomalies related to impact. Shock effects<br />
in impact structures can serve to increase or decrease magnetization<br />
levels. Thermal effects may result in the production<br />
of non-magnetic impact glasses (Pohl 1971) or in<br />
resetting magnetic minerals through thermoremanent<br />
magnetization in the direction of the Earth’s magnetic field<br />
at the time of impact. Chemical effects may result in the<br />
production of new magnetic phases, through elevated<br />
residual temperatures and hydrothermal alteration, leading<br />
to the acquisition of a chemical remanent magnetization in<br />
the direction of the ambient field.<br />
Seismic signature<br />
Reflection seismic surveys allow for detailed imaging<br />
of impact structure morphology and delineating zones of<br />
incoherent reflections that are characteristic of brecciation<br />
and fracturing. The disturbance of coherent subsurface reflectors<br />
is most prominent in the central uplift of complex<br />
structures and decreases outward and downward from this<br />
zone (Brenan et al. 1975). Reflection data can provide es-<br />
256
The recognition of terrestrial impact structures<br />
timates of such morphological parameters as the dimensions<br />
of the central uplift, annular trough and faulted<br />
blocks at the structural rim of complex structures (e.g.<br />
Morgan et al. 2002). The depth to horizontal reflectors that<br />
exist below the crater floor can be used to determine the<br />
amount of structural uplift.<br />
Electrical signature<br />
The presence of fluids in impact-induced fractures and<br />
pore spaces leads to decreased resistivity levels that can be<br />
mapped effectively by various electrical methods. The<br />
conductivity of rocks is heavily dependent on their water<br />
content: < 1% change in water content can produce more<br />
than an order of magnitude change in conductivity. The<br />
degree of fragmentation determines the amount and distribution<br />
of fluids within the rock and hence, its electrical<br />
properties.<br />
Where a distinct contrast exists between the allochthonous<br />
breccia deposits and the underlying autochthonous<br />
target rocks, electrical profiling using resistivity sounding<br />
can map the structure of the true crater floor (e.g. Vishnevsky<br />
and Lagutenko 1986). In order to determine the<br />
deeper electrical structure associated with impact, magnetotelluric<br />
surveys have been carried out (e.g. Zhang et al.<br />
1988, Campos-Enriquez et al. 1997).<br />
Geology of impact structures<br />
Although an anomalous circular topographic, structural,<br />
or geological feature may indicate the presence of an<br />
impact structure, there are other endogenic geological<br />
processes that can produce similar features in the terrestrial<br />
environment. An obvious craterform is an excellent indicator<br />
of a possible impact origin; particularly, if it has<br />
the appropriate morphometry, but as noted, such features<br />
are rare and short-lived in the terrestrial environment. The<br />
burden of proof for an impact origin generally lies with the<br />
documentation of the occurrence of shock-metamorphic<br />
effects.<br />
Few structures preserve physical evidence of the impacting<br />
body. Such structures are limited to small, young,<br />
simple structures, where the impacting body (or, more<br />
commonly, fragments of it) has been slowed by atmospheric<br />
deceleration and impacts at less than cosmic velocity.<br />
These are restricted generally to the impact of iron or<br />
stony-iron meteorites. Stony meteorites are weaker than<br />
their iron-bearing counterparts and small stones are generally<br />
crushed as a result of atmospheric interaction (Melosh<br />
1981). Larger impacting bodies (>100–150 m in diameter)<br />
survive atmospheric passage with undiminished impact<br />
velocity. Consequently, the peak shock pressures upon impact<br />
are sufficient, in most cases, to result in the melting<br />
and vaporisation of the impacting body, destroying it as a<br />
physical entity.<br />
On impact, the bulk of the impacting body’s kinetic<br />
Temperature (°C)<br />
10 000<br />
1 000<br />
100<br />
P-T field of<br />
endogenic<br />
metamorphism<br />
Shatter<br />
cones<br />
Rock<br />
melting<br />
Fused<br />
glasses<br />
Diaplectic<br />
glasses<br />
Planar<br />
features<br />
Vaporization<br />
Pressure post-shock<br />
temperature curve for<br />
shock metamorphism<br />
of granitic rocks<br />
1 10 100 1 000<br />
Pressure, GPa<br />
Figure 5. Temperature and pressure range of shock metamorphic effects<br />
compared to that of endogenic metamorphism. Planar features include<br />
planar deformation features (PDFs) and planar fractures (PFs). Scale is<br />
log-log. See text for details.<br />
energy is transferred to the target by means of a shock<br />
wave. This shock wave imparts kinetic energy to the target<br />
materials, which leads to the formation of a crater. It also<br />
increases the internal energy of the target materials, which<br />
leads to the formation of so-called shock-metamorphic effects.<br />
The details of the physics of impact and shockwave<br />
behavior can also be found in Melosh (1989), and references<br />
therein.<br />
Shock metamorphism is the progressive breakdown in<br />
the structural order of minerals and rocks due to the passage<br />
of a high-pressure shock wave and requires pressures<br />
and temperatures well above the pressure-temperature<br />
field of endogenic terrestrial metamorphism (Fig. 5). The<br />
dependence on high pressures for the formation of shockmetamorphic<br />
effects has been shown by their duplication<br />
in nuclear and chemical explosion craters, and in laboratory<br />
shock recovery experiments (e.g. Hörz 1968, Müller<br />
and Hornemann 1969, Borg 1972). Minimum shock pressures<br />
required for the production of diagnostic shockmetamorphic<br />
effects are 5–10 GPa for most silicate<br />
minerals. Strain rates produced by impact cratering<br />
process are of the order of 10 6 s -1 to 10 9 s -1 (Stöffler and<br />
Langenhorst 1994), many orders of magnitude higher than<br />
typical tectonic strain rates (10 -12 s -1 to 10 -15 s -1 ; e.g. Twiss<br />
and Moores 1992), and shock-pressure duration is measured<br />
in seconds, or less, in even the largest impact events<br />
(Melosh 1989). These physical conditions are not reproduced<br />
by endogenic geologic processes. They are unique<br />
to impact and, unlike endogenic terrestrial metamorphism,<br />
disequilibrium and metastability are common phenomena<br />
in shock metamorphism.<br />
The extreme pressures and high strain rates of shock<br />
deformation are fundamental differences from normal endogenic<br />
causes of compression (Ashworth and Schneider<br />
1985, Goltrant et al. 1991, 1992, Langenhorst 1994). A<br />
shock wave passing through a heterogeneous rock mass<br />
undergoes numerous modifications, as it interacts with<br />
grain boundaries, fractures, foliations, and different mineral<br />
species with different shock impedances within the<br />
257
Ann M. Therriault – Richard A. F. Grieve – Mark Pilkington<br />
Figure 6. Outcrop (~ 80 m high) of coherent impact melt rock at the Mistastin<br />
complex impact structure, Canada.<br />
rock. There is, thus, local variations in shock pressure. Petrographic<br />
study indicates that shock pressures may vary by<br />
a factor of two or more over distances ranging from millimeters<br />
to meters in outcrops (Grady 1977). Hence, each<br />
individual mineral grain experiences its own particular<br />
shock history based upon its physical properties and its relationship<br />
to both the adjacent grains and the overall structural<br />
character of the rock. A maximum shock effect in<br />
grains of a particular mineral species in a hand specimen<br />
may, thus, be a means of measuring relative deformation<br />
intensities throughout an impact structure. For example,<br />
shock pressures of at least ~ 5 GPa are required to produce<br />
PFs in quartz and greater than 10 GPa to produce PDFs in<br />
quartz or feldspars. This variation of shock deformation of<br />
important rock-forming minerals of the target rocks with<br />
increasing shock pressures have been used to delineate<br />
zones of shock metamorphism in the floor of a number of<br />
impact structures, e.g. Charlevoix, Canada (Robertson<br />
1968), Brent, Canada (Dence 1968), Ries, Germany (von<br />
Engelhardt and Stöffler 1968), and Manicouagan, Canada<br />
(Dressler 1990), with the intensity of deformation decreasing<br />
from the center outwards.<br />
The exact physical conditions on impact are a function<br />
of the specific impact parameters. The density of the impacting<br />
body and the target, and the impact velocity determine<br />
the peak pressure on impact. The shock wave<br />
attenuates with distance from the impact point with the kinetic<br />
energy of the impact event determining the absolute<br />
radial distance in the target at which a specific shock pressure<br />
is achieved and, thus, which specific shock-metamorphic<br />
effects occur. Shock-metamorphic effects are well<br />
described in papers by Chao (1967), Bunch (1968), Stöffler<br />
(1971, 1972, 1974), Stöffler and Langenhorst (1994),<br />
Grieve et al. (1996), French (1998), Langenhorst and<br />
Deutsch (1998), and Langenhorst (this volume). They are<br />
discussed here only in general terms.<br />
Impact melting<br />
During compression, considerable pressure-volume<br />
work is done and the pressure release occurs adiabatically.<br />
Heating of the target rocks, thus, occurs as not all this<br />
pressure-volume work is recovered upon pressure release<br />
and results in irreversible waste heat. Above 60 GPa, the<br />
waste heat is sufficient to cause whole-rock melting and,<br />
and at higher pressures, vaporisation of a certain volume<br />
of target rocks (Melosh 1989). This volume is a function<br />
of the impact velocity, physical properties of the impacting<br />
body and target, and, most importantly, the size of the impacting<br />
body (Grieve and Cintala 1992).<br />
Impact melt lithologies may occur as glass bombs in<br />
crater ejecta (von Engelhardt 1990), as dykes within the<br />
crater floor and walls, as glassy to crystalline pools and<br />
lenses within the breccia lenses of simple craters, or as coherent<br />
annular sheets (Fig. 6) lining the floor of complex<br />
craters and stratigraphically located immediately above<br />
breccias and/or brecciated basement rocks and overlain by<br />
breccias.<br />
When crystallized, impact-melt sheets have igneous<br />
textures, but tend to be heavily charged with clastic debris<br />
a<br />
b<br />
Figure 7. Photomicrographs of far-from-equilibrium textures examples in impact melts: (a) plagioclase crystals with swallow-tail texture, Boltysh impact<br />
melt sheet, Ukraine, plane light, field-of-view = 2.28 mm; (b) pyroxene-plagioclase spherulitic texture, Vredefort Granophyre impact melt dyke,<br />
South Africa, plane light, field-of-view = 5 mm.<br />
258
The recognition of terrestrial impact structures<br />
Figure 8. Photomicrograph of fused glass (lechatelierite), Ries, Germany,<br />
plane light, field-of-view = 2.5 mm.<br />
towards their lower and upper contacts. They may, therefore,<br />
have a textural resemblance to endogenic igneous<br />
rocks. Impact melts are superheated, reaching thousands<br />
of degrees Kelvin. Temperature differences with host<br />
rocks may result in rapid cooling of the melt leading to farfrom-equilibrium<br />
textures (Fig. 7). Grain-size in thick impact-melt<br />
sheets increases inwards from the contacts, but,<br />
in general, impact-melt rocks are usually fine-grained to<br />
glassy. An important textural property of impact-melt<br />
rocks is the presence of mineral and rock fragments, which<br />
have undergone shock metamorphism of different degrees,<br />
and have been variously reworked by the melt. The size of<br />
such fragments ranges from millimeters to several hundreds<br />
of meters, and gradational changes in inclusion content<br />
are observed in thick melt sheets, varying from one to<br />
several tens of percent (e.g. von Engelhardt 1984), with<br />
highest concentrations towards their lower and upper contacts.<br />
Impact-melt rocks can have an unusual chemistry compared<br />
with endogenic volcanic rocks, as their composition<br />
depends on the wholesale melting of a mix of target rocks,<br />
as opposed to partial melting and/or fractional crystallization<br />
relationships for endogenous igneous rocks. The composition<br />
of impact-melt rocks is characteristic of the target<br />
rocks and may be reproduced by a mixture of the various<br />
country rock types in their appropriate geological proportions.<br />
Such parameters as 87 Sr/ 86 Sr and 143 Nd/ 144 Nd ratios<br />
may also reflect the pre-existing target rocks within the<br />
impact-melt rocks composition (Jahn et al. 1978, Faggart<br />
et al. 1985). In general, unlike endogenous magmatic rock<br />
masses of comparable size (up to a few hundred meters<br />
thick), even relatively thick impact-melt sheets are chemically<br />
homogeneous over distances of millimeters to kilometers.<br />
In cases where the target rocks are not<br />
homogeneously distributed, this observation may not hold<br />
true, such as for Manicouagan, Canada (Grieve and Floran<br />
1978), Chicxulub (Kettrup et al. 2000) and Popigai (Kettrup<br />
et al. 2002). Differentiation is not a characteristic of<br />
relatively thick coherent impact-melt sheets (with the exception<br />
of the extremely thick, ~ 2.5 km, Sudbury Igneous<br />
Complex, Sudbury Structure, Canada; Ostermann 1996,<br />
Ariskin et al. 1999, Therriault et al. 2002).<br />
Enrichments above target rock levels in siderophile elements<br />
and Cr have been identified in some impact-melt<br />
rocks. These are due to an admixture of up to a few percent<br />
of meteoritic material from the impacting body. In<br />
some melt rocks, the relative abundances of the various<br />
siderophiles have constrained the composition of the impacting<br />
body to the level of meteorite class, (e.g. East<br />
Clearwater, Canada, was formed by a C1 chondrite, Palme<br />
et al. 1979). In other melt rocks, no siderophile anomaly<br />
has been identified. This may be due to the inhomogeneous<br />
distribution of meteoritic material within the impact-melt<br />
rocks and sampling variations (Palme et al.<br />
1981) or to differentiated, and, therefore, relatively nonsiderophile-enriched<br />
impacting bodies, such as basaltic<br />
achondrites. More recently, high precision osmium-isotopic<br />
analyses have been used to detect a meteoritic signature<br />
at terrestrial impact structures (e.g. Koeberl et al.<br />
1994). Unfortunately, Re-Os systematics are, in themselves,<br />
not an effective discriminator between meteorite<br />
classes.<br />
Fused glasses and diaplectic glasses<br />
In general, shock fused minerals are characterized<br />
morphologically by flow structures and vesiculation (Fig.<br />
8). Peak pressures required for shock melting of single<br />
crystals are in the order of 40 to 60 GPa (Stöffler 1972,<br />
1974), for which postshock temperatures (> 1000 °C) exceed<br />
the melting points of typical rock-forming minerals<br />
(Fig. 5). At these conditions, the minerals in the rock will<br />
melt immediately and independently after the passage of<br />
the shock wave. This melt has approximately the same<br />
composition as the original mineral before any flow or<br />
mixing takes place, and the melt regions are initially distributed<br />
through the rock in the same manner as the original<br />
mineral grains (French 1998). Melting is mineral<br />
selective, producing unusual textures in which one or more<br />
minerals show typical melting features; whereas, others,<br />
even juxtaposed ones, do not. One of the most common<br />
fused glasses observed at terrestrial impact structures is<br />
that of quartz, i.e. lechatelierite (e.g. Fig. 8).<br />
Conversion of minerals to an isotropic, dense, glassy<br />
phase at peak pressures of 30 to 50 GPa (Fig. 5) and temperatures<br />
well below their normal melting point is a shock<br />
metamorphic effect unique to framework silicates. These<br />
phases are called diaplectic (from the Greek “destroyed by<br />
striking”) glasses, which are produced by breakdown of<br />
long-range order of the crystal lattice without fusion.<br />
Although diaplectic forms may occur as the direct result of<br />
compression by the shock wave, they are probably more<br />
commonly produced by inversion from a high-pressure<br />
crystalline phase, which is unstable in the postshock P-T<br />
environment (Robertson 1973). Based on shock recovery<br />
experiments, the formation of diaplectic glass occurs between<br />
30 and 45 GPa for feldspar and 35 to 50 GPa for<br />
quartz (e.g. Stöffler and Hornemann 1972). The morphology<br />
of the diaplectic glass is the same as the original mineral<br />
crystal and shows no evidence of fluid textures (e.g.<br />
Grieve et al. 1996). Diaplectic glasses have densities low-<br />
259
Ann M. Therriault – Richard A. F. Grieve – Mark Pilkington<br />
Figure 9. Photomicrograph of partial conversion to maskelynite of plagioclase<br />
feldspar crystals, Manicouagan, Canada, cross-polarized light,<br />
field-of-view = 5 mm.<br />
er than the crystalline form from which they are derived,<br />
but higher than thermally melted glasses of equivalent<br />
composition (e.g. Stöffler and Hornemann 1972, Langenhorst<br />
and Deutsch 1994). With increasing pressure, the<br />
bulk density of diaplectic glass decreases. This decrease is<br />
due in part to progressively greater portions of the mineral<br />
having been converted to low density, disordered phases,<br />
but also to the fact that diaplectic phases exist in a<br />
sequence of intermediate structural states, whose refractive<br />
index and density decrease with increasing pressure<br />
and temperature (Stöffler and Hornemann 1972). The refractive<br />
index of diaplectic glasses is also generally higher<br />
than for synthetic, or thermally melted, glasses of<br />
equivalent composition (e.g. Robertson 1973, Grieve et al.<br />
1996). However, in the case of K-feldspar, its diaplectic<br />
glass has a slightly lower refractive index than the fused<br />
feldspar glass (Stöffler and Hornemann 1972). Maskelynite,<br />
the diaplectic form of plagioclase (Fig. 9), is the<br />
most common example from terrestrial rocks; diaplectic<br />
glasses of quartz (Chao 1967) and of alkali feldspar<br />
(Bunch 1968) are also reported but in lesser abundance.<br />
Diaplectic glasses of different minerals can exist adjacent<br />
to one another without mixing (e.g. Robertson 1973).<br />
High-pressure polymorphs<br />
Shock can result in the formation of metastable polymorphs,<br />
such as stishovite and coesite from quartz (Chao<br />
et al. 1962, Langenhorst this volume) and diamond and<br />
lonsdaleite from graphite (Grieve and Masaitis 1996, Masaitis<br />
1998, Langenhorst this volume). Coesite and diamond<br />
are also products of endogenic terrestrial geological<br />
processes, including high-grade metamorphism, but the<br />
paragenesis and, more importantly, the geological setting<br />
are completely different from that in impact events.<br />
Under high pressure, the mineral lattice is unstable and<br />
is converted to a more stable configuration. Such transformation<br />
begins at ~ 11.5 GPa for K-feldspars (Robertson<br />
1973) and at ~ 12 GPa for quartz (De Carli and Milton<br />
1965). With increasing pressure, a greater proportion of<br />
the mineral is converted to a high-pressure polymorph until<br />
complete transformation is achieved at ~ 30 GPa for<br />
feldspars (Ahrens et al. 1969) and ~ 35 GPa for quartz<br />
(Stöffler and Langenhorst 1994). Neither the high-pressure<br />
phase of K-feldspar, thought to be the dense hollandite-type<br />
structure with Al and Si in octahedral<br />
co-ordination, nor an equivalent plagioclase polymorph<br />
have been recovered from shock experiments or identified<br />
in non-impact terrestrial rocks (Robertson 1973). It would<br />
appear that these phases are very unstable in postshock environments<br />
and, more likely, invert to more disordered,<br />
metastable phases. The high-pressure polymorphs of<br />
quartz (i.e. stishovite and coesite) have only rarely been<br />
produced by laboratory shock recovery experiments (cf.<br />
Stöffler and Langenhorst 1994). Contrary to what is expected<br />
from equilibrium phase diagram, stishovite is<br />
formed at lower pressures (12–30 GPa) than coesite<br />
(30–50 GPa; Stöffler and Langenhorst 1994) in impact<br />
events. This is mainly due to the fact that stishovite is<br />
formed during shock compression, whereas, coesite crystallizes<br />
during pressure release. In terrestrial impact structures,<br />
these polymorphs occur in small or trace amounts as<br />
very fine-grained aggregates and are formed by partial<br />
transformation of the host quartz. In crystalline or dense<br />
rocks, coesite is found in quartz with planar deformation<br />
features (PDFs) and strongly lowered refractive index and,<br />
more commonly, in diaplectic glass; whereas, in porous<br />
sandstone, coesite co-exists with > 80% of quartz displaying<br />
planar fractures (PFs) and diaplectic quartz glass<br />
(Grieve et al. 1996). Stishovite occurs most commonly in<br />
quartz with PDFs and less frequently in diaplectic glass<br />
(Stöffler 1971). For details on the characteristics of coesite<br />
and stishovite, the reader is referred to Stöffler and Langenhorst<br />
(1994) and references therein.<br />
Planar microstructures<br />
The most common documented shock-metamorphic<br />
effect is the occurrence of planar microstructures in tectosilicates,<br />
particularly quartz (Hörz 1968). The utility of<br />
planar microstructures in quartz reflects the ubiquitous nature<br />
of the mineral and its stability, including the stability<br />
of the microstructures themselves, in the terrestrial environment,<br />
and the relative ease with which they can be documented.<br />
For details, the reader is referred to the<br />
accompanying paper by Langenhorst. Recent reviews of<br />
the nature of the shock metamorphism of quartz, with an<br />
emphasis on the nature and origin or planar microstructures<br />
in experimental and natural impacts, can be found in<br />
Stöffler and Langenhorst (1994) and Grieve et al. (1996).<br />
Planar deformation features (PDFs) in minerals are<br />
produced under pressures of ~ 10 to ~ 35 GPa (Fig. 5).<br />
Planar fractures (PFs) form under shock pressures ranging<br />
from ~ 5 GPa up to ~ 35 GPa (Stöffler 1972, Stöffler and<br />
Langenhorst 1994).<br />
260
The recognition of terrestrial impact structures<br />
Shatter cones<br />
The only known diagnostic shock effect that is megascopic<br />
in scale is the occurrence of shatter cones (Dietz<br />
1968). Shatter cones are unusual, striated, and horse-tailed<br />
conical fractures ranging from millimeters to meters in<br />
length produced in rocks by the passage of a shock wave<br />
(e.g. Sagy et al. 2002). The striated surfaces of shatter<br />
cones are positive/negative features and the striations are<br />
directional, i.e., they appear to branch and radiate along<br />
the surface of the cone. The acute angle of this distinctive<br />
pattern points toward the apex of the cone and the shatter<br />
cones themselves generally point upward with their axes<br />
lying at any angle to the original bedding. Once the host<br />
rocks are graphically restored to their original impact position,<br />
shatter cones indicate the point of impact.<br />
Shatter cones are initiated most frequently in rocks that<br />
experienced moderately low shock pressures, 2–6 GPa<br />
(Fig. 5), but have been observed in rocks that experienced<br />
~25 GPa (Milton 1977). These conical striated fracture<br />
surfaces are best developed in fine-grained, structurally<br />
isotropic lithologies, such as carbonates and quartzites.<br />
They do occur in coarse-grained crystalline rocks but are<br />
less common and poorly developed. They are generally<br />
found as individual or composite groups of partial to complete<br />
cones (Fig. 10) in place in the rocks below the crater<br />
floor, especially in the central uplifts of complex impact<br />
structures, and rarely in isolated rock fragments in breccia<br />
units. Shatter cones are used as a diagnostic field criterion<br />
to identify impact structures (e.g. Dietz 1947, Milton<br />
1977).<br />
Conclusion<br />
The detailed study of impact events on Earth is a relatively<br />
recent addition to the spectrum of studies engaged in<br />
by the geological sciences. More than anything, it was<br />
preparations for and, ultimately, the results of the lunar<br />
and the planetary exploration program that provided the<br />
initial impetus and rationale for their study. Some recent<br />
discoveries have resulted from the occurrence or re-examination<br />
of unusual lithologies, rather than an obvious circular<br />
geological or topographic feature. For example,<br />
unusual breccias at Gardnos, Norway and Lockne, Sweden<br />
had been known for some time, but their shock-metamorphic<br />
effects were documented only recently, and they<br />
are now associated with the remnants of impact structures<br />
(French et al. 1997, Lindström and Sturkell 1992).<br />
The level of knowledge concerning individual terrestrial<br />
impact structures is highly variable. In some cases, it<br />
is limited to the original discovery publication. In terms of<br />
understanding the terrestrial record, this is compensated,<br />
to some degree, by the fact that impact structures with similar<br />
dimensions and target rocks have the same major characteristics.<br />
Nevertheless, there is still much to be learned<br />
about impact processes from terrestrial impact structures,<br />
Figure 10. Complete shatter cone in limestone, Cap de la Corneille,<br />
Charlevoix, Canada.<br />
particularly with respect to details of the third dimension.<br />
This is the property that is unobtainable from impact structures<br />
on other bodies in the solar system, where it must be<br />
studied by remote-sensing methodologies.<br />
Apart from increasing our understanding of impact<br />
processes, the study of terrestrial impact structures has influenced<br />
the siting of significant economic deposits<br />
(Grieve and Masaitis 1994, Donofrio 1997, Grieve 1997).<br />
In addition, the documentation of the terrestrial impact<br />
record provides a direct measure of the cratering rate on<br />
Earth and, thus, a constraint on the hazard that impact<br />
presents to human civilization (Gehrels 1994). The K/T<br />
impact may have resulted in the demise of the dinosaurs as<br />
the dominant land-life form and, thus, permitted the ascendancy<br />
of mammals and, ultimately, humans. It is, however,<br />
inevitable that human civilization, if it persists long<br />
enough, will be subjected to an impact-induced environmental<br />
crisis of potentially immense proportions.<br />
Acknowledgements. We would like to thank J. Ormö and<br />
A. Deutsch for their critical reviews. This paper is GSC contribution<br />
No. 2002141.<br />
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Handling editor: Roman Skála<br />
263
Bulletin of the Czech Geological Survey, Vol. 77, No. 4, 265–282, 2002<br />
© Czech Geological Survey, ISSN 1210-3527<br />
Shock metamorphism of some minerals: Basic introduction and microstructural observations<br />
FALKO LANGENHORST<br />
Bayerisches Geoinstitut, University of Bayreuth, Universitätsstr. 30, D-95447 Bayreuth, Germany; e-mail: Falko.Langenhorst@uni-bayreuth.de<br />
Abstract. Minerals show a unique behaviour when subjected to shock waves. The ultradynamic loading to high pressures and temperatures<br />
causes deformation, transformation and decomposition phenomena in minerals that are unequivocal indicators of impact events. This paper introduces<br />
into the basics of shock compression, required to understand the formation and experimental calibration of these shock effects in minerals, and particularly<br />
focuses on the recent advances in the field of shock metamorphism achieved by the application of transmission electron microscopy (TEM).<br />
TEM studies underline that the way minerals respond to shock compression largely depends on their crystal structures and chemical compositions, as<br />
is illustrated here on the basis of four minerals: quartz, olivine, graphite and calcite.<br />
The crystal structure of a mineral exerts an important control on the shock-induced deformation phenomena, comprising one- to two-dimensional<br />
lattice defects, such as dislocations, mechanical twins, planar fractures, and amorphous planar deformation lamellae. For example, dislocations cannot<br />
be activated in quartz due to the strong covalent bonding, whereas the island silicate olivine easily deforms by dislocation glide.<br />
Transformation phenomena include phase transitions to (diaplectic) glass and/or high-pressure polymorphs. TEM studies reveal that high-pressure<br />
polymorphs such as coesite, stishovite and ringwoodite are liquidus phases, which form upon decompression by crystallization from high-pressure<br />
melts. The graphite-to-diamond transition is however a rare example for a solid-state transformation, taking place by a martensitic shear mechanism.<br />
Shock-induced decomposition reactions are typical of volatile-bearing minerals and liberate toxic gases that, in case of large impacts, may affect<br />
Earth’s climate. Shock experiments show that degassing of calcite does not take place under high pressure but can massively occur after decompression<br />
if the post-shock temperature is sufficiently high. A recombination reaction happens however if CaO and CO 2 are not physically separated.<br />
Key words: impact features, shock metamorphism, shock waves, minerals, crystal structure, defects, experimental study<br />
Introduction<br />
Number of craters (>1 km) per km 2<br />
0.04<br />
0.03<br />
0.02<br />
0.01<br />
0.00<br />
4 3 2 1 0<br />
Age (Ga)<br />
Apollo Luna Earth<br />
Fig. 1. Cratering statistics of the Moon-Earth system for the last 4 Ga<br />
years [data from Stöffler and Ryder (2001) and regression curve after<br />
Neukum et al. (2001)].<br />
Collisions of solid bodies played a crucial role in the<br />
formation of Earth and its subsequent evolution. The Proto-Earth<br />
accreted by collisions of planetesimals (Wetherill<br />
1984) and underwent, in Archean times, a very heavy<br />
bombardment (Melosh 1989). The high collision rate at<br />
the beginning of Earth was simply the consequence of the<br />
chaotic states in the orbital movements of early solid bodies.<br />
Subsequently, this early collision rate distinctly declined<br />
until about 2.5 Ga, and since then we have an<br />
essentially constant flux of bodies colliding with Earth<br />
(Fig. 1).<br />
This knowledge of the collision history of Earth is<br />
however not exclusively based on observations of terrestrial<br />
impact craters, as one would possibly expect, but it<br />
largely relies on the cratering history of the Moon (Chapman<br />
and Morrison 1994, Neukum et al. 2001, Stöffler and<br />
Ryder 2001). Due to the absence of an atmosphere (and<br />
hence weathering) and the early cessation of volcanic activity<br />
on Moon, impact craters accumulated, in nearly<br />
undisturbed fashion, particularly in the lunar highlands,<br />
where crater densities are highest. On the geologically<br />
very active Earth, the morphologic landforms of impact<br />
craters easily disappear beyond recognition due to erosion,<br />
plate tectonics and other exogenic and endogenic processes.<br />
Although four Archean impact layers have been reported<br />
(Byerly et al. 2002), we have no knowledge of an<br />
Archean crater (Fig. 2). According to the cratering statistics<br />
(Fig. 1), one would however expect that most craters<br />
formed during this early episode of Earth (Grieve and<br />
Shoemaker 1994).<br />
265
Falko Langenhorst<br />
Identified craters per 1 Ma<br />
1.0<br />
0.5<br />
0.0<br />
Cenozoic (0–65 Ma)<br />
Mesozoic (65–250 Ma)<br />
Impact events are however not only expressed at the<br />
large scale in the form of circular craters but they manifest<br />
also at microscopic scales in minerals. This article focuses<br />
on these microscopic traces in minerals termed shock or<br />
shock-metamorphic effects. Shock effects in minerals are<br />
an unequivocal fingerprint and, often, the last remnants of<br />
impact events. Even if the crater is completely erased,<br />
shocked minerals can be preserved in distal or global ejecta<br />
horizons, still providing evidence of the impact and its<br />
age. In case of the Cretaceous/Tertiary extinction (Alvarez<br />
et al. 1980), the discovery of shocked minerals in the KT<br />
boundary layer increased, for example, the efforts to find<br />
the corresponding impact structure (Bohor et al. 1984 and<br />
1987), subsequently identified as the Chicxulub crater<br />
(Hildebrand et al. 1991).<br />
In the last 10–15 years we have obtained new insights<br />
and a better understanding of the shock behaviour of minerals,<br />
mainly due to the increased use of transmission electron<br />
microscopy (TEM). In terms of spatial resolution, this<br />
technique is well superior to optical microscopy. Therefore,<br />
it became possible to decipher the nature of shock<br />
phenomena already known from optical studies (e.g. planar<br />
deformation features (PDFs)), to discover so-far unknown<br />
effects, and to understand their mechanisms of<br />
Paleozoic (250–570 Ma)<br />
Geological Era<br />
Fig. 2. The number of identified impact craters per Ma plotted for different<br />
eras in the Earth history. Note that despite the high cratering activity<br />
in the Archean we have no knowledge of an impact crater from this<br />
time period (cf. Fig. 1, data from http://gdcinfo.agg.nrcan.gc.ca/crater/<br />
world_craters_e.html).<br />
Proterozoic (570–2500 Ma)<br />
Archean (2500–4550 Ma)<br />
formation and subsequent alteration. This article does not<br />
aim to give a comprehensive review on shocked minerals;<br />
for a more detailed compilation the reader is referred to:<br />
e.g., French and Short (1968), Stöffler (1972, 1974), Stöffler<br />
and Langenhorst (1994), French (1998), Deutsch and<br />
Langenhorst (1998), Langenhorst and Deutsch (1998). It<br />
is merely an attempt to utilize instructive examples to explain<br />
the specific response of minerals to shock compression,<br />
which is distinctly different from the transformation<br />
and deformation behaviour of minerals in other geologic<br />
processes, principally of lower strain rate.<br />
Principles of shock waves<br />
From a basic understanding of shock waves it will be<br />
immediately clear why minerals respond differently to impact<br />
than to other geologic processes. It will also help to<br />
understand the mechanics of the large-scale crater-forming<br />
process (Roddy et al. 1977, Melosh 1989). A shock wave<br />
is an extreme compression wave that propagates with supersonic<br />
velocity, abruptly compresses, heats, and plastically<br />
deforms solid matter. In this respect, shock waves are<br />
fundamentally different from seismic (elastic) waves (e.g.<br />
Duvall and Fowles 1963).<br />
A shock wave is produced by the impact of a high-velocity<br />
projectile or the detonation of an explosive (Roddy<br />
et al. 1977, Asay and Shahinpoor 1993). In these processes,<br />
the time of load is extremely short and, therefore, the<br />
initial stress wave steepens immediately to an almost<br />
atomically sharp discontinuity, which separates highly<br />
compressed from uncompressed material. This so-called<br />
“shock front” represents consequently an infinite discontinuity<br />
in all state parameters (Duvall and Fowles 1963,<br />
Melosh 1989): pressure P, temperature T, specific volume<br />
V, and energy E. Minerals and rocks undergo some kind of<br />
a physical “shock”, because they have to instantly adapt to<br />
extreme P,T conditions with strain rates on the order of 10 6<br />
to 10 9 s -1 . Additionally, a shock wave is very short-lived<br />
with a typical pulse duration of about 1 second for a natural<br />
impact of a 10 km diameter projectile. It is due to these<br />
two time parameters, high strain rates and short shock duration,<br />
that minerals cannot respond by equilibrium reactions<br />
but rather by the activation of fast deformation and<br />
transformation mechanisms.<br />
The unusual properties of shock waves can be illustrated<br />
by a simple train model (Fig. 3). The cartoon shows<br />
the collision of a moving train (projectile) with a standing<br />
train (target). The collision leads to deformation and compression<br />
of the hitting locomotive and the wagons in two<br />
opposite directions. The two boundaries between compressed<br />
and uncompressed wagons are the shock fronts,<br />
which propagate with the shock velocity U. An additional<br />
effect of the compression is material flow in the direction<br />
of the target (see the displacement of the boundary between<br />
the hitting locomotive and the last target wagon).<br />
The material moves behind the shock wave into the target,<br />
266
time<br />
Shock metamorphism of some minerals: Basic introduction and microstructural observations<br />
at a particle velocity u p , which is distinctly smaller than<br />
the shock velocity U. As the process proceeds, more and<br />
more wagons are engulfed by the compression until the<br />
shock wave in the projectile is reflected as rarefaction<br />
wave at the free rear side of the projectile (Fig. 3). This<br />
leads to a backward acceleration of wagons and represents<br />
the ejection of material in natural impact cratering. As the<br />
rarefaction wave is propagating in already compressed<br />
material, it is faster than the shock wave in the target. Consequently,<br />
the shock wave will be overtaken at some depth<br />
by the rarefaction wave, i.e. it will decay.<br />
Both shock U and particle u p velocities characterise the<br />
state of material under shock compression and are related<br />
to pressure P, density ρ, and energy E via the Hugoniot<br />
equations (Duvall and Fowles 1963, Melosh 1989):<br />
ρ 0 U = ρ (U – u p ) (1)<br />
P – P 0 = ρ 0 U u p (2)<br />
P u p = ρ 0 U (u p2 /2) + ρ 0 U (E – E 0 ) (3)<br />
These equations express the conservation of mass, momentum,<br />
and energy across the shock front. By combining<br />
equations (1) to (3) the velocities can be eliminated to give<br />
the so-called Rankine-Hugoniot equation:<br />
E – E 0 = (P – P 0 ) (V 0 – V)/2 with V = 1/ρ (4)<br />
This is an equation of state, describing the physical<br />
states that can be achieved by shock waves of variable intensity<br />
in any solid. Commonly, the shock equation of state<br />
of a particular material is experimentally determined by<br />
measuring particle u p and shock U velocities. Since the zero-pressure<br />
densities ρ 0 of minerals are usually well known,<br />
pressures P and densities ρ (or specific volumes V) can be<br />
calculated with the above mentioned Hugoniot equations.<br />
As is usual for all equations of state, the shock data of<br />
a particular material are displayed in a pressure-specific<br />
volume plot, defining the so-called Hugoniot curve. The<br />
Hugoniot curves of rock-forming minerals are commonly<br />
characterised by kinks, i.e., discontinuous changes in the<br />
curve slope. One discontinuity is typically at 5–10 GPa,<br />
the so-called Hugoniot elastic limit, which is the yield<br />
strength of the material. Discontinuities at higher pressures<br />
were generally assumed to result from phase transformations<br />
to high-pressure polymorphs (e.g. Ahrens and<br />
Rosenberg 1968, Jackson and Ahrens 1979, Ahrens et al.<br />
1976, Melosh 1989). This interpretation is certainly correct<br />
for materials such as iron and graphite, which undergo<br />
martensitic (displacive) transformations, fast enough to<br />
take place under shock compression. It is however an inappropriate<br />
assumption for silicate materials such as<br />
quartz, feldspars and olivine. These minerals can only be<br />
converted into high-pressure polymorphs via reconstructive<br />
mechanisms. These mechanisms are however too<br />
time-consuming to occur under shock compression.<br />
Therefore, shock experiments on these minerals usually<br />
result in the formation of dense (diaplectic) glass with possibly<br />
five- and/or six-fold coordinated silicon or finely recrystallised<br />
low-pressure phase.<br />
U<br />
V 0 , E 0<br />
P 0 , T 0<br />
U<br />
P 1 , T 1<br />
V 1 , E 1<br />
shock front<br />
u p<br />
material<br />
front<br />
u p<br />
Experimental simulation<br />
shock front<br />
rarefaction front<br />
ejection<br />
Fig. 3. A train model illustrating the formation and propagation of shock<br />
and rarefaction waves and the associated material movement (from Langenhorst<br />
2000).<br />
Shock experiments are indispensable for understanding<br />
the formation of shock effects in minerals, because<br />
they are performed under controlled laboratory conditions<br />
and because they provide shocked minerals in their initial,<br />
unmodified state. This has two basic advantages. First,<br />
shock effects can be calibrated as function of pressure (or<br />
other factors) and the resultant barometers can then, with<br />
some care, be applied to nature (Stöffler and Langenhorst<br />
1994). Secondly, the study of pristine shock effects helps<br />
to understand possible post-shock modifications (annealing,<br />
chemical alteration etc.) in the natural impact environment<br />
(Grieve et al. 1996).<br />
The major disadvantage of shock experiments is their<br />
short pulse duration (< 1µs), which is at least 6 orders of<br />
magnitude shorter than the pressure pulse in a natural<br />
bolide impact (~ 1 s, Langenhorst et al. 2002a). The short<br />
pulse duration in an experiment is simply the result of the<br />
small size of the projectile. The pressure duration corresponds<br />
approximately to the time that a shock wave needs<br />
to travel through the projectile and back (i.e. 2 projectile<br />
diameters, Fig. 3).<br />
It may be some surprise, but pioneering, experimental<br />
work on impact processes started with Alfred Wegener<br />
(1921), the founder of plate tectonics. He simulated impact<br />
events by throwing cement powder in a tablespoon<br />
with his bare hand onto a target, which was also composed<br />
of cement powder. He was able to produce circular craters<br />
with central uplifts, resembling in shape and proportions<br />
those observed on the Moon. Since then, a large variety of<br />
sophisticated shock techniques has been developed to<br />
simulate cratering mechanics and shock metamorphism of<br />
267
Falko Langenhorst<br />
a<br />
b<br />
booster<br />
laser<br />
d<br />
D<br />
high explosive<br />
flyer plate<br />
spacing ring<br />
cover layer<br />
specimen<br />
Fe cylinder<br />
vacuum<br />
chamber<br />
lens<br />
mirrors<br />
sample<br />
steel blocks<br />
Fig. 4. Two different experimental designs to produce shock waves: (a) High-explosive device used at the Ernst-Mach-Institut, Efringen-Kirchen, Germany<br />
(modified after Langenhorst and Deutsch 1994) and (b) a laser irradiation setup with the sample being clamped into an Al block. The laser is focused<br />
on a thin Al foil, acting as flyer plate (modified after Langenhorst et al. 1999a and 2002a).<br />
minerals (e.g. French and Short 1968, Roddy et al. 1977,<br />
Asay and Shahinpoor 1993, Davison et al. 2002).<br />
Most experiments related to cratering mechanics employ<br />
spherical projectiles that produce and excavate some<br />
crater in an infinite half space medium via a spherically<br />
expanding shock wave. In contrast, most experiments related<br />
to shock metamorphism employ flat-plate projectiles<br />
that drive a planar shock wave through a similarly planar<br />
target; the thickness of the latter is typically less than projectile<br />
thickness to avoid measurable pressure decay<br />
across the sample (Barker et al. 1993). The target is usually<br />
a metallic container, encapsulating the sample in a fashion<br />
to allow its partial or complete recovery. The<br />
experiments may differ widely in the type of accelerating<br />
system (Fig. 4): powder and light-gas guns, high-explosive<br />
charges, electric discharge guns, and laser irradiation techniques<br />
have been used and tested to successfully reproduce<br />
shock effects in minerals (e.g. Milton and DeCarli<br />
1963, Müller and Hornemann 1969, Gratz et al. 1992,<br />
Stöffler and Langenhorst 1994, Langenhorst et al. 1999a,<br />
2002a). The principle of the electric gun is to vaporise a<br />
thin metal foil by rapid electric discharge of a capacitor.<br />
The high electrical current leads to the instantaneous vaporisation<br />
of the foil and the production of a shock wave<br />
(Langenhorst et al. 2002a). Laser irradiation experiments<br />
can be performed either with or without a projectile. In the<br />
latter case, the beam is directly focused on the sample surface<br />
(Langenhorst et al. 2002a), whereby the absorption of<br />
the laser energy generates rapidly exploding plasma that<br />
subsequently induces a shock wave. Such plasma techniques<br />
are capable to produce the highest shock pressures<br />
with an unbelievable world record of 750 Mbar (Cauble et<br />
al. 1993). However, higher shock pressures are commonly<br />
at the expense of shorter shock durations and smaller sample<br />
volumes. This is because higher impact velocities and<br />
hence higher shock pressures can only be achieved by reducing<br />
the size and weight of the projectile. Typical pressure<br />
pulses in laser irradiation, electric discharge and highexplosive<br />
experiments are approximately 1 ns, 10 ns, and<br />
1 µs with shocked sample volumes on the order of 0.1, 1,<br />
and 100 mm 3 , respectively (Langenhorst et al. 2002a).<br />
To determine pressures in shock experiments it is necessary<br />
to measure the velocities associated with the shock<br />
waves (projectile v, particle u and shock U velocities), using<br />
electrical pin contact, optical interferometry (VISAR)<br />
or similar techniques (Hornemann and Müller 1971, Barker<br />
et al. 1993). It is then possible to calculate the pressures<br />
temperature (°C)<br />
3000<br />
2500<br />
2000<br />
1500<br />
1000<br />
500<br />
quartz<br />
eclogite<br />
liquid<br />
coesite<br />
release<br />
paths<br />
stishovite<br />
porous sandstone<br />
0<br />
1 10<br />
100<br />
shock pressure (GPa)<br />
Fig. 5. Phase diagram depicting the pressure-temperature conditions<br />
reached in quartz, olivine (solid line), and porous sandstone (long dashed<br />
line) by shock compression (data after Wackerle 1962, Kieffer et al.<br />
1976, and Holland and Ahrens 1997). The release paths hold for porous<br />
quartz, which first melts on loading and then solidifies on cooling as coesite<br />
or stishovite. The equilibrium phase boundaries between quartz, coesite,<br />
stishovite and liquid are drawn as dashed lines. The grey<br />
pressure-temperature field represents the conditions reached in regional<br />
metamorphism; the solid line within this field depicts the pressure-temperature<br />
path of a diamond-bearing gneiss (Stöckhert et al. 2001).<br />
quartz<br />
olivine<br />
268
Shock metamorphism of some minerals: Basic introduction and microstructural observations<br />
by aid of the known Hugoniot relations of the materials involved<br />
(Marsh 1980). Thus, the determination of shock<br />
pressure is fundamentally different from the approach<br />
used in static compression techniques (e.g. piston cylinder,<br />
multi-anvil or diamond anvil cell experiments), in which<br />
the pressures are calibrated via properties and/or phase<br />
transformations of reference materials (e.g. Rubie 1999).<br />
The determination of temperatures is a less precise and<br />
more difficult undertaking. So far, pyrospectrometric techniques<br />
have been used to measure both shock and postshock<br />
temperatures (e.g. Raikes and Ahrens 1979, Holland<br />
and Ahrens 1997; Fig. 5). The knowledge of temperatures<br />
is however of fundamental importance for the determination<br />
of the melting temperatures of materials at very high<br />
pressures. For example, the precise measurement of the<br />
melting curve of iron enables the temperature at the<br />
boundary between Earth’s inner (solid) and outer (liquid)<br />
core to be determined (Brown and McQueen 1986), an<br />
important fix point of the geotherm.<br />
calcite graphite olivine quartz<br />
shock effects<br />
mechanical twins<br />
PF<br />
PDF<br />
mosaicism<br />
diaplectic glass \ lechatelierite<br />
stishovite \ coesite<br />
dislocations<br />
PF and PDF<br />
mosaicism<br />
recrystallisation and staining<br />
ringwoodite<br />
kink bands<br />
diamond<br />
mechanical twins<br />
dislocations<br />
decomposition and recombination products<br />
shock pressure (GPa)<br />
0 10 20 30 40 50 60<br />
0 10 20 30 40 50 60<br />
Shock effects in minerals<br />
Fig. 6. Compilation of the pressure intervals over which certain shock effects<br />
are formed in quartz, olivine, graphite and calcite (modified after<br />
Stöffler and Langenhorst 1994 and Langenhorst and Deutsch 1998). The<br />
diagram is based on shock experiments with non-porous samples.<br />
Shock-induced physical and chemical changes in minerals<br />
are collectively called shock effects or shock-metamorphic<br />
effects. This term is relatively broad and covers<br />
any type of shock-induced change, such as formation of<br />
lattice defects, phase transformations, decomposition reactions<br />
and resultant changes in physical and chemical properties.<br />
A great diversity of natural shock effects has been<br />
described on the basis of spectroscopic techniques, X-ray<br />
diffraction, and optical microscopy (Hörz and Quaide<br />
1973, Stöffler 1972 and 1974, Schneider 1978, Boslough<br />
et al. 1989). The physical nature of some of the effects was<br />
not completely clear and others were not even known until<br />
TEM was used to characterize the mineralogical effects<br />
at the nanometer scale. Based on TEM observations, the<br />
following simple subdivision of shock effects and processes<br />
occurring during shock compression and decompression<br />
has been proposed (Langenhorst and Deutsch 1998):<br />
(1) Deformation: formation of dislocations, planar microstructures<br />
(planar fractures and planar deformation<br />
features), mechanical twins, kink bands, and mosaicism<br />
(2) Phase transformations into high-pressure phases and<br />
diaplectic glass<br />
(3) Decomposition into a solid residue and a gaseous<br />
phase<br />
(4) Melting and vaporisation of entire mineral (subsequently<br />
quenched as shock-fused glass or polycrystalline<br />
aggregates)<br />
This simple list does not contain the post-shock thermal<br />
effects forming distinctly after the impact. In a wide<br />
sense, these effects may also be regarded as shock indicators,<br />
although they are not primary effects of shock compression<br />
and decompression and simply result from the<br />
high temperatures prevailing after an impact event. Examples<br />
of diagnostic post-shock effects are the formation of<br />
Ballen quartz and checkerboard feldspars in impact melts<br />
(Carstens 1975, Bischoff and Stöffler 1984) or the crystallization<br />
of highly oxidised Ni-rich spinels (magnesioferrites)<br />
in microtektites (Robin et al. 1992).<br />
We will focus here exclusively on the shock effects<br />
listed above. The deformation and transformation effects<br />
largely form during the compression phase of shock<br />
waves, whereas decomposition, melting and vaporisation<br />
are temperature dominated processes, which take place<br />
during the decompression phase when pressure declines to<br />
a larger extent than temperature. There is no single mineral<br />
that shows all of these effects (Fig. 6). The response of<br />
a mineral to shock compression largely depends on its<br />
crystal structure and composition. A mineral with strong<br />
three-dimensional covalent bonding between polyhedra in<br />
the crystal structure can, for example, not respond by dislocation<br />
glide. Also, minerals without volatile components<br />
cannot respond by decomposition reactions such as dehydration<br />
and decarbonation. To highlight these aspects and<br />
to illustrate the various types of shock effects in minerals<br />
we will concentrate on four minerals, differing largely in<br />
terms of crystal structure and composition.<br />
Quartz<br />
Among the rock-forming minerals, quartz (SiO 2 ) displays<br />
the widest variety of shock effects. It possesses a<br />
crystal structure, consisting of three-dimensionally linked,<br />
corner-shared SiO 4 -tetrahedra with strong covalent bonding.<br />
In the low-pressure regime (< 30 GPa), quartz can<br />
269
Falko Langenhorst<br />
(101 — 1)<br />
a<br />
50 µm<br />
0.2 µm<br />
b<br />
(0001)<br />
c<br />
0.5 µm<br />
100 nm<br />
d<br />
Fig. 7. Shock effects in quartz: (a) Optical micrograph of planar deformation features in shocked quartz in a garnet gneiss from the Popigai crater,<br />
Siberia, (b) bright-field TEM image of fresh, amorphous PDFs in shocked quartz from the Massignano outcrop, Italy (see Langenhorst 1996), (c) Darkfield<br />
TEM image of a mechanical Brazil twin in shocked quartz from the Mjølnir crater, Barents Sea and (d) dark-field scanning TEM image of numerous<br />
stishovite needles embedded in a glassy shock vein of the Zagami meteorite (see Langenhorst and Poirier 2000).<br />
therefore not react by dislocation glide, particularly because<br />
the activation and glide of dislocations is controlled<br />
by the diffusion of water-related defects (see McLaren<br />
1991 for “hydrolytic weakening”), which is a rather slow<br />
process compared to the short time frame of shock compression.<br />
Instead, quartz develops so-called planar microstructures<br />
(Grieve et al. 1990), which comprise planar fractures<br />
(PF), planar deformation features (PDFs), and mechanical<br />
twins (Stöffler and Langenhorst 1994). The mechanical<br />
twins were previously also regarded as PDFs, because a distinction<br />
on the basis of optical microscopy is impossible.<br />
PFs can basically be regarded as high-pressure cleavage<br />
planes that are only activated by dynamic shock loading;<br />
they are relatively widely spaced (> 5–20 µm). On the<br />
contrary, quartz has no cleavage at ambient conditions and<br />
fails by a glassy-like parting.<br />
PDFs were previously also called planar elements (Engelhardt<br />
and Bertsch 1969) and are thin (< 200–300 nm)<br />
amorphous lamellae with the same composition as the host<br />
crystal (Fig. 7b); at the TEM scale, their spacing (< 1 µm)<br />
is much smaller than that of PFs (Müller 1969, Ashworth<br />
and Schneider 1985, Gratz et al. 1992, Langenhorst 1994).<br />
PDF orientations are crystallographically controlled and<br />
show a pressure-dependent variation. Most PDFs are oriented<br />
parallel to rhombohedral planes such as {101 — 3} and<br />
{101 — 2}; other less abundant PDF orientations are given in<br />
Table 1 (see also Stöffler and Langenhorst 1994). In the<br />
low-pressure regime (< 30 GPa), PDF orientations are regarded<br />
as the most robust barometer, because even postshock<br />
annealing and alteration merely converts the PDFs<br />
into the “decorated” type (French 1969; Fig. 7a), but PDF<br />
orientations remain unchanged. The decoration of PDFs in<br />
naturally shocked quartz is due to recrystallization of the<br />
270
Shock metamorphism of some minerals: Basic introduction and microstructural observations<br />
Table 1. Compilation of the most abundant PDF orientations in shocked quartz.<br />
Miller indices {h k i l} Azimuth angle Pole distance ρ Symbol Form<br />
(0001) – 0° c basal pinacoid<br />
{101 — 3}, {011 — 3} p, n 30° 22.95° ω, ω’ rhombohedron<br />
{101 — 2}, {011 — 2} p, n 30° 32.42° π, π’ rhombohedron<br />
{101 — 1}, {011 — 1} p, n 30° 51.79° r, z rhombohedron<br />
{101 — 0} 30° 90° m hexagonal prism<br />
{404 — 1v, {044 — 1} p, n 30° 78.87° t rhombohedron<br />
{516 — 0}, {61 — 5 — 0} r, l 40° 90° k ditrigonal prism<br />
{516 — 1}, {61 — 5 — 1} p, n, r, l 40° 82.07° x trigonal<br />
{61 — 5 — 1}, {156 — 1} trapezoedron<br />
{314 — 1}, {43 — 1 — 1} p, n, r, l 45° 77.91° – trigonal<br />
{41 — 3 — 1}, {134 — 1} trapezoedron<br />
{213 — 1}, {32 — 1 — 1} p, n, r, l 50° 73.71° – trigonal<br />
{31 — 2 — 1}, {123 — 1} trapezoedron<br />
{112 — 2}, {21 — 1 — 2} r, l 60° 47.73° ξ trigonal dipyramid<br />
{112 — 1}, {21 — 1 — 1} r, l 60° 65.56° s trigonal dipyramid<br />
{112 — 0}, {21 — 1 — 0} r, l 60° 90.0° a trigonal prism<br />
{224 — 1}, {42 — 2 — 1} r, l 60° 77.20° trigonal dipyramid<br />
p = positive, n = negative, r = right, l = left<br />
amorphous lamellae and resultant exsolution<br />
of water. The exsolution of water can<br />
be attributed to the different solubility of<br />
water in silica glass and crystalline quartz.<br />
Therefore, the fluids mobilized in impact<br />
events can initially be dissolved in the<br />
amorphous PDFs but subsequent recrystallization<br />
of the glass expels the water in<br />
form of tiny voids (Goltrant et al. 1991,<br />
1992, Leroux and Doukhan 1996, Grieve et<br />
al. 1996, Langenhorst and Deutsch 1998).<br />
Sub-planar features of tectonic origin<br />
such as the so-called Böhm lamellae have<br />
been erroneously assigned as PDFs (Ernstson<br />
et al. 1985, Vrána 1987; Fig. 8a). TEM<br />
studies have deciphered the nature of these<br />
tectonic features, as being subgrain boundaries<br />
(Cordier et al. 1994, Langenhorst and<br />
Deutsch 1996, Joreau et al. 1997a). Subgrain<br />
boundaries are dislocation arrays,<br />
separating a crystal into sub-grains that are<br />
slightly tilted (< 5°) with respect to each other. They are<br />
the result of slow plastic deformation and recovery of deformed<br />
quartz in a tectonic environment. The deformation<br />
proceeds by the activation and emission of dislocations<br />
coupled with simultaneous or subsequent climb and recovery<br />
of dislocations into sub-grain boundaries (Fig. 8b;<br />
Poirier 1985). Water can easily penetrate along these internal<br />
boundaries leading to a decoration with water bubbles.<br />
A careful optical inspection of the suspected planar<br />
features in quartz will immediately reveal whether they are<br />
of endogenic or exogenic origin. Sub-grain boundaries<br />
show a sub-parallel arrangement but are not perfectly planar,<br />
unlike shock-produced PDFs. The spacing of tectonic<br />
features (usually > 5–10 µm) is larger than that of shockproduced<br />
PDFs (< 1 µm). Under crossed Nicols, the tectonically<br />
deformed quartz grains show undulatory extinction<br />
and can exhibit an anomalous optic axial angle of up<br />
to 10°. In contrast, shocked quartz usually shows a patchy<br />
extinction pattern, with extinct areas in different parts of<br />
the crystal. This behaviour is the so-called mosaicism. In a<br />
tectonic source rock, not all of the deformed quartz grains<br />
contain sub-grain boundaries in a sub-planar arrangement;<br />
many quartz grains may even be devoid of sub-grain<br />
boundaries. On the other hand, it would be rather unusual<br />
for an impact rock that only one or few quartz grains contain<br />
PDFs. If the quartz grains have experienced the same<br />
pressure-temperature conditions, then at least most of<br />
them should contain PDFs (Hörz 1968, Engelhardt and<br />
Bertsch 1969). The size and orientation of quartz grains<br />
with respect to the shock front has however an influence<br />
on the development of PDFs (Walzebuck and Engelhardt<br />
a<br />
50 µm 3 µm<br />
b<br />
Fig. 8. (a) Optical micrograph and (b) corresponding bright-field TEM image of subgrain boundaries in a tectonically deformed quartz from Azuara,<br />
Spain (see Langenhorst and Deutsch 1996).<br />
271
Falko Langenhorst<br />
1979). These effects may therefore be responsible for a<br />
heterogeneous PDF distribution throughout quartzose<br />
rocks, particularly at pressures required for incipient PDF<br />
formation (~ 10 GPa).<br />
Another important outcome of TEM studies was the<br />
discovery of mechanical Brazil twins (Leroux et al. 1994),<br />
which are exclusively oriented parallel to the basal plane<br />
(0001). Numerous partial dislocations in the twin boundaries<br />
indicate the mechanical nature of the twins (Fig. 7c).<br />
In contrast, the commonly known Brazil twins are hydrothermally<br />
grown twins, which lack partial dislocations<br />
and are always oriented parallel to (101 — 1) (McLaren and<br />
Pithkethly 1982, Langenhorst and Poirier 2002). Static deformation<br />
experiments have shown that a high shear stress<br />
of 3 to 4 GPa has to be applied to generate the mechanical<br />
Brazil twins parallel to (0001) (McLaren et al. 1967). In<br />
crustal rocks, such conditions are only met by an impact<br />
event. At the optical scale, the mechanical twins become<br />
only visible if they are decorated with water bubbles. The<br />
mechanical Brazil twins are more resistant to post-shock<br />
annealing and alteration. Long-term regional metamorphism<br />
with complete recrystallization of the shocked rock<br />
or melting is probably the only way to erase them. At the<br />
Vredefort structure, most of the PDFs in shocked quartz<br />
are lost by post-shock overprint but the Brazil twins are<br />
still present. This discovery could explain why the PDF<br />
orientations indicate an apparent decrease in shock pressure<br />
toward the center of the crater (Schreyer 1983, Nicolaysen<br />
and Reimold 1990).<br />
In the high-pressure regime (> 25–30 GPa), quartz is<br />
dominated by phase transformations either to diaplectic<br />
glass or to high-pressure polymorphs. Diaplectic glass is a<br />
densified glass, preserving the shape and sometimes even<br />
internal features of precursor grains (Engelhardt et al.<br />
1967, Stöffler 1984). X-ray studies demonstrate that the<br />
transition from crystalline quartz to diaplectic glass is<br />
marked by increasing mosaicism coupled with decreasing<br />
domain size (Dachille et al. 1968, Hörz and Quaide 1973,<br />
Hanns et al. 1978). The transition is also characterized by<br />
a decrease of refractive indices and densities but diaplectic<br />
glass has a density about 5% higher than that of synthetic<br />
silica glass (Langenhorst and Deutsch 1994). It is<br />
still not fully understood on whether the transformation<br />
represents a solid-state collapse (Stöffler 1984) or quenching<br />
of a liquid under high pressure (Langenhorst 1994).<br />
The latter seems to be more likely because diaplectic glass<br />
is often associated with coesite that crystallized from highpressure<br />
melt (see below).<br />
Solid-state phase transformations of quartz into the<br />
high-pressure polymorphs coesite and stishovite are reconstructive.<br />
This means that time is needed for the cooperative<br />
movement and diffusion of atoms. Consequently,<br />
the short duration of shock compression impedes a direct<br />
solid-state transformation of quartz into the high-pressure<br />
polymorphs. Instead, quartz has to be melted under high<br />
pressure and the high-pressure phases can then readily<br />
crystallize during the decompression phase (see release<br />
paths in Fig. 5). The latter means that coesite and<br />
stishovite form in their stability fields at pressures, which<br />
are smaller than the maximum shock pressure achieved<br />
during the compression phase. The very high temperatures<br />
needed for melting are reached locally within shocked<br />
rocks, e.g. at pores or along shock veins, which result from<br />
shear-induced frictional melting (Kieffer et al. 1976, Langenhorst<br />
and Poirier 2000). The crystallization of highpressure<br />
polymorphs from melt is much faster than a<br />
reconstructive solid-state transformation because the<br />
liquidus temperatures at high pressures are well above<br />
2000°C, where kinetics is very fast. Furthermore, it is<br />
known from NMR studies that compressed silicate melts<br />
contain five- and six-fold coordinated silicon (Xue et al.<br />
1989, Stebbins and Poe 1999), which should facilitate per<br />
se the crystallization of high-pressure polymorphs from<br />
such dense melts. Indeed, coesite and stishovite have always<br />
been found in conjunction with silica or rock glass<br />
(Kieffer et al. 1976, White 1993, Leroux et al. 1994, Langenhorst<br />
and Poirier 2000). Polycrystalline coesite aggregates<br />
occur in diaplectic silica glass (Hörz 1965, Stöffler<br />
1971), e.g. at the Ries and Popigai craters. The rapid crystallization<br />
led to the formation of numerous (100) rotation<br />
twins with the composition plane (010) (Leroux et al.<br />
1994, Grieve et al. 1996). These twins are known to represent<br />
growth defects (Bourret et al. 1986). Stishovite has<br />
been identified in the porous Coconino sandstone from the<br />
Barringer crater (Kieffer et al. 1976), in thin pseudotachylite<br />
veins in shocked basement rocks of the Vredefort<br />
structure, South Africa (Martini 1991, White 1993), as<br />
well as in shock veins in the Martian meteorite Zagami<br />
(Fig. 7d, Langenhorst and Poirier 2000). Recently, the discovery<br />
of post-stishovite polymorphs has been reported, as<br />
well (ElGoresy et al. 2000), but the high beam sensitivity<br />
prevented a thorough characterization of the phases (Sharp<br />
et al. 1999).<br />
Olivine<br />
Olivine is an island silicate with isolated SiO 4 tetrahedra<br />
that are joined by divalent cations. As a consequence,<br />
it is easier than in quartz to break bonds and to activate and<br />
move dislocations in this crystal structure. In the low-pressure<br />
regime, olivine deforms thus by dislocation glide. The<br />
Burgers vector b is always [001] (= c) but depending on<br />
the orientation of the olivine to the shock front, various<br />
slip planes can be activated, all sharing the c direction as<br />
zone axis (Fig. 9a): (010), (100), (110), (hk0) and symmetrically<br />
equivalent planes (Ashworth and Barber 1975,<br />
Langenhorst et al. 1995, Leroux et al. 1996, Joreau et al.<br />
1997b, Langenhorst and Greshake 1999). The dislocation<br />
densities can be as high as 2 × 10 14 m –2 (Madon and Poirier<br />
1983, Langenhorst et al. 1995, Leroux 2001), even in experimentally<br />
shocked olivine (Langenhorst et al. 1999a<br />
and 2002b). Experiments have also demonstrated that dislocations<br />
can propagate at approximately half the sound<br />
velocity (~ 3 km/s, Langenhorst et al. 1999a) and are<br />
272
Shock metamorphism of some minerals: Basic introduction and microstructural observations<br />
0.5 µm 0.2 µm<br />
a b<br />
Fig. 9. (a) Dark-field TEM image of numerous c dislocations and a planar fracture in a shocked olivine grain from the Tenham chondrite, (b) Brightfield<br />
TEM image of ringwoodite in a shock vein of the ordinary chondrite Acfer 90072. Note the numerous stacking faults parallel to {110} planes.<br />
probably hampered to reach this maximum speed due to<br />
interactions between themselves. The sources of dislocations<br />
seem to be the tips of forming planar fractures. When<br />
the planar fractures are formed, a high stress field is created<br />
at their tips, from which the dislocations are first emitted<br />
as loops. Since the edge component is distinctly faster<br />
than the screw component, the dislocations become very<br />
straight during further propagation, with the long dislocation<br />
line representing the screw segment.<br />
The PFs in olivine are indicative of shock as they are<br />
oriented parallel to rational crystallographic planes that<br />
are not known as normal cleavage planes of olivine. The<br />
PFs are typically parallel to low index planes (Müller and<br />
Hornemann 1969, Snee and Ahrens 1975, Reimold and<br />
Stöffler 1978, Bauer 1979, Langenhorst et al. 1995, Stöffler<br />
et al. 1991): (100), (010), (001), (130), and (110), belonging<br />
to pinacoidal and prismatic forms. Both, the<br />
internal fragmentation of olivine by fracturing and the<br />
high density of dislocations contribute to the patchy extinction<br />
behaviour under crossed Nicols, known as mosaicism.<br />
Observations on naturally and experimentally shocked<br />
olivine reveal that mosaicism increases distinctly in the<br />
high-pressure regime (> 25–30 GPa; Carter et al. 1968,<br />
Müller and Hornemann 1969, Snee and Ahrens 1975,<br />
Reimold and Stöffler 1978, Bauer 1979, Schmitt 2000).<br />
Additional shock phenomena in this pressure regime are<br />
staining, recrystallization, and transformation into the<br />
high-pressure polymorphs wadsleyite and ringwoodite<br />
(Fig. 9b). Although the production of glass has been reported<br />
in one experimental study (Jeanloz et al. 1977), diaplectic<br />
or shock-fused glasses are generally unknown for<br />
olivine.<br />
Brownish staining of olivine has been described for experimentally<br />
and naturally shocked olivine (Stöffler et al.<br />
1991, Schmitt 2000) but the reason for the colorization is<br />
unknown; a careful microstructural characterization is certainly<br />
required to unravel the nature of the staining effect.<br />
The term recrystallisation decribes the formation of<br />
fine-grained olivine (1–2 µm) aggregates, mostly in the<br />
vicinity of shock veins. Shock-induced recrystallisation of<br />
olivine is generally assumed to be a solid-state process<br />
(Carter et al. 1968, Ashworth and Barber 1975, Bauer<br />
1979, Stöffler et al. 1991). This interpretation actually<br />
makes sense, because recovery and polygonization of dislocations<br />
are expected to occur at elevated post-shock temperatures,<br />
resulting in fine-grained strain-free olivine<br />
aggregates with lattice-preferred orientation of subgrains<br />
(Lally et al. 1976).<br />
In analogy to quartz, the high-pressure transformations<br />
require first the production of an olivine melt, which has<br />
then to rapidly crystallize upon decompression as highpressure<br />
polymorphs. Such rapid crystallization is so far<br />
only manifested in shock veins of ordinary chondrites, i.e.<br />
in thin localized melt zones that are first formed by shearinduced<br />
frictional heating (Stöffler et al. 1991) and are<br />
then rapidly quenched by the surrounding cold host rock.<br />
The shock veins contain aggregates of tiny (~1 µm)<br />
wadsleyite and ringwoodite grains, together with other<br />
high-pressure phases (Binns et al. 1969, Putnis and Price<br />
1979, Madon and Poirier 1983, Langenhorst et al. 1995,<br />
Chen et al. 1996). Olivine melt crystallizing at pressures<br />
beyond the ringwoodite stability field yields for example<br />
an assemblage of silicate perovskite and magnesiowüstite<br />
(Sharp et al. 1997, Tomioka and Fujino 1997), the expected<br />
mineral assemblage in the Earth’s lower mantle. The<br />
coexistence of high-pressure phases that should not coexist<br />
under equilibrium indicates that the crystallization of<br />
shock veins probably happened during decompression, i.e.<br />
the phases crystallized progressively from the melt while<br />
the pressure declined.<br />
In ordinary chondrites, wadsleyite and ringwoodite are<br />
both characterized by numerous stacking faults. Wadsleyite<br />
develops faults parallel to the (010) plane (Madon<br />
and Poirier 1983) and ringwoodite parallel to {110} planes<br />
(Fig. 9b; Langenhorst et al. 1995, Chen et al. 1996). The<br />
273
Falko Langenhorst<br />
a<br />
Graphite<br />
b<br />
Diamond<br />
A<br />
C<br />
A<br />
c<br />
B<br />
B<br />
<br />
C<br />
C<br />
A<br />
Fig. 10. Crystal structures of (a) hexagonal (ABAB…) graphite and (b) cubic (ABCABC…) diamond showing the different stacking sequences in the<br />
[0001] and [111] directions, respectively.<br />
stacking faults are regarded as growth defects, i.e. they are<br />
an inevitable result of the short crystallization times. The<br />
time for crystallisation of shock veins depends primarily<br />
on the thickness of the vein and the initial temperature difference<br />
between vein and adjacent cold host rock. Recent<br />
calculations suggest that the times for crystallisation of<br />
high-pressure polymorphs are much shorter than the shock<br />
duration (Langenhorst and Poirier 2000).<br />
In terrestrial impact rocks, the high-pressure polymorphs<br />
of olivine have not been found yet, probably because<br />
of the lack of well-preserved, olivine-rich target<br />
rocks with thin shock veins.<br />
Graphite<br />
Graphite is composed of pure carbon and is an example<br />
of a mineral with a pronounced sheet structure (Fig.<br />
10a). Within the sheets, carbon atoms form hexagonal<br />
rings with very strong covalent bonds. Weak van-der-<br />
Waals bonding prevails between the sheets. For such a layered<br />
structure, it is characteristic to react to shock<br />
compression by kink or twin operations. In the low-pressure<br />
regime (< 25–30 GPa), graphite is usually assumed to<br />
kink but there are no exact measurements of rotation angles<br />
between different parts of shock-folded graphite crystals<br />
to exclude the possibility of twin operations (Stöffler<br />
1972).<br />
Graphite is of most interest for its phase transformation<br />
to diamond. In the context of impact events, the formation<br />
of diamond is a rare example for a solid-state transformation.<br />
Another mineralogical example for such a transformation<br />
is the conversion of zircon into the scheelite<br />
structured high-pressure polymorph reidite (Glass et al.<br />
2002). Two atomic operations are necessary to convert<br />
graphite into diamond (Fig. 10). The hexagonal carbon<br />
layers have to be brought together by compression along<br />
the c axis and the stacking sequence has to be changed<br />
from a hexagonal to a cubic array by shearing of the<br />
hexagonal carbon layers in their a-a plane. Neglecting the<br />
van-der-Waals bonds, it is not necessary to break any<br />
strong bonds within the layers. Such shear-induced transitions<br />
are called martensitic transformations. Even in short<br />
shock experiments it is possible to produce this martensitic<br />
transformation; this was first demonstrated by DeCarli<br />
and Jamieson (1961).<br />
In light of this first shock synthesis, the long-known diamonds<br />
in iron meteorites and ureilites (Erofeev and<br />
Lachinov 1888, Foote 1891) were reinterpreted as shock<br />
products (Lipschutz 1964). On Earth, a large number of<br />
impact craters and the K/T boundary are yet known as find<br />
locations of impact diamonds (Masaitis et al. 1990 and<br />
2000, Valter et al. 1992, Koeberl et al. 1997, Hough et al.<br />
1997). They were first discovered in the 100 km sized<br />
Popigai structure, Siberia (Masaitis et al. 1972), which is<br />
regarded as largest diamond deposit on Earth (Deutsch et<br />
al. 2000). In the Ries, impact diamonds were already<br />
found in 1978 by Rost et al., but it was not before 1995<br />
that this finding was noticed by a broader scientific community<br />
(Masaitis et al. 1995, Hough et al. 1995, El Goresy<br />
et al. 2001).<br />
The source rocks of diamonds from terrestrial impact<br />
craters are usually graphite-bearing gneisses or other crystalline<br />
rocks (Masaitis et al. 1990, ElGoresy et al. 2001).<br />
Graphite in these rocks was transformed within the very<br />
short time of shock compression. As a consequence of the<br />
short transformation time, impact diamonds are very defect-rich<br />
and inherited some features of the precursor<br />
graphite. They are birefringent (Fig. 11a), retain the tabular<br />
hexagonal and sometimes even preserve spectacular<br />
growth twins rotated about the c axis of graphite (Fig.<br />
11b). Therefore impact diamonds are regarded as para- or<br />
pseudomorphs after graphite and are called apographitic<br />
diamonds (Masaitis et al. 1990). At the TEM scale, these<br />
impact diamonds contain numerous kink or twin bands<br />
parallel to (h h 2 — h — l) planes of precursor graphite (Fig. 11c;<br />
Langenhorst et al. 1999b). The bands were generated<br />
274
Shock metamorphism of some minerals: Basic introduction and microstructural observations<br />
b<br />
0.1 mm a<br />
c<br />
Fig. 11. (a) Optical micrograph of a tabular impact diamond from the<br />
Ries crater, Germany. The anomalous interference colours are due to internal<br />
strain; crossed Nicols; (b) secondary electron scanning image of<br />
impact diamond from the Popigai impact crater, showing inherited twins<br />
of the precursor graphite, (c) Dark-field TEM image of an impact diamond<br />
from Popigai crater, showing mechanical twin bands that are inherited<br />
from precursor graphite.<br />
when the shock wave was transmitted into the graphite, i.e.<br />
directly before the phase transformation (Langenhorst<br />
2000). TEM studies failed, so far, to detect lonsdaleite although<br />
X-ray diffraction techniques indicate the presence<br />
of this high-pressure polymorph with a hexagonal stacking<br />
sequence (Frondel and Marvin 1967, Hannemann et al.<br />
1967, Masaitis et al. 1990). Instead, one observes that the<br />
diamonds are very disordered and contain numerous<br />
stacking faults, changing locally the cubic into a hexagonal<br />
stacking sequence (Langenhorst 2000). Diffuse X-ray<br />
scattering on these stacking faults is a way to explain the<br />
extra-peaks in X-ray diffraction patterns.<br />
Strongly corroded impact diamonds that are intergrown<br />
with moissanite (SiC) have been found at the Ries<br />
impact crater, Germany. Based on this finding, Hough et<br />
al. (1995) concluded that the diamonds formed by vapour<br />
condensation (so-called chemical vapour deposition<br />
(CVD) mechanism). Meanwhile, this idea has been discarded,<br />
because the moissanite may have formed by reaction<br />
of diamond with silica-rich impact melt (Langenhorst<br />
et al. 1999b). This reaction also forms the basis for the industrial<br />
production of SiC (Mehrwald 1992). Incorporation<br />
of impact diamonds into hot impact melt additionally<br />
provides an elegant explanation for the corroded surfaces.<br />
Calcite<br />
Calcite possesses a crystal structure with planar CO 3<br />
groups that are bridged via Ca atoms. The CO 3 groups are<br />
arranged in layers normal to the c-axis. The bonding between<br />
Ca cations and CO 3 groups is rather weak, allowing<br />
this structure to cleave as rhombohedra and to deform by<br />
mechanical twinning and dislocation glide (Nicolas and<br />
Poirier 1976). Static deformation experiments have shown<br />
that calcite can basically develop three types of mechanical<br />
twins (Barber and Wenk 1979a): e = {011 — 8}, r = {101 — 4}<br />
and f = {011 — 2} using the hexagonal unit cell setting with<br />
a = 4.99 Å and c = 17.06 Å. Little is known about the<br />
shock deformation of calcite but these twin laws apparently<br />
operate also under low to moderate shock pressures<br />
(Fig. 12a; Barber and Wenk 1979b, Langenhorst et al.<br />
2002a). At slightly higher pressures, the microstructure of<br />
shocked calcite becomes more dominated by dislocations<br />
(Fig. 12b; Barber and Wenk 1976, Langenhorst et al.<br />
2002a), occurring in a high density of up to 10 14 m -2 .<br />
X-ray line broadening observed for naturally shocked calcite<br />
might be due to such high dislocation densities (Skála<br />
and Jakeš 1999).<br />
Effects in the high-pressure regime are of fundamental<br />
importance, as calcite is known to decompose into solid<br />
CaO and gaseous CO 2 . The devolatilization of carbonates<br />
by impacts is considered to be important for the evolution<br />
of Earth’s atmosphere, climate, and life (Silver and<br />
Schultz 1980, Crutzen 1987). For example, the Chicxulub<br />
impact possibly perturbed the atmosphere with large<br />
amounts of CO 2 and SO x , changing its radiative balance<br />
and causing acid rain (Emiliani et al. 1981, Prinn and Fegley<br />
1987). This may have played an important role in the<br />
275
Falko Langenhorst<br />
3 µm 1 µm<br />
a<br />
b<br />
Fig. 12. Shock effects in calcite: (a) bright-field TEM image of crossing deformation twins in calcite shocked to 85 GPa using a high-explosive setup;<br />
(b) dark-field TEM image of numerous dislocations in a laser-shocked calcite (see Langenhorst et al. 2002a).<br />
mass extinction scenario at the Cretaceous-Tertiary<br />
boundary (Alvarez et al. 1980).<br />
Numerous shock experiments have recently been conducted<br />
to address the question of shock-induced devolatilization<br />
(Martinez et al. 1995, Skála et al. 2001,<br />
Ivanov et al. 2002, Langenhorst et al. 2002a). The experiments<br />
indicate that strongly shocked calcite can melt at<br />
high pressure but degassing probably takes only place<br />
after decompression if the post-shock temperatures are<br />
sufficiently high. This result is strengthened by theoretical<br />
calculations of the phase diagram of calcite (Ivanov and<br />
Deutsch 2002) and the discovery of quenched carbonate<br />
melts in suevites of the Ries and Chicxulub craters (Graup<br />
1999, Jones et al. 2000). Furthermore, experiments indicate<br />
that back reactions between the decomposition products,<br />
CO 2 and CaO, are fast and efficient and therefore<br />
have to be taken into account in any quantification of impact-released<br />
CO 2 (Agrinier et al. 2001). To avoid the back<br />
reaction it is necessary to spatially separate the decomposition<br />
products, which is another complexity in a natural<br />
environment.<br />
Shock-melted calcite develops upon quenching a<br />
feathery texture (Jones et al. 2000). Under the optical microscope,<br />
the feathery texture appears as aggregates of radiating,<br />
elongated calcite crystals. At the TEM scale,<br />
quench crystals of calcite are usually devoid of lattice defects,<br />
indicating that they went through the liquid state<br />
(Langenhorst et al. 2002a). On the other hand, incipient<br />
decomposition in shocked calcite is manifested by the<br />
presence of numerous tiny dislocation loops, indicative for<br />
the mobilization of CO 2 (Langenhorst et al. 2002a).<br />
Estimation of shock conditions<br />
A prerequisite for deciphering the shock-metamorphic<br />
history of minerals and their host rocks is an assessment of<br />
their pressure-temperature-time paths. It is important to remember<br />
here that polymict impact breccias consist of rock<br />
and mineral fragments that have suffered different degrees<br />
of shock metamorphism. Therefore it is necessary to consider<br />
each fragment separately.<br />
The estimation of the shock duration is rather difficult,<br />
since no mineralogical speedometer is available. However,<br />
one can obtain a rough idea of the shock pulse if the size<br />
of the projectile is known from e.g. crater size. The shock<br />
pulse corresponds substantially to the time that the shock<br />
wave needs to propagate to the rear surface of the projectile<br />
and back to the point of impact.<br />
The estimation of temperatures is a difficult task as<br />
well, because it is influenced by a number of factors such<br />
as porosity. In the context of shock metamorphism, one<br />
can, in principle, distinguish three different temperatures:<br />
(1) pre-shock, (2) shock and (3) post-shock temperatures.<br />
The pre-shock temperature is not directly related to shock<br />
metamorphism but elevated pre-shock temperatures have<br />
the effect to lower the threshold pressure for certain shockmetamorphic<br />
effects (Huffman et al. 1989, Langenhorst et<br />
al. 1992). It can be elevated due to regional metamorphism<br />
at the time of impact and the temperature could be determined<br />
via classical petrologic concepts (mineral assemblages,<br />
element partitioning between coexisting minerals).<br />
It is also known that PDF orientations in quartz significantly<br />
change at elevated pre-shock temperature, when<br />
quartz is shocked in the β high-temperature structure<br />
(> 573°C; Langenhorst and Deutsch 1994, Grieve et al.<br />
1996). Quartz experimentally shocked in the β stability<br />
field contains PDFs parallel to planes of hexagonal pyramids,<br />
whereas shocked α-quartz exhibits PDFs that only<br />
belong to one rhombohedron (for further details see Langenhorst<br />
and Deutsch 1994).<br />
Shock and post-shock temperatures are directly related<br />
to the magnitude of shock compression. The shock temperature<br />
is the maximum temperature achieved during<br />
shock compression, whereas the post-shock temperature is<br />
the temperature prevailing directly after decompression.<br />
276
Shock metamorphism of some minerals: Basic introduction and microstructural observations<br />
For compact materials, the pressure-dependence of shock<br />
and post-shock temperatures is fairly well known through<br />
calculations and pyrospectrometric measurements (e.g.,<br />
Wackerle 1962, Raikes and Ahrens 1969, Martinez et al.<br />
1995, Holland and Ahrens 1997; Fig. 5). Therefore, temperatures<br />
can be estimated from these reference data, if the<br />
shock pressure has been determined by applying a shock<br />
barometer.<br />
It is more difficult to assess the shock and post-shock<br />
temperatures in porous rocks/minerals, because porosity<br />
has the general effect to significantly increase both temperatures.<br />
Shock compression leads however to compaction<br />
of rocks and loss of pore space, making it difficult<br />
to assess the initial porosity of rocks. Therefore, one can<br />
only apply simple arguments to estimate the temperatures<br />
from observations. For example, in case of mineral melting,<br />
the post-shock temperature has certainly exceeded the<br />
melting point of the mineral at ambient pressure.<br />
The estimation of shock pressure relies on calibration<br />
data obtained in well-controlled shock experiments. Shock<br />
experiments have provided quantitative information on (1)<br />
co(existence) of shock effects in certain pressure ranges,<br />
(2) changes in physical (bulk) properties (e.g. refractive<br />
index and density), (3) variations in PDF orientations (Fig.<br />
13), and (4) degree of mosaicism (Stöffler 1972, Stöffler et<br />
al. 1988, Hanns et al. 1978, Stöffler and Langenhorst<br />
1994, Grieve et al. 1996, Langenhorst and Deutsch 1998).<br />
To obtain a rough estimate of the shock pressure, it is<br />
often enough to use the petrographic microscope and to<br />
observe the shock effects in coexisting minerals. Data on<br />
the (co)existence of pressure-specific shock effects is<br />
available for most rock-forming minerals; compilations<br />
can be found in (Fig. 5): Stöffler (1972), Stöffler et al.<br />
(1988) and (1991), Bischoff and Stöffler (1992), Langenhorst<br />
and Deutsch (1998).<br />
Better constraints on shock pressures can be obtained<br />
if the refractive indices or densities of quartz or feldspars<br />
were measured, using a spindle stage and a density gradient<br />
column (Fig. 13; Medenbach 1985, Langenhorst<br />
1993). The change in these physical properties reflects the<br />
gradual conversion of quartz or feldspars into diaplectic<br />
glasses. This technique applies only over a small pressure<br />
range and requires that the glass is unaffected by postshock<br />
annealing or alteration.<br />
A more robust and widely used technique is to determine<br />
PDF orientations in quartz with an universal-stage<br />
(see appendix and Fig. 13, Stöffler and Langenhorst 1994,<br />
Grieve et al. 1996). Statistical data on PDF orientations in<br />
quartz have been provided, as a function of pressure, by<br />
various U-stage studies (Hörz 1968, Müller and Defourneaux<br />
1969, Robertson and Grieve 1977, Langenhorst<br />
and Deutsch 1994). These measurements reveal, for example,<br />
that, at pressures of about 20 GPa, PDFs are predominantly<br />
oriented parallel to {101 — 3} planes but change at<br />
higher pressure to {101 —<br />
2} orientations. A practical description<br />
on how to identify PDF orientations with an U-<br />
stage is given in the appendix of this paper.<br />
Mean refractive index<br />
1.55<br />
1.50<br />
1.45<br />
PDFs<br />
(1013)<br />
(1011)<br />
(1122)<br />
PDFs<br />
(1012)<br />
(1013)<br />
(1011)<br />
(1122)<br />
X-ray diffractometer studies on shocked rock-forming<br />
minerals reveal an increasing degree of mosaicism with increasing<br />
shock pressure as expressed by decreasing diffraction<br />
peak amplitude and pronounced line-broadening<br />
(Hörz and Quaide 1973, Hanns et al. 1978). Although this<br />
technique is capable of yielding relatively accurate pressure<br />
determinations, it has never been widely applied because<br />
it requires fresh, unaltered samples.<br />
Concluding remarks<br />
transformation regime<br />
PDFs<br />
(1012)<br />
(1013)<br />
20 25 30 35<br />
Shock pressure (GPa)<br />
diaplectic<br />
glass<br />
Fig. 13. Refractive index, density and combinations of PDF orientations<br />
of experimentally shocked quartz as function of pressure (from Langenhorst<br />
and Deutsch 1994).<br />
In the past decade, we have made considerable<br />
progress in understanding the nature and formation mechanisms<br />
of shock effects in minerals. These advances are, to<br />
a large extent, due to TEM studies of shocked minerals,<br />
providing a thorough characterization of the defect microstructures.<br />
Minerals show a unique response when subjected to<br />
strong shock waves. The effects range from deformation<br />
and transformation phenomena to decomposition, melting<br />
and vaporisation. Which shock effects are activated at<br />
what pressures and temperatures depends on the crystal<br />
structure and chemical composition of the mineral studied.<br />
Most shock effects have been reproduced in short laboratory<br />
experiments with various designs, although the<br />
shock pulses in experiments can be more than 6 orders of<br />
magnitude shorter than those prevailing in nature. Experimental<br />
limits are however reached if more time-consuming<br />
processes are simulated, such as reconstructive phase<br />
transformations to high-pressure silicates. On the other<br />
hand, the experimental simulation is very successful in reproducing<br />
deformation defects in shocked minerals. Furthermore,<br />
experiments led also to a better understanding of<br />
post-shock modifications of mineralogical shock effects in<br />
the natural environment. Finally, the shock signature of<br />
minerals is not only an unequivocal indicator for hypervelocity<br />
impact but can also be used to obtain quantitative<br />
constraints on the pressures and temperatures in natural<br />
impacts.<br />
2.6<br />
2.4<br />
2.2<br />
Density (g/cm 2 )<br />
277
Falko Langenhorst<br />
Acknowledgements. I am grateful for the financial support<br />
provided by the Deutsche Forschungsgemeinschaft, which funded part of<br />
this work (grants DE 401/15, HO 1446/3, LA 830/4). I am also indebted<br />
to many colleagues who provided samples or collaborated with me on the<br />
subject of shock metamorphism: A. Bischoff, M. Boustie, A. Deutsch,<br />
J.-C. Doukhan, H. Dypvik, U. Hornemann, B. Ivanov, V. L. Masaitis,<br />
J.-P. Poirier, G. Shafranovsky, and D. Stöffler. I also wish to thank<br />
F. Hörz, H. Leroux, and R. Skala for their constructive reviews and<br />
J. Hopf for technical assistance.<br />
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Handling editor: Roman Skála<br />
The following is a simple description on how to determine the crystallographic<br />
orientation of PDFs in shocked quartz grains, using an universal<br />
stage (von Federov 1896, Reinhard 1931, Nikitin 1936, Emmons<br />
1943, Phillips 1971). Although the use of universal stages has considerably<br />
declined in structural geology, it remains the only method, which<br />
provides statistical data on the orientation of PDFs. Other techniques<br />
such as TEM are also capable of measuring PDF orientations but TEM<br />
measurements are too time-consuming to obtain statistically meaningful<br />
data.<br />
There are four fundamental practical steps in the determination of<br />
PDF orientations in shocked quartz. One has to locate the spatial orientation<br />
of (1) the optic axis (parallel to c axis) and (2) the normals to the<br />
PDF planes in the grain studied. Once these directions are known from<br />
measurements, they are plotted and transformed in a stereographic Wulff<br />
net (3) and can then be indexed by comparison with the standard stereographic<br />
projection of quartz (4).<br />
(1) Since quartz is an uniaxial (trigonal) mineral it is only possible to locate<br />
the c axis optically. The a axes are in the plane perpendicular to<br />
c but their exact positions within this plane are not measurable. This<br />
causes a problem for indexing a PDF plane because the angle to the<br />
c axis can be measured but not the angle to the a axes. To circumvent<br />
this problem in part one needs at least two or more crossing PDF sets<br />
in a single quartz grain. To explain on how to locate the c axis of<br />
quartz, we will follow here the Reinhard notation of rotation axes for<br />
a 4-axis or 5-axis universal stage (Reinhard 1931, Fig. 14). Depending<br />
on the orientation of the quartz grain studied, the optic axis can<br />
be brought either parallel to the M (microscope) axis or parallel to<br />
the K (control) axis (E-W). Hence the first step is to find out whether<br />
the optic axis of the quartz grain is highly inclined to (polar position)<br />
or lies almost within the plane (equatorial position) of the thin section.<br />
Polar position: Rotate about the M axis to the diagonal position (45°<br />
to E-W) and then rotate about the H axis until the grain extincts under<br />
crossed Nicols. If it remains light, the grain is in the equatorial position<br />
APPENDIX: How to determine PDF orientations ?<br />
(see below). Rotate about the M axis to restore the 0° position, but keep<br />
H at its inclined position. The grain will become light again (unless the<br />
optic axis is already parallel to M). Now rotate about the N axis to<br />
achieve again the extinction position. Finally, repeat all the steps until the<br />
grain remains extinct when rotated about the M axis.<br />
Equatorial position: Rotate first about the N axis until the quartz<br />
grain extincts and its optic axis is in the E-W plane. This is the case if<br />
the grain becomes light by a further rotation about the K axis. Rotate<br />
then about the H axis until the extinction position of the grain is restored.<br />
The grain will again become light by a further rotation about the<br />
K axis in opposite direction (unless the optic axis is already parallel to<br />
E-W). Finally, repeat all the steps until the grain remains extinct when<br />
tilted about the K axis. The equatorial position is the more common situation<br />
in PDF measurements, because PDF poles mostly form a small<br />
angle to the c axis.<br />
(2) To determine the orientation of a PDF plane it is necessary to bring<br />
its normal parallel to E-W. This is achieved by rotating about the N<br />
axis until the trace of the PDF plane is parallel to N-S. Rotate then<br />
about the H axis until the trace becomes as sharp as possible. One<br />
can test whether the plane is exactly vertical by defocusing the PDF.<br />
It is vertical if the trace of the PDF does not move. Another way to<br />
test for the vertical position is to tilt about the K axis. If the PDF<br />
plane is exactly vertical, its trace will remain in N-S orientation.<br />
(3) The two important rotation angles to be plotted in the stereonet are the<br />
azimuth angle (i.e. rotation about N) and the ρ angle (i.e. rotation<br />
about H). When plotting the values for the optic axis, it has to be remembered<br />
whether it was tilted vertically or horizontally. Additionally,<br />
one needs to keep in mind the sense of tilting about H. Detailed<br />
descriptions on the plotting of U-stage data can be found in Bloss<br />
(1961) and Phillips (1971). Once the orientation of the optic axis and<br />
the normals to PDF planes are plotted, they need to be transformed<br />
into the standard stereographic projection with the c axis in the center<br />
(Fig. 15). The pole of the optic axis is transformed along the<br />
equatorial line of the Wulff net toward the center, and the normals to<br />
281
Falko Langenhorst<br />
M<br />
A<br />
West<br />
K<br />
H<br />
K<br />
N<br />
K<br />
East<br />
1 (0001)<br />
2 {1013}<br />
3 {1012}<br />
4 {1011}<br />
5 {1010}<br />
6 {1122}<br />
7 {1121}<br />
8 {2131}<br />
9 {5161}<br />
10 {1120}<br />
a 3<br />
a 2<br />
left<br />
negative<br />
Fig. 14. Sketch of the rotation axes on a 5-axis universal stage. The notation<br />
of axes is according to Reinhard (1931): M = microscope axis,<br />
A = auxiliary axis, N = normal axis, H = horizontal axis, and K = control<br />
axis.<br />
a 1<br />
right<br />
positive<br />
Fig. 16. Standard stereographic projection of quartz with the c axis in the<br />
center. The circles have a 5° radius and mark the positions of the most<br />
abundant PDF orientations (modified after Stöffler and Langenhorst<br />
1994). Since quartz is trigonal, one can distinguish positive and negative<br />
(e.g., rhombohedra) as well as right and left (e.g. pyramids) forms.<br />
FN'<br />
ρ<br />
∆<br />
FN'<br />
' – transformed positions<br />
OA – optic axis<br />
FN – face normal<br />
∆ – azimuth difference<br />
ρ – pole distance<br />
ϕ – azimuth angle<br />
ρ OA<br />
OA'<br />
FN<br />
ρ FN'<br />
ρ OA<br />
ϕ FN<br />
– ϕ OA<br />
OA<br />
a 3<br />
a 1<br />
(1012)<br />
(1013)<br />
(1011)<br />
(2112)<br />
a 2<br />
{1013}<br />
{1011}<br />
{0112}<br />
{1122}<br />
120°<br />
Fig. 17. Example for PDF orientations in quartz experimentally shocked<br />
to 25 GPa (from Langenhorst and Deutsch 1994). The right-hand<br />
diagram depicts schematically the full symmetry of coexisting forms.<br />
Fig. 15. An example for the transformation of a PDF pole (FN) and the<br />
optic axis (OA) into the standard stereographic projection of quartz with<br />
the optic axis (=c axis) in the center.<br />
the PDF planes are transformed along small circles by the same angle<br />
(see also von Engelhardt and Bertsch 1969). You can read now<br />
the angle between the PDF normals and the c axis. Alternatively, one<br />
can calculate this angle by the following equation:<br />
cos ρ FN’ = cos ρ FN cos ρ OA + sin ρ FN sin ρ OA cos (ϕ FN – ϕ OA) (5)<br />
In the literature, one will often find histograms in which this angle<br />
is plotted as function of the frequency of PDFs. However, as the a-axes<br />
cannot be located by polarizing microscopy, the angle to the c axis alone<br />
is insufficient for unequivocal indexing of PDF planes. This problem<br />
cannot be solved if the quartz grain of interest contains only one set of<br />
PDFs. However, if the grain contains at least two sets of PDFs, the next<br />
analytical step probably yields a reliable indexing result.<br />
(4) In this final step, the transformed stereoplot is compared to the standard<br />
stereographic projection of quartz, displaying the orientation of<br />
known PDF planes (Fig. 16). The latter are drawn as 5° circles, representing<br />
the estimated errors in the measurements. Table 1 shows<br />
that not only the pole distance varies for the crystallographic PDF<br />
planes but also the azimuth angles, e.g. rhombedral forms lie 30° off<br />
the pyramidal forms because they do not belong to the same crystallographic<br />
zone. This is the basis for indexing the PDF planes. In<br />
practice, the stereographic projection of measured PDF poles is rotated<br />
until all poles fall into the circles of the standard stereographic<br />
projection (Fig. 16). Usually, there should be only one indexing<br />
solution; if the measurements are not precise enough, some PDFs<br />
can remain unindexed. The stereographic projection yields not only<br />
the Miller indices of PDF planes but also provides information on<br />
the coexistence of positive and negative or right and left forms (Langenhorst<br />
and Deutsch 1994). Figure 17 shows an example for typical<br />
PDF combinations in quartz shocked at a pressure of 25 GPa. It<br />
demonstrates that the positive rhombohedra {101 — 1} and {101 — 3} are<br />
combined with the negative rhombohedron {01 — 12} and the right<br />
pyramid {112 — 2}. It is of course not possible to distinguish between<br />
a negative and a positive form but when indexing a stereogram one<br />
has to make an arbitrary choice for the first PDF pole (positive or<br />
negative) and can then consistently index the following poles.<br />
282