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Microbial diversity on the Tatahouine meteorite
Karim BENZERARA1*, Virginie CHAPON2, David MOREIRA3,
Purificación LÓPEZ-GARCÍA3,
François GUYOT1, and Thierry HEULIN2
1Laboratoire de Minéralogie-Cristallographie, UMR 7590 and
Institut de Physique du Globe de Paris, 4 place Jussieu, 75252 Paris Cedex,
France
2CEA/Cadarache, DSV-DEVM, Laboratoire d’Ecologie Microbienne de
la Rhizosphère,
UMR 6191 CNRS-CEA-Université de la Méditerranée, F-13108 Saint-Paul-lez-Durance,
France
3Unité d’Ecologie, Systématique et Evolution, UMR CNRS 8079,
Université Paris-Sud, 91405 Orsay Cedex, France
*Corresponding author. E-mail:
benzerar@impmc.jussieu.fr
Biological processes can alter
the chemistry and mineralogy of meteorites in a very short time, even in
cold or hot deserts. It is thus important to assess the diversity of
microorganisms that
colonize meteorites in order to better understand their physiological
capabilities. Microscopy
observations of Tatahouine meteorite fragments that were exposed for 70
years in the Sahara desert showed that they were colonized by
morphologically diverse biomorphs. A molecular diversity study based on
16S rRNA gene amplification of DNA supported the conclusion that a huge
taxonomic diversity of prokaryotes colonized the Tatahouine meteorite in
less than 70 years in the Tatahouine sand. Eleven different bacterial
divisions were evidenced, among which Cytophaga-Flexibacter-Bacteroides (CFB),
Cyanobacteria, and Alpha-Proteobacteria were dominantly represented.
Crenarcheota were also detected. Most of the Tatahouine meteorite
phylotypes were related to sequences identified in the surrounding
Tatahouine more generally to sequences detected in soils. Some of them, in
particular many of the archaeal phylotypes, were detected in arid regions
in association with desert varnish. The results suggest that the diversity
of the clone library generated from the meteorite fraction was reduced
compared with that of the Tatahouine sand clone library, which can be
explained as the result of partial colonization of the meteorite and/or a
specific selection of colonizing bacteria by the substrate. We discuss the
possibility that several groups detected in this study may play a
prominent role in the various alteration processes detected at the surface
of the Tatahouine meteorite.
Spectral
properties of angrites
T. H. BURBINE1*, T. J. MCCOY2, J. L. HINRICHS3,
and P. G. LUCEY4
1Department of Astronomy, Mount Holyoke College, South Hadley,
Massachusetts 01075, USA
2Department of Mineral Sciences, National Museum of Natural
History, Smithsonian Institution, Washington, D.C. 20560–0119, USA
3NovaSol, 733 Bishop Street, Honolulu, Hawai’i 96813, USA
4Hawai’i Institute of Geophysics and Planetology, 1680
East-West Road, University of Hawai’i at Manoa, Honolulu, Hawai’i 96822,
USA
*Corresponding author. E-mail:
tburbine@mtholyoke.edu
Angrites are generally believed
to be fragments of a basaltic asteroid that differentiated under
relatively oxidizing conditions. Almost all angrites (e.g., D’Orbigny,
Lewis Cliff [LEW] 86010, and Sahara 99555) are composed predominately of
anorthite, Al-Ti diopside-hedenbergite, and Ca-rich olivine, except for
the type specimen, Angra dos Reis, which is composed almost entirely of
Al-Ti diopside-hedenbergite. D’Orbigny, LEW 86010, and Sahara 99555 also
have spectral properties very different from Angra dos Reis. These newly
measured angrites all have broad absorption features centered near 1 µm
with very weak to absent absorption bands at ∼2 µm, which is
characteristic of some clinopyroxenes. The spectrum of Angra dos Reis has
the characteristic 1 and 2 µm features due to pyroxene. One asteroid, 3819
Robinson, has similar spectral properties to the newly measured angrites
in the visible wavelength region, but does not appear to spectrally match
these angrites in the near-infrared.
Asteroid
3628 Božnémcová: Covered with angrite-like basalts?
Edward A. CLOUTIS1*, Richard P. BINZEL2, Thomas H.
BURBINE3, Michael J. GAFFEY4, and Timothy J. McCOY5
1Department of Geography, University of Winnipeg, Winnipeg,
Manitoba, R3B 2E9, Canada
2Department of Earth, Atmospheric and Planetary Sciences,
Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA
3Department of Astronomy, Mount Holyoke College, South Hadley,
Massachusetts 01075, USA
4Space Studies Department, University of North Dakota, Box
9008, Grand Forks, North Dakota 58202, USA
5Department of Mineral Sciences, National Museum of Natural
History, Smithsonian Institution, Washington, D.C. 20560–0119, USA
*Corresponding author. E-mail:
e.cloutis@uwinnipeg.ca
A detailed analysis of the
reflectance spectrum of asteroid 3628 Božnémcová,
previously identified as a possible ordinary chondrite parent body,
indicates that its surface consists of an assemblage dominated by
clinopyroxene and plagioclase feldspar. The clinopyroxene is Fe2+-bearing
(likely in the range Fs~10–20),
with >90% of the Fe2+ being present in the M1 crystallographic
site
(spectral type A). The clinopyroxene:plagioclase feldspar ratio is between
~2
and 3 (~55–75%
clinopyroxene, ~20–33%
plagioclase feldspar). If olivine is present, the clinopyroxene:olivine
ratio is
>~3
(<20% olivine). The derived mineralogy of Božnémcová
is most similar, but not identical, to the
known angrite meteorites. The data suggest that Božnémcová
formed by melting and differentiation
of an oxidized chondritic precursor and probably represents an unsampled
angrite-like body.
Frontier
Mountain 93001: A coarse-grained, enstatite-augite-oligoclase-rich,
igneous rock from the acapulcoite-lodranite parent asteroid
Luigi FOLCO1*, Massimo D’ORAZIO2, 3, and
Alessandro BURRONI1
1Museo Nazionale dell’Antartide, Università di Siena, Via
Laterina 8, 53100 Siena, Italy
2Dipartimento di Scienze della Terra, Università di Pisa, Via
S. Maria 53, 56126 Pisa, Italy
3Istituto di Geoscienze e Georisorse, C.N.R., Via Moruzzi 1,
I-56126 Pisa, Italy
*Corresponding author. E-mail:
folco@unisi.it
The Frontier Mountain (FRO)
93001 meteorite is a 4.86 g fragment of an unshocked, medium- to
coarse-grained rock from the acapulcoite-lodranite (AL) parent body. It
consists of anhedral orthoenstatite (Fs13.3 ± 0.4Wo3.1 ± 0.2), augite
(Fs6.1 ± 0.7Wo42.3 ± 0.9; Cr2O3 = 1.54 ± 0.03), and
oligoclase (Ab80.5 ± 3.3Or3.1 ± 0.6) up to >1 cm in size enclosing
polycrystalline aggregates of finegrained olivine (average grain size: 460
± 210 µm) showing granoblastic textures, often associated with Fe,Ni
metal, troilite, chromite (cr# = 0.91 ± 0.03; fe# = 0.62 ± 0.04),
schreibersite, and
phosphates. Such aggregates appear to have been corroded by a melt. They
are interpreted as
lodranitic xenoliths. After the igneous (the term “igneous” is used here
strictly to describe rocks or
minerals that solidified from molten material) lithology intruding an
acapulcoite host in Lewis Cliff
(LEW) 86220, FRO 93001 is the second-known silicate-rich melt from the AL
parent asteroid.
Despite some similarities, the silicate igneous component of FRO 93001
(i.e., the pyroxeneplagioclase mineral assemblage) differs in being
coarser-grained and containing abundant enstatite. Melting-crystallization
modeling suggests that FRO 93001 formed through high-degree partial
melting (≥35 wt%; namely, ≥15 wt% silicate melting and
~20
wt% metal melting) of an acapulcoitic source rock, or its chondritic
precursor, at temperatures ≥1200 °C, under reducing conditions. The
resulting magnesium-rich silicate melt then underwent equilibrium
crystallization; prior to complete crystallization at
~1040
°C, it incorporated lodranitic xenoliths. FRO 93001 is the
highest-temperature melt from the AL parent-body so far available in
laboratory. The fact that FRO 93001 could form by partial melting and
crystallization under equilibrium conditions, coupled with the lack of
quench-textures and evidence for shock deformation in the xenoliths,
suggests that FRO 93001 is a magmatic rock produced by endogenic heating
rather than impact melting.
Noble gas
space exposure ages of individual interplanetary dust particles
Karl KEHM1, 2*, George J. FLYNN3, and Charles M.
HOHENBERG4
1Department of Physics, Washington College, 300 Washington
Avenue, Chestertown, Maryland 21620, USA
2Department of Terrestrial Magnetism, Carnegie Institution of
Washington, 5241 Broad Branch Road NW, Washington, D.C. 20015, USA
3Department of Physics, State University of New
York–Plattsburgh, 101 Broad Street, Plattsburgh, New York 12901, USA
4Department of Physics, Washington University, Box 1105, One
Brookings Drive, Saint Louis, Missouri 63130, USA
*Corresponding author. E-mail:
kkehm2@washcoll.edu
The He, Ne, and Ar compositions
of 32 individual interplanetary dust particles (IDPs) were
measured using low-blank laser probe gas extraction. These measurements
reveal definitive evidence of space exposure. The Ne and Ar isotopic
compositions in the IDPs are primarily a mixture between solar wind
(SW) and an isotopically heavier component dubbed “fractionated solar”
(FS), which could be implantation-fractionated solar wind or a distinct
component of the solar corpuscular radiation previously identified as
solar energetic particles (SEP). Space exposure ages based on the Ar
content of individual IDPs are estimated for a subset of the grains that
appear to have escaped significant volatile losses during atmosphere
entry. Although model-dependent, most of the particles in this subset have
ages that are roughly consistent with origin in the asteroid belt. A short
(<1000 years) space exposure age is inferred for one particle, which is
suggestive of cometary origin. Among the subset of grains that show some
evidence for relatively high atmospheric entry heating, two possess
elevated 21Ne/22Ne ratios generated by extended
exposure to solar and galactic cosmic rays. The inferred cosmic ray
exposure ages of these particles exceeds 107 years, which tends
to rule out origin in the asteroid belt. A favorable possibility is that
these 21Ne-rich IDPs previously resided on a relatively stable
regolith of an Edgeworth-Kuiper belt or Oort cloud body and were
introduced into the inner solar system by cometary activity. These results
demonstrate the utility of noble gas measurements in constraining models
for the origins of interplanetary dust particles.
Laboratory
simulation of terrestrial meteorite weathering using the Bensour (LL6)
ordinary chondrite
Martin R. LEE1*, Caroline L. SMITH1†, Sarah H.
GORDON1‡, and Mark E. HODSON2
1Department of Geographical and Earth Sciences, University of
Glasgow, Gregory Building, Lilybank Gardens, Glasgow G12 8QQ, UK
2Department of Soil Science, School of Human and Environmental
Science, The University of Reading, Whiteknights, Reading RG6 6AB, UK
†Present address: Department of Mineralogy, The Natural History
Museum, Cromwell Road, London SW7 5BD, UK
‡Present address: Department of Earth Science and Engineering,
South Kensington Campus, Imperial College, London, UK
*Corresponding author. E-mail:
Martin.Lee@ges.gla.ac.uk
Laboratory dissolution
experiments using the LL6 ordinary chondrite Bensour demonstrate that
meteoritic minerals readily react with distilled water at low
temperatures, liberating ions into solution and forming reaction products.
Three experiments were performed, all for 68 days and at atmospheric fO2
but using a range of water/rock ratios and different temperatures.
Experiments 1 and 2 were batch experiments and undertaken at room
temperature, whereas in experiment 3, condensed boiling water was dripped
onto meteorite subsamples within a Soxhlet extractor. Solutions from
experiment 1 were chemically analyzed at the end of the experiment,
whereas aliquots were extracted from experiments 2 and 3 for analysis at
regular intervals. In all three
experiments, a very significant proportion of the Na, Cl, and K within the
Bensour subsamples
entered solution, demonstrating that chlorapatite and feldspar were
especially susceptible to
dissolution. Concentrations of Mg, Al, Si, Ca, and Fe in solution were
strongly affected by the
precipitation of reaction products and Mg and Ca may also have been
removed by sorption.
Calculations predict saturation of experimental solutions with respect to
Al hydroxides, Fe oxides,
and Fe (oxy)hydroxides, which would have frequently been accompanied by
hydrous aluminosilicates. Some reaction products were identified and
include silica, a Mg-rich silicate, Fe
oxides, and Fe (oxy)hydroxides. The implications of these results are that
even very short periods of subaerial exposure of ordinary chondrites will
lead to dissolution of primary minerals and
crystallization of weathering products that are likely to include
aluminosilicates and silicates, Mg-Ca
carbonates, and sulfates in addition to the ubiquitous Fe oxides and (oxy)hydroxides.
Synchrotron-based infrared microspectroscopy as a
useful tool to study hydration states of meteorite constituents
L. V. MOROZ1, 2*, M. SCHMIDT3, 4, U. SCHADE4,
T. HIROI5, and M. A. IVANOVA6
1Institute of Planetology, University of Münster, Wilhelm-Klemm-Strasse
10, D-48149, Münster, Germany
2German Aerospace Center (DLR), Institute of Planetary
Research, Rutherfordstrasse 2, D-12489, Berlin, Germany
3Applied Physical Chemistry, University of Heidelberg, Im
Neuenheimer Feld 253, D-69120, Heidelberg, Germany
4Berliner Elektronenspeicherring-Gesellschaft für
Synchrotronstrahlung m.b.H (BESSY),
Albert-Einstein-Strasse 15, Berlin D-12489, Germany
5Department of Geosciences, Brown University, Lincoln Field
Building, 324 Brook Street, Providence, Rhode Island 02912, USA
6Vernadsky Institute of Geochemistry and Analytical Chemistry,
Russian Academy of Sciences, Kosygin Street 19, Moscow 119991, Russia
*Corresponding author. E-mail:
Ljuba.Moroz@dlr.de
We present the results of the
infrared (IR) microscopic study of the anomalous carbonaceous chondrites
Dhofar (Dho) 225 and Dhofar 735 in comparison to typical CM2 chondrites
Cold Bokkeveld, Murray, and Mighei. The Fourier transform infrared (FTIR)
2.5–14 µm reflectance
measurements were performed on conventional polished sections using an
infrared microscope with a synchrotron radiation source. We demonstrate
that the synchrotron-based IR microspectroscopy is a useful,
nondestructive tool for studying hydration states of meteorite
constituents in situ. Our results show that the matrices of Dho 225 and
Dho 735 are dehydrated compared to the matrices of typical CM2 chondrites.
The spectra of the Dho 225 and Dho 735 matrices lack the 2.7–2.8 µm
absorption feature present in the spectra of Cold Bokkeveld, Murray, and
Mighei. Spectral signatures caused by Si-O vibrations in fine-grained,
Fe-rich olivines dominate the 10 µm spectral region in the spectra of Dho
225 and Dho 735 matrices, while the spectra of normal CM2 chondrites are
dominated by spectral signatures due to Si-O vibrations in phyllosilicates.
We did not detect any hydrated phases in the spectra of Dho 225 and Dho
735 polished sections. In addition, the near-infrared reflectance spectra
of Dho 225 and Dho 735 bulk powders show spectral similarities to the
Antarctic metamorphosed carbonaceous chondrites. We confirm the results of
previous mineralogical, chemical, and isotopic studies indicating that the
two meteorites from Oman are the first non-Antarctic metamorphosed
carbonaceous chondrites.
Carbon
isotopic composition of acetic acid generated by hydrous pyrolysis of
macromolecular organic matter from the Murchison meteorite
Yasuhiro OBA1 and Hiroshi NARAOKA2, 3*
1Graduate School of Natural Science and Technology, Okayama
University, 3-1-1 Tsushima-Naka, Okayama 700-8530, Japan
2Department of Earth Sciences, Okayama University, 3-1-1
Tsushima-Naka, Okayama 700-8530, Japan
3Institute of Space and Astronautical Science (ISAS), Japan
Aerospace Exploration Agency (JAXA), 3-1-1 Yoshinodai, Sagamihara,
Kanagawa 229-8510, Japan
*Corresponding author. E-mail:
naraoka@cc.okayama-u.ac.jp
Low molecular weight
monocarboxylic acids, including acetic acid, are some of the most abundant
organic compounds in carbonaceous chondrites. So far, the 13C-
and D-enriched signature
of water-extractable carboxylic acids has implied an interstellar
contribution to their origin. However,
it also has been proposed that monocarboxylic acids could be formed by
aqueous reaction on the
meteorite parent body. In this study, we conducted hydrous pyrolysis of
macromolecular organic
matter purified from the Murchison meteorite (CM2) to examine the
generation of monocarboxylic
acids with their stable carbon isotope measurement. During hydrous
pyrolysis of macromolecular
organic matter at 270–330 °C, monocarboxylic acids with carbon numbers
ranging from 2 (C2) to 5
(C5) were detected, acetic acid (CH3COOH; C2)
being the most abundant. The concentration of the
generated acetic acid increased with increasing reaction temperature; up
to 0.48 mmol acetic acid/g macromolecular organic matter at 330 °C. This
result indicates that the Murchison macromolecule has a potential to
generate at least ~0.4
mg acetic acid/g meteorite, which is about four times higher than the
amount of water-extractable acetic acid reported from Murchison. The
carbon isotopic composition of acetic acid generated by hydrous pyrolysis
of macromolecular organic matter is
~−27‰
(versus PDB), which is much more depleted in 13C than the
water-extractable acetic acid reported from Murchison. Intramolecular
carbon isotope distribution shows that methyl (CH3-)-C is more
enriched in 13C relative to carboxyl (-COOH)-C, indicating a
kinetic process for this formation. Although the experimental condition of
this study (i.e., 270–330 °C for 72 h) may not simulate a reaction
condition on parent bodies of carbonaceous chondrite, it may be possible
to generate monocarboxylic acids at lower temperatures for a longer period
of time.
Polygonal
impact craters in the Argyre region, Mars: Evidence for influence of
target structure on the final crater morphology
T. ÖHMAN1, 2*, M. AITTOLA2, V.-P. KOSTAMA2,
M. HYVÄRINEN2, and J. RAITALA2
1Department of Geosciences, Division of Geology, P.O. Box 3000,
FI-90014 University of Oulu, Oulu, Finland
2Department of Physical Sciences, Division of Astronomy, P.O.
Box 3000, FI-90014 University of Oulu, Oulu, Finland
*Corresponding author. E-mail:
teemu.ohman@oulu.fi
Impact craters that in plan
view are distinctly polygonal rather than circular or elliptical are
common on Mars and other planets (Öhman et al. 2005). Their actual
formation mechanism, however,
is somewhat debatable. We studied the polygonal craters of different
degradational stages in the
region of the Argyre impact basin, Mars. The results show that in the same
areas, heavily degraded,
moderately degraded, and fresh polygonal craters display statistically
similar strike distributions of
the straight rim segments. The fact that the strike distributions are not
dependent on lighting conditions was verified by using two data sets
(Viking and MOC-WA) having different illumination
geometries but similar resolutions. In addition, there are no significant
differences in the amount of
polygonality of craters in different degradational stages. These results
clearly imply that large-scale
polygonality is not caused by degradation, but originates from the
cratering process itself, concurring with the findings regarding lunar
craters by Eppler et al. (1983). The straight rims of polygonal craters
apparently reflect areal fracture patterns that prevail for a geologically
long time.
Chronostratigraphy,
composition, and
origin of Ni-rich spinel from the Late Eocene Fuente Caldera section in
Spain: One impact or more?
Eric ROBIN1* and Eustoquio MOLINA2
1LSCE/IPSL, UMR CEA/CNRS 1572, Avenue de la Terrasse 91190 Gif-sur-Yvette,
France
2Departamento de Ciencias de la Tierra, Universidad de
Zaragoza, 50009 Zaragoza, Spain
*Corresponding author. E-mail:
robin@lsce.cnrs-gif.fr
Here we report on the
stratigraphic distribution and chemical composition of Ni-rich
spinel, a specific mineral tracer of meteorite impacts, in the Fuente
Caldera section in Spain. A major peak in spinel abundance is observed in
a biostratigraphic interval defined by the last occurrence of the planktic
foraminifera Porticulasphaera semiinvoluta and the first occurrence of the
planktic foraminifera Turborotalia cunialensis. Two other peaks of lower
abundances are observed higher up in the same biostratigraphic interval,
but geochemical considerations suggest that they likely originate from
redeposition by turbiditic currents. Biostratigraphic correlations with
the global stratotype section and point for the Eocene/Oligocene boundary
of Massignano in Italy give an age of 35.4 ± 0.2 Ma (1σ) for the major
peak. This age is indistinguishable from the age of the impact horizon at
Massignano (35.5 ± 0.2 Ma) and within the age uncertainties for the
Popigai (35.7 ± 0.2 Ma) and Chesapeake Bay (35.5 ± 0.5 Ma) craters. The
Fuente Caldera spinel, as the Massignano spinel, is assumed to be a relic
mineral of microkrystites, which are believed to derive from a unique
source related to the Popigai impact crater. The morphologies and Cr
compositions of the Fuente Caldera and Massignano spinel crystals are
markedly different, however: the Fuente Caldera spinel occurs mostly as
octahedral and skeletal crystals with 85% of the grains belonging to the
Cr-rich magnetite series and 15% to the Fe-rich chromite series, whereas
the Massignano spinel occurs mostly as dendritic crystals with 90% of the
grains belonging to the Cr-poor magnetite series. It is unlikely that
these differences are the result of post-depositional alteration processes
because the compositions of the crystals, as well as their morphologies,
are in general very similar to those reported for primary spinel crystals,
i.e., spinel crystals present in meteorite fusion crust or synthetized
from meteoritic material. In addition, spinel crystals have quite
homogeneous compositions except for a few grains (<10%) showing Cr
zonations, but these are assigned to primary crystallization processes.
One possible explanation that is consistent with a single impact event
producing spatial variations in spinel compositions and morphologies is
that microkrystites are locally generated by the ablation in the
atmosphere of impact debris. An alternative explanation is that Fuente
Caldera and Massignano microkrystites derive from two closely spaced
impact events, which however requires another, so-far unknown source
crater for microkrystites.
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