The role of very fine particle sizes in the reflectance spectroscopy of plagioclase-bearing mixtures: new understanding for the interpretation of the finest sizes of the lunar regolith

1Giovanna Serventi, 2Cristian Carli
Icarus (in Press) Link to Article [http://doi.org/10.1016/j.icarus.2017.04.018]
1Department of Chemistry, Life Sciences and Environmental Sustainability, University of Parma, Viale delle Scienze 157/A Parma 43124, Italy
2IAPS-Inaf, Viale Fosso del Cavaliere Tor Vergata, Roma, 00133 Italy
Copyright Elsevier

The lunar surface consists of a regolith layer that covers the underlying bedrocks, and is generally characterized by particulates

The coarsest sizes of the regolith are chemically and mineralogically similar, while the finest fractions are more feldspathic, probably due to easier fracturing of plagioclase than mafic minerals.

Due to the more feldspathic nature of the very fine lunar soils, in this paper, we quantitatively investigate the influence of very fine (

(1) fine sizes act principally on reflectance and on spectral contrast (with the former increasing and the latter decreasing); (2) very fine plagioclase has a blue slope in the Near Infrared and very shallow 1250 nm band depth, close to zero; (3) consequently, the plagioclase band is always shallower than mafic bands; (4) in mixtures with olivine, the composite band center always shows the typical olivine value, differently from coarser mixtures; and (5) mafic materials have a blue slope in the Short Wavelength Infrared Region, a more V-shaped 1µm pyroxene absorption and the 1µm mafic band centers are shifted by ca. 40 nm vs. coarse sizes, reflecting a different weight within the crystal field absorption of the mafic component in very fine size. We also evidenced that a coarse plagioclase could be overestimated, while a very fine one could be underestimated if compared with the 63-125µm size.

Surface vitrification caused by natural fires in Late Pleistocene wetlands of the Atacama Desert

1Pierrick Roperch, 2Jérôme Gattacceca, 3Millarca Valenzuela, 2Bertrand Devouard, 4Jean-Pierre Lorand, 5Cesar Arriagada, 2Pierre Rochette,6,7Claudio Latorre, 8Pierre Beck
Earth and Planetary Science Letters 469, 15-26 Link to Article [http://doi.org/10.1016/j.epsl.2017.04.009]
1Géosciences Rennes, CNRS–INSU, Université de Rennes 1, Rennes, France
2CNRS, Aix Marseille Univ., IRD, Coll France, CEREGE, Aix-en-Provence, France
3Instituto de Astrofísica, P. Universidad Católica de Chile, Av. Vicuña Mackenna 4860, Santiago, Chile
4Laboratoire de Planétologie et Géodynamique, CNRS UMR 6112, Université de Nantes, 2 Rue la Houssinière, 44322, Nantes, France
5Departamento de Geología, Facultad de Ciencas Físicas y Matemáticas, Universidad de Chile, Plaza Ercilla 803, Santiago, Chile
6Centro UC del Desierto de Atacama and Departamento de Ecología, Pontificia Universidad Católica de Chile, Alameda 340, Santiago, Chile
7Institute of Ecology & Biodiversity (IEB), Santiago, Chile
8Institut de Planétologie et d’Astrophysique de Grenoble (IPAG), 414, Rue de la Piscine, Domaine Universitaire, 38400 St-Martin d’Hères, France
Copyright Elsevier

We describe extended occurrences of unusual silicate glass surface layers from the Atacama Desert (Chile). These glasses, found near the town of Pica at four localities separated by up to 70 km, are neither fulgurites, nor volcanic glasses, nor metallurgical slags related to anthropic activity, but show close similarities to other glasses that have been previously attributed to large airbursts created by meteoroids entering the Earth’s atmosphere. The glasses are restricted to specific Late Pleistocene terrains: paleo-wetlands and soils rich in organic matter with SiO2-rich plant remains, salts and carbonates. 14C dating and paleomagnetic data indicate that the glasses were formed during at least two distinct periods. This rules out the hypothesis of a single large airburst as the cause of surface melting. Instead, burning of organic-rich soils in dried-out grassy wetlands during climate oscillations between wet and dry periods can account for the formation of the Pica glasses. Large oases did indeed form in the hyperarid Atacama Desert due to elevated groundwater tables and increased surface discharge during the Central Andean Pluvial Event (roughly coeval with the Mystery interval and Younger Dryas). Finally, we discuss the implications of our results for the other surface glasses previously attributed to extraterrestrial events.

Park Forest (L5) and the asteroidal source of shocked L chondrites

1Matthias M. M. Meier,2Kees C. Welten,1,3My E. I. Riebe,4,5Marc W. Caffee,6,7,8Maria Gritsevich,1Colin Maden,1Henner Busemann
Meteoritics & Planetary Science (in Press) Link to Article [DOI: 10.1111/maps.12874]
1ETH Zurich, Institute of Geochemistry and Petrology, Zurich, Switzerland
2Space Sciences Laboratory, University of California, Berkeley, California, USA
3Department of Terrestrial Magnetism, Carnegie Institution of Washington, Washington, DC, USA
4Department of Physics and Astronomy, Purdue University, West Lafayette, Indiana, USA
5Department of Earth, Atmospheric and Planetary Sciences, Purdue University, West Lafayette, Indiana, USA
6Department of Physics, University of Helsinki, Helsinki, Finland
7Finnish Geospatial Research Institute, Masala, Finland
8Institute of Physics and Technology, Ural Federal University, Ekaterinburg, Russia
Published by arrangement with John Wiley & Sons

The Park Forest (L5) meteorite fell in a suburb of Chicago, Illinois (USA) on March 26, 2003. It is one of the currently 25 meteorites for which photographic documentation of the fireball enabled the reconstruction of the meteoroid orbit. The combination of orbits with pre-atmospheric sizes, cosmic-ray exposure (CRE), and radiogenic gas retention ages (“cosmic histories”) is significant because they can be used to constrain the meteoroid’s “birth region,” and test models of meteoroid delivery. Using He, Ne, Ar, 10Be, and 26Al, as well as a dynamical model, we show that the Park Forest meteoroid had a pre-atmospheric size close to 180 g cm−2, 0–40% porosity, and a pre-atmospheric mass range of ~2–6 tons. It has a CRE age of 14 ± 2 Ma, and (U, Th)-He and K-Ar ages of 430 ± 90 and 490 ± 70 Ma, respectively. Of the meteorites with photographic orbits, Park Forest is the second (after Novato) that was shocked during the L chondrite parent body (LCPB) break-up event approximately 470 Ma ago. The suggested association of this event with the formation of the Gefion family of asteroids has recently been challenged and we suggest the Ino family as a potential alternative source for the shocked L chondrites. The location of the LCPB break-up event close to the 5:2 resonance also allows us to put some constraints on the possible orbital migration paths of the Park Forest meteoroid.

The Allende multicompound chondrule (ACC)—Chondrule formation in a local super-dense region of the early solar system

1Addi Bischoff, 2Gerhard Wurm, 3Marc Chaussidon, 1Marian Horstmann, 1Knut Metzler, 4Mona Weyrauch, 1Julia Weinauer
Meteoritics & Planetary Science (in Press) Link to Article [DOI: 10.1111/maps.12833]
1Institut für Planetologie, Westfälische Wilhelms-Universität Münster, Münster, Germany
2Fakultät für Physik, Universität Duisburg-Essen, Duisburg, Germany
3Institut de Physique du Globe, Sorbonne Paris Cité, UMR CNRS 7154, Université Paris Diderot, Paris Cedex 05, France
4Institut für Mineralogie, Leibniz-Universität Hannover, Hannover, Germany
Published by arrangement with John Wiley & Sons

In Allende, a very complex compound chondrule (Allende compound chondrule; ACC) was found consisting of at least 16 subchondrules (14 siblings and 2 independents). Its overall texture can roughly be described as a barred olivine object (BO). The BO texture is similar in all siblings, but does not exist in the two independents, which appear as relatively compact olivine-rich units. Because of secondary alteration of pristine Allende components and the ACC in particular, only limited predictions can be made concerning the original compositions of the colliding melt droplets. Based on textural and mineralogical characteristics, the siblings must have been formed on a very short time scale in a dense, local environment. This is also supported by oxygen isotope systematics showing similar compositions for all 16 subchondrules. Furthermore, the ACC subchondrules are isotopically distinct from typical Allende chondrules, indicating formation in or reaction with a more 16O-poor reservoir. We modeled constraints on the particle density required at the ACC formation location, using textural, mineral-chemical, and isotopic observations on this multicompound chondrule to define melt droplet collision conditions. In this context, we discuss the possible relationship between the formation of complex chondrules and the formation of macrochondrules and cluster chondrites. While macrochondrules may have formed under similar or related conditions as complex chondrules, cluster chondrites certainly require different formation conditions. Cluster chondrites represent a mixture of viscously deformed, seemingly young chondrules of different chemical and textural types and a population of older chondrules. Concerning the formation of ACC calculations suggest the existence of very local, kilometer-sized, and super-dense chondrule-forming regions with extremely high solid-to-gas mass ratios of 1000 or more.

Mineralogical, crystallographic and redox features of the earliest stages of fluid alteration in CM chondrites

1Isabella Pignatelli, 1Yves Marrocchi, 2,3Enrico Mugnaioli, 4Franck Bourdelle, 5Matthieu Gounelle
Geochimica et Cosmochimica Acta (in Press) Link to Article [http://doi.org/10.1016/j.gca.2017.04.017]
1CRPG, UMR 7358, CNRS – Université de Lorraine, 54500 Vandoeuvre-lès-Nancy, France
2Dipartimento di Scienze Fisiche, della Terre e dell’Ambiente, Università degli Studi di Siena, Via Laterino 8, 53100 Siena, Italy
3Center for Nanotechnology Innovation@NEST, Istituto Italiano di Tecnologia, Piazza San Silvestro 12, 56127, Pisa, Italy
4LGCgE, Université de Lille 1, SN 5, 59655 Villeneuve d’Ascq, France
5IMPMC, MNHN, UPMC, UMR CNRS 7590, 61 rue Buffon, 75005 Paris, France
6InstitutUniversitaire de France, Maison des Universités, 103 bd. Saint-Michel, 75005 Paris
Copyright Elsevier

The CM chondrites represent the largest group of hydrated meteorites and span a wide range of conditions, from less altered (i.e., CM2) down to heavily altered (i.e., CM 1). The Paris chondrite is considered the least altered CM and thus enables the earliest stages of aqueous alteration processes to be deciphered. Here, we report results from a nanoscale study of tochilinite/cronstedtite intergrowths (TCIs) in Paris —TCIs being the emblematic secondary mineral assemblages of CM chondrites, formed from the alteration of Fe-Ni metal beads (type-I TCIs) and anhydrous silicates (type-II TCIs). We combined high-resolution transmission electron microscopy, scanning transmission X-ray microscopy and electron diffraction tomography to characterize the crystal structure, crystal chemistry and redox state of TCIs. The data obtained are useful to reconstruct the alteration conditions of Paris and to compare them with those of other meteorites. Our results show that tochilinite in Paris is characterized by a high hydroxide layer content (n = 2.1-2.2) regardless of the silicate precursors. When examined alongside other CMs, it appears that the hydroxide layer and iron contents of tochilinites correlate with the degree of alteration experienced by the chondrites. The Fe3+/ΣFe ratios of TCIs are high: 8-15% in tochilinite, 33-60% in cronstedtite and 70-80% in hydroxides. These observations suggest that alteration of CM chondrites took place under oxidizing conditions that could have been induced by significant H2 release during serpentinization. Similar results were recently reported in CR chondrites (Le Guillou et al., 2015), suggesting that the process(es) controlling the redox state of the secondary mineral assemblages were quite similar in the CM and CR parent bodies despite the different alteration conditions.

According to our mineralogical and crystallographic survey, the formation of TCIs in Paris occurred at temperatures lower than 100°C, under neutral, slightly alkaline conditions that favored the formation of both tochilinite and cronstedtite. During the course of alteration, the reduction in sulphur activity and/or the decrease of temperature prevented tochilinite crystallization and favoured the formation of cronstedtite and iron hydroxides. We suggest that iron hydroxides probably formed as ferrihydrite and then progressively converted to goethite between 50° and 80°C, a temperature range that is also favourable for cronstedtite formation. The presence of cronstedtite plays a key role in the reconstruction of the alteration history, demonstrating that the alteration of Paris took place by way of serpentinization processes similar to those described on the Earth.

Formation of unequilibrated R chondrite chondrules and opaque phases

1,2K.E. Miller, 1,2D.S. Lauretta, 2,3,4,5H.C. Connolly Jr., 6E.L. Berger, 7K. Nagashima, 2K. Domanik
Geochimica et Cosmochimica Acta (in Press) Link to Article [http://doi.org/10.1016/j.gca.2017.04.009]
1Space Sciences Division, Southwest Research Institute, San Antonio, TX 78238
2Lunar and Planetary Laboratory, University of Arizona, Tucson, AZ 85721, USA
3Department of Geology, School of Earth and the Environment, Rowan University, 201 Mullica Hill Road, Glassboro, N. J. 08028 USA
4Earth and Environmental Sciences, The Graduate Center of the City University of New York, Brooklyn, NY 10016, USA
5Earth and Planetary Science, American Museum of Natural History, Central Park West, New York, NY 10024, USA
6GeoControl Systems Inc. – Jacobs JETS – NASA Johnson Space Center, Houston, TX 77058, USA
7Hawai’i Institute of Geophysics and Planetology, University of Hawai’i at Manoa, Honolulu, HI 96822, USA
Copyright Elsevier

Sulfide assemblages are commonly found in chondritic meteorites as small inclusions in the matrix or in association with chondrules. These assemblages are widely hypothesized to form through pre-accretionary corrosion of metal by H2S gas or through parent body processes. We report here on two unequilibrated R chondrite samples that contain large, chondrule-sized sulfide nodules in the matrix. Both samples are from Mount Prestrud (PRE) 95404. Chemical maps and spot and broad-beam electron microprobe analyses (EMPA) were used to assess the distribution, stoichiometry, and bulk composition of sulfide nodules and silicate chondrules in the clasts. Oxygen isotope data were collected via secondary ion mass spectrometry (SIMS) to assess the relationship of chondrules to other chondrite groups. Scanning electron microscopy (SEM), focused ion beam (FIB), and transmission electron microscopy (TEM) analyses were used to assess fine-scale features and identify crystal structures in sulfide assemblages. Thermodynamic models were used to assess the temperature, sulfur fugacity (fS2), total pressure, dust-to-gas ratio, and oxygen fugacity (fO2) conditions during sulfide nodule and chondrule formation.

The unequilibrated clasts include a mixture of type I and type II chondrules, as well as non-porphyritic chondrules. Chondrule oxygen isotopes overlap with ordinary-chondrite chondrules. Sulfide nodules average 200 µm in diameter, have rounded shapes, and are primarily composed of pyrrhotite, pentlandite, and magnetite. Some are deformed around chondrules in a petrologic relationship similar in appearance to compound chondrules. Both nodules and sulfides in chondrules include phosphate inclusions and Cu-rich lamellae, which suggests a genetic relationship between sulfides in chondrules and in the matrix. Ni/Co ratios for matrix and chondrule sulfides are solar, while Fe and Ni are non-solar and inversely related.

We hypothesize that sulfide nodules formed via pre-accretionary melt processes. During chondrule formation, precursors composed of a mixture of silicate and sulfide material were heated to form immiscible melt droplets, which separated and cooled to form Si-rich chondrules and S-rich nodules. Sulfide melt was stabilized by a high total pressure (∼1 atm) in a dust- or ice-enriched environment. Heating of this material contributed to a high fS2 (2 × 10-3 atm at 1138 °C), and high fO2 (IW – 1 to IW – 4), in an environment with peak temperatures between 1539 °C and 1750 °C. Oxygen isotopic compositions in this region were similar to those recorded by the LL-chondrite chondrules.

The role of sulfides in the fractionation of highly siderophile and chalcophile elements during the formation of martian shergottite meteorites

1Raphael J. Baumgartner, 1Marco L. Fiorentini, 2Jean-Pierre Lorand, 3,4David Baratoux, 5Federica Zaccarini, 6Ludovic Ferrière, 7Marko K. Prašek,8Kerim Sener
Geochimica et Cosmochimica Acta (in Press) Link to Article [http://doi.org/10.1016/j.gca.2017.04.011]
1Centre for Exploration Targeting, School of Earth Sciences, ARC Centre of Excellence for Core to Crust Fluid Systems, University of Western Australia, 6009 Crawley, Australia
2Laboratoire de Planétologie et Géodynamique de Nantes, Université de Nantes and Centre National de la Recherche Scientifique, UMR 6112 44322 Nantes, France
3Géosciences Environnement Toulouse, CNRS, IRD and University of Toulouse, 31400 Toulouse, France
4Institut Fondamental d’Afrique Noire Cheikh Anta Diop, 5005 Dakar, Senegal
5Department of Applied Geological Sciences and Geophysics, University of Leoben, 8700 Leoben, Austria
6Natural History Museum Vienna, 1010 Vienna, Austria
7McGill University, Department of Earth and Planetary Sciences, H3A 0E8, Montreal, Canada
8Matrix Exploration Pty Ltd, 6112 Armadale, Australia
Copyright Elsevier

The shergottite meteorites are ultramafic to mafic igneous rocks whose parental magmas formed from partial melting of the martian mantle. This study reports in-situ laser ablation inductively coupled plasma mass spectrometry analyses for siderophile and chalcophile major and trace elements (i.e., Co, Ni, Cu, As, Se, Ag, Sb, Te, Pb, Bi, and the highly siderophile platinum-group elements, PGE: Os, Ir, Ru, Rh, Pt and Pd) of magmatic Fe-Ni-Cu sulfide assemblages from four shergottite meteorites. They include three geochemically similar incompatible trace element- (ITE-) depleted olivine-phyric shergottites (Yamato-980459, Dar al Gani 476 and Dhofar 019) that presumably formed from similar mantle and magma sources, and one distinctively ITE-enriched basaltic shergottite (Zagami). The sulfides in the shergottites have been variably modified by alteration on Earth and Mars, as well as by impact shock-shock related melting/volatilization during meteorite ejection. However, they inherit and retain their magmatic PGE signatures. The CI chondrite-normalized PGE concentration patterns of sulfides reproduce the whole-rock signatures determined in previous studies. These similarities indicate that sulfides exerted a major control on the PGE during shergottite petrogenesis. However, depletions of Pt (and Ir) in sulfide relative to the other PGE suggest that additional phases such discrete Pt-Fe-Ir alloys have played an important role in the concentration of these elements. These alloys are expected to have enhanced stability in reduced and FeO-rich shergottite magmas, and could be a common feature in martian igneous systems. A Pt-rich PGM was found to occur in a sulfide assemblage in Dhofar 019. However, its origin may be related to impact shock-related sulfide melting and volatilisation during meteorite ejection. In the ITE-depleted olivine-phyric shergottites, positive relationships exist between petrogenetic indicators (e.g., whole-rock Mg-number) and most moderately to strongly siderophile and chalcophile elements in sulfides. These variations extend to incompatible elements like Te and Pd. The whole-rock concentrations of Pd derived from mass-balance calculations decrease by one order of magnitude in the order Y-980459, DaG 476 and Dhofar 019, and broadly overlap the trends in previously published whole-rock analyses. Mantle heterogeneities, and the timing of sulfide saturation as function of mantle melting and/or magma fractionation following ascent from the mantle, may have been the controlling factors of the siderophile and chalcophile element systematics in the analyzed shergottites.

The origin of volatile element depletion in early solar system material: Clues from Zn isotopes in chondrules

1Emily A. Pringle, 1,2Frédéric Moynier, 2,3Pierre Beck, 4Randal Paniello, 5,6Dominik C. Hezel
Earth and Planetary Science Letters 468. 62-71 Link to Article [http://doi.org/10.1016/j.epsl.2017.04.002]
1Institut de Physique du Globe de Paris, Université Paris Diderot, Sorbonne Paris Cité, CNRS UMR 7154, 1 rue Jussieu, 75238 Paris, France
2Institut Universitaire de France, Paris, France
3Institut d’Astrophysique et de Planétologie de Grenoble, Université Grenoble Alpes, France
4Department of Earth and Planetary Sciences, Washington University in St. Louis, USA
5University of Cologne, Department of Geology and Mineralogy, Zülpicher Str. 49b, 50674 Köln, Germany
6Department of Mineralogy, Natural History Museum, Cromwell Road, London, SW7 5BD, UK
Copyright Elsevier

Volatile lithophile elements are depleted in the different planetary materials to various degrees, but the origin of these depletions is still debated. Stable isotopes of moderately volatile elements such as Zn can be used to understand the origin of volatile element depletions. Samples with significant volatile element depletions, including the Moon and terrestrial tektites, display heavy Zn isotope compositions (i.e. enrichment of 66Zn vs. 64Zn), consistent with kinetic Zn isotope fractionation during evaporation. However, Luck et al. (2005) found a negative correlation between δ66Zn and 1/[Zn] between CI, CM, CO, and CV chondrites, opposite to what would be expected if evaporation caused the Zn abundance variations among chondrite groups.

We have analyzed the Zn isotope composition of multiple samples of the major carbonaceous chondrite classes: CI (1), CM (4), CV (2), CO (4), CB (2), CH (2), CK (4), and CK/CR (1). The bulk chondrites define a negative correlation in a plot of δ66Zn vs 1/[Zn], confirming earlier results that Zn abundance variations among carbonaceous chondrites cannot be explained by evaporation. Exceptions are CB and CH chondrites, which display Zn systematics consistent with a collisional formation mechanism that created enrichment in heavy Zn isotopes relative to the trend defined by CI–CK.

We further report Zn isotope analyses of chondrite components, including chondrules from Allende (CV3) and Mokoia (CV3), as well as an aliquot of Allende matrix. All chondrules are enriched in light Zn isotopes (∼500 ppm on 66Zn/64Zn) relative to the bulk, contrary to what would be expected if Zn were depleted during evaporation, on the other hand the matrix has a complementary heavy isotope composition. We report sequential leaching experiments in un-equilibrated ordinary chondrites, which show sulfides are isotopically heavy compared to silicates and the bulk meteorite by ca. +0.65 per mil on 66Zn/64Zn. We suggest isotopically heavy sulfides were removed from either chondrules or their precursors, thereby producing the light Zn isotope enrichments in chondrules.

Primordial and cosmogenic noble gases in the Sutter’s Mill CM chondrite

1Ryuji Okazaki, 2,3Keisuke Nagao
Meteoritics & Planetary Science (in Press) Link to Article [DOI: 10.1111/maps.12819]
1Faculty of Sciences, Department of Earth and Planetary Sciences, Kyushu University, Nishi-ku, Fukuoka, Japan
2Graduate School of Science, Geochemical Research Center, University of Tokyo, Hongo, Bunkyo-ku, Tokyo, Japan
3Korea Polar Research Institute, Incheon, Yeonsu-gu, South Korea
Published by arrangement with John Wiley & Sons

The Sutter’s Mill (SM) CM chondrite fell in California in 2012. The CM chondrite group is one of the most primitive, consisting of unequilibrated minerals, but some of them have experienced complex processes occurring on their parent body, such as aqueous alteration, thermal metamorphism, brecciation, and solar wind implantation. We have determined noble gas concentrations and isotopic compositions for SM samples using a stepped heating gas extraction method, in addition to mineralogical observation of the specimens. The primordial noble gas abundances, especially the P3 component trapped in presolar diamonds, confirm the classification of SM as a CM chondrite. The mineralogical features of SM indicate that it experienced mild thermal alteration after aqueous alteration. The heating temperature is estimated to be 500 °C. The variation in the heating temperature of thermal alteration is consistent with the texture as a breccia. The heterogeneous distribution of solar wind noble gases is also consistent with it. The cosmic-ray exposure (CRE) age for SM is calculated to be 0.059 ± 0.023 Myr based on cosmogenic 21Ne by considering trapped noble gases as solar wind, the terrestrial atmosphere, P1 (or Q), P3, A2, and G components. The CRE age lies at the shorter end of the CRE age distribution of the CM chondrite group.

Annama H chondrite—Mineralogy, physical properties, cosmic ray exposure, and parent body history

1,2,3Tomáš Kohout et al (>10)*
Meteoritics & Planetary Science (in Press) Link to Article [DOI: 10.1111/maps.12871]
1Department of Physics, University of Helsinki, Finland
2Institute of Geology, The Czech Academy of Sciences, Praha, Czech Republic
3Finnish Fireball Network, Finland
*Find the extensive, full author and affiliation list on the publishers website
Published by arrangement with John Wiley & Sons

The fall of the Annama meteorite occurred early morning (local time) on April 19, 2014 on the Kola Peninsula (Russia). Based on mineralogy and physical properties, Annama is a typical H chondrite. It has a high Ar-Ar age of 4.4 Ga. Its cosmic ray exposure history is atypical as it is not part of the large group of H chondrites with a prominent 7–8 Ma peak in the exposure age histograms. Instead, its exposure age is within uncertainty of a smaller peak at 30 ± 4 Ma. The results from short-lived radionuclides are compatible with an atmospheric pre-entry radius of 30–40 cm. However, based on noble gas and cosmogenic radionuclide data, Annama must have been part of a larger body (radius >65 cm) for a large part of its cosmic ray exposure history. The 10Be concentration indicates a recent (3–5 Ma) breakup which may be responsible for the Annama parent body size reduction to 30–35 cm pre-entry radius.