¹Anna Milillo et al. (>10)
Icarus (in Press) Link to Article [https://doi.org/10.1016/j.icarus.2020.114179]
¹INAF/IAPS
Copyright Elsevier

The Na exosphere of Mercury is characterized by the variability of the emission lines intensity and of its distribution in time scales from less than one hour to seasonal variations. While the faster variations, accounting for about 10–20% of fluctuations are probably linked to the planetary response to solar wind and Interplanetary Magnetic Field variability, the seasonal variations (up to about 80%) should be explained by complex mechanisms involving different surface release processes, loss, source and migrations of the exospheric Na atoms. Eventually, a Na annual cycle can be identified. In the past, ground-based observations and equatorial density from MESSENGER data have been analyzed. In this study, for a more extensive investigation of the exospheric Na features, we have studied the local time and latitudinal distributions of the exospheric Na column density as a function of the True Anomaly Angle (TAA) of Mercury by means of the extended dataset of images, collected from 2009 to 2013, by the THEMIS solar telescope. Our results show that the THEMIS images, in agreement with previous results, registered a strong general increase in sodium abundance at aphelion and a dawn ward emission predominance with respect to dusk ward and subsolar region between 90° and 150° TAA. This behavior can be explained by desorption of a sodium surface reservoir consisting of sodium that is pushed anti-sunward and condenses preferentially in the coldest regions. Our analyses shows a predominance of subsolar line-of-sight column density along the rest of Mercury’s orbit. An unexpected relationship between Northward or Southward peak emission and both TAA and local time is also shown by our analysis. This result seems to contradict previous results obtained from different data sets and it is not easily explained, thus it requires further investigations.

¹Yohei Igami,^2,3Akira Tsuchiyama,⁴Tomoya Yamazaki,⁵Megumi Matsumoto,⁴Yuki Kimura
Geochimica et Cosmochimica Acta (in Press) Link to Article [https://doi.org/10.1016/j.gca.2020.10.023]
¹Division of Earth and Planetary Sciences, Graduate School of Science, Kyoto University, Kyoto 606-8502, Japan
²Research Organization of Science and Technology, Ritsumeikan University, Kusatsu 525-8577, Japan
³Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou, 510640, China
⁴Institute of Low Temperature Science, Hokkaido University, Sapporo 060-0819, Japan
⁵Department of Earth and Planetary Materials Science, Tohoku University, Sendai 980-8578, Japan
Copyright Elsevier

Amorphous silicates, abundant in primitive carbonaceous chondrites, are among the most primitive materials from the early Solar System. They show evidence of some aqueous alteration in the meteorite parent bodies, but it is not clear how this highly reactive material changed at an early stage after contact with water. Herein, we report in-situ experiments on the aqueous alteration of amorphous silicate nanoparticles (typically 70 nm in diameter); we used two different compositions that are similar to forsterite (MgO/SiO2 = 2.02) and enstatite (MgO/SiO2 = 1.15) in the simple MgO–SiO2 system to understand basic reaction principles at the onset of the aqueous alteration. The experiments were performed in pure water at room temperature using X-ray diffraction (XRD), transmission electron microscopy (TEM), and pH measurements. The in-situ TEM images of the nanoparticles—in particular those with the forsterite composition—gradually became difficult to recognize in water. The pH value of the water also increased with time, suggesting that preferential Mg2+ dissolution occurred from the amorphous silicates right after mixing with water. The in-situ XRD patterns showed that magnesium silicate hydrate (M-S-H), which is a poorly crystalline phase like a phyllosilicate, newly appeared. The M-S-H seems to have been formed via a dissolution–precipitation process. Its formation rate from amorphous silicates was considerably higher than from crystalline silicates, because amorphous silicates are highly metastable and have high solubility in water. M-S-H formation from the forsterite composition, which has a highly unstable amorphous structure, is ten times faster than from the enstatite composition. The M-S-Hs show string-like or tiny fragmental textures in the final dried products that are very similar to those observed in the matrices of some primitive carbonaceous chondrites. M-S-H would have been the initial product formed in the aqueous alteration of amorphous silicates in the meteorites; thus, it is an important tracer of early aqueous activity at low temperatures in the early Solar System. By comparing the in-situ observations with those obtained after drying the experimental samples, we found two types of M-S-Hs: epigenetic M-S-Hs—which have a slightly Si-rich composition—formed during drying, and syngenetic M-S-Hs formed by in-situ alteration. Carbonaceous chondrites may also contain these two types of hydrous silicates, and this should be investigated to understand the conditions for aqueous alteration in the early Solar System in more detail. The present study clearly showed the importance of Mg/Si ratio in the precursor materials, although the actual chondrites are in more complicated multi-component system. Future experiments based on the present results can extend the investigation to the system containing Fe, S, and other components as in carbonaceous chondrites.

¹Marine Paquet,¹James M.D.Day,²Arya Udry,¹Ruan Hattingh,¹Ben Kumler,²Rachel R.Rahib,³Kimberly T.Tait,⁴Clive R.Neal
Geochimica et Cosmochimica Acta (in Press) Link to Article [https://doi.org/10.1016/j.gca.2020.10.024]
¹Scripps Institution of Oceanography, University of California San Diego, La Jolla, CA 92093-0244, USA
²Department of Geoscience, University of Nevada, Las Vegas, 4505 S. Maryland Parkway, Las Vegas, NV 89154, USA
³Department of Natural History, Royal Ontario Museum, 100 Queens Park, Toronto, ON M5S 2C6, Canada
⁴Department of Civil Engineering and Geological Sciences, University of Notre Dame, Notre Dame, IN 46556, USA
Copyright Elsevier

Shergottite meteorites are ultramafic to mafic igneous rocks derived from partial melting of distinct regions of the martian mantle. As such, they trace magmatic processes, including fractional crystallization and mixing processes in Mars. New chalcophile (Cu, Se, Zn, Pb), siderophile (Ni, Co, W), and highly siderophile element (HSE: Au, Re, Pd, Rh, Pt, Ru, Ir, Os) abundance data are reported for sulfide assemblages in a suite of thirteen incompatible trace element depleted, intermediate and enriched shergottites, along with new whole-rock HSE abundance and 187Os/188Os data for seven shergottites. Sulfide grains in depleted and intermediate shergottites typically have the highest absolute abundances of the HSE, with broadly flat CI-chondrite normalized patterns. Enriched shergottite sulfide grains typically have highly variable Au, elevated Pd and Rh and are relatively depleted in Zn, Ir and Os. The new HSE whole-rock data for enriched (Northwest Africa [NWA] 7397, NWA 7755, NWA 11043), and intermediate shergottites (NWA 10961, NWA 11065, NWA 12241, and NWA 12536) are generally consistent with existing 187Os/188Os and HSE abundance data for these geochemical groupings. Enriched shergottites with > 1 ppb Os have measured 187Os/188Os ranging between 0.1296 and 0.1471, with variable Pd and Pt contents. Intermediate shergottites with > 1 ppb Os have chondrite-relative proportions of the HSE at ∼ 0.01 to 0.001 × CI chondrites and 187Os/188Os from 0.1284 and 0.1295. Sulfides are the major host of the HSE, and they control the behavior of the HSE during petrogenetic processes in shergottite magmas, enabling the determination of HSE compatibility for martian magmatism in the order: Os > Ir ≥ Ru ≥≥ Rh ≥ Pd ≥ Re ≥ Pt ≥ Au. Fractionation models of removal of an olivine-dominated cumulate recreate HSE patterns for the whole-rock shergottites. Enriched shergottites are best reproduced by 25 to 30% of fractionation from a degassed parent melt (250 ± 50 ppm of S), whereas depleted and intermediate shergottites can be explained by slightly lower fractionation (10 to 15%) from higher S content parent melts (350 ± 100 ppm of S). Sulfur contents in the melt ∼ 50% higher than these estimates yield earlier S-saturation during fractional crystallization, leading to an abrupt decrease of the more compatible HSE (Ru, Ir, Os), which is not observed. These results indicate that the martian mantle and partial melts from it, are probably not anomalously enriched in S, and instead are similar to slightly higher than those of the terrestrial mantle and its partial melts.

¹Addi Bischoff et al. (>10)
Geochimica et Cosmochimica Acta (in Press) Link to Article [https://doi.org/10.1016/j.gca.2020.10.014]
¹Institut für Planetologie, University of Münster, Wilhelm-Klemm Str. 10, D-48149 Münster, Germany
Copyright Elsevier

On September 12, 2019 at 12:49:48 (UT) a bolide was observed by hundreds of eye-witnesses from the Netherlands, Germany, Belgium, Denmark and the UK. One day later a small meteorite stone was found by accident in Flensburg. The presence of short-lived cosmogenic radionuclides with half-lives as short as 16 days proves the recent exposure of the found object to cosmic rays in space linking it clearly to the bolide event. An exceptionally short exposure time of ∼5000 years was determined. The 24.5 g stone has a fresh black fusion crust, a low density of <2 g/cm3, and a magnetic susceptibility of logχ= 4.35 (χ in 10-9 m3/kg). The rock consists of relict chondrules and clusters of sulfide and magnetite grains set in a fine-grained matrix. The most abundant phases are phyllosilicates. Carbonates (∼3.9 vol.%) occur as calcites, dolomites, and a Na-rich phase. The relict chondrules (often surrounded by sulfide laths) are free of anhydrous silicates and contain abundant serpentine. Lithic clasts are also surrounded by similar sulfide laths partly intergrown with carbonates. 53Mn-53Cr ages of carbonates in Flensburg indicate that brecciation and contemporaneous formation of the pyrrhotite-carbonate intergrowths by hydrothermal activities occurred no later than 4564.6±1.0 Ma (using the angrite D’Orbigny as the Mn-Cr age anchor). This corresponds to 2.6±1.0 or 3.4±1.0 Ma after formation of CAIs, depending on the exact absolute age of CAIs. This is the oldest dated evidence for brecciation and carbonate formation, which likely occurred during parent body growth and incipient heating due to decay of 26Al. In the three oxygen isotope diagram, Flensburg plots at the 16O-rich end of the CM chondrite field and in the transition field to CV-CK-CR chondrites. The mass-dependent Te isotopic composition of Flensburg is slightly different from mean CM chondrites and is most similar to those of the ungrouped C2 chondrite Tagish Lake. On the other hand, 50Ti and 54Cr isotope anomalies indicate that Flensburg is similar to CM chondrites, as do the ∼10 wt.% H2O of the bulk material. Yet, the bulk Zn, Cu, and Pb concentrations are about 30% lower than those of mean CM chondrites. The He, Ne, and Ar isotopes of Flensburg show no solar wind contribution; its trapped noble gas signature is similar to that of CMs with a slightly lower concentration of 20Netr. Based on the bulk H, C, and N elemental abundances and isotopic compositions, Flensburg is unique among chondrites, because it has the lightest bulk H and N isotopic compositions of any type 1 or 2 chondrite investigated so far. Moreover, the number of soluble organic compounds in Flensburg is even lower than that of the brecciated CI chondrite Orgueil. The extraordinary significance of Flensburg is evident from the observation that it represents the oldest chondrite sample in which the contemporaneous episodes of aqueous alteration and brecciation have been preserved. The characterization of a large variety of carbonaceous chondrites with different alteration histories is important for interpreting returned samples from the OSIRIS-REx and Hayabusa 2 missions.

^1,2Phillip R.Heck et al. (>10)
Meteoritics & Planetary Science (in Press) Link to Article [https://doi.org/10.1111/maps.13584]
¹Robert A. Pritzker Center for Meteoritics and Polar Studies, Negaunee Integrative Research Center, The Field Museum of Natural History, 1400 South Lake Shore Drive, Chicago, Illinois, 60605 USA²Chicago Center for Cosmochemistry and Department of the Geophysical Sciences, The University of Chicago, 5734 South Ellis Avenue, Chicago, Illinois, 60637‐1433 USA
Published by arrangement with John Wiley & Sons

The Hamburg meteorite fell on January 16, 2018, near Hamburg, Michigan, after a fireball event widely observed in the U.S. Midwest and in Ontario, Canada. Several fragments fell onto frozen surfaces of lakes and, thanks to weather radar data, were recovered days after the fall. The studied rock fragments show no or little signs of terrestrial weathering. Here, we present the initial results from an international consortium study to describe the fall, characterize the meteorite, and probe the collision history of Hamburg. About 1 kg of recovered meteorites was initially reported. Petrology, mineral chemistry, trace element and organic chemistry, and O and Cr isotopic compositions are characteristic of H4 chondrites. Cosmic ray exposure ages based on cosmogenic 3He, 21Ne, and 38Ar are ~12 Ma, and roughly agree with each other. Noble gas data as well as the cosmogenic 10Be concentration point to a small 40–60 cm diameter meteoroid. An 40Ar‐39Ar age of 4532 ± 24 Ma indicates no major impact event occurring later in its evolutionary history, consistent with data of other H4 chondrites. Microanalyses of phosphates with LA‐ICPMS give an average Pb‐Pb age of 4549 ± 36 Ma. This is in good agreement with the average SIMS Pb‐Pb phosphate age of 4535.3 ± 9.5 Ma and U‐Pb Concordia age of 4535 ± 10 Ma. The weighted average age of 4541.6 ± 9.5 Ma reflects the metamorphic phosphate crystallization age after parent body formation in the early solar system.

¹Yong Xiong,^1,2Ai‐Cheng Zhang,³Noriyuki Kawasaki,⁴Chi Ma, ⁵Naoya Sakamoto,⁵Jia‐Ni Chen,⁶Li‐Xin Gu,^3,5Hisayoshi Yurimoto
Meteoritics & Planetary Science (in Press) Link to Article [https://doi.org/10.1111/maps.13575]
¹State Key Laboratory for Mineral Deposits Research, School of Earth Sciences and Engineering, Nanjing University, Nanjing, 210023 China
²CAS Center for Excellence in Comparative Planetology, Hefei, China
³Department of Natural History Sciences, Hokkaido University, Sapporo, 060‐0810 Japan
⁴Division of Geological and Planetary Sciences, California Institute of Technology, Pasadena, California, 91125 USA
⁵Isotope Imaging Laboratory, Creative Research Institution Sousei, Hokkaido University, Sapporo, 001‐0021 Japan
⁶Institute of Geology and Geophysics, Chinese Academy of Sciences, Beijing, 100029 China
Published by arrangement with John Wiley & Sons

Calcium‐aluminum‐rich inclusions (CAIs) are the first solid materials formed in the solar nebula. Among them, ultrarefractory inclusions are very rare. In this study, we report on the mineralogical features and oxygen isotopic compositions of minerals in a new ultrarefractory inclusion CAI 007 from the CV3 chondrite Northwest Africa (NWA) 3118. The CAI 007 inclusion is porous and has a layered (core–mantle–rim) texture. The core is dominant in area and mainly consists of Y‐rich perovskite and Zr‐rich davisite, with minor refractory metal nuggets, Zr,Sc‐rich oxide minerals (calzirtite and tazheranite), and Fe‐rich spinel. The calzirtite and tazheranite are closely intergrown, probably derived from a precursor phase due to thermal metamorphism on the parent body. The refractory metal nuggets either exhibit thin exsolution lamellae of Fe,Ni‐dominant alloy in Os,Ir‐dominant alloy or are composed of Os,Ir,Ru,Fe‐alloy and Fe,Ni,Ir‐alloy with troilite, scheelite, gypsum, and molybdenite. The later four phases are apparently secondary minerals. The Zr,Sc,Y‐rich core is surrounded by a discontinuous layer of closely intergrown hibonite and spinel. The CAIs are rimmed by Fe‐rich spinel and Al‐rich diopside. Perovskite has high concentrations of the most refractory rare earth elements (REEs) but is relatively depleted in the moderately refractory and volatile REEs, consistent with the ultrarefractory REE pattern. Based on this unusual Zr,Sc,Y‐rich mineral assemblage, the layered distribution in CAI 007, and the REE concentrations in perovskite, we suggest that CAI 007 is an ultrarefractory inclusion of condensation origin. In CAI 007, hibonite, spinel, and probably Al‐rich diopside are ¹⁶O‐rich (Δ¹⁷O ~–22‰) whereas perovskite and davisite are ¹⁶O‐poor (Δ¹⁷O ~–3‰). Such oxygen isotope heterogeneity suggests that the UR inclusion formed in the various degrees of ¹⁶O‐rich nebular setting or was originally ¹⁶O‐rich and then experienced oxygen isotope exchange with ¹⁶O‐poor fluid on the CV3 chondrite parent body.

¹Aleksandra N. Stojic et al. (>10)
Icarus (in Press) Link to Article [https://doi.org/10.1016/j.icarus.2020.114162]
¹Institut für Planetologie, Westfälische Wilhelms Universität Münster, Wilhelm-Klemm-Str. 10, D-48149 Münster, Germany
Copyright Elsevier

We conducted classic dynamic high – pressure experiments on porous San Carlos (SC) olivine powder to examine if and how different shock stages modify corresponding reflectance mid – infrared (MIR) spectra. Microscopic investigation of the thin sections produced of our shocked samples indicates local peak pressures of >60 GPa along with all lower grade shock stages. Spectral analyses of optically identified shock areas were documented and compared in terms of Christiansen Feature (CF) and the position of olivine – diagnostic Reststrahlenbands (RBs). We found that one RB (fundamental vibrations of the orthosilicate – ion) of olivine occurring at 980 cm−1 (corresponding to ≈ 10.2 μm) shows the least energetic shift in the investigated MIR spectra and could therefore serve as a proxy for the presence of olivine in remote sensing application. Furthermore, a peak located at ≈ 1060 cm−1 (≈ 9.4 μm) shows a significant intensity change probably related to the degree of shock exposure or grain orientation effects, as we observe a decline in intensity of this band from our averaged reference olivine spectra of our IRIS database (diffuse reflectance measurement) down to spectra of grains showing mosaicism and recrystallized areas. We also report the presence of a weak band in some of the olivine spectra located at ≈ 1100 cm−1 (9.1 μm) that has an influence on the position of the CF when spectral data of olivine are averaged.

¹Naoki Hirakawa,¹Yoko Kebukawa,¹Kensei Kobayashi,²Hideyuki Nakano
Icarus (in Press) Link to Article [https://doi.org/10.1016/j.icarus.2020.114167]
¹Graduate School of Engineering Science, Yokohama National University, 79-5 Tokiwadai, Hodogaya-ku, Yokohama 240-8501, Japan
²Faculty of Culture and Sport Policy, Toin University of Yokohama, 1614 Kurogane-cho, Aoba-ku, Yokohama 225-8503, Japan
Copyright Elsevier

Molecular structures and chemical compositions of organic matter in primitive meteorites reflect the conditions of the parent bodies, as well as the preaccretional history. During the parent body processing, co-existing minerals could have effects on structural changes of organics, in addition to temperature and redox state. Here, we performed heating experiments of a primordial organic matter analog with and without minerals to understand the effects of minerals on organic matter in conditions simulating metamorphism in thermally metamorphosed type 3 chondrites. The primordial analog materials were heated up to 400 °C, and the experimental products were analyzed using X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and gas chromatography mass spectrometry (GC/MS). Montmorillonite and olivine, particularly montmorillonite, enhanced decomposition of oxygen containing species due to decarboxylation and/or cracking, while olivine enhanced esterification at lower temperature. Our results further imply that the variations of insoluble organic matter in CV, CO, and type 3 ordinary chondrites could be partially due to different mineral compositions. We also tested the effects of pressure on the degradation of the organic matter at 400 °C up to 268 atm, however no significant pressure effects were observed by FTIR and GC/MS.

^1,2J.Pape,¹Å.V.Rosén,¹K.Mezger,³M.Guillong
Geochimica et Cosmochimica Acta (in Press) Link to Article [https://doi.org/10.1016/j.gca.2020.10.019]
¹Institute of Geological Sciences, University of Bern, Baltzerstrasse 1+3, CH-3012 Bern, Switzerland
²Institut für Planetologie, University of Münster, Wilhelm-Klemm-Str. 10, 48149 Münster, Germany
³Institute of Geochemistry and Petrology, ETH Zurich, Clausiusstrasse 25, 8092 Zurich, Switzerland
Copyright Elsevier

Chondrules from unequilibrated ordinary chondrites are among the oldest Solar system materials and preserve mineralogical, chemical and isotopic signatures that link them to their primary formation mechanisms and environments in the early Solar System. Some chondrules record features indicating modifications by high- to low-temperature processes throughout their residence time in the protoplanetary disk. Chondrules that were partially modified after their primary formation record chemical, isotopic and textural information on their initial formation conditions and subsequent reprocessing that are essential to reconstruct their formation environments and interpret the ages recorded by individual chondrules correctly.

The detailed textural and major, minor and trace element analyses of two type-I chondrules from the low petrologic type ordinary chondrites MET 00526 and MET 00452 (L/LL3.05) reveal complex chemical and textural systematics bearing testimony of their multi-stage high temperature evolution, including reheating and partial remelting, in the evolving protoplanetary disk prior to accretion into their parent bodies. During primary crystallization of chondrule MET00526_Ch43, mineral growth, including incipient formation of feldspar in the outer parts of the chondrule, led to the fractionation of melt, eventually resulting in a chemical gradient in the mesostasis. During a later punctuated reheating that ultimately led to partial remelting of the outer parts of the chondrule, mesostasis and low-Ca pyroxene remelted partially. This partial remelting enhanced the chemical differences within the mesostasis and led to the formation of two chemically distinct mesostases in the inner and the outer zone of the chondrule with almost complementary abundances of Rb, Na, K, Ba, Sr and Eu. The calculated bulk mesostasis composition reveals chondritic relative abundances of these elements in the bulk chondrule with a slight depletion of the most volatile elements. Chemical and textural observations further indicate that this disequilibrium remelting occurred under more reducing conditions than the primary melting event preserved in the chondrule centre, allowing for the crystallization of a second generation of low-Ca pyroxene in the outer parts of the chondrule. Very similar processes are also recorded in chondrule MET00452_Ch22 with the degree of remelting being more extensive.

A previously determined young 26Al-26Mg age of ∼3 Ma after CAIs determined for chondrule MET00452_Ch22 dates the time of the chondrule remelting rather than its primary formation. This is evidence for a late thermal event in the protoplanetary disk and generally indicates that multiple, distinct thermal pulses occurred in the chondrule forming region of the protoplanetary disk throughout the time of chondrule formation. The nonconcentric secondary outer zone around a spherical inner zone may indicate a directed heat source as the cause of partial remelting and reprocessing of primary chondrules.

¹Zuriñe Yoldi,¹Antoine Pommerol,^1,2Olivier Poch,¹Nicolas Thomas
Icarus (in Press) Link to Article [https://doi.org/10.1016/j.icarus.2020.114169]
¹Physikalisches Institut, Universität Bern and NCCR PlanetS, Sidlerstrasse 5, 3012 Bern, Switzerland
²Univ. Grenoble Alpes, CNRS, IPAG, 38000 Grenoble, France
Copyright Elsevier

The reflectance of water ice and dust mixtures depends, amongst other parameters, on how the components are mixed (e.g. intimate mixture, areal mixture or coating) (Clark, 1999). Therefore, when inverting the reflectance spectra measured from planetary surfaces to derive the amount of water ice present at the surface, it is critical to distinguish between different mixing modes of ice and dust. However, the distinction between mixing modes from reflectance spectra remains ambiguous. Here we show how to identify some water ice/soil mixing modes from the study of defined spectral criteria and colour analysis of laboratory mixtures. We have recreated ice and dust mixtures and found that the appearance of frost on a surface increases its reflectance and flattens its spectral slopes, whereas the increasing presence of water ice in intimate mixtures mainly impacts the absorption bands. In particular, we provide laboratory data and a spectral anal