MITM10 | Laboratory experiments in support of ground observations and space missions (sample return, analogs, analytical workflow etc.)

MITM10

Laboratory experiments in support of ground observations and space missions (sample return, analogs, analytical workflow etc.)
Conveners: Alessandro Pisello, Giovanni Poggiali, Koki Yumoto, Antonin Wargnier
Orals WED-OB3
| Wed, 10 Sep, 11:00–12:30 (EEST)
 
Room Venus (Veranda 3)
Orals FRI-OB2
| Fri, 12 Sep, 09:30–10:30 (EEST)
 
Room Mercury (Veranda 4)
Orals FRI-OB3
| Fri, 12 Sep, 11:00–12:30 (EEST)
 
Room Mercury (Veranda 4)
Posters TUE-POS
| Attendance Tue, 09 Sep, 18:00–19:30 (EEST) | Display Tue, 09 Sep, 08:30–19:30
 
Finlandia Hall foyer, F125–137
Wed, 11:00
Fri, 09:30
Fri, 11:00
Tue, 18:00
Most of our knowledge about the origin and the evolution of the Solar System comes from our ability to decipher the processes that formed and processed planetary materials. These materials have diverse physical (grain size, roughness etc.) and chemical properties (composition, mineralogy, volatile/refractory content, organic/inorganic compounds) and are mixed in various ways.

In the laboratory, the analyses of cosmo-materials coming from planetary or asteroidal objects (that felt on Earth or returned by space missions) as well as analyses on analogues reproducing their physical/chemical properties, are both essential for the understanding of the history of planets and small bodies.
The results of these laboratory experiments are essential for the interpretations of measurements obtained by ground-based observations and space missions. They are also necessary for planning and preparing future in situ and sample-return space missions, ensuring their success in collecting valuable samples and data.

In this session, we invite submissions related to the analysis of cosmo-materials and to the production, evolution and analysis of planetary and small bodies analogues (interpretation of chemical/physical properties, predictions, preparation of analytical tools or space instruments, preparation of analytical chain for sample return analyses, etc.). Laboratory experiments necessary to interpret data of any past, present and future space missions will be particularly encouraged.

Session assets

Orals WED-OB3: Wed, 10 Sep, 11:00–12:30 | Room Venus (Veranda 3)

Chairpersons: Antonin Wargnier, Koki Yumoto, Giovanni Poggiali
11:00–11:12
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EPSC-DPS2025-735
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ECP
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On-site presentation
Oliver Gaida, Olfa D'Angelo, Jonthan E. Kollmer, and Jens Teiser


Rheological models applicable on Earth tend to fail in reduced gravity. Below a critical gravitational acceleration, cohesive forces become predominant. For granular processing in space, notably to sustain human presence on the Moon, this can have disastrous consequences: it can lead to clumping of the material, unexpected clogging of hoppers, and in the end, compromises the complete processing pipeline. Yet, the influence of (low) gravity on granular flows is not accounted for in most existing models.

The Granular Rheology in Space (GRIS) project aims to contribute to the development of  rheological models applicable to lunar regolith, in space environment (including reduced gravity and low pressure). This contribution will present results from hourglass experiments, conducted in low gravity using an active drop tower and parabolic flights. To access partial gravity, a centrifuge is placed inside the plane, allowing us to generate gravities from 0.1g to 1g (where g is the Earth gravity). The flow rate and clogging probability were measured for different regolith simulants and analysed dependent on the granular Bond number. We generalise the granular behaviour in reduced gravity for all simulants studied, by scaling the clogging probability using the granular Bond number. We also propose an explanation for the deviations observed from the gravity-scaling of the Beverloo equation.

How to cite: Gaida, O., D'Angelo, O., Kollmer, J. E., and Teiser, J.: Flow Behaviour of Lunar Regolith in a Low-Gravity Environment, EPSC-DPS Joint Meeting 2025, Helsinki, Finland, 7–13 Sep 2025, EPSC-DPS2025-735, https://doi.org/10.5194/epsc-dps2025-735, 2025.

11:12–11:24
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EPSC-DPS2025-113
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ECP
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On-site presentation
Alexia Duchêne, Jeanne Bigot, Michał Stankiewicz, Sarah Dghais, Colas Robin, Arnaud Wilhelm, Jonathan E. Kollmer, and Naomi Murdoch

Understanding the physics of granular materials in a low gravity and vacuum environment is essential to predict the regolith behavior on the Moon and asteroids. Cohesive forces - interparticle attractive forces, are an important parameter to consider in the regolith dynamics. A given cohesive force may be considered negligeable in Earth’s gravity but become dominant when the gravitational acceleration is reduced (e.g. [1]). The surface properties, such as cohesion, influence the response of planetary surfaces (e.g., will an object sink or bounce?) and the performance of space missions (e.g., will a lander sink or bounce, how will a sampling arm perform?). The sinkage of an object, such as a CubeSat after landing or a boulder resting on fine regolith, enables estimates to be made of the bearing capacity of the surface – maximum load the surface can withstand before rupturing.

To quantify the importance of cohesive forces on the sinkage depending on the gravitational acceleration, sinkage experiments into granular materials were performed at different levels of cohesion and gravitational acceleration. The experiment campaign named SILOE (Surface Investigation in Low gravity Environment) was conducted in December 2024 in the GraviTower Bremen Pro at the ZARM drop tower facility (Bremen, Germany). The sinkage experiments were performed in terrestrial gravity (9.8 m/s²) and in two reduced gravitational accelerations: Mars gravity (3.8 ± 0.2 m/s²), and Moon gravity (1.8 ± 0.2 m/s²). These two levels of low gravity are achieved using the GraviTower in partial gravity.

The SILOE sinkage experiments (fig. 1) consist in the release of a spherical projectile (D = 25 mm, stainless steel) into a tray filled with a granular material. The projectile is released from a constant drop height of 6 mm above the surface. The associated collision velocities range from 0.1 to 0.5 m/s, depending on the gravitational acceleration. The experiments are conducted under low to medium vacuum conditions (50 – 400 Pa), to remove the interstitial air pockets and water molecules inside the material.

Figure 1: Design of the SILOE experiment.

The granular materials (fig. 2) studied are glass beads (120 µm) and quartz sand (500 µm). To increase the cohesive forces of the glass beads, the material was covered by a polymer coating enabling the addition of liquid capillary forces [2]. The cohesive force is controlled by the coating thickness applied to the beads. Glass beads with three levels of cohesion were produced following the preparation technique presented in Gans et al. (2020) [2]: at 50, 200, and 400 Pa (cohesive shear stress).

Figure 2: Granular materials used in the SILOE experiments.

 

The sinkage, defined as the final penetration depth of the projectile, is measured by tracking the vertical displacement of the projectile using a camera (sampling rate: 240 Hz) and a laser profilometer (sampling rate: 340 Hz), placed on the side and top of the chamber, respectively.

Cohesion increases the surface strength, which leads to smaller sinkage (fig. 3). In low gravity, the importance of cohesive forces increases, and smaller sinkage are observed for an identical material when the gravity is reduced. In the case of the very cohesive glass beads, rebounds can be observed (fig. 4).

Figure 3: Images captured with the camera after the projectile is dropped and finished sinking into the glass beads of different levels of cohesion (from cohesionless to very cohesive).

 

Figure 4: Projectile vertical displacement with respect to the surface (surface height at 0 mm) in vacuum and Earth gravity condition into the different cohesive glass beads.

 

The results of the SILOE drop tower campaign, and additional sinkage experiments performed at varied ambient pressure, will be presented during the conference. In addition to bringing a better understanding of cohesive forces with respect to gravity, the SILOE results will help to improve interpretations of the data from the upcoming ESA Hera mission (in particular with the CubeSat landings on asteroids Didymos and Dimorphos [3], and boulder tracks [4]), and the JAXA MMX mission (in particular the IDEFIX rover [5] on Phobos).

 

References

[1] Scheeres, et al. (2010). Scaling forces to asteroid surface: the role of cohesion. Icarus, 210, 2.

[2] Gans, Pouliquen, and Nicolas (2020). Cohesion-controlled granular material. Physical review E, 101:032904.

[3] Michel, et al. (2022). The ESA Hera mission: Detailed Characterization of the DART Impact Outcome and the Binary Asteroid (65803) Didymos. The Planetary Science Journal, 3:160.

[4] Bigot, Lombardo, et al. (2024). The bearing capacity of asteroid (65803) Didymos estimated from boulder tracks. Nature Communications, 15:6204.

[5] Michel, et al. (2022), The MMX rover: performing in situ surface investigations on Phobos. Earth, Planets and Space, 74:2.

 

Acknowledgements

This project is carried out with the support of the Education Office of the European Space Agency (ESA) under the educational Experiments Programme. This project received funding through the grant EUR TESS N°ANR-18-EURE-0018 in the framework of the Programme des Investissements d’Avenir, and the Bourse Espace 2024 scholarship by the Fondation Ailes de France. A.D. acknowledges PhD funding from University of Toulouse III, and C.R. acknowledges PhD funding from CNES and ISAE SUPAERO. This project benefitted from funding from CNES in the context of the Hera mission and the MMX rover/wheelcams, the French ANR (ANR-23-ERCC-0003-01), and the European Research Council (ERC) GRAVITE project (Grant Agreement N°1087060).

 

 

How to cite: Duchêne, A., Bigot, J., Stankiewicz, M., Dghais, S., Robin, C., Wilhelm, A., Kollmer, J. E., and Murdoch, N.: Sinking or bouncing in low gravity environments?, EPSC-DPS Joint Meeting 2025, Helsinki, Finland, 7–13 Sep 2025, EPSC-DPS2025-113, https://doi.org/10.5194/epsc-dps2025-113, 2025.

11:24–11:36
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EPSC-DPS2025-129
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ECP
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On-site presentation
Zac Amato, Tom F. Headen, Lorna Dougan, Mark G. Fox-Powell, Helen J. Fraser, Rachael E. Hamp, Harrison Laurent, and Christoph G. Salzmann

Neutrons are a powerful probe and vital tool for a wide range of scientific and industrial fields. Neutron scattering is used to obtain a direct and detailed insight into the structure and dynamics of condensed matter – matching dimensions in space from single atoms to macromolecules and in time from atomic vibrations to diffusion of large molecular units – all depending on the instrument and facility used. Compared to other scattering probes, neutrons are non-interacting and scatter off of the nucleus - allowing for much deeper penetration. This unique mechanism gives it the ability to ‘see’ hydrogen with high sensitivity, which is present in most molecules relevant to planetary and interstellar environments, and allows it to differentiate between isotopes. By exploiting the isotopic differentiation, such as using selective H/D substitution, we can also highlight interatomic correlations of interest. Another important advantage is that complex sample environments can be used, such as vacuum chambers and pressure cells, to recreate the conditions across various regions. This range of techniques has much to offer the Planetary Sciences and Astrochemistry communities and there is much to be gained from its increased use/collaboration. In this presentation, I will present what is on offer to these communities, starting with an introduction to the main techniques (diffraction, small-angle, dynamics, spectroscopy and imaging) and then I will go through examples of neutron work we have previously and are currently undertaking with relevance to both the Solar System and the Interstellar Medium (ISM).

The presentation will focus on some recent examples in detail. We have uniquely employed an in-situ ice vapour-deposition experiment (high vacuum) on the instruments NIMROD and Sans2d, at the ISIS Neutron and Muon Source in the UK, to study the structure of Amorphous Solid Water (ASW), as a function of growth and thermal evolution.1–3 Neutrons gave us the ability to directly probe (non-destructively) the general bulk structure of ASW, along with its porosity (volume fraction, pore sizes, shapes etc.), surface area and crystallinity, and how this all evolves with time and temperature. Altogether, the results converge to form a new picture of the ASW structure and nanoporosity during growth and annealing, involving microporous islands with voids between them (see Fig.1). This work has drastically changed our picture of ice astrophysics and the role it plays in planet- and star-formation processes.

Figure 1. Cartoon representation of the structure of ASW theorised in this work – islands/grains with voids between them (not to scale).

Another avenue of ice studies conducted using NIMROD and Polaris at the ISIS Facility led to the discovery of a new metastable dihydrate of sodium chloride at ambient pressure.2,4,5 Neutrons were key here with their particular sensitivity to the position of hydrogen, which makes up a large part of the NaCl water ice mixture. This dihydrate should be stable at the surfaces of icy worlds, such as Europa and Enceladus, and if it were detected then that would indicate regions of recent activity where subsurface brines have frozen rapidly, which are priorities for upcoming planetary missions, such as ESA’s JUICE and NASA’s Europa Clipper.

NIMROD and SANDALS at the ISIS Facility specialise in studying disordered materials such as liquids and glasses.2,7 They allow for the full structural characterisation of such a material and the interactions between all its components. One example of long-term work using both instruments is the study of the role of magnesium perchlorate (Mg(ClO4)2) in the subsurface water on Mars. Initially, it was found that the presence of Mg(ClO4)2 has a significant effect on the structure of water, making it appear as though it is under massive pressure, even when no external pressure is applied.6 Although this is the case, it was still found in a follow up study that amino acids, such as glycine in this case, can still self-assemble under these conditions, even though the Mg(ClO4)2 disrupts its hydration and hydrogen bonding ability.8 This happened more readily at low temperatures and so it seems possible to have biological molecules forming in the Martian environment. Finally, it was recently found that the presence of the osmolyte trimethylamine N-oxide (TMAO) could undo the pressuring effect of Mg(ClO4)2 on water, which would help prevent damage to biological systems.9

References
[1] Z. Amato, T. F. Headen, S. G ¨artner, P. Ghesqui `ere, T. G. A. Youngs, D. T. Bowron, L. Cavalcanti, S. E. Rogers, N. Pascual, O. Auriacombe, E. Daly, R. E. Hamp, C. R. Hill, R. K. TP and H. J. Fraser, Phys. Chem. Chem. Phys., 2025, 27, 6616–6627.
[2] ISIS, NIMROD, 2025, https://www.isis.stfc.ac.uk/Pages/nimrod.aspx, Accessed: 02-04-2025.
[3] ISIS, Sans2d, 2025, https://www.isis.stfc.ac.uk/Pages/Sans2d.aspx, Accessed: 02-04-2025.
[4] R. E. Hamp, C. G. Salzmann, Z. Amato, M. L. Beaumont, H. E. Chinnery, P. Fawdon, T. F. Headen,
P. F. Henry, L. Perera, S. P. Thompson and M. G. Fox-Powell, The Journal of Physical Chemistry Letters, 2024, 15, 12301–12308.
[5] ISIS, Polaris, 2025, https://www.isis.stfc.ac.uk/Pages/Polaris.aspx, Accessed: 02-04-2025.
[6] S. Lenton, N. H. Rhy, J. J. Towey, A. K. Soper and L. Dougan, Nat Commun, 2017, 8, 919.
[7] ISIS, SANDALS, 2025, https://www.isis.stfc.ac.uk/Pages/sandals.aspx, Accessed: 02-04-2025.
[8] H. Laurent, A. K. Soper and L. Dougan, Molecular Physics, 2019, 117, 3398–3407.
[9] H. Laurent, T. G. A. Youngs, T. F. Headen, A. K. Soper and L. Dougan, Communications Chemistry, 2022, 5, 116.

How to cite: Amato, Z., Headen, T. F., Dougan, L., Fox-Powell, M. G., Fraser, H. J., Hamp, R. E., Laurent, H., and Salzmann, C. G.: Neutron Scattering as a Powerful Tool for Studying Multi-Scale Structure for Planetary Sciences, EPSC-DPS Joint Meeting 2025, Helsinki, Finland, 7–13 Sep 2025, EPSC-DPS2025-129, https://doi.org/10.5194/epsc-dps2025-129, 2025.

11:36–11:48
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EPSC-DPS2025-493
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On-site presentation
Mariana Reis, Erika Kaufmann, David Haack, and Axel Hagermann

Enceladus is famous for its geyser-like plumes of water vapour and ice particles on its south pole, titled as ”tiger stripes”. They are predominantly released from fractures, and some of the ejected material falls back onto Enceladus’ surface, coating it with fresh ice grains that keep its albedo high [1]. Enceladus and other icy satellites like Europa, are believed to have salty subsurface oceans. Sodium salts such as NaCl, NaHCO₃ and Na₂CO₃ have been suggested as salts present in Enceladus’ [2,3] surface and ocean. Recently, Postberg et al. 2023 [4], re-examined Cassini's Cosmic Dust Analyzer data and denoted the presence of sodium phosphate salts in high amounts on Enceladus’s surface and ocean, Na₃PO₄ and Na₂HPO₄.

At present we have missions like JUICE and Europa Clipper with the goals of studying in depth icy moons surfaces and its connections with their subsurface oceans. This work intends to support the interpretation of data from these missions, as well as to provide insights that might help shape the design and emphasis of future icy satellites investigations. We experimentally investigate energy balances and space weathering on Enceladus’ surface, with a focus on how contaminants affect energy transfer and structural evolution, processes that are also relevant to other icy moons with sub-surface oceans. We prepare granular intra-mixtures of water ice and salts, and insolate them in a pre-cooled vaccum chamber to analyse how they evolve overtime. In our experiments, we monitor temperature variations and light transmission through analogue surface materials during irradiation in the vacuum chamber. Additionally, we analyse microstructural and spectral changes by comparing each sample before and after solar exposure. This includes microscopic imaging to track surface evolution and reflectance spectroscopy to assess changes in optical properties. We also measure the hardness profile of the sample to understand structural evolution through sintering.

 

References:

[1] Porco, C. C., “Cassini Observes the Active South Pole of Enceladus”, Science, vol. 311, no. 5766, pp. 1393–1401, 2006. doi:10.1126/science.1123013.

[2] Postberg, F., “Sodium salts in E-ring ice grains from an ocean below the surface of Enceladus”, Nature, vol. 459, no. 7250, pp. 1098–1101, 2009. doi:10.1038/nature08046

[3] Postberg, F., Schmidt, J., Hillier, J., Kempf, S., and Srama, R., “A salt-water reservoir as the source of a compositionally stratified plume on Enceladus”, Nature, vol. 474, no. 7353, pp. 620–622, 2011. doi:10.1038/nature10175.

[4] Postberg, F., “Detection of phosphates originating from Enceladus's ocean”, Nature, vol. 618, no. 7965, pp. 489–493, 2023. doi:10.1038/s41586-023-05987-9.

How to cite: Reis, M., Kaufmann, E., Haack, D., and Hagermann, A.: Microstructural and Optical Evolution of Icy Moons Surface Analogues in Space Conditions, EPSC-DPS Joint Meeting 2025, Helsinki, Finland, 7–13 Sep 2025, EPSC-DPS2025-493, https://doi.org/10.5194/epsc-dps2025-493, 2025.

11:48–12:00
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EPSC-DPS2025-774
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On-site presentation
Yaël Bourgeois and Stéphanie Cazaux

Once a mighty giant follower of Kronos in the Gigantomachy, crushed beneath Mount Etna by Athena, Enceladus now slumbers in the icy grip of Saturn’s embrace. Its cryovolcanic plumes, rich in water vapour and organic molecules, rise like spectral echoes of its mythical past, making this enigmatic moon a beacon in the search for life beyond Earth. Both the European Space Agency (ESA) and NASA are planning missions to return to the Cronian system, via a large-class mission and a flagship mission respectively, aiming to unravel the mysteries of this icy moon.

To support such efforts, experimental modeling is essential, providing critical data to guide mission planning and maximise the scientific return of future in situ observations. In this context, the Crevasse Laboratory Analogue for icy Moons (CLAM) experimental setup, presented in this work, offers valuable insight into water vapour flow conditions inside the ice shell fractures of Enceladus.

The setup uses 3D-printed straight cylindrical channels, designed using key dimensionless scaling parameters, the Reynolds, Knudsen, Prandtl, and Eckert numbers, to serve as crevasse analogues. Each channel is mounted atop a cylindrical reservoir filled with demineralised water and placed inside our environmental chamber, PISCES (Plumes and Ices Simulation Chamber for Enceladus and other moonS). The channel is instrumented with differential pressure sensors and thermocouples to monitor the evolution of vapour flow as the chamber pressure is reduced to sub-millibar levels (~5×10-2  mbar). It is also externally cooled to sub-zero temperatures (~255 K) using frozen aluminium pellets. Finally, the velocity of the emerging plume is measured using an L-shaped Prandtl (Pitot-static) tube.

Our results present how plumes develop in different channels at cold temperature (~255 K), and which velocities are reached within the channel and at the vent. We show that channel temperatures have an important effect on the velocities of plumes, and discuss these effects. Notably, supersonic gas plumes were observed in several cases, with some configurations reaching supersonic speeds within the channel while others accelerated beyond the vent.

How to cite: Bourgeois, Y. and Cazaux, S.: CLAM: a Crevasse Laboratory Analogue for icy Moons to recreate and study plumes, EPSC-DPS Joint Meeting 2025, Helsinki, Finland, 7–13 Sep 2025, EPSC-DPS2025-774, https://doi.org/10.5194/epsc-dps2025-774, 2025.

12:00–12:12
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EPSC-DPS2025-116
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On-site presentation
Fulvio Franchi, Marianna Túri, Gergö Lakatos, Kumar Rahul, Duncan Mifsud, Giuliana Panieri, Richárd Rácz, Sándor Kovács, Enikö Furu, Róbert Huszánk, Robert Mccullough, and Zoltán Juhász

Introduction. Seep and vent environments on Enceladus would be ideal to sample by future astrobiological missions, although this may not be possible due to technological limitations [1, 2]. Searching for biosignatures in the more readily sampled Enceladus’ icy shell is preferable. In this regard, the Arctic Ocean is a unique terrestrial analogue of Enceladus. For this reason here we try to determine whether any geochemical biosignatures associated with methane cycling can be detected in Arctic ice using mass spectrometric techniques similar to those likely to be included in the payloads of planned missions to Enceladus.

Study Area and samples. The site investigated lies at the southernmost extent of the Vestnesa Ridge, on the Svalbard continental slope (Figure 1) and it was visited in May 2022 during the AKMA2-OceanSenses Research Expedition [3]. Gas hydrates are very common in the area as revealed by several seismic studies and direct sampling [4]. The Vestnesa Ridge system interacts with warm fluids whose circulation is driven by hydrothermal activity [5].

Ice and surface water from the drill holes were sampled from the ice pack (Figure 1). Samples of deep water were collected from another location nearby at a depth of 1392 m using a conductivity, temperature, and depth (CTD) probe (Figure 1). Shallow (<1 m from the sediment-water interface) gas hydrates were sampled in the same area using a gravity corer (Figure 1).

Figure 1. Study area and sampling sites: IC = ice samples; CTD = water samples collected using a CTD probe; GC = gas hydrate sample. From [6].

 

Methods. The hydrogen and oxygen stable isotopic compositions of the melted ice samples were determined at the HUN-REN Institute for Nuclear Research in Debrecen, Hungary, using off-axis integrated-cavity output spectroscopy (OA-ICOS).

The relative composition of gases emitted during the melting of the Arctic ice samples was measured via 70 eV electron impact quadrupole mass spectrometry (QMS) across a mass range of 1-50 amu at the HUN-REN Institute for Nuclear Research (Figure 2). Ice samples were analysed following an ad hoc protocol presented in Franchi et al. [6]. QMS analysis was performed by measuring integer masses sequentially using an ion counting secondary electron multiplier (SEM).

 

Figure 2. Apparatus used to measure the mass spectra of gases emitted by melted ice samples (top-right) and seawater and gas samples (bottom-right) using an ultrahigh-vacuum chamber fitted with a QMS (left).

 

Results and Interpretation. The measured isotopic compositions of the ice and seawater revealed that the surface water sample exhibited δ2H and δ18O values comparable to the standard. The ice sample collected at the water – ice interface exhibited significant enrichments of 2H and moderate-to-large enrichments of 18O, with δ2H and δ18O values of 17.43‰ and 1.959‰, respectively. These results are likely indicative of the isotopic fractionation effect that occurs during the freezing of water in which heavy isotopes are preferentially incorporated into the ice phase [7]. The deep ocean water exhibited noticeably negative δ2H and δ18O values. On Earth, this may be attributed to biological activity in the oceans, since living organisms preferably built in the lighter isotopes in their body, and after their death, the dead matter enriches the deep waters at the bottom with light isotopes.

The abundances of several gas species of interest (CH4, C2H6, H2, N2, O2, CO2, Ar and Ne) trapped or dissolved within the Arctic water and ice samples was assessed by QMS. The composition of the gases emitted from one ice sample collected at the water – ice interface showed close similarity to that of air, with the notable exception of a relatively high molecular hydrogen abundance, and small quantities of methane and ethane.

Two samples of ice collected from another location, one acquired from the ice-seawater interface and one at the air-ice interface, showed higher concentrations of CO2 consistent with their relatively low pH values. This observation is consistent with either: (i) these ice samples containing atmospheric CO2 dissolved in the ocean water; or (ii) the oxidation of CH4 released at the seafloor [6]. To ascertain the source of C, the δ13C values of carbon dioxide were studied using the signal intensities at the 44 (12C16O2) and 45 (13C16O2) amu mass channels. All Arctic samples exhibited δ13C values ranging between -2.4 and +2.3‰. Negative value was obtained for the deep sea water sample, which is in line with biological activity [8].

Our experiments have tentatively demonstrated that the concentration of molecular hydrogen in one ice sample is ca. 3.6%, which is about 175 times higher than its concentration in laboratory air control samples, and ca. 2.5-10 times higher than concentrations observed in the plume of Enceladus [9]. This high concentration of molecular hydrogen in Arctic ice could possibly be sourced from hydrothermal activity linked to serpentinization along the Arctic mid-oceanic ridge. Hence, hydrothermal activity within the global ocean of Enceladus might be inferred from excesses of molecular hydrogen within its ice shell.

Furthermore, our results demonstrate that QMS measurements similar to ours, which were and will be obtainable by past and future space missions at icy moons can detect possible biosignatures when gas components and isotopic ratios are carefully extracted from the data.

 

References: 1. McKay, CP., et al. 2012. Planetary and Space Science 71, 73; 2. Carrizo, D., et al. 2022. Astrobiology 22, 552; 3. Panieri, G., et al. 2022. CAGE22-2 Scientific Cruise Report: AKMA 2/Ocean Senses. CAGE – Centre for Arctic Gas Hydrate, Environment, and Climate Report Series 10; 4. Panieri, G., et al. 2017. Marine Geology 390, 282-300; 5. Bünz, S., et al. 2012. Marine Geology 332-334, 187-197; 6. Franchi, F., et al. 2025. Planetary and Space Science 257, 106051; 7. Toyota, T., et al. 2013. Journal of Glaciology 59, 697-710; 8. Kroopnick, P. M. 1985 Deep-Sea Research, 32, 57- 84,.9. Waite, J.H., et al. 2017. Science 356, 155.

How to cite: Franchi, F., Túri, M., Lakatos, G., Rahul, K., Mifsud, D., Panieri, G., Rácz, R., Kovács, S., Furu, E., Huszánk, R., Mccullough, R., and Juhász, Z.: Investigation of Arctic Ice in preparation for the Future Exploration of Biosignatures on Enceladus and other icy moons, EPSC-DPS Joint Meeting 2025, Helsinki, Finland, 7–13 Sep 2025, EPSC-DPS2025-116, https://doi.org/10.5194/epsc-dps2025-116, 2025.

12:12–12:24
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EPSC-DPS2025-172
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ECP
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Virtual presentation
Patrick Tribbett, Yukiko Yarnall, Reggie Hudson, Perry Gerakines, and Christopher Materese

Simple nitrogen (N-) heterocycles are expected to be an abundant class of molecules within the interstellar medium (ISM).  Computational and laboratory studies have demonstrated previously that these molecules likely form during the polymerization of acetylene in the presence of hydrogen cyanide (Ricca et al. 2001, Hamid et al. 2014), a process expected to occur in the stellar outflows of carbon-rich AGB stars.  This production pathway is analogous to the formation of benzene, which has been detected in the presence of polyacetylenic chains (Cernicharo et al. 2001).   Additionally, laboratory studies have demonstrated that N-heterocycles readily form during the irradiation of icy materials.  Specifically, Materese et al. 2015 identified pyridine and isoquinoline in the room-temperature residues formed from photolyzed and warmed ices containing water, ammonia, and benzene or naphthalene.  More recently, Wang et al. 2024 identified pyrrole and indole in electron-irradiated acetylene and ammonia ice mixtures.

N-heterocycles are also present in meteoritic materials and in the samples returned from carbonaceous asteroids.  All five nucleobases (adenine, cytosine, guanine, thymine and uracil) and many other N-heterocycles were detected in extracts of an aggregate sample returned from asteroid Bennu by NASA’s OSIRIS-Rex (Glavin et al. 2025).  Many of these N-bearing species are critical compounds to terrestrial biology, and an extraterrestrial origin informs our understanding of prebiotic astrochemistry.  Simple N-heterocycles (pyridine, diazines, etc.) might be the prerequisite molecules for the formation of nucleobases present on the surfaces of small, outer Solar System objects.  However, despite the expectation of abundant N-heterocycles, these molecules have not been detected remotely in the ISM or the outer Solar System.  Several observational studies have provided upper limits on the abundances of pyridine and pyrimidine (Kuan et al. 2003, Cordiner et al. 2017).

A possible reason for the non-detections of N-heterocycles could be a difference in radiolytic stability compared to other aromatic compounds (e.g., benzene).  Peeters et al. 2005 previously explored this hypothesis demonstrating the photo-destruction of matrix-isolated pyridine, pyrimidine, and s-triazine and found that these molecules can be destroyed in diffuse regions of the ISM (higher UV fluxes), but the molecules should survive in dense molecular clouds, which can provide some UV shielding.  However, galactic cosmic rays (GCRs) readily penetrate dense interstellar clouds and continuously irradiate the surfaces of outer Solar System objects (e.g., TNOs), which likely contain primitive organic materials and possibly N-heterocycles.  Using facilities in NASA’s Cosmic Ice Laboratory and techniques described previously (e.g., Gerakines et al. 2022, Tribbett et al. 2024), we demonstrate the radiation-driven destruction of several simple N-heterocycles (pyridine, pyrimidine, pyridazine, pyrazine, and s-triazine) when embedded in a water-ice matrix.  We use infrared spectroscopy to quantify the radiolytic destruction of these molecules in water ices at 15 K and report their destruction rate constants and radiolytic half-lives.  We extrapolate these half-lives to the expected radiation doses received in interstellar dense molecular clouds (Moore et al. 2001) and on or within the surfaces of outer Solar System objects (Loeffler et al. 2020).  We also discuss the implications of our results in the context of the recent detections of N-heterocycles in the Bennu samples returned by OSIRIS-Rex.

 

References:

Cernicharo et al., ApJ546, L123 (2001).

Cordiner et al., ApJ. 850, 187 (2017).

Glavin et al., Nat. Astron. 9, 199 (2025).

Gerakines et al., Astrobio. 22, 233 (2022).

Hamid et al., J. Phys. Chem Lett. 5, 3392 (2014).

Kuan et al., MNRAS. 345, 650 (2003).

Loeffler et al., Icarus 351, 113943 (2020).

Materese et al., ApJ. 800, 116 (2015).

Moore et al., Spectrochim. Act. A 57, 843 (2001).

Peeters et al., Astron. Astrophys. 433, 583 (2005).

Ricca et al., Icarus 154, 516 (2014).

Tribbett et al., Astrobio. 24, 1085 (2024).

Wang et al., JACS. 146, 28437 (2024).

How to cite: Tribbett, P., Yarnall, Y., Hudson, R., Gerakines, P., and Materese, C.: Radiation-driven Destruction of N-heterocycles in H2O-ice mixtures, EPSC-DPS Joint Meeting 2025, Helsinki, Finland, 7–13 Sep 2025, EPSC-DPS2025-172, https://doi.org/10.5194/epsc-dps2025-172, 2025.

12:24–12:30

Orals FRI-OB2: Fri, 12 Sep, 09:30–10:30 | Room Mercury (Veranda 4)

Chairpersons: Giovanni Poggiali, Alessandro Pisello, Koki Yumoto
09:30–09:42
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EPSC-DPS2025-809
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ECP
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On-site presentation
Emma Caminiti, Pierre Beck, Lydie Bonal, Bernard Schmitt, and Tomohiro Usui

Introduction:
The VNIR reflectance spectrum of a surface depends on its composition, physical properties, and the interactions between the surface and the environment. The temperature dependence of spectral properties may complicate the interpretation of planetary surfaces’ reflectance, but can also provide valuable information about their composition and state.

The VNIR reflectance spectra of common rock-forming minerals vary with temperatures [1][2][3][4], and these spectral changes can bias the interpretation of remote sensing data [5][6][4]. For example, Lucey et al. [7] showed that the A-type asteroids' spectra differ from those of olivines under terrestrial conditions but are consistent with those of olivines at the low surface temperatures expected on the main belt asteroids. Thereafter, Lucey et al. [8] detected temperature-dependent variations in the spectral properties of Eros, highlighting the importance of considering the effect of low temperatures on surface properties.

However, less has been done concerning carbonaceous chondrites. In this study, we report comparative low-temperature laboratory measurements of a panel of meteorites. This work may help us to understand the mineralogy of meteorites, but also to gain a better understanding of the solar system small bodies.

 Samples:
We studied carbonaceous chondrites from four different groups (CI, CM, CV, and CO), one ungrouped carbonaceous chondrite (UCC), an ordinary chondrite, and a HED meteorite (diogenite). More specifically, we used the CI Orgueil, the CMs Murchison and DOM 08003, the CVs QUE 94688 and Axtell, and the CO ALH 85003. The meteorite Tarda was used (UCC). Additionally, we studied the ordinary chondrite LL Saint-Severin and the diogenite Bilanga, whose possible parent body is the differentiated asteroid Vesta.

Measurements:
Low-temperature reflectance spectroscopy measurements were acquired at IPAG (France) using the bidirectional reflectance spectrogonio-radiometer SHINE (SpectropHotometer with variable INcidence and Emergence) [9]. Spectra were acquired from 400 to 4000 nm with an incidence angle of 0° and an emission angle of 20°. SHINE was coupled with the double environmental chamber CarboN-IR [10]. With this setup, we performed measurements from about 280 K to a minimum of 70 K with several intermediate temperature steps. The temperature error is estimated to be 1 K and the measurements were led in an Ar-filled inner cell, ensuring good thermalization to the granular samples. All of our samples were in the form of powder.

Results and implications for space missions:
Spectral changes induced by temperature were observed for all classes of meteorites, and these changes were generally linear as a function of temperature.

With decreasing temperatures, the band at 1000 nm associated with olivine and/or pyroxene generally becomes deeper (Bilanga, Axtell, QUE 94688) and narrower (Bilanga, Saint Severin, Axtell) (Figure 1 A, D). There is no trend in the change in minimum reflectance values associated with temperature variations, but the position of the minimum may shift towards longer (Axtell) or shorter (Bilanga) wavelengths.

Concerning the band at 2000 nm associated with pyroxene, although the minimum reflectance values do not seem to vary with temperature, the band shifts towards shorter wavelengths (Bilanga, Saint Severin, ALH 85003) (Figure 1 B, E). In addition, the band deepens (Bilanga, Saint Severin, ALH 85003) with decreasing temperatures. The only significant change in bandwidth is for Bilanga, for which the band becomes narrower.

With decreasing temperatures, the band at 3000 nm shifts towards longer wavelengths (Bilanga, DOM 08003, Tarda). In general, the band deepens (Bilanga and DOM 08003) and becomes narrower (Orgueil, Bilanga, Axtell, and DOM 08003). The slope between 2900 and 3900 nm increases at low temperatures (Orgueil, Bilanga, Saint-Severin, ALH 85003, QUE 94688, Murchison, DOM 08003) (Figure 1 C, F).

Other spectral features can be impacted by changes in temperature such as the maxima at 550 nm and 1500 nm, and the band at 700 nm.

Our results are important for the analysis of sample returns from the Hayabusa, Hayabusa2, and OSIRIS-REx missions, and the remote sensing measurement interpretations of the JAXA/MMX, ESA/Hera, ESA/Ramses, and JAXA Hayabusa2 extended missions. For example, the spectral properties of Phobos in the VNIR show that it could be analogous to a carbonaceous chondrite. Its surface temperatures vary significantly from 130 K to 350 K [11]. For a correct interpretation of the surface properties by the MMX Infrared Spectrometer (MIRS) [12], it is necessary to consider the spectral variations induced by temperature variations.

           

Figure 1: Reflectance spectra at different temperatures of (A) Bilanga, (B) Saint-Severin, and (C) DOM 08003. (D) shows the 1000 nm bandwidth changes for Bilanga. (E) shows the minimum reflectance of the 2000 nm band of Saint-Severin, and (F) shows the slope changes for DOM 08003.

 

Conclusion:
Our work shows the importance of surface temperature in the interpretation of VNIR reflectance spectra. Based on our present sample set, it seems that the spectral alterations generally show similar trends between ordinary chondrites, carbonaceous chondrites and achondrites. The data interpretation of several space missions may be affected by the present work, and future improvements of the quality and spectral resolution of the space mission measurements will increasingly necessitate taking into account the spectral alteration due to surface temperature.

 

References:
[1] Singer, R. B., & Roush, T. L. (1985).
[2] Roush, T. L., & Singer, R. B. (1986).
[3] Schade, U., & Wäsch, R. (1999).
[4] Moroz, L., Schade, U., & Wäsch, R. (2000).
[5] Roush, T. L., & Singer, R. B. (1987).
[6] Hinrichs, J. L., Lucey, P. G., Robinson, M. S., Meibom, A., & Krot, A. N. (1999).
[7] Lucey, P. G., Keil, K., & Whitely, R. (1998).
[8] Lucey, P. G., Hinrichs, J., Kelly, M., Wellnitz, D., Izenberg, N., Murchie, S., ... & Bell III, J. F. (2002).
[9] Brissaud, O., Schmitt, B., Bonnefoy, N., Doute, S., Rabou, P., Grundy, W., & Fily, M. (2004).
[10] Beck, P., Schmitt, B., Cloutis, E. A., & Vernazza, P. (2015).
[11] Giuranna, M., Roush, T. L., Duxbury, T., Hogan, R. C., Carli, C., Geminale, A., & Formisano, V. (2011).
[12] Barucci, M. A., Reess, J. M., Bernardi, P., Doressoundiram, A., Fornasier, S., Le Du, M., ... & Zeganadin, D. (2021).

 

How to cite: Caminiti, E., Beck, P., Bonal, L., Schmitt, B., and Usui, T.: Low-temperature reflectance spectra of meteorites: implications for space missions, EPSC-DPS Joint Meeting 2025, Helsinki, Finland, 7–13 Sep 2025, EPSC-DPS2025-809, https://doi.org/10.5194/epsc-dps2025-809, 2025.

09:42–09:54
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EPSC-DPS2025-1008
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ECP
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On-site presentation
Christopher Cox, Christopher Edwards, Jean-Francois Smekens, Mark Salvatore, Christopher Haberle, and Christopher Rose

Background and Motivation

Decades of space missions have advanced our understanding of planetary surfaces through remote sensing and in-situ spectroscopy [1, 2, 3]. These efforts produce high-quality data but suffer from observational limitations and often requiring complex models and lab validation [4, 5, 6]. A major source of uncertainty is the effect of viewing geometry on spectral measurements, causing modifications in spectral features such as shape, depth, and slope, among others [7, 8, 9, 10]. This can cause various issues with misidentification of surface materials [11, 12]. Phase angle variations influence surface brightness and albedo, complicating surface temperature measurements from instruments like Diviner on the Lunar Reconnaissance Orbiter [10]. These complications have also been seen on Mars as phase reddening and variable brightness temperatures [13, 14]. Here, we present our Spectrogoniometer designed to measure effects of varying phase angles on spectral measurements and the ”first-light” data.

The instrument presented here supports both reflectance and emission measurements. In reflectance mode, the viewing geometry is defined by the phase angle (ϕ, Figure 1), which depends on the incidence angle (i, Figure 1), emergence angle (α, Figure 1), and their respective azimuthal directions (θ, Figure 1) [4]. In emission, it is characterized by the emission angle (e, Figure 1) [4]. Laboratory studies of viewing angle effects are limited due to challenges in instrumentation and automation. Most lab measure ments use fixed geometries (e.g., 30◦ phase angle with no azimuthal offset), while mission data has often relied heavily on modeled data for interpretation [15, 16]. Efforts to characterize these effects have focused primarily on the visible (VIS) and short-wave
IR (SWIR) ranges, with growing work in longer IR wavelengths (e.g. Figure 1) [17, 18]. Additionally, most existing setups only utilize reflectance, lacking emission capabilities [e.g. 18].

To support spacecraft data, lab measurements must replicate similar phase angles. Rovers and landers, unlike orbiters, frequently view surfaces at high emergence/emission angles. These large phase angles complicate comparison to nadir-viewing instruments and hinder data interpretation by affecting the angular distribution of scattered light, which depends on grain size, shape, and internal structure [5, 6]. Absorbing surface layers and small geometric changes at high angles further amplify scattering complexities and cause significant variations in the phase curve, making accurate analysis more difficult [6].

Due to the lack of well-characterized spectral measurements across varying phase angles, high-phase-angle data is often interpreted through complex models that rely heavily on estimations and assumptions. While a dedicated phase angle measurement campaign won’t eliminate these complexities, it can provide valuable constraints and improve model accuracy, enhancing space craft data interpretation.

With the growing volume of spacecraft observations and measurements, including past, current, and future missions, the need to collect lab data that matches observation geometries is increasingly important. Figure 2 ([19]) illustrates limited laboratory measurements across a small phase angle range, but it highlights an example of phase angle characterization in a laboratory setting. Even in the case of a few phase angles measured, there are spectral features that are changing or in some cases disappearing from the spectra.

Spectrogoniometers capable of measuring variable phase angles do exist [e.g. 17, 18], but [18] is restricted to VIS and SWIR ranges. Though helpful, current instruments have limited capacity to support a broad range of mission science objectives. Specifically, phase angle measurements in the thermal IR (TIR) remain largely unsupported in a laboratory setting. The instrument described in [17] was originally designed to cover both VIS and IR, but [20] notes the
IR capability is no longer functional. Improved characterization of phase angle effects across a wider spectral range will enhance the support and accuracy of modeling efforts used in the interpretation of both remote sensing and in-situ data.

Methodology and Instrument Description

The spectrogoniometer used in this work (Figure 3) is a multi-wavelength spectrogoniometer with a measurable spectral range of .285 μm - 18 μm with a spectral resolution of approximately 1cm−1. The instrument utilizes a dual arm design. One arm, the receiving arm (Rx Arm) "A", uses a series of relay optics "B" to collect light reflected or emitted from the sample to the detector. The transmit arm (Tx Arm) "C", holds the light source "D" used in reflectance measurements. The motion of each arm is depicted in Figure 4. Both arms have an approximate elevation angle range of ±70◦. The Tx arm has an azimuth range of 230◦. The sample tray "F" contains four fixed positions and rotates to bring each position under the arms. It contains the sample and three calibration targets. This design allows for efficient measurements and immediate calibration as needed for both reflectance and emission modes.

Data collection and calibration was performed using an automated system developed for the instrument. The Rx arm moves incrementally over its whole range then the Tx arm increments and the Rx arm repeats its range. After the Tx arm completes its elevation range, it moves in azimuth and the process is repeated until a measurement is performed at each combination of arm elevations and azimuth. In total, 14 incidence angles, 23 incidence azimuths, 14 emergence angles, and 28 emission angles are characterized per material. Each sample measured produces 4508 reflectance spectra and 28 emission spectra at various phase angle combinations. Data are processed using a pipeline developed for the instrument. For each material analyzed, a hyperspectral reflectance spectrum, a hyperspectral emission spectrum, and visible images are produced. Those data products will be used to identify
modifications (among other things) in spectra as phase angles change. Well characterized materials (e.g. olivine, pyroxenes, clays, etc.) were selected for the initial characterization of this instrument. Later, other materials commonly found in spectral databases (e.g. ASU spectral library [21]) will be analyzed to provide a number of phase angle characterizations for these already well characterized materials. The data produced by this instrument will be analyzed and produce science products which will aid in interpretations of spacecraft-based measurements (e.g. identify commonly altered spectral features, identify phase reddening in materials, surface brightness temperatures, etc.).

How to cite: Cox, C., Edwards, C., Smekens, J.-F., Salvatore, M., Haberle, C., and Rose, C.: A Novel Instrument Design for Studying Photometric Effects in Reflectance and Emission Data in Visible and Mid-IR Wavelengths, EPSC-DPS Joint Meeting 2025, Helsinki, Finland, 7–13 Sep 2025, EPSC-DPS2025-1008, https://doi.org/10.5194/epsc-dps2025-1008, 2025.

09:54–10:06
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EPSC-DPS2025-1700
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On-site presentation
Simone De Angelis, Francesca Altieri, Eliana La Francesca, Maria Cristina De Sanctis, Marco Ferrari, Eleonora Ammannito, Jeremy Brossier, Enrico Bruschini, Michelangelo Formisano, Alessandro Frigeri, and Janko Trisic-Ponce

Introduction: 

Studying Martian Meteorites in the laboratory provides fundamental clues about the surface composition as well as the evolution of Mars. Spectroscopic and geochemical investigations furnish valuable insight both regarding the planet composition and information related to secondary processes (i.e. aqueous alteration) [1,2] SNCs meteorites have compositions that are mafic to ultramafic [1,2] essentially basalts or basaltic cumulates. Spectroscopic investigations in the VIS-NIR moreover provide important laboratory data for comparison with rover missions that currently are exploring the Martian surface with in situ spectrometers at even higher spatial resolutions with respect to past instruments.

Here we present reflectance spectroscopic measurements on a large sample of Martian Shergottite, North West Africa (NWA) 13367, by using the VIS-IR hyperspectral imaging technique. The sample has been investigated in the range of 0.35-5.1 micron by means of the SPIM setup at IAPS-CLab [5,6].

Setup and sample description:  the meteorite slab has been investigated with the Spectral Imager (SPIM) instrument in use at C-Lab laboratory at INAF-IAPS. The facility consists in an imaging spectrometer operative in the 0.35-5.1 micron-range [5,6], and contains the laboratory spare of VIR spectrometer onboard the Dawn mission [7]. The setup includes two bidimensional focal planes, a CCD (0.35-1 micron) and an HgCdTe (1-5.1 micron) detectors both hosted, together with the spectrometer, inside a liquid N2 cooled Thermal Vacuum Chamber. The entry slit is 9x0.038 mm corresponding to a single acquired image on the sample of 256 px, with spatial resolution of 38 micron/px on the target. The sample to analyze is placed outside the TVC on a 3-axis motorized stage: by moving the target at 38 micron-steps and acquiring consecutive frames it is possible to construct a hyperspectral cube of 876 spectral bands and the desired number of lines.

The analyzed sample is a slab of about 5x5 cm. According to the Meteoritical Bulletin, this sample is constituted mainly of olivine (50%), pyroxene (40%), and 5-10% maskelynite, and is characterized by ophitic/poikilitic texture. Pyroxenes range from a low Ca/Fe-rich pigeonite to a Ca-rich augite. Other phases include Fe-Ti oxides, sulfides, and merrillite (Ca-rich phosphate containing Na and Mg).

Measurements and Results: Two scans covering each an area of about 9x6 mm2 have been acquired on the same meteorite face. Each image has been constructed by acquiring 150 consecutive frames at 38-micron steps (dimension along the vertical axis). Here we focus on the first of the two scans. To obtain a first preliminary view of the spectral data, several band parameters maps have been retrieved. In particular, here we show the map of (i) band depth at 1 micron [Fig.1], and (ii) band depth at 0.65 micron [Fig.2]. The first map is related to the distribution of iron silicates (pyroxenes and olivine), and as can be seen, these phases cover the almost totality of the distribution map (Fig.1). Nevertheless most of the spectra resemble at first glance those of pyroxenes, characterized by the occurrence of the two Fe2+ bands at 1 and 2 micron (fig.3), with the second band varying between 2-2.3 micron.

Fig.1. Map of band depth at 1 mm for NWA 13367 cube, indicative of pyroxene/olivine distribution. This map and the following ones have dimensions of 9 mm x 5.7 mm.

 

In Fig.2 the distribution map of 0.65 micron band depth is shown. Although this absorption band could be consistent with spin-forbidden transition in Ti3+ in augite as reported in [8], here it appears, when present, broad and intense. Moreover, it seems to correlate with the 1-micron band more shifted towards longer wavelengths, pointing to a more Fe-rich composition. However it is evident how this phase forms outer rims (yellowish in this map) around core pyroxene grains with different composition (zonation) (Fig.2).

 

Fig.2. Map of band depth at 0.65 mm for NWA 13367 cube. This feature is related to Fe and/or Ti present in clinopyroxene.

 

A first tentative identification of spectral endmembers has been made by using the K-Means classification available on ENVI software. Spectral classes and relative representative endmembers are displayed in fig.3. Here spectra corresponding to pyroxene mineralogy are identified, with different levels of reflectance and also pyroxene composition, as suggested by the changing position of the 1 and 2-mm bands. The other two main classes identified likely represent a hydrated Fe-oxyde and a dark/opaque phase. In some locations spectra characterized by intense organic (C-H) features in the 3-4 micron region are identified (fig.4).

 

Fig.3. Spectral endmembers extracted as a first preliminary analysis through K-Means classification.

Fig.4. Selected spectra showing intense organic absorption features in the 3-4 micron region.

 

Conclusions and Future Work:

We started to investigate by means of VIS-IR imaging spectroscopy a Martian Shergottite (NWA 13367) at the spatial resolution of 38 mm. As preliminary spectral analysis, we retrieved several maps, for example at 1 micron (Fe silicates) and 0.65 micron (Ti or Fe-rich clinopyroxene). In particular, in some zones, the pyroxenes show zonation, with a likely Fe-rich outer rim. The correlation of 0.65-micron band depth with 1-micron band position will be further investigated. The 38-micron spatial resolution will allow to investigate in detail both the mineralogy of this sample and also at least some aspects related to the texture at the sub-mm scale. Moreover, additional analyses will be performed on a portion of this sample by means of coupled FTIR spectroscopy and mass spectrometry.

 

References: [1] Udry A. et al. JGR Planets 125 2020. [2] Treiman A H et al PSS, 48 1213 1230 2000 [3] Hicks L.J. et al. Geoc. Et Coscmoc. Acta, 136 194 210 2014. [4] Bishop J. L. et al. 80th Met. Soc. 6115 2017. [5] Coradini A. et al., Vol. 6, EPSC-DPS2011-1043, 2011. [6] De Angelis S. et al., Rev.Sci.Instr. 86, 093101, 2015. [7] De Sanctis M.C. et al., Space Sc. Rev., 163:329–369, 2011. [8] Klima R.L., et al., M&PS, 42, n.2, 235-253, 2007.

 

Acknowledgements: Scientific activities with SPIM are funded within the ExoMars program by the Italian Space Agency (ASI).

How to cite: De Angelis, S., Altieri, F., La Francesca, E., De Sanctis, M. C., Ferrari, M., Ammannito, E., Brossier, J., Bruschini, E., Formisano, M., Frigeri, A., and Trisic-Ponce, J.: Investigation of NWA13367 Martian Shergottite by means of VIS-IR imaging spectroscopy, EPSC-DPS Joint Meeting 2025, Helsinki, Finland, 7–13 Sep 2025, EPSC-DPS2025-1700, https://doi.org/10.5194/epsc-dps2025-1700, 2025.

10:06–10:18
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EPSC-DPS2025-1471
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ECP
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On-site presentation
Yan Zhuang, Hao Zhang, Pierre Beck, Sylvain Douté, Bernard Schmitt, and Yeming Liu

1. Introduction

The surfaces of many solar system airless bodies are covered by a layer of fine regolith formed by long-term space weathering processes, and traditional planetary remote sensing studies primarily focused on the research of optical properties of regolith layers. With the recent advances in space explorations, more disk-resolved spectral imagery data of the Moon, Mars, and asteroids have been returned and there is an increasing need to understand the reflectance properties of rocks and complex mixtures of rocks, fragments and powders (Pieters & Noble, 2016). The optical properties of rocks covered by fine dust layers can be very different from that of the layers and the underlying material (Kiddell et al. 2018; Johnson & Grundy, 2001; Johnson et al., 2002,). Therefore, it is important to understand the spectral, photometric and polarimetric properties of igneous rocks covered by powders with various thicknesses.

2. Samples and methods

We measured the reflectance of four igneous rocks (Trachyte, Peridotite, Diabase, Picrite Porphyrite, ranging from high to low reflectance) as bare slabs and slabs covered with powder layers of varying thicknesses (0.1 mm, 0.2 mm, 1 mm, and 2 mm) and particle sizes (0–45 µm, 90–125 µm).

We used two spectro-goniometric systems and one spectrometer to obtain the bidirectional reflectance spectra. CUG spectro-goniometric system: The emergence zenith angle varied from 0° to 70°, and the relative azimuth angle from 0° to 360° (Jiang et al., 2022). This configuration yields 121 viewing geometries for an incidence angle of 0° and 165 geometries for 55°. The spectral range covered is 0.35-2.1 µm. SHADOWS: We selected 15 specific wavelengths between 0.4 and 4.2 µm and collected 71 viewing geometries (Potin et al., 2018). SHINE spectrometer: This instrument measures spectra across a wavelength range of 0.35-4.2 µm with an incident angle of 30° and an emergency angle of 0° (Brissaud et al., 2004).

3. Result

Fig. 1 and Fig. 2 show the upper hemisphere reflectance and spectra of four rock slabs and the slab covered with varying powder layer thicknesses. The results demonstrate that rock slabs exhibit low reflectance and strong forward scattering, and even very thin dust layers (0.1mm) can significantly alter the overall reflectance and mask the strong forward scattering of rock slabs. Reflectance increases with powder thickness until reaching a "saturation thickness", after which further coating has little effect on reflectance spectra. Larger particles (90-125 µm) reach “saturation” faster than smaller ones (0-45 µm). Lower reflectance rocks and spectral regions are more susceptible to surface scattering effects than higher-reflectance rocks.

Fig. 3 displays the dependent of the phase angle on the spectral slope (0.6-1.8 µm) of the four rocks. It shows that rock slabs exhibit strong specular reflection and little phase reddening up in small phase angle, while powder-coated surfaces show a gradual and linear increase in spectral slope with phase angle. We analyzed the 2.7 µm hydration feature for Peridotite and the results show 2.7 µm hydration band decreases in strength with increasing phase angle and is weaker under strong specular reflection angle.

Using the Hapke two-layer model and Planet-GLLiM tool (Hapke, 2012; Douté et al., 2023), we retrieved the phase function parameters and optical constants of Peridotite, and reconstructed the spectra and bidirectional reflectance for bare and powder-coated slabs. Fig. 4 illustrates the dependence of reflectance on thickness, showing that reflectance increases exponentially with increasing optical thickness. We calculate the ratios of surface scattering to total scattering and retrieved the relationship of phase function parameters, indicate stronger surface scattering and forward scattering in bare rocks compared to powder-coated samples.

4. Conclusion:

We have measured the reflectance of four igneous rocks—Trachyte, Peridotite, Diabase, and Picrite Porphyrite—as bare slabs and as slabs coated with powder layers of four varying thicknesses and two particle sizes. We found that even very thin powder layers can significantly alter the reflectance and photometric behavior of rock surfaces. Reflectance increases with powder thickness until reaching a "saturation thickness", with larger particles reaching this threshold more quickly. And powder coatings reduce strong forward scattering. Bare rock slabs exhibit little phase reddening up in small phase angle, while powder-coated surfaces show a gradual and linear increase in spectral slope with phase angle. Modeling results reveal that reflectance grows exponentially with optical thickness, and that coated powder layers reduce surface scattering and weaken forward scattering behavior.

Fig. 1. Reflectance comparison of four rocks covered with different thicknesses of powder and bare rock slab. Purple: bare rock slab; Red: 0.1 mm powder layer coated; Orange: 0.2 mm; Blue: 1 mm; Dark blue: 2 mm.

Fig. 2. Reflectance spectra of the 4 igneous rocks and their powders in 2 size fractions. i = 0°, e = 30°.

Fig. 3. Phase angle dependent of the spectra l slope in the 0.6 to1.8 µm region of particle coated rock.

Fig. 4. The dependence of reflectance on optical thickness for Peridotite. (a) and (b) correspond to 0-45 µm size distribution, and (c) and (d) to 90-125 µm size distribution.

 

 

Reference:

Douté, S., Forbes, F., Borkowski, S., Heidmann, S. & Meyer, L. Massive analysis of multidimensional astrophysical data by inverse regression of physical models. (2023).

Hapke, B. Theory of Reflectance and Emittance Spectroscopy. (Cambridge University Press, 2012).

Johnson, J. R., Christensen, P. R. & Lucey, P. G. Dust coatings on basaltic rocks and implications for thermal infrared spectroscopy of Mars. J.‐Geophys.‐Res. 107, (2002).

Johnson, J. R. & Grundy, W. M. Visible/near‐infrared spectra and two‐layer modeling of palagonite‐coated basalts. Geophysical Research Letters 28, 2101–2104 (2001).

Jiang, T. et al. Bi-directional reflectance and polarization measurements of pulse-laser irradiated airless body analog materials. Icarus 331, 127–147 (2019).

Kiddell, C. B. et al. Spectral Reflectance of Powder Coatings on Carbonaceous Chondrite Slabs: Implications for Asteroid Regolith Observations. JGR Planets 123, 2803–2840 (2018).

Pieters, Carle M., and Sarah K. Noble. Space weathering on airless bodies. Journal of Geophysical Research: Planets 121.10 (2016): 1865-1884.

Potin, S. et al. SHADOWS: a spectro-gonio radiometer for bidirectional reflectance studies of dark meteorites and terrestrial analogs: design, calibrations, and performances on challenging surfaces. Appl. Opt. 57, 8279 (2018).

How to cite: Zhuang, Y., Zhang, H., Beck, P., Douté, S., Schmitt, B., and Liu, Y.: Effects of Powder Coatings on the Reflectance Spectra and Photometric Properties of Igneous Rocks, EPSC-DPS Joint Meeting 2025, Helsinki, Finland, 7–13 Sep 2025, EPSC-DPS2025-1471, https://doi.org/10.5194/epsc-dps2025-1471, 2025.

10:18–10:30
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EPSC-DPS2025-1581
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ECP
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On-site presentation
Eliana La Francesca, Simone De Angelis, Maria Cristina De Sanctis, Marco Ferrari, Eleonora Ammanito, Mauro Ciarniello, Gianrico Filacchione, and Andrea Raponi

Introduction:

Recent planetary missions such as Dawn at Ceres [1], Hayabusa2 at Ryugu [2], and OSIRIS-REx at Bennu [3]  have revealed the widespread occurrence of OH-bearing, hydrated, and ammonium-bearing minerals. Ammonia-rich compounds have also been identified on distant bodies including Pluto, Charon [4,5], and Umbriel [6], suggesting a broader presence of ammoniated materials in the outer solar system. These discoveries provide critical constraints on the origin and chemical evolution of planetary bodies.

Forthcoming instruments like the MWIR Imaging Spectrometer for Target-Asteroids (MIST-A) [7] on the Emirates Mission to the Asteroid Belt  (EMA)[8] are expected to provide valuable insights into the presence and distribution of these compounds in that region.

The detection and quantification of volatiles such as OH, H₂O, and NH₃ are fundamental for reconstructing the evolutionary history of planetary surfaces and subsurfaces with implications for astrobiology [9].

Estimating the abundance of these species provides critical constraints on (i) formation and accretion processes, (ii) their surface and subsurface distribution, and (iii) potential associations with possible tenuous exospheres. While laboratory reflectance studies quantifying H₂O content exist [10], relatively few have examined ammonium-bearing compounds (mainly in the VIS-NIR) [11–16], and even fewer have used mid-IR transmittance spectroscopy to determine NH₄⁺ concentrations [17]. This work focuses on quantifying ammonium abundance in controlled two-component mixtures via IR reflectance spectroscopy over the 1.4–11.5 μm range.

Experimental setup and Samples:

Measurements were performed in the 1.4–11.5 μm range using the CAPSULA setup at IAPS CLAB [18,19]. A Bruker INVENIO FTIR spectrometer equipped with a liquid nitrogen-cooled Mercury Cadmium Telluride (MCT) detector, operating at a spectral sampling of 0.13 nm, was employed. The internal SiC lamp of the FTIR system, suitable for mid-IR measurements, provided illumination. Light was transmitted through a CaF₂ viewport into a TVC chamber, where a system of mirrors collected the reflected signal. The measurement geometry was set to i= 45° and e = 0°.

The samples comprised binary mixtures of a synthetic ammonium salt and a second endmember. The considered Ammonium salts are: Ammpnium Sulfate, Ammonium chloride, and monoammonium phosphate. Unlike previous work focused on specific planetary analogues (e.g. Ceres [12,14]), the second component was selected based on its spectral properties—specifically, its flatness in spectral regions where ammonium features occur.

Two materials were chosen as second endmember: Glencoe Rhyolite (Scotland) and Magnetite, representing bright and dark endmembers respectively, both with grain sizes <50 µm. Mixtures were prepared by weight, varying the proportions of ammonium salt and the selected endmember.

An example of studied mixtures is reported in the following table.

Mix 1

Endmember 1

(Rhyolite)

Endmember 2

(NH4)2SO4

End1

100%

0%

Mix1-A

80%

20%

Mix1-B

60%

40%

Mix1-C

40%

60%

Mix1-D

20%

80%

End2

0%

100%

Results:  As an illustrative case, Figure 1 presents the reflectance spectra of mixtures of Glencoe Rhyolite and ammonium sulfate measured with CAPSULA.

Figure 1: Reflectance spectra of Glencoe Rhyolite and Ammonium Sulfate mixtures in air, spanning 1–11 μm. Data normalized at 1.45 μm. Red and blue lines represent the pure endmembers.

It is evident that rhyolite exhibits slight hydration, as indicated by the 3 μm absorption feature, along with several absorptions at longer wavelengths, notably the fundamental SiO₂ band complex near 8–9 μm [20], where the rhyolite background is flat, and there is minimal overlap with water absorptions.

However, it remains spectrally flat between 1–2.5 μm. In the first mixture (Mix 1-A), where ammonium sulfate constitutes 20% by weight (equivalent to 5% NH₄⁺ by weight in the mixture), ammonium absorption bands become clearly discernible. The black arrow in Fig. 1 indicates the increasing of NH4+ amount in the spectra from top to bottom. This effect is especially pronounced in the bands at 1.6 μm and 2.1 μm (Fig.2). This facilitates the identification and analysis of NH₄⁺ features.

 

Figure 2: Continuum-removed spectra of Glencoe Rhyolite and Ammonium Sulfate mixtures in air. The upper panel highlights NH₄⁺ vibrational mode 2𝜈3, while the lower panel shows additional NH₄⁺ features (𝜈2 + 𝜈3 and 𝜈3 + 𝜈4 vibrational modes) [12,16].

Figure 3 shows the correlation between NH₄⁺ abundance (wt%) and the corresponding spectral band area for three different mixtures of ammonium salts and rhyolite (Mix 1, Mix 2, and Mix 3). The observed positive linear trend indicates that increasing NH₄⁺ concentrations are associated with a proportional increase in the band area, suggesting a consistent and quantifiable spectral response to ammonium content within these mixtures. This relationship provides a basis for interpreting ammonium-related absorptions in planetary remote sensing datasets.

Figure 3: Correlation between NH₄⁺ abundance (wt%) and the corresponding spectral band area for three laboratory-prepared mixtures of ammonium salts with rhyolite (Mix 1, Mix 2, and Mix 3). Data points include 1σ uncertainties on both axes.

Future work: All mixtures will also be analysed in vacuum and heated to high temperature for volatile analysis by mass spectrometry. This process can be useful, particularly at 3 μm, to distinguish the contribution of water from that of ammonia. 

References: [1] De Sanctis M.C. et al., Nature Letter 528, 241-244, 2015. [2] Kitazato K., et al., Science, 364, 272-275, 2019. [3] Hamilton V.E., et al., Nature Astronomy, 2019. [4] Cook J.C., et al., Icarus 315 (2018) 30–45. [5] Cruikshank D.P. et al., 2019, Icarus, 330, 155-168. [6] Cartwright R.J. et al., The Planetary Science Journal, 4:42 (28pp), 2023. [7] Filacchione G., et al., ACM 2023 (LPI Contrib. No. 2851). [8] Al Mazmi et al., 2024, COSPAR, b1.1-0036. [9] Glavin, Daniel P., et al.  Nature Astronomy (2025): 1-12. [10] Milliken R.E.,  (2006). [11] Bishop, J. L., et al., PSS 50 (2002) 11-19. [12] Berg B. L., et al., Icarus 265 (2016) 218-237. [13] Ferrari M., et al., Icarus 321 (2019) 522-530. [14]Poch et al., Science 367, 1212 (2020). [15] De Angelis S., et al., JGR Planets, 126.5 (2021). [16] Fastelli M., et al., Icarus 382 (2022) 105055. [17] Busigny V. et al., American Mineralogist, Volume 89, pages 1625-1630 (2004). [18] De Angelis S., et al. (2022): 16, EPSC2022-540. [19] De Angelis S., et al., Memorie S.A.It, 2024. [20] Salisbury J.W., et al., Journal of Geophysical 94 (1989) 9192-9202.

Acknowledgments: This work has been funded by AMMONHIA (Abundance Mass spectrometry Measurements Of NH In Analogues materials) “Bando Ricerca Fondamentale  INAF 2023”.

The experimental setup used has been funded with the Agreement ASI-INAF n.2018-16-HH.0.

How to cite: La Francesca, E., De Angelis, S., De Sanctis, M. C., Ferrari, M., Ammanito, E., Ciarniello, M., Filacchione, G., and Raponi, A.:  IR Reflectance measurements and quantitative analysis of ammonium abundance in two-component mixtures , EPSC-DPS Joint Meeting 2025, Helsinki, Finland, 7–13 Sep 2025, EPSC-DPS2025-1581, https://doi.org/10.5194/epsc-dps2025-1581, 2025.

Orals FRI-OB3: Fri, 12 Sep, 11:00–12:30 | Room Mercury (Veranda 4)

Chairpersons: Alessandro Pisello, Giovanni Poggiali, Koki Yumoto
11:00–11:12
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EPSC-DPS2025-171
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ECP
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On-site presentation
William Burris, Mark Loeffler, and Stephen Tegler

To date, there have been no detections of solid phase O2 in interstellar space via its forbidden transition at 6.447𝜇m (1551 cm-1). However, with the new James Webb Space Telescope (JWST), detections of these types of species (homonuclear molecules) may be possible in the future. To assist future observing efforts, we have measured the band strength of the O2 absorption at 6.447𝜇m in different astrophysical ice environments. Specifically, our experiments focused on binary ice mixtures of O2 and H2O, CO2, or CO. We also studied whether varying the concentration of O2 and/or annealing the mixture had a significant effect on the measured band strength.  

 

These new band strength values will be important for any future observing campaign of solid phase O2, as they will enable future observers to estimate time-on-target requirements for a detection. Finally, in the event of a detection, these values will allow for the quantification of O2, or if not detected, they will allow scientists to place appropriate upper limits on its abundance. 

How to cite: Burris, W., Loeffler, M., and Tegler, S.: Infrared Band Strength of Molecular Oxygen in Astrophysical Ices, EPSC-DPS Joint Meeting 2025, Helsinki, Finland, 7–13 Sep 2025, EPSC-DPS2025-171, https://doi.org/10.5194/epsc-dps2025-171, 2025.

11:12–11:24
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EPSC-DPS2025-1720
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ECP
|
On-site presentation
Massimo Germanà, Adam Vyjidak, Giuseppe Antonio Baratta, Barbara Michela Giuliano, Carlotta Scirè, Tommaso Grassi, Pavol Jusko, Daniele Fulvio, Riccardo Giovanni Urso, Paola Caselli, and Maria Elisabetta Palumbo

Introduction

     Organic refractory materials are present in several Solar System small bodies, including comets and Trans Neptunian Objects (TNOs) [1, 2]. Recent observations by the JWST of TNOs reveal the presence of various compounds on their surfaces, including N2, CO and CH4 [3-5]. The icy surfaces of TNOs and comets in the Oort cloud are affected by energetic charged particles, that together with heating that bodies can experience in space determine the formation of organic refractory materials [6]. Experiments show that the irradiation of C-rich icy mixtures, followed by heating, determines the formation of organic refractory materials [7-9].

     High doses of irradiation to organic refractories lead to the formation of amorphous carbon (αC) [10-13]. Experiments also show that αC can form after ion bombardment of C-bearing ices [14]. Hence, the surface of outer Solar System bodies might contain αC. However, αC cannot be detected by IR spectroscopy. We thus use laboratory analogues of the refractory organics that could be present at the surface of TNOs and comets, namely organic refractory residues (ORRs), to study the formation of αC after their exposure to energetic processing.

     Samples are characterized by Raman spectroscopy, providing insights into the structural properties and degree of disorder of carbonaceous materials [15-17].

     Our aim is to shed light on the origins and properties of refractory carbon in Solar System primitive bodies. We also inform on the origin of refractory carbon in the cold and dense regions of the interstellar medium, e.g., the central regions of pre-stellar cores, where volatiles are frozen onto dust grains, just before forming protoplanetary disks. Their exposure to energetic processing and heating can thus occur.

 

Methods

     ORRs were produced at the Laboratory for Experimental Astrophysics at INAF-OACT (Catania, Italy), after the irradiation with 200 keV ions at 18 K and subsequent warm-up to room temperature of icy mixtures in a ultra-high vacuum chamber(P ≤ 10-9 mbar). ORRs differ in the initial icy mixture and/or irradiation conditions. The icy mixtures (consisting of N2, CH4 and CO) mimic the surface composition of TNOs and comets in the Oort cloud [18]. Once at room temperature, some samples were exposed to further bombardment with 200 keV ions.

     Raman spectra were acquired at the Center for Astrochemical Studies of the Max-Planck Institute for Extraterrestrial Physics (Garching, Germany) by means of a spectrometer equipped with a 488 nm laser. Several spots on each sample were probed with low laser power (P=0.1 mW), and further spectra were collected at increasing laser power.

 

Results 

      We searched for amorphous carbon (αC) by looking for its bands, the D (disorder) line at ~1360 cm-1 and the G (graphitic) line at ~1580 cm-1 [10] in our samples.  We reveal that icy mixtures exposed to low dose (~120 eV/16u) lead to the formation of ORRs that do not show any features attributed to αC  (Fig. 1, red curve). Contrariwise, ORRs which were further irradiated (up to relatively high doses) exhibit a clear αC band signature (hereafter we refer to these ORRs as αC-ORRs) as seen on the blue curve of Fig. 1.

     Since the profile of the αC band reflects the structural properties of the carbonaceous material, we have used a Lorentz + Breit-Wigner-Fano fit to obtain the parameters of D and G lines [19], which in turn inform on the dimension of the αC sp2 clusters (La). Samples analysed at a laser power of 0.1 mW show values of La ranging between 5-11 Å, meaning that sp2 clusters are relatively small and the degree of disorder is high. The distribution of fitting parameters suggests a dependence on the initial icy mixture of the αC-ORRs.

     Raman spectra of αC-ORRs acquired at increasing laser power (0.2-0.5 mW) exhibit significant annealing effects attributed to the graphitization of the αC structure: conversion from sp³ to sp² bonds takes place, La increases.      

Figure 1. Raman spectra of ORRs produced from N₂ : CH₄ : CO + 200 keV He⁺ up to 120 eV/16u. Red curve: as formed ORR showing only the high fluorescence continuum; blue curve αC-ORR further exposed to +200 keV He⁺ reveals the αC band.

Conclusions 

      We shed light on the properties of carbonaceous refractory materials possibly present at the surface of outer solar system bodies. Due to their remote location, the characterization of their composition is mainly achieved in the IR. However, our data shows that IR-inactive αC can form from the exposure of complex organics to the high extent of energetic processing suffered by icy surfaces.

 

 

Acknowledgements

     MG acknowledges the Società Italiana di Scienze Planetarie - Angioletta Coradini (SISP-AC) through the call “Bando per la mobilità di giovani ricercatori e dottorandi 2024” and the support of Max Planck Society and the CAS group at Max-Planck Institute for Extraterrestrial Physics. This work is supported by the Istituto Nazionale di Astrofisica (INAF) through the funds provided for the PhD in Physics, XXXIX cycle, Università degli Studi di Catania.

 

References

[1] Quirico E. et al. (2016), Icarus, 272, 32.

[2] Grundy W. M. et al. (2020), Science, 367, eaay3705.

[3] Pinilla-Alonso N. et al. (2024), Nat. Astron., 9, 230.

[4] Emery J. P. et al. (2024), Icarus, 414, 116017.

[5] Brunetto R. et al. (2025), ApjL, 982, L8.

[6] Urso R. G et al. (2020), A&A, 644, A115.

[7] Accolla M. et al. (2018), A&A, 620, A123.

[8] Baratta G. A. et al. (2019), Astrobiology, 19, 1018.

[9] Potapov A. et al. (2022), Apj, 935, 158.

[10] Baratta G. A. et al. (2004), J. Raman Spec., 35, 487.

[11] Palumbo M. E. et al., (2004), Adv. Space Res., 33, 49.

[12] Brunetto R. et al. (2009), Icarus200, 323.

[13] Strazzulla G. and Baratta G. A. (1992), A&A, 266, 434.

[14] Ferini G. et al. (2004), A&A, 414, 757.

[15] Rotundi A. et al. (2008), MaPS, 43, 367.

[16] Brunetto R. et al. (2011), Icarus, 212, 896.

[17] Bower D. M. et al. (2013), Astrobiology13, 103.

[18] Baratta G. A. et al. (2015), Planet. Space Sci., 118, 211.
[19] Ferrari A. C. and Robertson J. (2000), Phys. Rev. B, 61, 14095.

 

How to cite: Germanà, M., Vyjidak, A., Baratta, G. A., Giuliano, B. M., Scirè, C., Grassi, T., Jusko, P., Fulvio, D., Urso, R. G., Caselli, P., and Palumbo, M. E.: RAMAN ANALYSIS OF ORGANIC REFRACTORY MATERIALS AFTER ENERGETIC PROCESSING. IMPLICATIONS FOR COMETS AND TNOs., EPSC-DPS Joint Meeting 2025, Helsinki, Finland, 7–13 Sep 2025, EPSC-DPS2025-1720, https://doi.org/10.5194/epsc-dps2025-1720, 2025.

11:24–11:36
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EPSC-DPS2025-1366
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ECP
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On-site presentation
Lorenzo Rossi, Alessandro Frigeri, Francesca Altieri, and Maria Cristina De Sanctis

Rosalind Franklin’s drill
The Rosalind Franklin rover, scheduled for launch in 2028, will drill into the Martian ground in its quest to unravel the planet’s history and search for biomarkers. Equipped with a drilling system capable of reaching depths of up to two meters, it will record hyperspectral measurements along the borehole and collect samples for analysis with experiments within the body of the rover [1].

Drill telemetry analysis for subsurface investigation
To improve and extend the characterization of the subsurface, the instruments’ measurements can be complemented with information about the mechanical behaviour of drilled materials. While the rover’s science payload does not include any dedicated instrument for directly measuring rock mechanical properties, we can use the drill itself for this purpose: useful information can be retrieved from housekeeping telemetry data generated while drilling [2,3]. During its operation, the drill system records parameters useful for geotechnical characterization of the rocks, including temperature, force, torque, and speed readings.
To prepare for the scientific analyses and interpretations of these data, we are developing dedicated data analysis techniques and tools [3].

Developing an instrumented laboratory drill
The development of dedicated data analysis tools and techniques and their validation requires a reference dataset that encompasses a wide range of different drilling conditions and rock samples. So far, we’ve been using drill telemetry data recorded during drilling tests conducted with the rover GTM (Ground Test Model), an almost identical replica of the flight model rover. Further development of analysis techniques would greatly benefit form a larger and more varied reference dataset.
To build an additional, extensive reference dataset, we are developing an instrumented laboratory drill. This will allow us to easily test drilling operations in the lab and collect data on a variety of rock samples. This laboratory drill is equipped with sensors that will record a range of important quantities that are also reported in Rosalind Franklin’s drill telemetry and employed in our analyses.
This laboratory drill will help us improve our understanding of rock drilling and support the development of data analysis techniques. Data collected with it will complement telemetry data stemming from GTM drilling tests. It will contribute to expand the range of drilling scenarios in our reference dataset. We intend to use this data to improve and validate our analysis techniques and machine learning models. We will then work to adapt some of the best performing techniques to the specifics of Rosalind Franklin’s drill and employ them for the investigation of the Martian subsurface.

Design concept
The design of this first iteration of the laboratory drill does not aim to reproduce exactly the mechanics of the rover’s drill nor to exactly simulate drilling telemetry generated by the rover’s drilling system. Rather, our goal is to develop a simple and versatile laboratory instrument that can be easily adapted to various drilling scenarios.
The laboratory drill is powered by an electric motor coupled to a planetary gearhead. The motor also includes a rotary encoder for the precise measurement of its rotation speed by its control electronics. Drilling torque and vertical force are measured by two dedicated strain-gauge load cells. A linear encoder measures the vertical position of the drill with respect to its stationary frame as it slides on a linear rail. This will provide a measure of the drill tip depth and of the rate of penetration (ROP), an important drilling performance parameter.

Looking forward
The procurement of components needed to build the first iteration of the laboratory setup is currently underway. Once it is assembled and tested, it will be used on a variety of rock samples returned from geologic fieldwork, building a library of observation on rocks and soils with analogies in their composition or evolution to the rock we observe from remote sensing at the landing site. The resulting data will support the development of our data analysis techniques. Further evolutions of the instrument’s design will build on the experience gained with the first design and expand its capabilities and representativeness, with the goal of eventually resulting in a portable instrument that can also be used in the field.

References
[1]    Vago J.L. et al, Astrobiology, vol 17, n.6-7 (2017), https://doi.org/10.1089/ast.2016.1533
[2]    Altieri F. et al., Advances in Space Research (2023), https://doi.org/10.1016/j.asr.2023.01.044
[3]    Rossi L. et al., Proceedings of IAC2024, https://doi.org/10.52202/078357-0048

How to cite: Rossi, L., Frigeri, A., Altieri, F., and De Sanctis, M. C.: An Instrumented Laboratory Drill to Investigate Mechanical Properties of Rocks with Rover Drilling Systems, EPSC-DPS Joint Meeting 2025, Helsinki, Finland, 7–13 Sep 2025, EPSC-DPS2025-1366, https://doi.org/10.5194/epsc-dps2025-1366, 2025.

11:36–11:48
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EPSC-DPS2025-953
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On-site presentation
Fiona Thiessen, Michael T. Thorpe, Elliot Sefton-Nash, Andrea D. Harrington, Marine Ciocco, Agata Krzesinska, Stephanie Werner, Luke Griffiths, T. Dylan Mikesell, Alvin L. Smith, Lindsay E. Hays, and Gerhard Kminek

Introduction:  Samples collected by NASA’s Mars 2020 Perseverance rover that are intended for return to Earth would be analyzed based on the highest priority recommendations of the international science community. The samples collected at Jezero crater by Perseverance consist of a variety of rocks (e.g., sedimentary and volcanic), regolith, and atmospheric gas [1-4]. With each additional sample, the potential cache continues to become more scientifically valuable. Regardless of the additional samples, even the current suite of samples represents a scientifically return-worthy cache [5].

Before these precious samples are investigated in state-of-the-art laboratories on Earth, extensive testing of analogues is necessary to fully prepare for engineering, science, curation, and planetary protection needs. Therefore, multiple teams branching from the Mars Sample Return (MSR) Campaign Science Group (MCSG) have been chartered to strategically select natural samples from the field that best represent discrete components of the Jezero samples. Collectively, these samples make up the Analogue Sample Library (ASL), set up to support MSR, and jointly hosted by NASA and ESA. The ASL is designed to serve as a resource for preparations to receive and analyse returned samples and support the broader scientific community in research, communication and outreach. Samples in the ASL collection are curated at and distributed from the Natural History Museum in Oslo in collaboration with the University of Oslo (UiO). This activity is supported by the Norwegian Space Agency (NOSA) and ESA.

Current ASL Collection:  In late 2022 an external expert science group, the ‘Rock Sample Team’ was appointed by the MSR Joint Science Office for various project needs. They were tasked to identify terrestrial analogue sites for four different lithologies based on the samples placed in the first sample depot on Mars at Three Forks.

These samples include (letters correlate to Fig. 1): (A) holocrystalline basalts, both aphyric and plagioclase-phyric, from Oregon, USA, (B) carbonate cemented and (C) carbonate-gypsum cemented fine sandstones/siltstones from California, and (D) eolian volcanic sands from Iceland, and (E) olivine cumulates from Scotland. The Rock Sample Team solicited input from the community and developed an extensive list of potential analogues before narrowing down to five candidates [6]. With field teams built from both NASA and ESA representatives, local geologists, as well as members from the Mars 2020 Science team, the first samples for the ASL were collected during the field campaign 2023 (Fig. 1).

Figure 1. Map displaying the sites of the field campaign 2023 (red stars) and newly proposed field sites (yellow stars; [7]). Pictures from the field teams of each field site are shown in inserts A-E.

Allocation of analogue samples: On November 14th, 2024, the ASL was officially opened at the Natural History Museum, Oslo. Analogue samples can be requested from the ASL. Proposals for allocation are evaluated according to priority of the proposed activity, which are (1) preparatory work for sample receiving, (2) the scientific community, and (3) public relations and outreach. The sample allocation process is managed by the NASA-ESA MSR Analogue Sample Allocation Panel (ASAP, Fig.2). Requests for analogue samples can be made via a web-interface (sample request) and are processed in a timely manner. The ASL also includes comprehensive baseline sample characterization by the Norwegian Geotechnical Institute (NGI), with reports available to the community.

Figure 2. Organizational flowchart for ASL sample management from collection and sample characterization to allocation and curation [6,7].

Ongoing and future work:  The MCSG chartered a new sub-team, the MCSG Analogue Team, which is tasked to critically evaluate the current collection and identifying any areas that need to be supplemented. One of the first tasks of the Analogue Team was to reevaluate the sedimentary analogue samples and subsequently, two new field sites were identified in Italy and Iceland (Fig. 1) to collect (1) a sandstone with basaltic provenance and (2) sandstone to pebble conglomerates with an ultramafic provenance. These analogues will be collected during the 2025 field campaign, funded by ESA and NASA. Their addition to the ASL will make the analogue collection more comprehensive. The Analogue Team also plans to re-examine both the igneous and regolith sample analogs. Finally, the team plans to continuously build the ASL as the Perseverance rover continues to diversify its cache.

The ASL represents a key resource for the preparation to study returned samples from Mars, as it enables wide availability of terrestrial analogue samples that are strategically selected to best represent the properties of diverse Mars samples at Jezero crater and collected by the Perseverance Rover.

Acknowledgments: The authors would like to thank the members of the “Rock Sample Team” for their recommendations on terrestrial analogue sample. We also would like to thank the members of the field campaign 2023 for their effort to collect the analogue samples.

 Disclaimer: The decision to implement Mars Sample Return will not be finalized until NASA’s completion of the National Environmental Policy Act (NEPA) process. This document is being made available for informational purposes only.

 

How to cite: Thiessen, F., Thorpe, M. T., Sefton-Nash, E., Harrington, A. D., Ciocco, M., Krzesinska, A., Werner, S., Griffiths, L., Mikesell, T. D., Smith, A. L., Hays, L. E., and Kminek, G.: Mars Analogue Sample Library, EPSC-DPS Joint Meeting 2025, Helsinki, Finland, 7–13 Sep 2025, EPSC-DPS2025-953, https://doi.org/10.5194/epsc-dps2025-953, 2025.

11:48–12:00
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EPSC-DPS2025-1445
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ECP
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On-site presentation
Marine Ciocco, Agata Krzesinska, Stephanie C. Werner, Axel B. Müller, Sofia Julve-Gonzalez, Marco Veneranda, Guillermo Lopez-Reyes, Fiona Thiessen, Elliot Sefton-Nash, T. Dylan Mikesell, and Luke Griffiths

NASA-ESA Mars Analogue Sample Library (ASL) officially opened in 2024 at the Natural History Museum of Oslo. ASL aims to provide the scientific community with samples analogous to those sampled by Mars 2020 Perseverance in Jezero Crater during the Crater Floor and Delta Front campaigns.  The goal is to prepare for operations and research relating to Mars, particularly on the eventually returned samples of Mars Sample Return[1], as well as outreach activities.

To assess analogue fidelity [2,3] tests are needed: among others, extensive mineralogical, petrological, chemical and mechanical characterization. Furthermore, in order to facilitate the comparison between the martian samples and the terrestrial analogues, characterization of the analogues via in-situ techniques used onboard Mars2020 is necessary. This study aims to analyze the ASL analogues with Raman Spectroscopy and Laser Induced Breakdown Spectroscopy (LIBS).  Raman spectroscopy, in particular, has been a crucial tool in the detection of many minerals on Mars [4], while LIBS gives a first order indication of the sample geochemistry.

ASL includes five sites with two representative samples of Jezero crater floor, one regolith analogue, and two samples aiming to represent the delta sediments [5,6, https://www.mn.uio.no/geo/english/research/projects/msr-asl-analogue-sample-library/msr-asl/]. 

Olivine cumulates from the Isle of Rum (Scotland) share similarities with cumulates found in Séítah formation and corresponding Robine, Malay, Salette and Coulettes samples. Aphyric (HMA) and phyric (HMP) holocrystalline basalts from Hart Mountain (HM), Oregon, USA, are the selected analogues for Máaz formation (samples Montdenier, Montagnac, Ha'ahóni, Atsá). Basaltic lithic sand from Lambahraun (Iceland) is intended to emulate Martian regolith (samples Atmo Mountain and Crosswind Lake). Finally, sandstones were sampled at Salton Sea and Ridge Basin (California) in order to represent the Delta Front Skinner Ridge, Wildcat Ridge and Amalik formations (samples Hazeltop, Bearwallow, Skyland, Swift Run, Shuyak and Mageik).

 

SimulCam, the heavy-duty laboratory emulator supporting SuperCam science [7], has been used to collect coaligned, time-resolved Raman and LIBS analyses from ~3-5 cm bulk samples. For each sample, 5–10 spots have been analyzed at 2m distance to disclose the mineralogical and geochemical complexity of the materials. Additionally, thin sections have been prepared for EDX mapping to provide laboratory ground-truth for observations made by Raman and LIBS. These measurements complement the baseline laboratory characterisation, which includes X-ray diffraction, X-ray fluorescence, and measurements of calcium carbonate content, particle size distribution and shape.

 

In Rum, olivine is abundant, as in Séítah, evidenced by Raman spectrometry (Fig. 1): the distinct olivine doublet peak correlates with the Raman spectrum acquired by SuperCam on Dourbes. Furthemore, the olivines appear to chemically match estimations of the forsterite% for Séítah samples Salette and Coulettes [8], but look partially serpentinized, whereas no serpentine was detected in Séítah. Carbonates, widespread in Séítah, appear as up to 10% in Rum. Rum is a good textural analogue to Séítah, with olivine grains of the same size (1-3 mm) and similar poikilitic texture.

As a representative case study, spectroscopic analyses of Rum performed by SimulCam revealed elemental and molecular compositions similar to those of targets investigated by SuperCam at Séítah. In this context, the combined interpretation of LIBS and Raman features could be employed to develop and test methods for quantifying fayalite–forsterite ratios in olivines, a key focus of the ongoing work by the SuperCam science team.

Figure 1: Séítah Raman spectra at Dourbes abrasion patch in Brac outcrop (top), and Simulcam spectra of Rum (bottom), indicating the presence of the typical olivine doublet peaks (shaded area).

 

Basalts from Hart Mountain (Máaz analogues), are composed of plagioclase and pyroxene. Texturally, HMA samples are representative of the samples Montdenier and Montagnac. HMP presents a larger porphyric texture, though the plagioclase crystals are one order of magnitude too large compared to Ha'ahóni and Atsá.

Lambahraun sand is composed of basaltic grains close in size and composition to what has been observed in Crosswind Lake and Atmo Mountain. In particular, one of the aims of sampling a megaripple was to sample the <150 micron size range [9] to characterize the global regolith of Mars. Such small particles appear to constitute >20% of Lambahraun samples, making it a good engineering analogue. It is well-sorted, rather coincident with the moderately to well-sorted martian samples. Their grain shape is consistent both in sphericity and roundness.

The sandstones analogous to Delta Front rocks contain carbonate and/or sulfate cement in varying amounts, but their clastic material is predominantly quartz and feldspars, unlike basaltic grains on Mars. Texturally, Ridge Basin can be analogous to the well-sorted material of Shuyak and Mageik, as well as the carbonate-rich laminations of Skyland and Swift Run. Salton Sea appears richer in sulfates, while still containing carbonates, making its cement analogous to Bearwallow and Hazeltop cores.

 

ASL analogues are extensively tested to evaluate their relevance to mission science preparations. While laboratory analyses provide ground-truth characterization of the analogue material, evaluation of the analogues with SimulCam allows more direct comparison with data collected in situ on Mars. Furthermore, such results combined with extensive ongoing characterization of analogues via laboratory techniques can support interpretation of martian formations, as the results highlight capabilities and limitations of the Perseverance instruments in detecting and characterizing mineralogical and geochemical details of encountered rocks.

Disclaimer: The decision to implement Mars Sample Return will not be finalized until NASA’s completion of the National Environmental Policy Act (NEPA) process. This document is being made available for informational purposes only.

Acknowledgments: Curation of Mars ASL is financed by ESA and NoSA (PRODEX) project.

References: [1] Tait. K. et al. (2022) Astrobiology 22(S1), S-57 [2] Foucher F. et al. (2021) Planetary and Space Science, 197, 105162. [3] Thorpe M. T. et al. (2025) LPI Contributions, Abstract #2109. [4] Lopez-Reyes, G. et al. (2025) Authorea Preprints, ESS Open Archive [5]Thiessen F. et al. (2024) LPI Contributions 3036, Abstract #6173. [6] Thiessen F. et al. (2025) EPSC-DPS2025-953 [7] Manrique J. et al (2024) Advances in Space Research, 74(8), 3855-3876 [8] Beyssac O. et al (2023) Journal of Geophysical Research: Planets 128 (7), e2022JE007638 [9] Hausrath E. M. et al. (2025) Journal of Geophysical Research: Planets, 130(2), e2023JE008046.

 

How to cite: Ciocco, M., Krzesinska, A., Werner, S. C., Müller, A. B., Julve-Gonzalez, S., Veneranda, M., Lopez-Reyes, G., Thiessen, F., Sefton-Nash, E., Mikesell, T. D., and Griffiths, L.: Three Forks Depot Analogues in Mars Analogue Sample Library – Representativity Assessment via Raman and LIBS Spectroscopy , EPSC-DPS Joint Meeting 2025, Helsinki, Finland, 7–13 Sep 2025, EPSC-DPS2025-1445, https://doi.org/10.5194/epsc-dps2025-1445, 2025.

12:00–12:12
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EPSC-DPS2025-828
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ECP
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On-site presentation
Andrew Alberini and the rest of the team

To assess the astrobiological significance of Martian samples collected by NASA’s Mars 2020 Perseverance rover at Jezero crater, the primary criterion lies in identifying minerals with a high potential to preserve biosignatures and organic compounds. By abrading rock surfaces and analyzing the underlying material with its scientific payload, Perseverance examines their mineralogical and organic composition. The SHERLOC instrument [1], onboard Perseverance, found interesting Raman features in the organic spectral range, spatially co-located with sulfates in abrasion patches among the Jezero crater floor, likely originating from aromatic organic compounds [2], e.g. in the Polar bear spot on Quartier abrasion (Fig. 1).

Because of operational constraints, the abraded surfaces are left exposed to Martian environmental conditions for at least one Martian day (“1 sol,” equivalent to 24 hours and 38 minutes on Earth) before analysis with proximity science instruments. During this period, solar ultraviolet (UV) photons could modify or degrade potential organic matter within the abraded patches [3,4]. To shed light on the nature of these Raman features, it's crucial to assess whether aromatic organic compounds can be photostable under Martian-like UV irradiation for at least 1 sol and whether sulfates can play a photoprotective role towards them. In this study, we explored the molecular photostability by irradiating two carboxylic acids (phthalic acid and mellitic acid) that are metastable products of the generic oxidation of meteoritic organic compounds [5,6], and two PAHs (2,6-dihydroxynaphthalene and benzo[a]pyrene) that can be delivered by Interplanetary Dust Particles (IDPs) and (micro)meteorites [7,8]. Because of the sulfate spatially co-located Raman signals, the potential photoprotective effect of magnesium sulfate heptahydrated (epsomite), widespread at Jezero crater [9], is investigated. Therefore, we irradiated these organic molecules even when adsorbed or embedded on epsomite, and subsequently compared the results with those obtained from irradiation of the pure molecules. To simulate natural interactions in an early Martian aqueous environment, the Martian analog samples (molecule-mineral complexes) were prepared by suspending the mineral powder in an aqueous solution containing the molecule, followed by a desiccation process [10]. The Martian analog samples were characterized using Diffuse Reflectance Infrared Fourier Transform (DRIFT) collected by a Bruker VERTEX 70v FTIR interferometer to investigate molecule-mineral interactions. Subsequently, the irradiations were performed using a Newport Oriel 300W Xenon discharge lamp (spectral range 200-930 nm) interfaced with the Bruker VERTEX 70v interferometer allowing to study the kinetics of degradation live on the sample without removing it from the sample compartment. To estimate the organics Martian survivability, half-lifetimes were scaled on the Jezero Crater’s UV flux, calculated using the radiative transfer model COMIMART [12], which includes state-of-the-art dust radiative properties, and is fed with Mastcam-Z opacities[13]. The pure molecule irradiation shows half-lifetimes t1/2 between ~ 0.5 and 7 sols of their molecular structures, regarding mostly the COOH functional groups for the two carboxylic acids [14], CH groups for benzo[a]pyrene and OH/CH groups for 2,6-dihydroxynaphthalene (Figure 2).

On the other hand, when these organic compounds are adsorbed/embedded on epsomite, no significant degradation is observed during UV irradiation, suggesting a photoprotective behavior of the mineral. Finally, photoproducts were detected. These intriguing findings support the key role of sulfates in Martian organic preservation and suggest that SHERLOC Raman signals spatially co-located with sulfates could potentially originate from aromatic organic compounds. Additionally, the photo-protective properties of sulfates may explain why the strongest SHERLOC Raman signals have been observed in association with sulfates rather than other minerals with photocatalytic properties that may degrade organics prior to SHERLOC analysis. These limitations of in-situ investigations highlight the need for Mars Sample Return (MSR) to accurately evaluate the organic content of the Martian samples collected by Perseverance.

References: [1] Bhartia R. et al. (2021), Space Sci Rev 217, 58. [2] Sharma S. et al. (2023), Nature, 619(7971), 724-732. [3] Fornaro T. et al. (2018), Life, 8(4), 56. [4] Bernard S. et al. (2024), LPI, Pasadena, pp. 3068. [5] Benner S.A. et al. (2000), PNAS, 97(6) 2425-2430. [6] Millan M. et al. (2022), J Geophys Res Planets, 127. [7] Kopacz N. et al. (2023), Icarus, Volume 394. [8] Flynn, G. J. & Durda, D. D. (2004), Planet Space Sci. 52, 1129–1140. [9] Siljeström S. et al. (2024), J Geophys Res Planets, 129, 1. [10] Fornaro T. et al. (2020), Frontiers in Astronomy and Space Sciences, 7, 539289. [11] Patel M. R. (2002), Planet Space Sci. 50, 915–927. [12] Vicente-Retortillo Á. et al. (2015), J. Spac Weather Space Clim. 5. [13] Vicente-Retortillo Á. et al. (2024), Geophys Res Lett. 51. [14] Alberini A. et al. (2024), Sci Rep, 14, 1.

Acknowledgements: ASI/INAF Agreement 2023-3-HH.

How to cite: Alberini, A. and the rest of the team: The potential of hydrated magnesium sulfates to preserve organics on Mars: spectroscopic analysis under simulated Martian UV exposure , EPSC-DPS Joint Meeting 2025, Helsinki, Finland, 7–13 Sep 2025, EPSC-DPS2025-828, https://doi.org/10.5194/epsc-dps2025-828, 2025.

12:12–12:24
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EPSC-DPS2025-1634
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On-site presentation
John Robert Brucato, Teresa Fornaro, Cristina Garcia Florentino, Andrew Alberini, Sole Biancalani, Ophélie McIntosh, Francesco Renzi, and Ilaria Bergamo

The detection and identification of organic compounds on Mars is one of the main goals of the NASA Mars 2020 and ESA ExoMars exploration programs. It is therefore important to understand the environment in which organic matter evolves on the Martian surface. In particular, minerals may play a crucial role in the processes experienced by organic molecules on Mars, influencing their chemical evolution. The preservation state of organic molecules is often controlled by their interaction with the mineral phase in which they are embedded. Therefore, the detection of organic molecules on the Martian surface requires a complementary approach with the instruments on board the rovers. One aspect that is of great interest to the scientific community is the interaction between organic and inorganic matter. Martian rocks may, in fact, play multiple roles in both preserving organic molecules over time and, conversely, promoting their degradation. The thin Martian atmosphere allows ionizing particle and UV radiation to reach the surface, affecting the stability of organic compounds.

We know that in several paleoenvironments on Earth, the long-term preservation of terrestrial biosignatures has been attributed to sedimentary materials, particularly phosphates, silica, clays, carbonates and metalliferous materials. It is also thought that the most suitable conditions for the preservation of organic compounds on Mars are found in the subsurface, protected from radiation. To aid interpretation of the data that ExoMars/Rosalind Franklin rover will provide, we have begun a comprehensive investigation of the catalytic and protective properties of various Martian analogue minerals. However, it is not possible to simply classify Martian minerals as catalytic or protective, because the behaviour of minerals under Martian conditions depends strongly on the organic molecules involved and their specific interactions with the mineral surface sites. It is therefore important to study the response of specific molecule-mineral complexes to UV and ion irradiation. In this sense, and to maximise the chances of detecting organic compounds on Mars, it is crucial to study the effect of ionising radiation on organic compounds adsorbed in minerals that may represent Martian soils. This may also help in the identification of the molecules adsorbed on the minerals, and may also help in understanding the nature of the interactions between the mineral and the biomolecule to better understand the mechanisms involved in the preservation of biomolecules in different types of minerals against UV radiation. This is important for identifying mineral targets in Mars missions that are more likely to have preserved the organic molecules.

An important parameter affecting the way molecules interact with mineral surfaces is the acidity of the solution. The pH is responsible for the protonation state of the molecules and the charge of the mineral surface, and hence the molecule-mineral interactions and spectroscopic properties. Different possible pH-dependent protonation states can influence the nature of the binding of biomolecules to the mineral. It was observed that adenine was almost completely intercalated in the clay montmorillonite when adsorbed at acidic pH in the positively charged state, whereas almost no adenine was intercalated in the mineral when adsorbed at a pH where adenine was neutral. The same result was obtained by our group with L-histidine adsorbed in saponite, where the positively charged amino acid (acidic pH) is adsorbed in the interlayer by cation exchange, while the negatively charged amino acid (basic pH) is bound to the edge groups of the mineral. In addition, at basic pH, the organic molecules are rapidly desorbed and released from the interlayer of the mineral, which on Mars means greater exposure to Martian UV radiation due to the loss of mechanical shielding by the clay mineral.

We will show infrared and Raman spectroscopy of different classes of biomolecules, such as amino acids, nucleobases, fatty acids, PAHs adsorbed at variable pHs on clays, sulfates and phosphates, with the aim of obtaining a spectroscopic database that may be useful for correctly interpreting spectra collected on Mars. We will also present recent results on the preservation of biomolecules despite Martian chemical weathering by high-energy irradiation, which could be observed by analytical techniques on board the Rosalind Franklin rover.

How to cite: Brucato, J. R., Fornaro, T., Garcia Florentino, C., Alberini, A., Biancalani, S., McIntosh, O., Renzi, F., and Bergamo, I.: Stability of biomolecules under energetic processes on Mars, EPSC-DPS Joint Meeting 2025, Helsinki, Finland, 7–13 Sep 2025, EPSC-DPS2025-1634, https://doi.org/10.5194/epsc-dps2025-1634, 2025.

12:24–12:30

Posters: Tue, 9 Sep, 18:00–19:30 | Finlandia Hall foyer

Display time: Tue, 9 Sep, 08:30–19:30
F125
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EPSC-DPS2025-507
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ECP
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On-site presentation
Camilla Cioria, Jean-Philippe Perrillat, and Giuseppe Mitri

Under the reducing conditions of the inner region of stellar nebulae (Cartier and Wood, 2019), thermodynamic calculations have shown that rocky planetary mantles could be dominated by pyroxenes instead of olivine (Cioria et al., 2024). This mineralogical composition would have geodynamic implications such as low mantle viscosity and reduced solidus temperature compared to peridotitic mantles, as on Earth and Venus. In this preliminary work, we perform high pressure- temperature experiments in a Paris-Edinburgh press to investigate the subsolidus and melting phase relations of CB (Bencubbin like) bulk silicate composition at conditions corresponding to the crust- mantle interface and core-mantle boundary in Mercury. The objective is also to experimentally constrain and anchor the previous thermodynamic calculations of Cioria et al. (2024), focusing particularly on the mineral constituents of the crusts and mantles of reduced bodies.

Synthetic samples (CB1, CB2) have been prepared using the average bulk silicate fraction of CB chondrites as proposed by Malavergne et al. (2010) and Brown and Elkins-Tanton (2008). Starting powders were prepared from high purity oxide mixtures, according to Cioria et al., 2024 Model 2, with 67.9 wt% SiO2, 0.2 wt% TiO2, 3.1 wt% Al2O3, 1.1 wt% Cr2O3, 0.3 wt% FeO, 0.1 wt% MnO, 25 wt% MgO, 2.6 wt% CaO, 0.1 wt% Na2O and 0.01 wt% K2O. Paris-Edinburgh press experiments were conducted in standard 10/3.5mm (sample CB1) and 7/2.4 mm (sample CB2) cell assemblies, using boron epoxy transmitting medium and graphite furnace heaters. Powders were loaded into a double capsule with a graphite inner wall and boron nitride outer wall. Samples were subjected to 2 GPa–1300K (CB1) and 5 GPa–1700K (CB2), for durations ranging from 3hours to 24 hours, respectively; in order to achieve equilibrium conditions. These P-T ranges are the same used in Cioria et al. (2024) as boundary conditions in thermodynamic modelling. Recovered charges were mounted, polished, and optical observations shown that run-products have coarse-grained texture, where large, euhedral crystals are embedded in a fine-grained matrix. The detailed analysis is under progress and scanning electron microscopy (SEM) are planned to characterize textures, phase assemblages, major element distributions, and constrain oxygen fugacity conditions - fO2 - using relevant phase equilibria buffers. Results will be compared with thermodynamic models (Cioria et al., 2024) and experimental studies by Berthet et al., (2009) and Boujibaar et al. (2025), to understand any differences between products derived from CB and EH compositions, respectively. Further works will involve synthesis under larger P-T conditions as well as investigating sulfur-bearing compositions under various oxygen fugacity conditions in order to assess the building materials and differentiation processes of Mercury-like planets and small bodies in the early solar system.

Acknowledgments

G.M. and C.C. acknowledge support from the Italian Space Agency (2022-16-HH.1-2024). 

References

Berthet, S., Malavergne, V., & Righter, K. (2009). Melting of the Indarch meteorite (EH4 chondrite) at 1 GPa and variable oxygen fugacity: Implications for early planetary differentiation processes. GCA73(20), 6402-6420.

Boujibar, A., Righter, K., Fontaine, E., Collinet, M., Lambart, S., Nittler, L. R., & Pando, K. M. (2025).  A Pyroxenite mantle on Mercury? Experimental insights from enstatite chondrite melting at pressures up to 5 GPa. Icarus, 116602.

Brown, S., & Elkins‐Tanton, L. T. (2009). Compositions of Mercury's earliest crust from magma ocean models. EPSL , 286(3-4), 446-455.

Cartier, C., & Wood, B. J. (2019).  The role of reducing conditions in building Mercury. Elements,15(1), 39-45.

Cioria, C., Mitri, G., Connolly, J. A. D., Perrillat, J.-P., & Saracino, F. (2024).  Mantle mineralogy of reduced sub‐Earths exoplanets and exo‐Mercuries.  JGR:Planets, 129.

Connolly, J. A. D. (1990). Multivariable phase diagrams; an algorithm based on generalized thermodynamics. Am. J. Sci., 290(6), 666- 718.

Malavergne, V., Toplis, M. J., Berthet, S., & Jones, J. (2010). Highly reducing conditions during core formation on Mercury: Implications for internal structure and the origin of a magnetic field . Icarus, 206(1), 199–209.

 

How to cite: Cioria, C., Perrillat, J.-P., and Mitri, G.: Exploring Pyroxene-Rich Planetary Mantles: Experimental Insights from CB Chondrites  , EPSC-DPS Joint Meeting 2025, Helsinki, Finland, 7–13 Sep 2025, EPSC-DPS2025-507, https://doi.org/10.5194/epsc-dps2025-507, 2025.

F126
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EPSC-DPS2025-1619
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ECP
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On-site presentation
Fernando Alberquilla, Leire Coloma, Julene Aramendia, Irantzu Martínez Arakarazo, Iratxe Población, Gorka Arana, Kepa Castro, and Juan Manuel Madariaga

The fusion crust of meteorites is a thin, thermally altered surface layer formed during atmospheric entry. In stony meteorites, this layer typically comprises olivine, silicate glass, wüstite, and other iron oxides from the magnetite series, and generally does not exceed 1–2 mm in thickness. The meteorite NWA 10495, discovered in southern Morocco in 2015, is classified as a lunar feldspathic breccia. This specimen comprises several brown-gray stones with a total mass of 15.6 kg and according to the Meteoritical Society, it lacks a fusion crust. All pieces display a fine-grained texture, with larger white clasts visible within a dark gray matrix [1,2]. For this study, 2 grams of the NWA 10495 meteorite were analyzed to perform a multianalytical characterization of its primary mineral phases and secondary alteration products, aiming to determine the presence or absence of a fusion crust. For elemental characterization, a Bruker M4 TORNADO (Bruker Nano GmbH, Germany) X-ray fluorescence spectrometer was used. For the molecular characterization, the equipment used was an inVia confocal micro-Raman instrument (Renishaw, UK), provided with 532, 633 and 785 nm excitation lasers and a Peltier-cooled charge-coupled device detector. The instrument is coupled to a Leica DMLM microscope (Bradford, UK) and has different lenses (5x, 20x, 50x and 100x) for the visualization and focusing of the sample. To obtain Raman images, the high-resolution StreamLine technology (Renishaw) and the map image acquisition tools were used. The measurement was made using 532 and 785 nm excitation laser with 5% laser power and 50x or 100x lenses. The measurement conditions were 5–15 s of exposure time, 1 or 2 accumulations and a spatial resolution of 0.5–0.75 μm depending on the laser and the objective used. The results obtained through µ-EDXRF (Figure. 1) have shown that the outer part of the meteorite exhibits a significantly higher silicon (Si) content when compared to the data from the inner parts of the meteorite, where the Si content decreases and is replaced by other elements, such as calcium (Ca) and iron (Fe), which become more abundant.

Figure. 1 µ-EDXRF results obtained from the inner part (upper)  and the outer part (bottom) of the meteorite NWA 10495.

Regarding the results obtained through Raman spectroscopy, it was difficult to assign specific bands in the outer regions of the meteorite due to the high fluorescence associated with each spectrum. This is a common occurrence in the analysis of volcanic glasses or fusion crusts. Nonetheless, some main mineral phases such us piroxene and secondary alteration phases are identifiable, such as calcite (CaCO₃), which is the main alteration mineral observed in NWA 10495.

The inner area of the meteorite, in contrast, exhibits a wide mineralogical diversity. As shown in Figure 2, calcite stands out as a prominent phase. Although it is presumably a secondary alteration product and not native to the lunar surface, its distribution throughout the meteorite is evident, as nearly all the analyzed spectra show characteristic signals of this mineral at 153, 281, 714, and 1086 cm⁻¹. Another secondary alteration phase identified is barite (BaSO4), characterized by its main Raman band at 988 cm⁻¹. Regarding the primary mineralogy, plagioclase ((Na,Ca)(Si,Al)3O8) with main bands at 486, 504 cm-1  is notably abundant, which is consistent with the classification of the sample as a feldspathic breccia. Other commonly observed minerals include Ti-rich hematite, Fe2O3 (672 cm-1), augite-type pyroxene ((Ca,Mg,Fe)2(Si,Al)2O6), and olivine ((Mg,Fe)2SiO4).

Figure. 2 Raman spectroscopy results obtained in the inner part of the meteorite

It seems obvious that at least this small fragment of the meteorite has been affected by terrestrial alteration processes, as evidenced by the detection of calcite or barite within it. However, if we look at Figure 3, although there are concentrations or hotspots of elements that could be associated with further alteration—such as Cl or Mn—others, such as Fe, Ti, Si, or K, are more likely related to a fusion crust.

Figure. 3 µ-EDXRF image highlighting the signal intensity of elements such as Si, Fe, Mn, Cl, K, and Ti in the outer crust of the meteorite

Potassium is particularly interesting in this context because the heterogeneous enrichment in potassium (on the exterior and not the interior), together with the detection of shifted feldspar bands, stands as strong evidence for the presence of  high-pressure feldspar phases such as maskelynite. The formation of maskelynite  (Figure. 4) is linked to melting followed by rapid quenching under high pressure. It is important to note that when maskelynite coexists with any crystalline phases in the area sampled by the excitation laser beam, the Raman signal from maskelynite tends to be masked (Figure. 4) by the spectral background of the crystalline phases and is difficult to extract [3].

Figure. 4 Image obtained through Raman spectroscopy highlighting the presence of feldspars altered under high pressure and temperature.

In conclusion, the results suggest that an external fusion crust may indeed be present on the NWA 10495 meteorite, contrary to previous assumptions. Raman spectroscopy and µ-EDXRF analyses have revealed clear mineralogical differences between the interior and exterior surfaces. These include the identification of high-pressure, high-temperature minerals typically associated with fusion processes, as well as elevated concentrations of elements such as Si and K, commonly found in glassy materials within fusion crusts of other meteorites.

Acknowledgements: Work supported through the PAMMAT project (Grant No. PID2022-142750OB-I00), funded by the Spanish Agency for Research (through the Spanish Ministry of Science and Innovation, MCIN, and the European Regional Development Fund, FEDER).

 

References:

[1] Korotev, R. L., & Irving, A. J. (2021). Lunar meteorites from northern Africa. Meteoritics & Planetary Science56(2), 206-240.

[2] Bouvier, A., Gattacceca, J., Grossman, J., & Metzler, K. (2017). The meteoritical bulletin, No. 105. Meteoritics & Planetary Science52(11), 2411-2411.

[3] Wang, A., Kuebler, K., Jolliff, B., & Haskin, L. A. (2004). Mineralogy of a Martian meteorite as determined by Raman spectroscopy. Journal of Raman Spectroscopy35(6), 504-514.

How to cite: Alberquilla, F., Coloma, L., Aramendia, J., Martínez Arakarazo, I., Población, I., Arana, G., Castro, K., and Madariaga, J. M.: High-Resolution Spectroscopy Analysis of the Lunar Meteorite NWA 10495: Comparative Study of Fusion Crust and inner zone Alterations, EPSC-DPS Joint Meeting 2025, Helsinki, Finland, 7–13 Sep 2025, EPSC-DPS2025-1619, https://doi.org/10.5194/epsc-dps2025-1619, 2025.

F127
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EPSC-DPS2025-494
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On-site presentation
Anna Galiano, Fabrizio Dirri, Marco Ferrari, Cristian Carli, Marianna Angrisani, Ernesto Palomba, Elisabetta De Angelis, and Lavinia Arpaia

Introduction

The surface of Mercury as seen by the MESSENGER spacecraft is mostly featureless in the Visible-to-Near-Infrared range (VIS-to-NIR) [1-4], except for some restricted locations [5,6], making it difficult to constrain its mineralogical composition. However, ground-based measurements of the planet in the Mid-Infrared (MIR) range suggest the occurrence of labradorite (a plagioclase with Anorthite 70-50) and enstatite (a Mg-rich orthopyroxene) on its surface [7], also supported by spectral modelling [8]. Thus, it was suggested that enstatite-rich meteorites (aubrites) could be potential analogues of Mercury [9], generally made of iron-free enstatite, sulfides and metallic iron [10]. 

The spectrometer MASCS [11] and the camera MDIS [12] onboard MESSENGER provided featureless spectra with a red slope on the entire surface of Mercury and with an average reflectance level of 4% in the VIS range [13]. Given the close vicinity to the Sun and the lack of an atmosphere, Mercury is constantly exposed to Space Weathering (SpWe) processes such as solar wind irradiation and micro-meteoritic impacts, which can alter the spectral properties of its surface, producing a reddening and darkening, as well as removing absorption bands [14,15,4].

SpWe processes are usually reproduced in the laboratory with ion irradiation and laser bombardment. In this work, we irradiated the enstatite achondrite meteorite NWA 13278 with He+ to simulate solar wind irradiation on Mercury’s surface. Spectral variations caused by the experiment are analysed.

 

NWA 13278

The sample was purchased with dimensions of 8.0×5.0 cm, and a small piece of 1.0×0.9 cm and a thickness of 0.3 cm was obtained for the investigationFrom a petrological analysis, the sample is a breccia with large clasts of enstatite and forsterite (Mg-rich olivine) within a finer-grained matrix composed of enstatite, sodic plagioclase (albite), Cr-troilite, niningerite and Si-bearing kamacite. Diopside (clinopyroxene) is also present through geochemical analysis [16]. The mineralogical composition of Mercury, as spectrally modelled by [17], is quite similar, including orthopyroxene, olivine, Mg-rich clinopyroxene, Na-rich plagioclase, orthoclase, and Fe-Ti agglutinic glasses.

 

Ion irradiation experiment and spectral acquisition

The sample was irradiated in vacuum (pressures of 10-7 mbar) at the Ion and Energetic Neutral Atoms (I-ENA) facility with a beam of 4.5 keV He+ ions. The beam spot size was around 2.5 mm in diameter (Fig.1). Full details of the I-ENA facility can be found in the abstract in the same session (Richards, G., 2025, Planetary space weather experiments at the I-ENA facility, EPSC-DPS Joint Meeting 2025).  After about 40 hours of irradiation, the maximum fluence reached was 4×1014 ions/cm2.

Several reflectance spectra in the VIS-NIR and MIR range of the virgin and processed sample were acquired in the irradiated area to evaluate spectral variations. Average spectra are then obtained. The VIS-NIR spectra were acquired at “SLAB” (Spectroscopy Laboratory), while the MIR data were obtained at “SPARK LAB” (Space Rocks Key Analysis), both at IAPS-INAF.

The VIS-NIR bidirectional reflectance spectra (i=30°, e=0°)  cover the 0.4-2.5 µm spectral range with a spectral resolution of 3 nm in the VIS range and 10 nm in the NIR one. The spot of the acquisition is 6 mm. The MIR spectra (i=0°) acquired in diffused reflectance cover the 3-14 µm spectral range with a spectral resolution of 4 cm-1 and a spot of 2.5 mm.

 

 

Results

The irradiated sample shows a spectral brightening and a slight bluing in the VIS range with respect to the spectrum of the virgin one, and a spectral reddening in the NIR range (Fig. 2). The reflectance at 0.55 µm increases from 0.124 to 0.128 and the VIS slope in the 0.5-0.8 µm range, estimated as in [13], changes from -0.38 to -0.39 µm-1. The NIR slope estimated as a linear fit in the 0.8-1.2 µm range reddens from -0.24 to -0.20 µm-1.

 

The MIR spectrum of the meteorite shows Reststrahlen peaks at ∼8.6 µm, ∼9.0 µm and ∼10.6 µm (due to plagioclase), ∼9.3 µm, ∼10.4 µm and ∼11.6 µm (diopside), ∼9.8 µm and ∼11.1 µm (enstatite), ∼10.2 µm (due to the combination of the peaks of enstatite and plagioclase) (Fig.3). The Christiansen Feature is at 7.60 µm, coherent with plagioclase. After irradiation, the strongest peaks at ∼9.0 µm and ∼9.3 µm shift longwards of about 20 nm, following previous experiments [18,19], while a shift of 30 nm is observed for the peaks at ∼10.4 µm, ∼10.6 µm, and ∼11.1 µm. The other peaks show either a shift toward shorter wavelengths or no variation in their position.

Discussion and future works

The irradiation experiment performed on the NWA 13278 aimed to simulate the solar wind irradiation on Mercury’s surface. The spectral reddening in the NIR range caused by the He+ exposition is coherent with the spectral behaviour observed on Mercury, where older and more degraded terrains are spectrally redder than younger ones [1, 20]. Anyway, the spectrum of the irradiated meteorite shows a blue spectral slope, conversely to Mercury’s spectra. It is worth noting that we simulated an exposure to SpWe of about a few hundred years, thus we reproduced the onset of spectral degradation. To better reproduce hermean spectra, we will perform a laser bombardment to simulate the effects caused by micro-meteoritic impacts.

 

References

[1] Robinson et al., Science 321 (2008). [2] Murchie et al., Science 321 (2008). [3] Denevi et al., Science 324 (2009). [4] Blewett et al., EPSL 285 (2009). [5] Vilas et al., Geophys. Res. Lett. 43 (2016). [6] Lucchetti et al., JGR: Planets 123 (2018). [7] Sprague and Rousch, Icarus 133 (1998). [8] Warell and Blewett, Icarus 168 (2004). [9] Burbine et al., LPI 1097 (2001). [10] Watters 10th LPSC (1979). [11] McClintock and Lankton SSR 131 (2007).  [12] Hawkins et al., SSR 131 (2007).  [13] Galiano et al, Icarus 388 (2022).  [14] Hapke, JGR 106 (2001).[15] Brunetto and Strazzulla, Icarus 179 (2005). [16] Gattacceca et al., MAPS 56 (2021). [17] Warell et al., Icarus 209 (2010) [18] Brunetto et al., PSS 158 (2018). [19] Lantz et al., Icarus 285 (2017).  [20] Domingue et al. SSR 181 (2014).

 

Acknowledgements

The measurements described are part of the “SIMILIS” project, in the outcome of "Mini Grants INAF 2023”.

How to cite: Galiano, A., Dirri, F., Ferrari, M., Carli, C., Angrisani, M., Palomba, E., De Angelis, E., and Arpaia, L.: Space Weathering simulation on the Aubrite meteorite NWA 13278, putative analogue of Mercury, EPSC-DPS Joint Meeting 2025, Helsinki, Finland, 7–13 Sep 2025, EPSC-DPS2025-494, https://doi.org/10.5194/epsc-dps2025-494, 2025.

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EPSC-DPS2025-2034
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On-site presentation
Alessandro Pisello, Maximiliano Fastelli, Enrico Scricciolo, Gabriele Scognamiglio, Marco Baroni, Alessandro Musu, Paola Comodi, Massimiliano Porreca, Diego Perugini, and Angelo Zinzi

Magmatism and volcanism are key processes that shaped the surface of rocky planets in the Solar System, and understanding how magmatism occurred on these planets is essential to reconstruct their geological histories.  It is very likely that volcanic terrains on planetary surfaces are covered by products that have a porphyric, aphanitic or hyalocrystalline texture, in which crystalline phases represent only a fraction of the rocks that are mainly composed by amorphous materials such as glasses.

Remote investigation of planetary surfaces combines geomorphological analysis with spectral data. Regarding the latter, the interpretation of spectral information from planetary terrains needs to be based on the comparison with reference material.

Up to now, libraries and  repositories are mostly report information about so-called planetary analogues consisting of crystalline materials rather than amorphous products. This happens because of the lack of spectral features of amorphous products. However, a the presence of amorphous material together with crystalline phases deeply influence the spectral response of the latter [1].

For this reason, the Petro-Volcanology Research Group at the University of Perugia started to build up a spectral database of volcanic rocks, both natural and synthetic, to understand how and how much are crystalline and amorphous products influencing each other in determining the spectral response of a rock/terrain. In this work we report the spectral characterization of various products within two ranges: Visible and Near Infrared (VNIR) and Mid-Infrared (MIR).

The accounted products consist of:

- Synthetic silicate glasses with wide range of chemical composition [2,3]

- Synthetic planetary analogues consisting of rocky materials containing both amorphous and crystalline products [4]

- Natural volcanic rocks

The overall analysis of the spectral response shows that, within the MIR, it is relatively easy to link the wavelength position of well-known spectral features (Christiansen feature, Reststrahlen Bands, Transparency features) to the silica content of the product itself, no matter which crystalline phases are present within the rock. This finding is of pivotal importance since the determination of silica content is fundamental for a characterization of volcanic products.

On the other hand, investigations and analyses on VNIR spectra show that the interpretation within such is more complicated. Indeed, a small presence of Iron-bearing crystals can deeply influence the VNIR spectrum. However, some constrains can be build using empirical parameters and machine-learning approaches.

All the spectra produced and published by our research group is or will be made available to everyone, open-source, within the platform hosted by ASI-SSDC (www.ssdc.asi.it/rockspectra/), making it possible for scientist from all-over the world to integrate such data in other researches or to directly compare planetary spectra to laboratory data [4].

[1]  Horgan, B. H., Cloutis, E. A., Mann, P., & Bell III, J. F. (2014). Near-infrared spectra of ferrous mineral mixtures and methods for their identification in planetary surface spectra. Icarus234, 132-154.
[2] Pisello, A., Ferrari, M., De Angelis, S., Vetere, F. P., Porreca, M., Stefani, S., & Perugini, D. (2022). Reflectance of silicate glasses in the mid-infrared region (MIR): Implications for planetary research. Icarus388, 115222.
[3] Pisello, A., De Angelis, S., Ferrari, M., Porreca, M., Vetere, F. P., Behrens, H., ... & Perugini, D. (2022). Visible and near-InfraRed (VNIR) reflectance of silicate glasses: Characterization of a featureless spectrum and implications for planetary geology. Icarus374, 114801.
[4] Pisello, A., Zinzi, A., Bisolfati, M., Porreca, M., & Perugini, D. (2022). A new spectral database for silicate glasses: a fundamental resource to interpret characteristics of volcanic terrains on planetary bodies (No. EPSC2022-539). Copernicus Meetings.

How to cite: Pisello, A., Fastelli, M., Scricciolo, E., Scognamiglio, G., Baroni, M., Musu, A., Comodi, P., Porreca, M., Perugini, D., and Zinzi, A.: The interaction of crystalline and amorphous phases in the determination of VNIR and MIR  spectral signatures: insights from the PVRG rock spectra database, EPSC-DPS Joint Meeting 2025, Helsinki, Finland, 7–13 Sep 2025, EPSC-DPS2025-2034, https://doi.org/10.5194/epsc-dps2025-2034, 2025.

F129
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EPSC-DPS2025-1534
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On-site presentation
Baptiste Gaudart, Océane Barraud, Bernard Charlier, Olivier Namur, Greta Lamers, Alessandro Maturilli, and Solmaz Adeli

Introduction

Mercury, the closest planet to the Sun, has been studied by two NASA missions: Mariner 10 and MESSENGER (Mercury Surface, Space Environment, Geochemistry, and Ranging). They provided much information about the surface of the planet including the unique surface composition—characterized by a strong depletion in iron for example—and the identification of distinct regions with varying chemical compositions. However, one remaining question about Mercury is the mineralogical composition of its surface. Visible to near-infrared observations from the Mercury Atmospheric and Surface Composition Spectrometer (MASCS) aboard MESSENGER lack absorption features of mafic minerals. One hypothesis for the absence of spectral signatures typically associated with mafic minerals is the low abundance of FeO [1]. Furthermore, Mercury's complex geological history, involving extensive volcanic activity, impact melting, and intense space weathering, likely resulted in the production of substantial amounts of glass at the surface, which may significantly influence the planet's spectral properties [2]. The ESA’s BepiColombo mission, launched in 2018, will soon be in its polar orbit around Mercury. Two key instruments will help characterize the surface mineralogy of the planet: MERTIS (Mercury radiometer and thermal infrared spectrometer), a radiometer and thermal infrared spectrometer operating between 7 and 14 µm and SIMBIO-SYS (Spectrometers and Imagers for MPO BepiColombo Integrated Observatory System), a high-resolution camera, a stereo camera and a near infrared hyperspectral imager operating between 0.4 and 2 µm. The aim of this study is to spectrally characterize glassy synthetic analogs with compositions similar to the five main geochemical regions of Mercury. This work is done at the Planetary Spectroscopy Laboratory (PSL) of the German Aerospace Center (DLR), Berlin. The spectral measurements will be compared to MASCS data and used for the interpretation of SIMBIO-SYS and MERTIS data. Thus, it will be possible to identify the effect of volcanic glass and their specific compositions characterized by a range of MgO content and low FeO.

Samples

The samples used in this study have been synthesized at the University of Liège by mixing high purity oxides and melting them in a Platinum crucible at 1500°C for 1 hour. The silicate melts were quenched in water to produce glass beads, similar to the volcanic glass expected on Mercury. The compositions are analogs to five hermean regions [3]: the Low-Mg Northern Volcanic Plains (Low-Mg-NVP), the High-Mg Northern Volcanic Plains (High-Mg NVP), the Smooth Plains, High-Mg Province and the Intermediate Terrains (ICP-HCT). The geochemical compositions of the samples are given in Table 1. In order to investigate the effect of glass particle size, each sample has been crushed in two different grain sizes: <125 µm  and 125-250 µm, thus a total of 10 samples have been measured.

Table 1: Selected chemical compositions of glassy analogues (in wt%) [3].

Region

SiO2

Al2O3

MgO

CaO

Na2O

Total

Low-Mg NVP

63.36

14.40

10.21

5.78

6.25

100.00

Smooth Plains

59.90

16.03

11.40

7.35

5.32

100.00

High-Mg NVP

60.43

12.31

16.89

6.44

3.92

99.99

ICT HCT

55.76

12.70

21.73

5.70

4.11

100.00

High-Mg Province

55.82

7.05

26.80

7.14

3.19

100.00

 

Experimental procedure

Firstly, the bidirectional reflectance of the samples has been measured in a range of ultraviolet (UV) to the mid-infrared (MIR) to cover the wavelength domains of MESSENGER’s (0.3 to 1.45 µm) and BepiColombo’s instruments (0.4 to 2 µm and 7 to 14 µm). Several illumination conditions and viewing geometries have been used to obtain bidirectional reflectance spectra in the same conditions of MASCS and SIMBIO-SYS observations. The reflectance measurements were supplemented with hemispherical reflectance data acquired in the MIR domain. Then, the samples have been heated up at temperatures from 250°C to 450°C to simulate the surface temperature of Mercury, and measure the emissivity every 50°C in the MIR - spectral range of the MERTIS instrument. After heating the samples, reflectance measurements in the UV to MIR were acquired again, to investigate the effect of the heating at Mercury’s day-side temperature. All the measurements have been performed under vacuum to simulate Mercury’s surface conditions. 

Preliminary results

After calibrating and merging the different wavelengths for the bidirectional reflectance, we obtained the spectra shown in Figure 1. A decrease of reflectance is visible when the phase angle increases before and after heating. After heating, the sample ICP-HCT shows an increase of the reflectance in the visible to NIR and a decrease of the hemispherical reflectance in the MIR spectral domain. In the MIR, the sample exhibits a strong Christiansen Feature (CF) - reflectance minimum - at around 8.25 µm. Calibration and processing of the emissivity measurement data are currently in progress.

Figure 1 : (a) Bidirectional reflectance of ICP-HCT (125-250 µm) before heating (solid line) and after heating (dashed line) at 3 different geometries in the UV, visible and near-infrared. (b) Hemispherical reflectance of the same sample before and after heating in the MIR spectral domain. 

Conclusion

In this study we measured unique samples simulating volcanic glass of different geochemical regions of Mercury. We obtained the reflectance of the samples before and after heating at Mercury’s day-side temperature, through different illumination and viewing geometries, in a wavelength range covering the range of both MESSENGER’s and BepiColombo’s instruments. Emissivity spectra were also completed while heating the samples to simulate the temperature of Mercury’s surface.The measurements will be compared to MASCS/MESSENGER observations and will be used for the interpretation of SIMBIO-SYS and MERTIS observations by the BepiColombo spacecraft.

References

1. Murchie, S. L., et al. (2015). Icarus, 254, 287-305.

2. Pisello, A., et al. (2022). Icarus, 388, 115222.

3. Namur, O. & Charlier, B. Nat. Geosci. 10, 9–13 (2017). 

How to cite: Gaudart, B., Barraud, O., Charlier, B., Namur, O., Lamers, G., Maturilli, A., and Adeli, S.: Spectral analysis of silicate glasses analog of Mercury’s geochemical terrains and comparison with MESSENGER and BepiColombo data, EPSC-DPS Joint Meeting 2025, Helsinki, Finland, 7–13 Sep 2025, EPSC-DPS2025-1534, https://doi.org/10.5194/epsc-dps2025-1534, 2025.

F130
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EPSC-DPS2025-671
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On-site presentation
Alice Amsili, Naomi Murdoch, Panos Delton, and Cecilia Da Silva Alves

Many celestial bodies in our Solar System, such as the Moon, Mars and small bodies, are covered with a layer of regolith. Numerous current and upcoming space missions aim to interact with these surfaces such as the IDEFIX rover of the Martian Moons eXploration (MMX) mission [1] and the Hera mission [2]. Some instruments, such as the instrument InSight HP³ mole, have even failed to perform as expected [3], highlighting the importance of understanding the geotechnical behavior of regolith surfaces. Due to the limited accessibility and high cost of in situ missions, laboratory experiments using regolith simulants are crucial for the preparation of surface operations like landing, mobility, and sampling. Different extraterrestrials simulants have been developed and characterized regarding the mineralogical, granulometric and some geotechnical properties [e.g., 4-7]. Here we present the results of additional characterisation experiments focussing on the dynamic angle of repose and the cohesive properties of the simulants. A rotating drum experiment has been developed to measure bulk properties of different planetary simulants in low consolidation conditions. The setup is presented in Figure 1. The simulant is placed in a cylinder container of  4 cm diameter and 5 cm depth so that the container is half full with the granular material. Two PMMA windows are mounted on the front and back of the container, to be able to see through the system. The sample container is attached to a drive shaft which allows it to rotate around its axis. A CCD camera (mvBlueFox-120aG) is fixed facing the front window to image the granular material. An LED panel illuminates the experiment from behind allowing a shadometry image analysis to be performed. The rotational speed of the motor is controlled by an Arduino card. The gear ratio between the motor and the container allows it to rotate between 10 and 70 rotations per minute (RPM).

Figure 1: The rotating drum experiment at ISAE-SUPAERO.

The motor rotational speed is varied and 10 images are taken for each speed with a frame rate of 20 Hz. A binarization of the image is performed followed by an edge detection which automatically detects the surface of the material. This process is shown in Figure 2 for glass beads at two different rotational speeds. It is performed on the 10 images, and for each rotational speed, as illustrated in Figure 3.

Figure 2: Surface detection for glass beads at two different rotational speeds.

Figure 3: Surface profiles for 10 images at different rotational speeds for glass beads.

By measuring the surface slope close to the center of the drum, the dynamic angle of repose for each rotational speed can be determined. This result is presented in Figure 4 for three different granular materials: quartz sand with a mean particle diameter of 500 µm, glass beads with a diameter between 90 and 150 µm and Mars Global (MGS-1) High-Fidelity Martian Regolith Simulant. 

Figure 4: Dynamic angle of repose as a function of the rotational speed. The error bars represent the standard deviation of the angle of repose measured in 10 different images at each rotation speed.

This experimental set-up also allows for a characterisation of the cohesive properties of the granular material. The rugosity of the surface at each rotational speed can be used to compute the cohesive index, an adimensional number directly linked to the total cohesive force [8]. This gives a comparative measurement of the cohesion of the different simulants.

In summary, we have developed a rotating drum experiment to characterise different planetary simulants. Two main material parameters can be extracted: a cohesive index, which is an adimensional number directly linked to the total cohesive forces, and the dynamic angle of repose. The set-up has already been tested with three different materials (glass beads, quartz sand and Mars Global (MGS-1) High-Fidelity Martian Regolith Simulant). The results of the rotating drum characterisation of the Exolith planetary simulants - Lunar Highlands (LHS-1) High-Fidelity Regolith Simulant, Lunar Mare (LMS-1) High-Fidelity Regolith Simulant, Carbonaceous Chondrite (CI-E) High-Fidelity Asteroid Regolith Simulant and Carbonaceous Chondrite (CM-E) High-Fidelity Asteroid Regolith Simulant - will be presented during the conference.

References:

[1] Michel, Patrick, et al. "The MMX rover: performing in situ surface investigations on Phobos." earth, planets and space 74 (2022): 1-14.

[2] Michel, Patrick et al. (2022). The ESA Hera mission: Detailed Characterization of the DART Impact Outcome and the Binary Asteroid (65803) Didymos. The Planetary Science Journal, 3:160.

[3] Spohn, Tilman, et al. "The InSight-HP3 mole on Mars: Lessons learned from attempts to penetrate to depth in the Martian soil." Advances in Space Research 69.8 (2022): 3140-3163.

[4] Long-Fox, Jared M., et al. "Geomechanical properties of lunar regolith simulants LHS-1 and LMS-1." Advances in Space Research 71.12 (2023): 5400-5412

[5] Cannon, Kevin M., et al. "Mars global simulant MGS-1: A Rocknest-based open standard for basaltic martian regolith simulants." Icarus 317 (2019): 470-478

[6] Yin et al., “Shear Properties of LHS-1 and LMS-1 Lunar Regolith Simulants”. Planetary and Space Science 2023, 226, 105630. https://doi.org/10.1016/j.pss.2022.105630.

[7] Just, G. H.et al., “Geotechnical Characterisation of Two New Low-Fidelity Lunar Regolith Analogues (UoM-B and UoM-W) for Use in Large-Scale Engineering Experiments”. Acta Astronautica 2020, 173, 414–424. https://doi.org/10.1016/j.actaastro.2020.04.025.

[8] Neveu, A., F. Francqui, and Geoffroy Lumay. "Measuring powder flow properties in a rotating drum." Measurement 200 (2022): 111548

Acknowledgements

This project is carried out with the support of the European Research Council (ERC) GRAVITE project (Grant Agreement N°1087060), and from CNES in the context of the Hera mission and the MMX rover/wheelcams.

 

How to cite: Amsili, A., Murdoch, N., Delton, P., and Da Silva Alves, C.: Characterisation of planetary simulants using a rotating drum experiment, EPSC-DPS Joint Meeting 2025, Helsinki, Finland, 7–13 Sep 2025, EPSC-DPS2025-671, https://doi.org/10.5194/epsc-dps2025-671, 2025.

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EPSC-DPS2025-1244
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ECP
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On-site presentation
Thilo Witzel, Rok Šeško, and Philipp Reiss

Introduction

A good understanding of the properties of water-ice and regolith mixtures is of paramount importance to support the development of upcoming scientific missions to the Moon and for future in-situ resource utilization (ISRU). Although water was already detected on the Moon by remote sensing observations and in impact ejecta (Colaprete et al. 2010), ground truth based on in-situ measurements is still missing. Water is a valuable resource for both human and robotic space exploration as it can be used as a propellant to fuel rockets or consumable for astronauts. Here, we present the development of a dusty thermal vacuum chamber (DTVC) at the Technical University of Munich (TUM) that will be used to qualify instrumentation developed for future Moon missions and to thermal ice extraction in relevant environments ( mbar, 150K).

Experiment Description

The state-of-the-art facility can reach vacuum levels down to  mbar. To prevent sublimation of ice particles, the regolith sample is cooled by a laboratory thermostat to a minimum temperature of 150 K. The cold plate can host a variety of sample geometries up to a size of 590 mm x 240 mm x150 mm (Figure 1). As the cooling system does not rely on consumables like liquid Nitrogen, the sample cooling can theoretically be sustained for several days.

Figure 1: The cold plate of the experiment with different regolith containers.

The samples can be illuminated by a calibrated halogen lamp with a light power of up to 50 W in the visible range. The position of the collimated light beam (Ø 50mm) is controlled by a movable mirror (see Figure 2). This allows for a maximum illuminated sample region with a diameter of 275 mm. The resulting temperature distribution in the sample is measured by sensors inside the sample as well as an infrared camera.

Figure 2: Overview of the vacuum chamber with illumination (marked in red) and ice retrieval (marked in pink) sections. A zoomed view on the mirror assembly indicates the position control of the mirror.

Planned Experimental Campaigns

In the near future, several novel experiments are planned to use this DTVC setup:

Investigation of Solar Heating for Thermal Ice Extraction:

As part of the EIC pathfinder project Ice2Thrust, this experiment will study the heat distribution in response to solar surface heating and the interaction of water vapor with a cold trap in close vicinity to the surface. The illumination can provide light power up to 20 solar constants, which allows an investigation of various surface power densities on the temperature distribution and water sublimation rates. A separate assembly is mounted on the side of the main chamber to retrieve the ice collected on the cold plate with a linear feed-through. It can be isolated with gate valves, allowing the pressurization and subsequent liquefaction of the collected water ice. The extracted liquid water will be fed to an electrolyser and subsequently be split into Hydrogen and Oxygen to generate thrust in a chemical thruster. This experiment will serve as the world’s first ISRU end-to-end demonstration from extraction up to utilization.

Qualification of Sensors for Water Ice Detection on the Moon:

TUM is developing several permittivity sensor for the detection of water on the lunar surface. These sensors measure the water content by detecting changes in the electric permittivity of the lunar surface via electrodes in direct contact with the soil (Gscheidle et al. 2024). The RPS sensor suite currently developed for ESA uses electrodes mounted on a rover wheel and will undergo development and qualification testing in the DTVC. As part of another development for ESA, an instrumented drill for volatiles and water ice prospecting will also be tested in the DTVC (Biswas et al. 2020).

As the interaction of ice, rocks, and sunlight is also relevant in cometary research (Kreuzig et al. 2021, Knoop et al. 2024), the DTVC facility can also be used to study related physical phenomena relevant to other icy moons and comets.

Investigation and Development of Dust-resistant Mechanisms:

Lunar and planetary regolith are composed of abrasive particles in several size ranges which can significantly impact the lifetime of space mechanisms. Qualification and test of mechanisms in a relevant environment is crucial to ensure proper lifetime on the lunar surface. The DTVC offers this test capability and will also be used to qualify a newly developed slip ring within the RPS project funded by ESA (Sesko et al., 2025).

Conclusion

The DTVC facility is crucial for advancing lunar exploration and ISRU in ongoing research projects. By enabling experiments on water-ice and regolith mixtures, it supports the development of key technologies for detecting lunar water, thermal ice extraction, and durable instrument components. These efforts are essential for the success of future lunar and planetary science missions and developments leading to the utilization of lunar resources.

References

Colaprete, A., et al. (2010). Detection of Water in the LCROSS Ejecta Plume. In Science (Vol. 330, Issue 6003, pp. 463–468). American Association for the Advancement of Science (AAAS). https://doi.org/10.1126/science.1186986

Kreuzig, C., et al. (2021). The CoPhyLab comet-simulation chamber. In Review of Scientific Instruments (Vol. 92, Issue 11). AIP Publishing. https://doi.org/10.1063/5.0057030

Knoop, C., et al. (2024). Experimental results from the CoPhyLab -Detection of the influences of surface structureson particle ejection in comet-simulationexperiments. Copernicus GmbH. https://doi.org/10.5194/epsc2024-499

Sesko, R., et al. (2025) A dust-tolerant slip ring for Lunar rover wheel-mounted permittivity sensors, accepted talk at European Space Mechanisms and Tribology Symposium, Lausanne, Switzerland

Biswas, J., et al. (2020). Searching for potential ice-rich mining sites on the Moon with the Lunar Volatiles Scout. In Planetary and Space Science (Vol. 181, p. 104826). Elsevier BV. https://doi.org/10.1016/j.pss.2019.104826

Gscheidle, C., et al. (2024). Permittivity sensor development for lunar and planetary surface exploration. In Frontiers in Space Technologies (Vol. 4). Frontiers Media SA. https://doi.org/10.3389/frspt.2023.1303180

Acknowledgements

The authors gratefully acknowledge the financial support of the European Union (GA number 101161690) for the project Ice2Thrust (S4I2T)

How to cite: Witzel, T., Šeško, R., and Reiss, P.: Experimental Investigation of Regolith-Ice Mixtures under Cryogenic Vacuum Conditions for Lunar and Planetary Exploration, EPSC-DPS Joint Meeting 2025, Helsinki, Finland, 7–13 Sep 2025, EPSC-DPS2025-1244, https://doi.org/10.5194/epsc-dps2025-1244, 2025.

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EPSC-DPS2025-1298
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ECP
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On-site presentation
Grace Richards, Alessandro Brin, Elisabetta De Angelis, Rosanna Rispoli, Martina Moroni, Roberto Sordini, Luca Colasanti, Nello Vertolli, Fabrizio Nuccilli, Anna Milillo, Alessandro Mura, Stefano Orsini, Stefano Massetti, and Cristina Leto

Introduction

The Ion and Energetic Neutral Atom (I-ENA) beam facility at INAF-IAPS provides a unique platform to investigate the interaction of modifiable ion and neutral beams with a wide range of samples and detectors [1, 2]. For over two decades, this facility has supported studies on the interaction of the solar wind with planetary environments, with particular emphasis on ENA detection and charge exchange processes. Recently, the scientific focus has been related to backscattered and sputtered particle yields, as well as exosphere refilling processes [3, 4]. These efforts have contributed to the characterisation, testing, and calibration of the SERENA particle packed of the cornerstone space mission, BepiColombo, to Mercury [5]. Today, the I-ENA facility supports active space missions (e.g., BepiColombo/SERENA/ELENA), early-phase instrument developments (e.g., SWEATERS [6]), and testing campaigns for materials, detectors, and subsystems, particularly in the context of low-energy (0.5–5 keV) interaction processes.

 

I-ENA facility

The I-ENA laboratory includes two high vacuum chambers (10-7 mbar), each with a respective ion source. The first chamber is equipped with a He+/Ar ion source (Penning-type cold cathode) with an energy range of 0.5-5 keV, and is capable of producing fluences of 1014 ions/cm2 over a 12 hr irradiation period. This source can be modulated in intensity using various pinholes and an Einzel lens system. ENAs may be generated using a charge exchange cell. Within the chamber, there is a translation-rotation stage, to move samples horizontally, vertically, and rotate them through 360°. This chamber is currently equipped with a Quadrupole Mass Spectrometer (QMS), with a mass range up to 200 u and a sensitivity down to partial pressures of 10-14 mbar. The QMS is used for residual gas measurements and to investigate volatile species within the chamber.  An image and schematic of this chamber is shown in Figure 1.

Figure 1. One of the I-ENA high vacuum chambers, and schematic of the set up.

The second, newest chamber hosts a higher intensity He+/Ar source, capable of producing beams with fluences of 1018 ions/cm2 over a 12 hr irradiation period. Consequently, this beam is more suited to experiments requiring higher fluences to replicate geological timescales on planetary bodies. The chamber is also within a clean (ISO 7) environment, suitable for testing instrumentation for space applications.   

 

Experiments

The I-ENA laboratory facilitates calibrations of particle detectors and controlled experiments using ion/neutral beams to irradiate diverse surface analogues for investigating planetary space weather. A core activity of the lab has been the development and testing of space instrumentation. Notably, ELENA (Emitted Low-Energy and Neutral Atoms), part of the SERENA suite onboard BepiColombo, was developed, tested, and calibrated at I-ENA and the University of Bern. ELENA detects backscattered ENAs as well as magnetospheric and solar wind ions in the 10 eV–5 keV energy range. The ELENA Flight Spare (FS) is still housed in the lab and will be used in upcoming experiments to investigate ion-surface interactions with Mercury analogues. These studies aim to provide ground truth for interpreting data collected by BepiColombo.

The I-ENA lab team is currently expanding its capabilities to establish an irradiation facility for analogue testing. These experiments are designed to investigate irradiation-driven processes, building on our expertise in planetary space weather. By collaborating with external facilities that specialise in sample analysis, we aim to study the coupled exosphere–magnetosphere–surface system as a whole. Current experiments include collaborations within INAF, for example irradiating the enstatite achondrite meteorite, NWA 13278, using a He beam of 4.5 keV to simulate the solar wind irradiating Mercury’s surface. Full details of this experiment can be found in the abstract in this session (Galiano, A., et al. (2025). Space weathering simulation on the Aubrite meteorite NWA 13278, putative analogue of Mercury. EPSC-DPS Joint Meeting 2025). Current work involves investigating release processes on different materials using the QMS, and using the ELENA FS to investigate backscattering processes of the solar wind, in collaboration with other BepiColombo teams [7].

 

Acknowledgements: This Activity is supported by ASI contract SERENA/BepiColombo Fase E.

 

References

[1] De Angelis, E., et al. (2009). A facility to study the particles released by ion-sputtering process. European Planetary Science Congress (EPSC), Potsdam.

[2] De Angelis, E., et al. (2024). Accelerated ion-ENA beam for planetary space weather. Congresso Nazionale di Scienze Planetarie (CNSP), Bormio.

[3] Milillo, A., et al. (2005). Surface-Exosphere-Magnetosphere System of Mercury. Space Science Reviews, 117, 397–443. https://doi.org/10.1007/s11214-005-3593-z

[4] Mura, A., et al. (2006). Neutral Atom Emission from Mercury. Advances in Geosciences, 3. https://doi.org/10.1142/5913-vol3

[5] Orsini, S., et al. (2021). SERENA: Particle Instrument Suite for Determining the Sun–Mercury Interaction from BepiColombo. Space Science Reviews, 217, 19. https://doi.org/10.1007/s11214-021-00801-9

[6] De Angelis, E., et al. (2022). An innovative ENA instrument for space weather monitoring: SWEATERS (Space WEATher ENA Radiation Sensors) project. 44th COSPAR Scientific Assembly.

[7] Barraud, O., et al. (2025). Mercury-Y Lab: A scientific rehearsal for future BepiColombo observations. Lunar and Planetary Science Conference (LPSC).

How to cite: Richards, G., Brin, A., De Angelis, E., Rispoli, R., Moroni, M., Sordini, R., Colasanti, L., Vertolli, N., Nuccilli, F., Milillo, A., Mura, A., Orsini, S., Massetti, S., and Leto, C.: Planetary space weather experiments at the I-ENA facility at INAF-IAPS in Rome, EPSC-DPS Joint Meeting 2025, Helsinki, Finland, 7–13 Sep 2025, EPSC-DPS2025-1298, https://doi.org/10.5194/epsc-dps2025-1298, 2025.

F133
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EPSC-DPS2025-1513
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On-site presentation
Riccardo Giovanni Urso, Giuseppe Antonio Baratta, Giulia Alemanno, Paola Caselli, Daniele Fulvio, Massimo Germanà, Barbara Michela Giuliano, Joern Helbert, Alessandro Maturilli, Maria Elisabetta Palumbo, and Carlotta Scirè

Introduction
Complex organic matter revealed in primitive small bodies shows evidences of early origins from physico-chemical processes taking place in the interstellar medium (ISM) and in the protosolar cloud [1, 2]. In this regard, a relevant contribution to the formation of organic molecules is expected from the exposure of simple H-, C-, N-, and O-bearing ISM ices to low-energy Galactic cosmic rays (GCR) [3, 4]. In the further stages of the Solar System formation, the diffusion and desorption of most volatile species from processed ices, possibly supported by their heating, lead to the production of complex refractory organics [5]. Later on, significant changes are expected to take place in the protoplanetary disk, where thermal processing to high temperatures can determine the formation of amorphous carbon [6] and the loss of astrobiologically-relevant compounds possibly present in pristine organic matter.

We simulate in the laboratory the formation of complex organic matter from the exposure of laboratory analogues of ISM ices to energetic charged particles, their subsequent heating to room temperature to form organic refractory residues (ORRs), and their further thermal processing to higher temperatures, with the aim to shed light on the alteration of pristine complex organic matter.

Methods
Ice mixtures containing (i) H2O, CH3OH, NH3, and (ii) CO, CH4, and N2 are exposed to 200 keV H+ and He+ ions, respectively, at the Laboratory for Experimental Astrophysics (LASp) at INAF-Osservatorio Astrofisico di Catania (Italy). Ices are deposited in an ultra-high vacuum chamber (P ≤10-9 mbar) at low temperature (18 K) on MgF2 inert substrates. After the ion bombardment, ices are warmed up to 300 K, leading to the formation of complex refractory organic matter [4]. These materials, named organic refractory residues (ORRs), are considered analogues of the pristine complex organic matter that can form in space. Thus, their characterization allows us to shed light on the properties of pristine organics, including the presence of compounds relevant in astrobiology [7].

ORRs then undergo thermal annealing by means of a vacuum (P≤10-2 mbar) oven available at the Planetary Spectroscopy Laboratory (PSL) at the DLR Berlin. The annealing is performed with a constant heating rate of 3 K min-1 and up to about 970 K.

During the experiments, we use Fourier-transform Infrared Spectroscopy (FT-IR) in the mid-IR and in transmittance mode to monitor the changes induced by ion bombardment and thermal annealing.

We also analyze ORRs by means of Raman spectrometers equipped with 532 and 488 nm excitation lasers available at LASp and at the Max-Planck-Institut für Extraterrestrische Physik, respectively, to shed light on the presence and properties of amorphous carbon.

Results & Discussion
The mid-IR spectra of the icy mixtures deposited at 18 K show the typical absorption of the deposited species. During the ion bombardment, we observe a decrease in the band area of the features attributed to the deposited species and the appearance of new IR bands due to the formation of new molecular species in the processed ices. The warm-up to room temperature determines further spectral changes induced by the desorption of volatile species and the formation of new compounds. At room temperature, we observe the IR spectrum of ORRs, with the most intense absorption feature centered at about 6 µm that includes the contributions from C=C, C=O, and C=N bearing compounds. The Raman spectra of these samples only show a strong fluorescence that is due to the presence of H bonded in the C-rich matrix. During thermal annealing, IR spectra acquired at increasing temperature show  the severe variation in the profile of all the IR features, with their intensity decreasing following a linear trend. IR absorption bands are observed up to about 700 K. ORRs annealed up to 970 K do not show any IR absorption feature, although their Raman spectra show the presence of the typical features associated with amorphous carbon, that is, the D and G bands at about 1360 and 1590 cm-1, respectively.

 Conclusions
Our experiments allow us to simulate the origin of pristine organic materials and to characterize their evolution in protoplanetary disks. The analysis of annealed ORRs provides information on the spectral changes induced by heating. In the IR spectra, we observe the ORR’s 6 µm feature up to about 700 K, while at higher temperature (973 K) we observe the presence of amorphous carbon, an IR inactive material that in our samples is revealed only by means of Raman spectroscopy. We use our data to shed light on the evolution of organic matter in protoplanetary disks and on how thermal annealing can determine the present physico-chemical properties of organics trapped in meteorites.

Acknowledgements
This work is supported by  the Istituto Nazionale di Astrofisica (INAF) through the grant Organic Refractories Sustaining microOrganisms - ORSO, CUP C63C23001250005 and through the grant “Misure in riflettanza di campioni extraterrestri e analoghi di superfici planetarie”, CUP C63C24001150005.

 

References

[1] Encrenaz, T., Puget, J. L., & D’Hendecourt, L. 1991, Space Sci. Rev., 56, 83

[2] Oba, Y., Takano, Y., Dworkin, J. P., & Naraoka, H. 2023, Nature Communications, 14, 3107

[3] Palumbo, M. E., Ferini, G., & Baratta, G. A. 2004, Advances in Space Research, 33, 49

[4] Urso, R. G., Hénault, E., Brunetto, R., et al. 2022, A&A, 668, A169

[5] Mispelaer, F., Theulé, P., Aouididi, H., et al. 2013, A&A, 555, A13

[6] Gail, H- P., Trieloff, M., A&A, 606, A16

[7] Baratta, G. A., Accolla, M., Chaput, D. et al. 2019, Astrobiology, 19, 8

How to cite: Urso, R. G., Baratta, G. A., Alemanno, G., Caselli, P., Fulvio, D., Germanà, M., Giuliano, B. M., Helbert, J., Maturilli, A., Palumbo, M. E., and Scirè, C.: The role of thermal processing in the alteration of complex organic matter, EPSC-DPS Joint Meeting 2025, Helsinki, Finland, 7–13 Sep 2025, EPSC-DPS2025-1513, https://doi.org/10.5194/epsc-dps2025-1513, 2025.

F134
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EPSC-DPS2025-293
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Virtual presentation
Jonathan Merrison, Jens Jacob Iversen, and Keld Rasmussen

Abstract

This unique and now improved planetary simulation facility is capable of re-creating extreme Terrestrial, Martian and now Lunar-like environments. It has been supported by various EU networking activities including Europlanet 2024 RI and continuing through the Europlanet Society. This facility is also used by ESA and NASA and has recently become an ESA Ground Based Facility making it possible to apply for funding from ESA to access this facility for Space related research projects (up to 50keuros) [1].

1  Europlanet Transnational Access

 

This environmental simulator facility is utilized for a broad range of research programs including; the study of other planets (such as Mars), for recreating extreme terrestrial environments, or in specific investigations involving aerosols and other forms of Aeolian particulate transport. The facility has been involved in the Europlanet 2024 Research Infrastructure through which a trans-national access program has allowed numerous research groups access to this facility. Some selected recent projects are listed below;

  • Sand transport and ripples on Mars [3,7]
  • Dust aerosols at low pressure. [2,6]
  • Polar CO2 ice on Mars (USA) [5]
  • LIBS system on Mars2020 (ISAE France) [4]
  • In-situ utilization on Mars2020 and dust loading. Imperial College UK [8]

 

These activities continue through the Europlanet Society pilot trans-national access scheme.

Other activities include the development, testing and calibration of sensor and planetary lander systems, both for ESA and NASA. Testing for missions ExoMars 2020 and Mars Perseverance were carried out.

Figure 1 The main Planetary Simulation Facility [1-8], guests carrying out a Europlanet2022RI funded experiment involving sand transport under Martian and terrestrial conditions [3] 2022.

2 Design and operation

 

The simulator consists of a 35m3 environmental (thermal-vacuum) chamber within which a re-circulating wind tunnel is housed. The wind is generated by a set of two fans which draw flow down the 2m×1m tunnel section and return it above and below. Wind speeds in the range 1-40 m/s have been demonstrated. Cooling is achieved by a novel liquid nitrogen flow system which has achieved temperatures below -160ºC. The inner chamber is thermally isolated from the vacuum chamber. An atmospheric cooling system allowing independent control of the air temperature (tested to -50°C) and a range of particle imaging, microscopy and laser based techniques allow study of aerosols [2].

 

Recent Improvements: Major recent improvements to the facility (funded by Europlanet 2024RI) include; an additional Roots and turbo-pump system allowing pressures below 10-4 mbar to be achieved (important for lunar simulation). An additional test section has been constructed, dedicated to lunar/icy-moon simulations. An advanced cooling/heating element has been constructed funded by ESA and improved aerosolization systems for dust and ice studies. Additional recent sensor systems include a new Laser Doppler Velocimeter system, a unique optical transmission (opacity) sensor array for studying sand/aerosol properties and a prototype flow sensor array (micro- Pitot tubes) [2,8].

Figure 2 Additional pump system (left) and a new test section (right)

 

Lunar simulation: Although the pressure achievable at this facility (10-4mbar) is far larger than that of the lunar surface, for dust transport / exposure research (or testing) it is sufficient that dust grain trajectories are unaffected by drag i.e. the scattering length is larger than the size of the chamber. The large volume of this chamber also allows relatively large scale regolith simulation. This could for example aid in development/testing of in-situ resource utilization technologies.

 

 

 

Figure 3 studying resuspended dust using prototype a light transmission (opacity) system and micro-Pitot tube wind flow sensors [8].

3 Sand, dust and ices on Mars

 

With control of wind flow at low pressure and temperature this facility is well suited for recreating the environment at the surfaces of terrestrial type planets such as Mars, Earth and icy moons. The interaction of wind and the planetary surface, specifically the transport of sand and dust is fundamental to understanding the evolution of the planets’ surface and atmosphere. Laboratory studies of the entrainment, flow, deposition and erosion are scarce and empirical in nature. The effects of low atmospheric pressure, composition, temperature can now be studied in detail.

This laboratory has been part of an EU supported European collaboration called ROADMAP including groups from BIRA in Belgium, CSIC in Spain and UDE in Germany, to study dust aerosols on Mars [Home (aeronomie.be)].

4 Conclusion

 

This planetary simulation facility has many unique and recently improved features which make it well suited for both planetary research applications and the development/testing of instrumentation. Details of some of the most recent and upcoming collaborative research activities will be summarized. For information on access to this facility please contact the author.

Acknowledgements

This laboratory is a member of Europlanet 2024 RI which has received funding from the European Union's Horizon 2020 research and innovation programme under grant agreement No 871149.

The laboratory is also a member of the ROADMAP  project which has received funding from the European Union’s Horizon 2020 research and innovation programme under grant agreement No 101004052.

References

[1]https://scispace.esa.int/scispace-platforms/ground-based-facility-gbf/

[2]A. Waza et al., (2023) PSS 227, 105638.

[3]Yizhaq, H., et al., Nat. Geosci. 17, 66–72 (2024)

[4] Murdoch, N., et al., PSS, 165 (2019) 260-271

[5] G. Portyankina et al., Icarus 322, 210–220 (2019)

[6] E. del Bello, et al., Scientific Reports, 8, 14509 (2018)

[7] Andreotti and Claudin et al.. PNAS 5, 118 (2021)

[8]K.R.Rasmussen et al., Flow Measurement and Instrumentation 101C (2025) 102750.

 

How to cite: Merrison, J., Iversen, J. J., and Rasmussen, K.: A European Planetary and Lunar Simulation Facility, EPSC-DPS Joint Meeting 2025, Helsinki, Finland, 7–13 Sep 2025, EPSC-DPS2025-293, https://doi.org/10.5194/epsc-dps2025-293, 2025.

F135
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EPSC-DPS2025-1605
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ECP
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On-site presentation
Valeria De Santis, Giovanni Pratesi, Annarita Franza, and Gabriele Giuli

Introduction: Lunar soil simulants have been produced since 1971, as the upcoming space missions needed astronauts to be trained in conducting scientific field works on the Moon’s surface. [1] However, the first lunar soil simulants were not satisfactory in terms of chemical composition and mineralogy, as they were focused on having the proper engineering properties [2].

Due to the scarcity and limited accessibility of real lunar soils and rocks samples, and as the interest in lunar colonization with In-Situ Resource Utilization (ISRU) is growing, the production of lunar soil simulants has increased over the years [2].

The objective of our work is to develop a new lunar regolith simulant providing a reliable analog in terms of both mineralogy and bulk chemical composition that could be used for experiments on element extraction and for sintering experiments aimed at the production of building materials.

Anorthositic rocks are major constituents of the highland regions of the Moon [3], so we aim at reproducing the composition of a regolith whose major component is anorthositic. 

As lunar meteorites give access to unsampled areas of the Moon’s surface [4], we analyzed microchemically and mineralogically feldspathic lunar breccias and use their chemical composition and modal mineralogy as a reference.

Samples and Methods: We performed microchemical and mineralogical characterization of some lunar feldspathic breccias, specifically of samples of the meteorites NWA 7948 [5], NWA 11273 [6], Bechar 007 [7] and Gadamis 004 [8], four feldspathic lunar breccias with low weathering grade [5-8]. The samples were analyzed through FE-SEM at the University of Camerino and the University of Perugia and FE-EMPA analyses are planned at the University of Firenze. Operation conditions were working distance of 8.5 mm and accelerating voltage of 15 and 20 kV.

We started with synthesizing anorthite plagioclase and fluorapatite. We plan to synthetize glass whose composition resembles that of impact glass, vescicular glass of the agglutinates, and volcanic spherules found on lunar rocks and lunar meteorites. The next step will be to find natural terrestrial pyroxenes and olivines of suitable chemical composition and to add them in adequate amounts.

Results: Petrographic and microchemical investigations on the cited meteorites revealed the dominance of anorthitic plagioclase with average composition An96.1Ab3.7Or0.2 and therefore we focused on the synthesis of anorthite microcrystalline powders with this chemical composition using a muffle furnace in air. Synthesis of fluorapatite is currently ongoing, as is the analysis of terrestrial pyroxenes and olivines.

Acknowledgments: This study was carried out within the Space It Up project funded by the Italian Space Agency, ASI, and the Ministry of University and Research, MUR, under contract n. 2024-5-E.0 - CUP n. I53D24000060005.

References: [1] Slabic A. et al. (2024), NASA Technical Reports Server (NTRS) [2] Taylor L. A., et al. (2016) Planetary and Space Science, 126, 1–7 [3] Jaumann R. et al. (2012) Planetary and Space Science, 74, 15-41 [4] Korotev R. L. (2005) Chemie der Erde, 65, 297-346 [5] Zeng, X. et al. (2018), Meteoritic Planetary Science, 53: 1030-1050. Doi: 10.1111/maps.13049 [6] Huidobro J. et al. (2021), ACS Earth Space Chem, 5: 1333-1342. Doi:10.1021/acsearthspacechem.0c00032. [7] Gattacceca J., et al. (2019), Meteorit Planet Sci, 54: 469-471 doi:10.1111/maps.13215 [8] Gattacceca J. et al. (2023), Meteorit Planet Sci, 58: 901-904 doi:10.1111/maps.13995

How to cite: De Santis, V., Pratesi, G., Franza, A., and Giuli, G.: Microchemical and mineralogical characterization of lunar meteorites aimed at the production and testing of lunar regolith simulants, EPSC-DPS Joint Meeting 2025, Helsinki, Finland, 7–13 Sep 2025, EPSC-DPS2025-1605, https://doi.org/10.5194/epsc-dps2025-1605, 2025.

F136
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EPSC-DPS2025-1355
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On-site presentation
Arnaud Wilhelm and Naomi Murdoch

Microgravity platforms such as drop towers [1], sounding rockets, the International Space Station (ISS), and parabolic flights offer varying levels of low gravity conditions, typically ranging from 10-4 – 10-6g, where g represents Earth’s gravitational acceleration. Certain platforms—such as Blue Origin’s suborbital rocket system—are also able to recreate partial gravity environments, enabling experiments under conditions that replicate e.g., lunar gravity. Partial gravity can also be generated during specific parabolic flight maneuvers [2], or using small centrifuges placed within microgravity platforms [3]. The 40-meter Einstein Elevator, for example, can support large-scale experiments (up to 1.7 meters in diameter) under partial gravity, but only down to 0.1g [4,5]. Similarly, the 16-meter ZARM GraviTower Pro [6] offers both lunar (1/6 g) and Martian (1/3 g) gravity conditions, as well as microgravity. However, this facility presently lacks the capability to produce intermediate levels of partial gravity.

We are currently building a new variable gravity laboratory at ISAE-SUPAERO that is complementary to these existing facilities. The facility will be capable of providing a wide range of gravity conditions (0.3 – 10-3g) for short duration (~0.7 s), large-scale (~0.9 x 1.5 m) experiments under vacuum conditions. The experience gained during the development and operation of an Atwood machine for creating partial gravity conditions [7-9], contributed significantly to our understanding of the design challenges for such a facility and the improvements that are necessary to increase the performance of the new variable gravity laboratory. The new variable gravity facility is currently under development and the first scientific experiments are expected to be performed early 2026.

Figure 1: The variable gravity laboratory and its cradle. The tower is 7m high.

The core principle of the variable gravity laboratory involves a vertically moving cradle inside a tower (Fig. 1). Placed in the cradle, the payload experiences reduced gravity due to the cradle’s acceleration relative to the Earth's inertial frame. When the cradle is stationary with respect to the tower, it experiences normal Earth gravity (1g). However, when the cradle accelerates at a rate of ac​, the effective gravity inside becomes geff = g + ac​. For example, a downward acceleration of 1g (ac = -1g) cancels the effect of gravity, resulting in an effective gravity of 0 m/s2. The effective gravity within the cradle is therefore controlled by adjusting the cradle’s acceleration, which can be set in advance by the experimenter. The cradle is designed to accommodate various payloads – up to 250 kg – without the need for structural modifications, enabling a modular setup where different experiments can be designed for use within the facility.

The laboratory will use high-precision linear motors to control the cradle’s motion. Unlike conventional electric motors that generate rotational torque, linear motors are essentially "unrolled" to produce direct linear force through electromagnetic interaction. This design, combined with advanced control systems, enables precise regulation of the cradle's acceleration throughout the experiment. Furthermore, as the cradle will be magnetically guided this will also significantly reduce the frictional forces and enhance the system performance. At the end of its assisted fall, the cradle will be slowed by shock absorber cylinders, and brought to a stop with a deceleration lower than 15 g. On the cradle, two 220V sockets and 4 cables linked to an acquisition system are planned. The system will also provide measurements of accelerations and vibrations of the cradle, and configurable trigger signals.

To come even closer to space environment conditions, a vacuum tight container is designed to fit on the cradle (Fig. 2). This container will be able to accommodate experiments of ~0.7 x 1 m and up to 100 kg, and its transparent PMMA body enables to place monitoring equipment (e.g. cameras or laser measurements systems) outside vacuum. Pass-through ports are also available on the top of the container, for equipment placed under vacuum.

Figure 2: The vacuum tight container. Its internal diameter is 0.76m.

References

[1]           ZARM, 2022. Bremen Drop Tower – Payload Unser’s Guide v 1.2. https://www.zarm.uni-bremen.de/fileadmin/user_upload/drop_tower/ZARM_BDT_PUG_ver1.2.pdf

[2]           Pletser, V., et al. The First Joint European Partial-G Parabolic Flight Campaign at Moon and Mars Gravity Levels for Science and Exploration. Microgravity Sci. Technol. 24, 383–395 (2012).

[3]           Collins, P.J., Grugel, R.N. and Radlińska, A., 2021. The Influence of Variable Gravity on the Microstructural Development of Tricalcium Silicate Pastes. In Earth and Space 2021 (pp. 59-66).

[4]           Lotz, C., et al. (2017). Einstein-Elevator: A New Facility for Research from μ to 5. Gravitational and Space Research, 5(2), 11-27.

[5]          Reitz, B., et al. Additive Manufacturing Under Lunar Gravity and Microgravity. Microgravity Sci. Technol. 33, 25 (2021). https://doi.org/10.1007/s12217-021-09878-4

[6]           Gierse, A. et al., « The GraviTower Bremen Pro – Experiences with a next-generation drop tower system », 73rd International Astronautical Congress (IAC), Paris, France, 18-22 September 2022, IAC-22-A2-5-4-x6756.

[7]           Sunday, C., et al. 2016. A novel facility for reduced-gravity testing: A setup for studying low-velocity collisions into granular surfaces. Review of Scientific Instruments, 87(8), p.084504.

Acknowledgements

The authors thank LateSys, the GRAVITE facility project team, and the project review board for their important contributions to this project.  Funding support is acknowledged from the French ANR (ANR-23-ERCC-0003-01), and the European Research Council (ERC) GRAVITE project (Grant Agreement N°1087060).

How to cite: Wilhelm, A. and Murdoch, N.: The GRAVITE tower: Design updates for the new variable gravity facility, EPSC-DPS Joint Meeting 2025, Helsinki, Finland, 7–13 Sep 2025, EPSC-DPS2025-1355, https://doi.org/10.5194/epsc-dps2025-1355, 2025.

F137
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EPSC-DPS2025-841
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On-site presentation
Máté Kerényi and Stas Barabash

Building on more than 60 years of success in experimental space research, the Swedish Institute of Space Physics (IRF) has developed a comprehensive test, qualification, and calibration infrastructure known as IRF SpaceLab. This facility supports the development and manufacturing of space hardware.

IRF SpaceLab includes the following capabilities:

  • Co-60 Irradiation Facility:
    Provides dose rates ranging from 1 kR over 3.5 days to 1 kR in 5 hours, depending on the distance to the source. These moderate dose rates make the facility ideal for realistic radiation testing of space hardware.
  • Radioactive Isotope Collection:
    Features a wide array of isotopes for detector characterization, including Co-60, Cs-137, Ni-63, H-3, Ba-133, and Ra-226.
  • Thermal-Vacuum Chambers:
    Offers three chambers designed for testing hardware at different scales: board level, instrument level (<50 cm), and nano/microsatellite scale (<1 m). The latter chamber is equipped with an LN2-cooled shroud and solar flux simulators, suitable for thermal balance tests.
  • Shaker (35 kN):
    Capable of mechanical testing of objects up to 100 kg in a cleanroom environment.
  • Ion (±), Neutral, and Electron Beam Facility:
    Operates over an energy range of 50 eV to 50 keV and includes a 4-degree-of-freedom turntable.
  • Particle–Surface Interaction Facility:
    Designed for surface characterization, particularly for surface-based ion mass analyzers.

One of the key advantages of IRF SpaceLab is the integration of these diverse facilities within a single premises, operated within a small research institute environment. This setup minimizes formalities and administrative overhead.

IRF SpaceLab is open to external users in support of space and planetary exploration initiatives:  https://spacelab.irf.se/

How to cite: Kerényi, M. and Barabash, S.: IRF SpaceLab – a Swedish open research infrastructure to support space and planetary exploration, EPSC-DPS Joint Meeting 2025, Helsinki, Finland, 7–13 Sep 2025, EPSC-DPS2025-841, https://doi.org/10.5194/epsc-dps2025-841, 2025.