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The question about the stability of certain biomolecules is directly connected to the life-detection missions aiming to search for past or present life beyond Earth. The extreme conditions experienced on extraterrestrial planet surface (e.g. Mars), characterized by ionizing and non-ionizing radiation, CO2-atmosphere and reactive species, may destroy the hypothetical traces of life. In this context, the study of the biomolecules behaviour after ionizing radiation exposure could provide support for the onboard instrumentation and data interpretation of the life exploration missions on other planets. Here, as a part of STARLIFE campaign, we investigated the effects of gamma rays on two classes of fungal biomolecules–nucleic acids and melanin pigments – considered as promising biosignatures to search for during the ‘in situ life-detection’ missions beyond Earth.

Biosignatures are widely sought after within the solar system and exoplanet communities. But what are we talking about, when we talk about biosignatures?The concept of a “biosignature” is widely used to suggest a link betweenanobservation and a biological cause,depending on thecontext. The term itself has, however,been defined and used in differentways in each of the differentparts of the scientific community involved in the search for past or present life on Earth and beyond. With the ongoing acceleration in the search for lifein our solar system and on exoplanets, there is a need for clarity and accuracy in the formulation and reporting of claims.This includes the discussion of false positives as well as false negatives. In this talk, resulting from the ISSI Tracers team,wediscussan inventory of questionsthat scientists and other interested parties should ask when assessing any reported detection of a “biosignature” to better understand exactly what is being claimed.This would improve clarity and accuracy in the formulation of claims and subsequent technical and public communication about some of the most profound and important questions in science and society.&nbsp

Xanthoria parietina (L.) Th. Fr. is a widely spread foliose lichen showing high tolerance against UV-radiation thanks to parietin, a secondary lichen substance. We exposed samples of X. parietina under simulated Martian conditions for 30 days to explore its survivability. The lichen’s vitality was monitored via chlorophyll a fluorescence that gives an indication for active light reaction of photosynthesis, performing in situ and after-treatment analyses. Raman spectroscopy and TEM were used to evaluate carotenoid preservation and possible variations in the photobiont’s ultrastructure respectively. Significant differences in the photo-efficiency between UV irradiated samples and dark-kept samples were observed. Fluorescence values correlated with temperature and humidity day-night cycles. The photo-efficiency recovery showed that UV irradiation caused significant effects on the photosynthetic light reaction. Raman spectroscopy showed that the carotenoid signal from UV exposed samples decreased significantly after the exposure. TEM observations confirmed that UV exposed samples were the most affected by the treatment, showing chloroplastidial disorganization in photobionts’ cells. Overall, X. parietina was able to survive the simulated Mars conditions, and for this reason it may be considered as a candidate for space long-term space exposure and evaluations of the parietin photodegradability.

The Moon is characterized by extremely harsh conditions due to ultraviolet irradiation, wide temperature extremes, vacuum resulting from the absence of an atmosphere and high ionizing radiation. Therefore, its surface may provide a unique platform to investigate the effects of such conditions. For lunar exploration with the Lunar Gateway platform, exposure experiments in Low Earth Orbit are useful testbeds to prepare for lunar space experiments and to understand how and if potential biomarkers are influenced by extra-terrestrial conditions. During the BIOMEX (BIOlogy and Mars EXperiment) project, dried colonies of the fungus Cryomyces antarcticus grown on Lunar Regolith Analogue (LRA) were exposed to space conditions for 16 months aboard the EXPOSE-R2 payload outside the International Space Station. In this study, we investigated the stability/degradation of fungal biomarkers in LRA after exposure to (i) simulated space and (ii) real space conditions, using Raman spectroscopy, gas chromatography-mass spectrometry and DNA amplification. The results demonstrated that fungal biomarkers were detectable after 16 months of real space exposure. This work will contribute to the interpretation of data from future biological experiments in the Cislunar orbit with the Lunar Gateway platform and/or on the lunar surface, in preparation for the next step of human exploration.

In 2022 JAXA issued an Announcement of Opportunity (AO) for receiving Hayabusa2 samples returned to Earth. We responded to the AO submitting a proposal based on using a multi-prong approach to achieve two main goals. The first goal is to address the subdued contrast of remote-sensing observations compared to measurements performed under laboratory conditions on analog materials. For this we will link the hyperspectral and imaging data collected from the spacecraft and the in-situ observations from the MASCOT lander instruments (MARA and MASCam) with laboratory-based measurements of Hayabusa2 samples using bi-directional reflectance spectroscopy under simulated asteroid surface conditions from UV to MIR/FIR achieved using three Bruker Vertex 80 V spectrometers in the Planetary Spectroscopy Laboratory. The second goal is the investigation of the mineralogy and organic matter of the samples collected by Hayabusa2, to better understanding the evolution of materials characterizing Ryugu and in general of protoplanetary disk and organic matter, investigating the aqueous alteration that took place in the parent body, and comparing the results with data collected from pristine carbonaceous chondrite analog meteorites. Spectral data will be complemented by Raman spectroscopy under simulated asteroid surface conditions, X-ray diffraction, would also allow us to define the bulk mineralogy of the samples as well as investigate the presence and nature of organic matter within the samples. In situ mineralogical and geochemical characterization will involve a pre-characterization of the sample fragments through scanning electron microscopy low voltage electron dispersive X-ray (EDX) maps, and micro IR analyses of the fragments. If allowed, a thin section of one grain will be used for electron microprobe analyses to geochemically characterize its mineralogical composition. To train our data collection and analysis methods on a realistic sample, we selected a piece of the Mukundpura meteorite, as one of the closer analogs to Ryugu’s surface (Ray et al., Planetary and Space Science, 2018, 151, 149–154). The Mukundpura chunk we selected for this study measures 3 mm in its maximum dimension, and we chose it so to have a test sample of the same size as the Hayabusa2 grain we requested in our proposal to JAXA’s AO. The test gave us confidence that we can measure with good SNR measurements in bi-directional reflectance for samples around 3 mm in size (see Figures 3, 4 below). To address our second goal the spectral data was complemented by Raman spectroscopy measured again under simulated asteroid surface conditions in our Raman Mineralogy and Biodetection Laboratory at DLR.