The theory of lithopanspermia proposes the natural exchange of organisms between solar system bodies through meteorites. The focus of this theory comprises three distinct stages: planetary ejection, interplanetary transit and planetary entry. However, it is debatable whether organisms transported within the ejecta can survive all three stages. If the conjecture is granted, that life can indeed be safely transmitted from one world to another, then it is not only a topic pertaining to planetary science but also biological sciences. Hence, these stages are only the first three factors of the equation. The other factors for successful lithopanspermia are the quality, quantity and evolutionary strategy of the transmitted organisms. When expanding into new environments, invading organisms often do not survive in the first attempt and usually require several attempts through propagule pressure to obtain a foothold. There is a crucial difference between this terrestrial situation and the one brought about by lithopanspermia. While invasive species on Earth repeatedly enters a new habitat, a species pragmatically arrives on another solar system body only once; thus, an all-or-nothing response will be in effect. The species must survive in the first attempt, which limits the probability of survival. In addition, evolution sets a boundary through the existence of an inverse proportionality between the exchanges of life between two worlds, thus further restricting the probability of survival. However, terrestrial populations often encounter unpredictable and variable environmental conditions, which in turn necessitates an evolutionary response. Thus, one evolutionary mode in particular, bet hedging, is the evolutionary strategy that best smooth out this inverse proportionality. This is achieved by generating diversity even among a colony of genetically identical organisms. This variability in individual risk-taking increases the probability of survival and allows organisms to colonize more diverse environments. The present analysis to understand conditions relevant to a bacterial colony arriving in a new planetary environment provides a bridge between the theory of bet hedging, invasive range expansion and planetary science.

In the space experiment ‘Spores in artificial meteorites’ (SPORES), spores of the fungus Trichoderma longibrachiatum were exposed to low-Earth orbit for nearly 2 years on board the EXPOSE-R facility outside of the International Space Station. The environmental conditions tested in space were: space vacuum at 10−7–10−4 Pa or argon atmosphere at 105 Pa as inert gas atmosphere, solar extraterrestrial ultraviolet (UV) radiation at λ > 110 nm or λ > 200 nm with fluences up to 5.8 × 108 J m−2, cosmic radiation of a total dose range from 225 to 320 mGy, and temperature fluctuations from −25 to +50°C, applied isolated or in combination. Comparable control experiments were performed on ground. After retrieval, viability of spores was analysed by two methods: (i) ethidium bromide staining and (ii) test of germination capability. About 30% of the spores in vacuum survived the space travel, if shielded against insolation. However, in most cases no significant decrease was observed for spores exposed in addition to the full spectrum of solar UV irradiation. As the spores were exposed in clusters, the outer layers of spores may have shielded the inner part. The results give some information about the likelihood of lithopanspermia, the natural transfer of micro-organisms between planets. In addition to the parameters of outer space, sojourn time in space seems to be one of the limiting parameters.

The experiment SPORES ‘Spores in artificial meteorites’ was part of European Space Agency's EXPOSE-R mission, which exposed chemical and biological samples for nearly 2 years (March 10, 2009 to February 21, 2011) to outer space, when attached to the outside of the Russian Zvezda module of the International Space Station. The overall objective of the SPORES experiment was to address the question whether the meteorite material offers enough protection against the harsh environment of space for spores to survive a long-term journey in space by experimentally mimicking the hypothetical scenario of Lithopanspermia, which assumes interplanetary transfer of life via impact-ejected rocks. For this purpose, spores of Bacillus subtilis 168 were exposed to selected parameters of outer space (solar ultraviolet (UV) radiation at λ>110 or >200 nm, space vacuum, galactic cosmic radiation and temperature fluctuations) either as a pure spore monolayer or mixed with different concentrations of artificial meteorite powder. Total fluence of solar UV radiation (100–400 nm) during the mission was 859 MJ m−2. After retrieval the viability of the samples was analysed. A Mission Ground Reference program was performed in parallel to the flight experiment. The results of SPORES demonstrate the high inactivating potential of extraterrestrial UV radiation as one of the most harmful factors of space, especially UV at λ>110 nm. The UV-induced inactivation is mainly caused by photodamaging of the DNA, as documented by the identification of the spore photoproduct 5,6-dihydro-5(α-thyminyl)thymine. The data disclose the limits of Lithopanspermia for spores located in the upper layers of impact-ejected rocks due to access of harmful extraterrestrial solar UV radiation.

The lichen Xanthoria elegans has been exposed to space conditions and simulated Mars-analogue conditions in the lichen and fungi experiment (LIFE) on the International Space Station (ISS). After several simulations and short space exposure experiments such as BIOPAN, this was the first long-term exposure of eukaryotic organisms to the hostile space conditions of the low Earth orbit (LEO). The biological samples were integrated in the EXPOSE-E facility and exposed for 1.5 years outside the ISS to the combined impact of insolation, ultraviolet (UV)-irradiation, cosmic radiation, temperatures and vacuum conditions of LEO space. Additionally, a subset of X. elegans samples was exposed to simulated Martian environmental conditions by applying Mars-analogue atmosphere and suitable solar radiation filters. After their return to Earth the viability of the lichen samples was ascertained by viability analysis of LIVE/DEAD staining and confocal laser-scanning microscopy, but also by analyses of chlorophyll a fluorescence. According to the LIVE/DEAD staining results, the lichen photobiont showed an average viability rate of 71%, whereas the even more resistant lichen mycobiont showed a rate of 84%. Post-exposure viability rates did not significantly vary among the applied exposure conditions. This remarkable viability is discussed in the context of particular protective mechanisms of lichens such as anhydrobiosis and UV-screening pigments.