Comets are a source of prebiotic molecules that likely enriched the early Earth during the Late Heavy Bombardment period. Laboratory experiments that replicate cometary conditions may facilitate understanding of the chemical reactions and supplement observational studies of these icy bodies. Prebiotic compounds, such as formic acid and formaldehyde, have been observed in comets. Furthermore, these compounds can easily be formed in experimental models using a variety of gas combinations and energy sources. We conducted experimental cometary simulations using radiation chemistry tools to obtain insight into the possible fate of formic acid and formaldehyde. The main results suggest a redundant system, signifying that the irradiation of formic acid forms formaldehyde molecules and vice versa. This phenomenon ensures the permanence of prebiotic molecules in high-radiation environments. Additionally, the potential role of forsterite and graphite was explored in cometary simulations. Our experimental results show the differential formation of aldehydes and other carbonyl-containing compounds dependent on the mineral phase present.

The observation of life on Earth is commonly believed to be uninformative regarding the probability of abiogenesis on other Earth-like planets. This belief is based on the selection effect of our existence. We necessarily had to find ourselves on a planet where abiogenesis occurred, thus nothing can be inferred about the probability of abiogenesis from this observation alone. This argument was first formalized in a Bayesian framework by Brandon Carter. Though we definitely had to find ourselves on a planet where abiogenesis occurred, I argue here that (1) the Carter conclusion is based on what is known as the ‘Old Evidence Problem’ in Bayesian Confirmation Theory and that (2) taking this into account, the observation of life on Earth is not neutral but evidence that abiogenesis on Earth-like planets is relatively easy. I then give an independent timescale argument that quantifies the prior probabilities, leading to the inference that the timescale for abiogenesis is less than the planetary habitability timescale and therefore the occurrence of abiogenesis on Earth-like planets is not rare.

Interplanetary spacecraft are assembled with thousands of parts composed of many diverse materials. Little is known on whether any of the spacecraft materials are biocidal to the typical microbiomes that develop on spacecraft during pre-launch processing. During ongoing experiments to examine the interactive effects of solar UV irradiation, solar heating, ionizing radiation, and vacuum, we observed that bacterial spores of three Bacillus spp. were killed when incubated within small vacuum chambers for 5 days – without exposure to the aforementioned factors. Eight potential spacecraft materials were tested within the vacuum chambers for biocidal activities against spores of B. atrophaeus ATCC 9372, B. pumilus SAFR-032 and B. subtilis 168. All three species were fully inactivated (i.e., no survivors detected) by machined parts manufactured from Delrin®; a thermoplastic polyacetal polymer. Although not tested here, it is known that Delrin can off-gas formaldehyde, and thus, we hypothesize that this volatile organic compound (VOC) was responsible for the biocidal activity of the material. Knowledge of the biocidal nature of routinely used spacecraft materials might offer diverse methods to inactivate deeply embedded or shielded microbiota within spacecraft via the release of biocidal VOCs.

A formalization of Fermi paradox inside the environment of classical propositional logic is proposed. The notion of Silentium Universi set is launched in order to establish that the Fermi paradox is truly paradoxical. Combining consistent explanatory hypotheses is taken into consideration and discussed inside this framework explaining what would count as a solution to the paradox. By the end, it is argued that Fermi paradox is an unsolvable problem in the domain of science.

If human population growth is not controlled, natural areas must be sacrificed. An alternative is to create more habitat, terraforming Mars. However, this requires establishment of essential, ecosystem services on a planet currently unamenable to Terran species. Shorter term, assembling Terran-type ecosystems within contained environments is conceivable if mutually supportive species complements are determined. Accepting this, an assemblage of organisms that might form an early, forest environment is proposed, with rationale for its selection. A case is made for developing a contained facsimile, old growth forest on Mars, providing an oasis, proffering vital ecosystem functions (a forest bubble). It would serve as an extraterrestrial nature reserve (ETNR), psychological refuge and utilitarian botanic garden, supporting species of value to colonists for secondary metabolites (vitamins, flavours, perfumes, medicines, colours and mood enhancers). The design presented includes organisms that might tolerate local environmental variance and be assembled into a novel, bioregenerative forest ecosystem. This would differ from Earthly forests due to potential impact of local abiotic parameters on ecosystem functions, but it is argued that biotic support for space travel and colonization requires such developments. Consideration of the necessary species complement of an ETNR supports a view that it is not humanity alone that is reaching out to space, it is life, with all its diverse capabilities for colonization and establishment. Humans cannot, and will not, explore space alone because they did not evolve in isolation, being shaped over aeons by other species. Space will be travelled by a mutually supportive system of Terran organisms amongst which humans fit, exchanging metabolites and products of photosynthesis as they have always done.

The Drake equation has proven fertile ground for speculation about the abundance, or lack thereof, of communicating extraterrestrial intelligences (CETIs) for decades. It has been augmented by subsequent authors to include random variables in order to understand its probabilistic behaviour. However, in most cases, the emergence and lifetime of CETIs are assumed to be independent of each other. In this paper, we will derive several expressions that can demonstrate how CETIs may relate to each other in technological age as well as how the dynamics of the concurrent CETI population change under basic models of interaction, such as the Allee effect. By defining interaction as the change in the expected communication lifetime with respect to the density of CETI in a region of space, we can use models and simulation to understand how the CETI density can promote or inhibit the longevity and overall population of interstellar technological civilizations.