The presence of viable, but non-cultureable, bacteria on membranes through which stratospheric air samples were passed has been confirmed using viable fluorescent staining.

Hypervelocity impacts (HVIs) where organic-bearing ice constitutes the target material are important in several aspects of planetary and space science: (1) sampling of planetary surfaces using a hypervelocity projectile to impact the surface and eject surface materials for measurement or collection by a spacecraft; (2) the transfer of organic material between planetary bodies; and (3) providing energy for chemical processes involving surface materials. While small organic molecules (~6 carbon atoms), if present in surface materials, will likely be present in HVI-ejecta, uncertainty remains for larger organic molecules. It is the larger molecular weight compounds which could constitute direct evidence of life, and thus their survival within an HVI-ejecta plume is of key importance when evaluating strategies for life detection on icy bodies. It is not currently known what large organic molecules, and in what concentrations, may be present on icy bodies in the Solar System, but it is highly likely some will be more chemically stable during a HVI than others. Accordingly, in this study we examined a range of chemicals (β,β carotene, stearic acid and anthracene) with molecular weights between 178 and 536 daltons, and three different types of chemical structure. The compounds were solvated in a dimethylsulfoxide/water mixture and frozen. The frozen targets were impacted with steel spheres 1 and 1.5 mm in diameter at velocities of about 4.9 km s−1. Ice ejected during the impact was collected and underwent chemical analysis. The most labile compound (β,β carotene) was only detected (in small amounts) in the ejecta (and only that emitted at the lowest angles of ejection), although the other compounds were present in larger quantities and at a range of ejection angles. A concentration gradient was observed within the ejecta as a function of angle of ejection. This was not the same for both stearic acid and anthracene: the greatest concentrations of stearic acid were found at shallow angles of ejection whereas anthracene was most abundant at both intermediate and large angles of ejection, implying an inverted concentration gradient. These observations may indicate that organic compounds are variably altered and destroyed during a HVI with ice and that the ejecta plume does not sample the original materials equally at all angles of ejection. Future work is planned and will evaluate fractional survival for a greater range of compound types, impact materials and velocities.

We numerically model the dynamics of the Enceladus plume ice grains and define our nominal plume model as having a particle size distribution n(R) ~ R−q with q = 4 and a total particulate mass rate of 16 kg s−1. This mass rate is based on average plume brightness observed by Cassini across a range of orbital positions. The model predicts sample volumes of ~1600 µg for a 1 m2 collector on a spacecraft making flybys at 20–60 km altitudes above the Enceladus surface. We develop two scenarios to predict the concentration of amino acids in the plume based on these assumed sample volumes. We specifically consider Glycine, Serine, α-Alanine, α-Aminoisobutyric acid and Isovaline. The first ‘abiotic’ model assumes that Enceladus has the composition of a comet and finds abundances between 2 × 10−6 to 0.003 µg for dissolved free amino acids and 2 × 10−5 to 0.3 µg for particulate amino acids. The second ‘biotic’ model assumes that the water of Enceladus's ocean has the same amino acid composition as the deep ocean water on Earth. We compute the expected captured mass of amino acids such as Glycine, Serine, and α-Alanine in the ‘biotic’ model to be between 1 × 10−5 to 2 × 10−5 µg for dissolved free amino acids and dissolved combined amino acids and about 0.0002 µg for particulate amino acids. Both models consider enhancements due to bubble bursting. Expected captured mass of amino acids is calculated for a 1 m2 collector on a spacecraft making flybys with a closest approach of 20 km during mean plume activity for the given nominal particle size distribution.

In a series of recent papers and in a book, this author put forward a mathematical model capable of embracing the search for extra-terrestrial intelligence (SETI), Darwinian Evolution and Human History into a single, unified statistical picture, concisely called Evo-SETI. The relevant mathematical tools are:

1. (1) Geometric Brownian motion (GBM), the stochastic process representing evolution as the stochastic increase of the number of species living on Earth over the last 3.5 billion years. This GBM is well known in the mathematics of finances (Black–Sholes models). Its main features are that its probability density function (pdf) is a lognormal pdf, and its mean value is either an increasing or, more rarely, decreasing exponential function of the time.

2. (2) The probability distributions known as b-lognormals, i.e. lognormals starting at a certain positive instant b>0 rather than at the origin. These b-lognormals were then forced by us to have their peak value located on the exponential mean-value curve of the GBM (Peak-Locus theorem). In the framework of Darwinian Evolution, the resulting mathematical construction was shown to be what evolutionary biologists call Cladistics.

3. (3) The (Shannon) entropy of such b-lognormals is then seen to represent the ‘degree of progress’ reached by each living organism or by each big set of living organisms, like historic human civilizations. Having understood this fact, human history may then be cast into the language of b-lognormals that are more and more organized in time (i.e. having smaller and smaller entropy, or smaller and smaller ‘chaos’), and have their peaks on the increasing GBM exponential. This exponential is thus the ‘trend of progress’ in human history.

4. (4) All these results also match with SETI in that the statistical Drake equation (generalization of the ordinary Drake equation to encompass statistics) leads just to the lognormal distribution as the probability distribution for the number of extra-terrestrial civilizations existing in the Galaxy (as a consequence of the central limit theorem of statistics).

5. (5) But the most striking new result is that the well-known ‘Molecular Clock of Evolution’, namely the ‘constant rate of Evolution at the molecular level’ as shown by Kimura's Neutral Theory of Molecular Evolution, identifies with growth rate of the entropy of our Evo-SETI model, because they both grew linearly in time since the origin of life.

6. (6) Furthermore, we apply our Evo-SETI model to lognormal stochastic processes other than GBMs. For instance, we provide two models for the mass extinctions that occurred in the past: (a) one based on GBMs and (b) the other based on a parabolic mean value capable of covering both the extinction and the subsequent recovery of life forms.

7. (7) Finally, we show that the Markov & Korotayev (2007, 2008) model for Darwinian Evolution identifies with an Evo-SETI model for which the mean value of the underlying lognormal stochastic process is a cubic function of the time.

Future space missions that aim to detect life should search for molecules that are vital to all living organisms. Although the Viking landers did not find any signs of organic molecules on Mars, signatures of past and/or present life may still exist in the Martian regolith. In this paper, we describe amino acid analyses performed in several Martian analogue soil samples collected close to the Mars Desert Research Station (MDRS), Utah, during the International Lunar Exploration Working Group (ILEWG) EuroGeoMars campaign in February 2009. The Utah desert around Hanksville is characterized as shale desert and is cold and arid with an average annual temperature of 12°C. It is subjected to wind erosion and was shaped by fluvial erosion. The data show large differences in the total amino acid abundances between all the collected soil samples, with values ranging from non-detectable to 100 000 parts per billion (ppb). These results are explained in the context of mineralogical differences (namely different clay content) among the soil samples. The data have implications for future life-detection missions and the target mineralogy that may host biological signatures.

Evolution, broadly construed, has become a powerful unifying concept in much of science – not only in the biological evolution of plants and animals, but also in the physical evolution of stars and planets, and the cultural evolution of society and its many varied products. This paper (1) explores the bulk structure and functioning of open, non-equilibrium, thermodynamic systems relevant to the interdisciplinary field of astrobiology, (2) places the astrobiological landscape into an even larger, cosmological context, (3) defines life, complexity and evolution writ large, (4) claims that life depends ultimately on the expansion of the Universe and the flow of energy derived therefrom and (5) proposes a quantitative metric to characterize the rise of complexity throughout all of natural history. That metric is neither information nor negentropy, for these inveterate yet qualitative terms cannot be quantified, nor even defined, to everyone's satisfaction in today's scientific community. Rather, the newly proposed metric is normalized energy flow, a revision of a long-cherished term – energy – that is physically intuitive, well defined and readily measurable. All ordered systems – from rocky planets and shining stars, to buzzing bees and redwood trees – can be best judged empirically and uniformly by gauging the amount of energy acquired, stored and expressed by those systems. Appeals to anthropism are unnecessary to appreciate the impressive hierarchy of the cosmic evolutionary narrative, including a technological civilization that now embraces an energetics agenda designed to better understand, and perhaps to unify, all the natural sciences.

Efficient life support systems are needed to maintain adequate oxygen, water and food for humans in extraterrestrial conditions. On the near-Earth missions, these are supplied by transport from the Earth, and by physical and chemical cleaning and recycling, but on long-term missions to far-away destinations, such as Mars, on-site production of the consumables may be required. Molecular oxygen and organic biomass can be most efficiently produced biologically, i.e. by photosynthesis. The conditions on Mars are distinctly harsh, and they strictly limit the growth and survival of any photosynthetic organisms to artificially maintained containments. For obtaining most economical growth conditions, minimal parameters need to be determined which still allow efficient growth of photosynthetic organisms. In this work we are testing how reduced air pressures (hypobaria) and increased CO2 concentrations, i.e. features typical for Martian conditions, affect the durability, growth and photosynthesis of laboratory strains of cyanobacteria, a group of prokaryotic organisms capable of plant-like photosynthesis. Our preliminary results show that air pressures down to 0.1 atm or CO2 concentrations up to 20% have no harmful effect on the photosynthetic oxygen production or growth rate of the cyanobacterial model species, Synechocystis sp. PCC 6803.

Planets with masses between 0.1 and 10 M⊕ are believed to host dense atmospheres. These atmospheres can play an important role on the planet's spin evolution, since thermal atmospheric tides, driven by the host star, may counterbalance gravitational tides. In this work, we study the long-term spin evolution of Earth-sized exoplanets. We generalize previous works by including the effect of eccentric orbits and obliquity. We show that under the effect of tides and core–mantle friction, the obliquity of the planets evolves either to 0° or 180°. The rotation of these planets is also expected to evolve into a very restricted number of equilibrium configurations. In general, none of these equilibria is synchronous with the orbital mean motion. The role of thermal atmospheric tides becomes more important for Earth-sized planets in the habitable zones of their systems; so they cannot be neglected when we search for their potential habitability.

We examined the environmental stresses experienced by cyanobacteria living in endolithic gneissic habitats in the Haughton impact structure, Devon Island, Canadian High Arctic (75° N) and compared them with the endolithic habitat at the opposite latitude in the Dry Valleys of Antarctica (76° S). In the Arctic during the summer, there is a period for growth of approximately 2.5 months when temperatures rise above freezing. During this period, freeze–thaw can occur during the diurnal cycle, but freeze–thaw excursions are rare within higher-frequency temperature changes on the scale of minutes, in contrast with the Antarctic Dry Valleys. In the Arctic location rainfall of approximately 3 mm can occur in a single day and provides moisture for endolithic organisms for several days afterwards. This rainfall is an order of magnitude higher than that received in the Dry Valleys over 1 year. In the Dry Valleys, endolithic communities may potentially receive higher levels of ultraviolet radiation than the Arctic location because ozone depletion is more extreme. The less extreme environmental stresses experienced in the Arctic are confirmed by the presence of substantial epilithic growth, in contrast to the Dry Valleys. Despite the more extreme conditions experienced in the Antarctic location, the diversity of organisms within the endolithic habitat, which includes lichen and eukaryotic algal components, is higher than observed at the Arctic location, where genera of cyanobacteria dominate. The lower biodiversity in the Arctic may reflect the higher water flow through the rocks caused by precipitation and the more heterogeneous physical structure of the substrate. The data illustrate an instance in which extreme climate is anti-correlated with microbial biological diversity.

If life occurs elsewhere in the Solar System, there is a strong likelihood that it occurs in a deep biosphere beneath the planetary surface. The evidence for methane in the martian atmosphere has drawn attention to the possible role of serpentinites in fuelling a deep biosphere through the generation of hydrogen and/or methane. Serpentinites represent a good target for the search for biosignatures in a range of reaction products. Isotopic measurements in each of methane, sulphide and carbonate in serpentinites can help determine evidence of biological activity. We show that ancient terrestrial serpentinites retain methane that could be subject to the measurement of carbon and hydrogen isotopes. There is, therefore, potential to sample serpentinites on Mars and test for evidence of life in the deep geological record of Mars.

Hot Lake (Oroville, WA) is an athalassohaline epsomite lake that can have precipitating concentrations of MgSO4 salts, mainly epsomite. Little biotic study has been done on epsomite lakes and it was unclear whether microbes isolated from epsomite lakes and their margins would fall within recognized halotolerant genera, common soil genera or novel phyla. Our initial study cultivated and characterized epsotolerant bacteria from the lake and its margins. Approximately 100 aerobic heterotrophic microbial isolates were obtained by repetitive streak-plating in high-salt media including either 10% NaCl or 2 M MgSO4. The collected isolates were all bacteria, nearly evenly divided between Gram-positive and Gram-negative clades, the most abundant genera being Halomonas, Idiomarina, Marinobacter, Marinococcus, Nesterenkonia, Nocardiopsis and Planococcus. Bacillus, Corynebacterium, Exiguobacterium, Kocuria and Staphylococcus also were cultured. This initial study included culture-independent community analysis of direct DNA extracts of lake margin soil using PCR-based clone libraries and 16S rRNA gene phylogeny. Clones assigned to Gram-positive bacterial clades (70% of total clones) were dominated by sequences related to uncultured actinobacteria. There were abundant Deltaproteobacteria clones related to bacterial sulphur metabolisms and clones of Legionella and Coxiella. These epsomite lake microbial communities seem to be divided between bacteria primarily associated with hyperhaline environments rich in NaCl and salinotolerant relatives of common soil organisms. Archaea appear to be in low abundance and none were isolated, despite near-saturated salinities. Growth of microbes at very high concentrations of magnesium and other sulphates has relevance to planetary protection and life-detection missions to Mars, where scant liquid water may form as deliquescent brines and appear as eutectic liquids.

The concept of sustainability is widely acknowledged as a political guideline. Economic, ecological, social and cultural aspects of sustainability are already under discussion. Current space mining efforts demand that the discussion become a broader one about ‘planetary sustainability’, including the space surrounding Earth. To date, planetary sustainability has mainly been used with reference to Earth only and I will extend it here, elaborating on a similar NASA initiative. This article (1) sketches the contemporary economic–political initiatives which call for a special reflection of Earth's location in space, and then (2) discusses the meaning of the concept of sustainability in this context. Next, (3) I relate the discussion to the issue of planetary and environmental protection, before, (4) finally, presenting a philosophical and theological perspective that seems particularly able to broach the issue of the multiple dimensions of sustainability in this context. This is the concept of constructive-critical realism. My overview of the topic concludes with (5) a summarizing outlook.

In this paper, we describe the development of an International Space Station experiment, BioRock. The purpose of this experiment is to investigate biofilm formation and microbe–mineral interactions in space. The latter research has application in areas as diverse as regolith amelioration and extraterrestrial mining. We describe the design of a prototype biomining reactor for use in space experimentation and investigations on in situ Resource Use and we describe the results of pre-flight tests.

I propose a unified framework for a joint analysis of the Drake equation and the Fermi paradox, which enables a simultaneous, quantitative study of both of them. The analysis is based on a simplified form of the Drake equation and on a fairly simple scheme for the colonization of the Milky Way. It appears that for sufficiently long-lived civilizations, colonization of the Galaxy is the only reasonable option to gain knowledge about other life forms. This argument allows one to define a region in the parameter space of the Drake equation, where the Fermi paradox definitely holds (‘Strong Fermi paradox’).

Chemical and microbiological studies of the impact of terrestrial contamination of the lunar surface during the Apollo missions could provide valuable data to help refine future Mars surface exploration plans and planetary protection requirements for a human mission to Mars. NASA and ESA have outlined new visions for solar system exploration that will include a series of lunar robotic missions to prepare for and support a human return to the Moon, and future human exploration of Mars and other destinations. Under the Committee on Space Research's (COSPAR's) current planetary protection policy for the Moon, no decontamination procedures are required for outbound lunar spacecraft. Nonetheless, future in situ investigations of a variety of locations on the Moon by highly sensitive instruments designed to search for biologically derived organic compounds would help assess the contamination of the Moon by lunar spacecraft and Apollo astronauts. These studies could also provide valuable ‘ground truth’ data for Mars sample return missions and help define planetary protection requirements for future Mars bound spacecraft carrying life detection experiments.

Cosmic rays may be linked to the formation of volatiles necessary for prebiotic chemistry. We explore the effect of cosmic rays in a hydrogen-dominated atmosphere, as a proof-of-concept that ion–neutral chemistry may be important for modelling hydrogen-dominated atmospheres. In order to accomplish this, we utilize Monte Carlo cosmic ray transport models with particle energies of 106 eV<E<1012 eV in order to investigate the cosmic-ray enhancement of free electrons in substellar atmospheres. Ion–neutral chemistry is then applied to a Drift–Phoenix model of a free-floating giant gas planet. Our results suggest that the activation of ion–neutral chemistry in the upper atmosphere significantly enhances formation rates for various species, and we find that C2H2, C2H4, NH3, C6H6 and possibly C10H are enhanced in the upper atmospheres because of cosmic rays. Our results suggest a potential connection between cosmic-ray chemistry and the hazes observed in the upper atmospheres of various extrasolar planets. Chemi-ionization reactions are briefly discussed, as they may enhance the degree of ionization in the cloud layer.

In this paper, in this edition of the Journal commemorating the life and work of David Wynn-Williams, we consider approaches to the astrobiological investigation of Mars. We provide a brief account of the scientific rationale behind the approach presented here. In particular, we outline the capabilities of the Raman spectrometer for the detection of biomarkers. David Wynn-Williams was an active champion of this instrument who was keen to field-qualify a version in Antarctica with a view to flying a Raman instrument onboard a Mars-bound space mission. We examine a scenario for the deployment of such an instrument in conjunction with other instrumentation and argue that subsurface deployment of scientific instruments is essential if we are to succeed in detecting any evidence that may exist for former life on Mars. We outline a mission scenario – Vanguard – which represents a novel but low-risk, low-cost approach to Mars exploration that was conceived and developed jointly by one of the authors (Ellery) and the late David Wynn-Williams.

The National Aeronautics and Space Administration (NASA) and the European Space Agency (ESA) are studying how samples might be brought back to Earth from Mars safely. Backward planetary protection is key in this complex endeavour, as it is required to prevent potential adverse effects from returning materials to Earth's biosphere. As the question of whether or not life exists on Mars today or whether it ever did in the past is still unanswered, the effort to return samples from Mars is expected to be categorized as a ‘Restricted Earth Return’ mission, for which NASA policy requires the containment of any unsterilized material returned to Earth. NASA is investigating several solutions to contain Mars samples and sterilize any uncontained Martian particles. This effort has significant implications for both NASA's scientific mission, and the Earth's environment; and so special care and vigilance are needed in planning and execution in order to assure acceptance of safety to Earth's biosphere. To generate a technically acceptable sterilization process across a wide array of scientific and other stakeholders, on 30–31 January 2019, 10–11 June 2019 and 19–20 February 2020, NASA informally convened a Sterilization Working Group (SWG) composed of experts from industry, academia and government to assess methods for sterilization and inactivation, to identify future work needed to verify these methods against biological challenges, and to determine their feasibility for implementation on robotic spacecraft in deep space. The goals of the SWG were:

1. (1) Understand what it means to sterilize and/or inactivate Martian materials and how that understanding can be applied to the Mars Sample Return (MSR) mission.

2. (2) Assess methods for sterilization and inactivation, and identify future work needed to verify these methods.

3. (3) Provide an effective plan for communicating with other agencies and the public.

This paper provides a summary of the discussions and conclusions of the SWG over these three workshops. It reflects a consensus position based on qualitative discussion of how agencies might approach the problem of sterilization of Mars material. The SWG reached a consensus that sterilization options can be considered on the basis of biology as we know it, and that sterilization modalities that are effective on terrestrial materials and organisms should be part of the MSR planetary protection strategy. Conclusions pointed to several industry standards for sterilization to include heat, chemical, UV radiation and low-heat plasma. Technical trade-offs for each sterilization modality were discussed while simultaneously considering the engineering challenges and limitations for spaceflight. Future work includes more in-depth discussions on technical trade-offs of sterilization modalities, identifying and testing Earth analogue challenge organisms and proteinaceous molecules against chosen modalities, and executing collaborative agreements between NASA and external working group partners to help close data gaps, and to establish strong, scientifically grounded sterilization and inactivation standards for MSR.

The astonishing capability of life to adapt to extreme conditions has provided a new perspective on what ‘habitable’ means. On Earth extremophiles thrive in hostile habitats, such as hot and cold deserts or Antarctic sub-glacial lakes considered as Earth analogues of Mars and icy moons of Jupiter and Saturn. Recently desert cyanobacteria were exposed to ground-based simulations of space and Martian conditions and to real space and Martian conditions simulated in low Earth orbit using facilities attached outside the International Space Station. When exposure to such conditions does not exceed repair capabilities, more data are available regarding the physico-chemical constraints that life can withstand. When the accumulated damage exceeds the survival potential, the persistence of biomarkers contributes to the search for life elsewhere. Knowledge concerning the endurance of desert cyanobacteria under space and Martian conditions contributes to the development of life support systems.

The adsorption of organic molecules on mineral matrices might have played a fundamental role in processes that led to the emergence of life. We investigated the adsorption properties of the nucleobases adenine, cytosine, uracil and hypoxanthine on magnesium oxide (MgO), determining the single solute batch equilibrium adsorption isotherms. Langmuir-type isotherms were fitted to data, assuming a rapid reversible equilibration of adsorption, demonstrated effectively through desorption experiments. The Langmuir equilibrium adsorption constant K and the amount of the solute per unit of adsorbent mass necessary to complete the monolayer b were calculated. The results indicate that MgO is a good adsorbent for nucleobases (adenine > uracil > hypoxantine > cytosine), suggesting a role of metal oxides in concentrating biomolecules in prebiotic conditions that might have favoured the passage from geochemistry to biochemistry.