Many experiments were carried out in order to evaluate the survival capacity of extremotolerant lichens when facing harsh conditions, including those of outer space or of simulated Martian environment. For further progress, a deeper study on the physiological mechanisms is needed that confer the unexpected levels of resistance detected on these symbiotic organisms. In this work, the response of the lichenized green algae Trebouxia sp. (a predominant lichen photobiont) to increasing doses of UV-C radiation is studied. UV-C (one of the most lethal factors to be found in space together with vacuum and cosmic-ionizing radiation with high atomic number and energy (HZE) particles) has been applied in the present experiments up to a maximum dose analogue to 67 days in Low Earth Orbit (LEO). For that purpose we selected two extremotolerant and space-tested lichen species in which Trebouxia sp. is the photosynthetic partner: the crustose lichen Rhizocarpon geographicum and the fruticose lichen Circinaria gyrosa. In order to evaluate the effect of the physiological state of the lichen thallus (active when wet and dormant when dry) and of protective structures (cortex and photoprotective pigments) on the resistance of the photobiont to UV-C, four different experimental conditions were tested: (1) dry intact samples, (2) wet intact samples, (3) dry samples without cortex/acetone-rinsed and (4) wet samples without cortex/acetone-rinsed. After irradiation and a 72 hours period of recovery, the influence of UV-C on the two lichen's photobiont under each experimental approach was assessed by two complimentary methods: (1) By determining the photosystem II (PSII) activity in three successive 24 hours intervals (Mini-PAM fluorometer) to investigate the overall state of the photosynthetic process and the resilience of Trebouxia sp. (2) By performing high performance liquid chromatography (HPLC)-quantification of four essential photosynthetic pigments (chlorophyll a, chlorophyll b, β-carotene and lutein) of one sample of each species and dose. Results indicate that the physiological state of the thallus is the most important factor impairing the tolerance of Trebouxia sp. to UV-C radiation in both lichen species. Desiccated thalli were demonstrated to be more resistant to UV-C. No clear influence of UV-C radiation on the carotenoid content was detected. Comparing the respective doses applied, the individuals of R. geographicum are more sensitive than C. gyrosa.

M-dwarf stars are more abundant than G-dwarf stars, so our position as observers on a planet orbiting a G-dwarf raises questions about the suitability of other stellar types for supporting life. If we consider ourselves as typical, in the anthropic sense that our environment is probably a typical one for conscious observers, then we are led to the conclusion that planets orbiting in the habitable zone of G-dwarf stars should be the best place for conscious life to develop. But such a conclusion neglects the possibility that K-dwarfs or M-dwarfs could provide more numerous sites for life to develop, both now and in the future. In this paper we analyse this problem through Bayesian inference to demonstrate that our occurrence around a G-dwarf might be a slight statistical anomaly, but only the sort of chance event that we expect to occur regularly. Even if M-dwarfs provide more numerous habitable planets today and in the future, we still expect mid G- to early K-dwarfs stars to be the most likely place for observers like ourselves. This suggests that observers with similar cognitive capabilities as us are most likely to be found at the present time and place, rather than in the future or around much smaller stars.

We study the orbital evolution of a three-planet system with masses in the super-Earth regime resulting from the action of tides on the planets induced by the central star which cause orbital circularization. We consider systems either in or near to a three-body commensurability for which adjacent pairs of planets are in a first-order commensurability. We develop a simple analytic solution, derived from a time averaged set of equations, that describes the expansion of the system away from strict commensurability as a function of time, once a state where relevant resonant angles undergo small amplitude librations has been attained. We perform numerical simulations that show the attainment of such resonant states focusing on the Kepler 60 system. The results of the simulations confirm many of the scalings predicted by the appropriate analytic solution. We go on to indicate how the results can be applied to put constraints on the amount of tidal dissipation that has occurred in the system. For example, if the system has been in a librating state since its formation, we find that its present period ratios imply an upper limit on the time average of 1/Q′, With Q′ being the tidal dissipation parameter. On the other hand if a librating state has not been attained, a lower upper bound applies.

Mars analogue sites represent vital tools in our continued study of the Red Planet; the similar physico-chemical processes that shape a given analogue environment on Earth allow researchers to both prepare for known Martian conditions and uncover presently unknown relationships. This review of organic host analogues – sites on Earth that mimic the putatively low organic content of Mars – examines specific locations that present particular Mars-like obstacles to biological processes. Low temperatures, aridity, high radiation and oxidizing soils characterise modern-day Mars, while acid–saline waters would have presented their own challenges during the planet's warmer and wetter past. By studying each of these hurdles to life on Earth, scientists can prepare instruments headed for Mars and identify the best locations and approaches with which to look for biological signatures. As our use of organic host analogues becomes increasingly sophisticated, researchers will work to identify terrestrial sites exhibiting multiple Mars-like conditions that are tailored to the distinct mineralogical and physical characteristics of Martian locations. Making use of organic host analogues in these ways will enhance the search for signs of past or present life on Mars.

Investigations of the effects of solar radiation combined with the spaceflight factors on biological objects were performed in the «EXPOSE-R» experiment on the outer surface of ISS. After more than 1 year of outer space exposure, the spores of microorganisms and fungi, as well as two species of plant seeds were analysed for viability and the set of biological properties. The experiment provided evidence that not only bacterial and fungal spores but also dormant forms of plants had the capability to survive a long-term exposure to outer space.

The biosignatures of life on Earth do not remain static, but change considerably over the planet's habitable lifetime. Earth's future biosphere, much like that of the early Earth, will consist of predominantly unicellular microorganisms due to the increased hostility of environmental conditions caused by the Sun as it enters the late stage of its main sequence evolution. Building on previous work, the productivity of the biosphere is evaluated during different stages of biosphere decline between 1 and 2.8 Gyr from present. A simple atmosphere–biosphere interaction model is used to estimate the atmospheric biomarker gas abundances at each stage and to assess the likelihood of remotely detecting the presence of life in low-productivity, microbial biospheres, putting an upper limit on the lifetime of Earth's remotely detectable biosignatures. Other potential biosignatures such as leaf reflectance and cloud cover are discussed.

We develop a polarimetry-based remote-sensing method for detecting and identifying life forms in distant worlds and distinguishing them from non-biological species. To achieve this we have designed and built a bio-polarimetric laboratory experiment BioPol for measuring optical polarized spectra of various biological and non-biological samples. Here we focus on biological pigments, which are common in plants and bacteria that employ them either for photosynthesis or for protection against reactive oxygen species. Photosynthesis, which provides organisms with the ability to use light as a source of energy, emerged early in the evolution of life on Earth. The ability to harvest such a significant energy resource could likely also develop on habited exoplanets. Thus, we investigate the detectability of biomolecules that can capture photons of particular wavelengths and contribute to storing their energy in chemical bonds. We have carried out laboratory spectropolarimetric measurements of a representative sample of plants containing various amounts of pigments such as chlorophyll, carotenoids and others. We have also measured a variety of non-biological samples (sands, rocks). Using our lab measurements, we have modelled intensity and polarized spectra of Earth-like planets having different surface coverage by photosynthetic organisms, deserted land and ocean, as well as clouds. Our results demonstrate that linearly polarized spectra provide very sensitive and rather unambiguous detection of photosynthetic pigments of various kinds. Our work paves the path towards analogous measurements of microorganisms and remote sensing of microbial ecology on the Earth and of extraterrestrial life on other planets and moons.

On Earth, microorganisms living under intense ultraviolet (UV) radiation stress can adopt endolithic lifestyles, growing within cracks and pore spaces in rocks. Intense UV irradiation encountered by microbes leads to death and significant damage to biomolecules, which also severely diminishes the likelihood of detecting signatures of life. Here we show that porous rocks shocked by asteroid or comet impacts provide protection for phototrophs and their biomolecules during 22 months of UV radiation exposure outside the International Space Station. The UV spectrum used approximated the high-UV flux on the surface of planets lacking ozone shields such as the early Earth. These data provide a demonstration that endolithic habitats can provide a refugium from the worst-case UV radiation environments on young planets and an empirical refutation of the idea that early intense UV radiation fluxes would have prevented phototrophs without the ability to form microbial mats or produce UV protective pigments from colonizing the surface of early landmasses.

This paper investigates the possible use of space probes to explore the Milky Way, as a means both of finding life elsewhere in the Galaxy and as finding an answer to the Fermi paradox. Exploration of the Galaxy is simulated by first examining how long time it takes a given number of space probes to explore 40 000 stars in a box from −300 to 300 pc above the Galactic thin disc, as a function of Galactic radius. The Galaxy is then modelled to consist of ∼260 000 of these 40 000 stellar systems all located in a defined Galactic Habitable Zone and how long a time it takes to explore this zone is shown. The result is that with eight probes, each with eight subprobes, ∼4% of the Galaxy can be explored in 2.92×108 years. Increasing the number of probes to 200, still with eight subprobes each, reduces the exploration time to 1.52×107 years.

Conventionally, intelligence is seen as a property of individuals. However, it is also known to be a property of collectives. Here, we broaden the idea of intelligence as a collective property and extend it to the planetary scale. We consider the ways in which the appearance of technological intelligence may represent a kind of planetary scale transition, and thus might be seen not as something which happens on a planet but to a planet, much as some models propose the origin of life itself was a planetary phenomenon. Our approach follows the recognition among researchers that the correct scale to understand key aspects of life and its evolution is planetary, as opposed to the more traditional focus on individual species. We explore ways in which the concept may prove useful for three distinct domains: Earth Systems and Exoplanet studies; Anthropocene and Sustainability studies; and the study of Technosignatures and the Search for Extraterrestrial Intelligence (SETI). We argue that explorations of planetary intelligence, defined as the acquisition and application of collective knowledge operating at a planetary scale and integrated into the function of coupled planetary systems, can prove a useful framework for understanding possible paths of the long-term evolution of inhabited planets including future trajectories for life on Earth and predicting features of intelligentially steered planetary evolution on other worlds.

The work reported here represents a study into the total fluorescence exhibited by a broad selection of model, extremophilic and photosynthetic bacterial strains, over a great range of excitation and emission wavelengths from ultraviolet (UV) through visible to near infrared. The aim is to identify distinctive fluorescent features that may serve as detectable biosignatures of remnant microbial life on the Martian surface. A lab-bench fluorescence spectrometer was used to generate an excitation–emission matrix (EEM) for the unpigmented Escherichia coli, radiation-resistant Deinococcus radiodurans, Antarctic Dry Valley isolates Brevundimonas sp. MV.7 and Rhodococcus sp. MV.10, and the cyanobacterium Synechocystis sp. PCC 6803. Detailed EEMs, representing the fluorescence signature of each organism, are presented, and the most significant features suitable for biosignature surveys are identified, including small-molecule cellular metabolites, light-harvesting photosynthetic pigments and extracellular UV-screening compounds. E. coli exhibits the most intense emission from tryptophan, presumably due to the absence of UV-screening pigments that would shield the organism from short-wavelength light-exciting intracellular fluorescence. The efficacy of commonly available laser diodes for exciting cellular fluorescence is treated, along with the most appropriate filter wavelengths for imaging systems. The best combination of available laser diodes and PanCam filters aboard the ExoMars probe is proposed. The possibility of detecting fluorescence excited by solar UV radiation in freshly exposed surface samples by imaging when both sunlit and shadowed, perhaps by the body of the rover itself, is discussed. We also study how these biological fluorophore molecules may be degraded, and thus the potential biosignatures erased, by the high flux of far-ultraviolet light on Mars.

Monocyanopolyynes are formed by arcing graphite electrodes in ammonia. This work completes the parallelism existing between the polyynes formed by laser ablation experiments of graphite targets and those produced from the submerged electric arc. In both cases the same products are obtained. The products consist of hydrogen-terminated polyynes if water is present, monocyanopolyynes (mixed with hydrogen-terminated polyynes) if the carbon arc is sparked in acetonitrile or ammonia and dicyanopolyynes if the arc is struck in liquid nitrogen. The mechanism of formation of polyynes in the submerged carbon arc involves essentially neutral species; similar species and pathways may also occur in the circumstellar environment where polyynes have been detected by radioastronomy. It is shown that the relative abundances of the polyynes formed in the submerged carbon arc or in a carbon arc in vacuum decrease by a factor between three and five as the chain length increases by a C2 unit. Exactly the same trend has been observed by radioastronomy both for polyynes and cyanopolyynes in the circumstellar environment around red giants and asymptotic giant branch (AGB) stars. This fact may be a simple coincidence or may suggest that the mechanism of formation of the polyynes in the carbon arc is the same as that occurring in the surroundings of carbon-rich stars.

The carboxylic acids produced by the reductive tricarboxylic acid (rTCA) cycle are possibly a biosynthetic core of initial life, although several steps such as the reductive kinetics of oxaloacetate (OAA) to malate (MA) are problematic by conventional chemical routes. In this context, we studied the kinetics of this reaction as promoted by ZnS mineral photoelectrochemistry. The quantum efficiency φMA of MA production from the photoelectrochemical reduction of OAA followed φMA=0.13 [OAA] (2.1×10−3+[OAA])−1 and was independent of temperature (5 to 50°C). To evaluate the importance of this forward rate under a prebiotic scenario, we also studied the temperature-dependent rate of the backward thermal decarboxylation of OAA to pyruvate (PA), which followed an Arrhenius behavior as log (k−2)=11.74–4956/T, where k−2 is in units of s−1. These measured rates were employed in conjunction with the indirectly estimated carboxylation rate of PA to OAA to assess the possible importance of mineral photoelectrochemistry in the conversion of OAA to MA under several scenarios of prebiotic conditions on early Earth. As an example, our analysis shows that there is 90% efficiency with a forward velocity of 3 yr/cycle for the OAA→MA step of the rTCA cycle at 280 K. Efficiency and velocity both decrease for increasing temperature. These results suggest high viability for mineral photoelectrochemistry as an enzyme-free engine to drive the rTCA cycle through the early aeons of early Earth, at least for the investigated OAA→MA step.

54 strains of viable green algae and 26 strains of viable cyanobacteria were recovered from 128 and 56 samples collected from Siberian and Antarctic permafrost, respectively, with ages from modern to a few million years old. Although species of unicellular green algae belonged to Chlorococcales were subdominant inside permafrost, green algae Pedinomonas sp. were observed in Antarctic permafrost. Filamentous cyanobacteria of Oscillatoriales, Nostocales were just found in Siberian permafrost. Algal biomass in the permanently frozen sediments, expressed as concentration of chlorophyll a, was 0.06–0.46 μg g−1. The number of viable algal cells varied between <102 and 9×103 cfu g−1, but the number of viable bacterial cells was usually higher from 102 to 9.2×105 cfu g−1. Frozen but viable permafrost algae have preserved their morphological characteristics and photosynthetic apparatus in the dark permafrost. In the laboratory, they restored their photosynthetic activity, growth and development in favourable conditions at positive temperatures and with the availability of water and light. The discovery of ancient viable algae within permafrost reflects their ability to tolerate long-term freezing. In this study, the tolerance of algae and cyanobacteria to freezing, thawing and freezing–drying stresses was evaluated by short-term (days to months) low-temperature experiments. Results indicate that viable permafrost microorganisms demonstrate resistance to such stresses. Apart from their ecological importance, the bacterial and algal species found in permafrost have become the focus for novel biotechnology, as well as being considered proxies for possible life forms on cryogenic extraterrestrial bodies.

A number of studies have demonstrated that bacteria and fungi are present in the stratosphere. Since the tropopause is generally regarded as a barrier to the upward movement of particles it is difficult to see how such microorganisms can reach heights above 17 km. Volcanoes provide an obvious means by which this could be achieved, but these occur infrequently and any microorganisms entering the stratosphere from this source will rapidly fall out of the stratosphere. Here, we suggest mechanisms by which microorganisms might reach the stratosphere on a more regular basis; such mechanisms are, however, likely only to explain how micrometre to submicrometre particles could be elevated into the stratosphere. Intriguingly, clumps of bacteria of size in excess of 10 μm have been found in stratospheric samples. It is difficult to understand how such clumps could be ejected from the Earth to this height, suggesting that such bacterial masses may be incoming to Earth. We suggest that the stratospheric microflora is made up of two components: (a) a mixed population of bacteria and fungi derived from Earth, which can occasionally be cultured; and (b) a population made up of clumps of, viable but non-culturable, bacteria which are too large to have originated from Earth; these, we suggest, have arrived in the stratosphere from space. Finally, we speculate on the possibility that the transfer of bacteria from the Earth to the highly mutagenic stratosphere may have played a role in bacterial evolution.

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.

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

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.

If an industrial civilization had existed on Earth many millions of years prior to our own era, what traces would it have left and would they be detectable today? We summarize the likely geological fingerprint of the Anthropocene, and demonstrate that while clear, it will not differ greatly in many respects from other known events in the geological record. We then propose tests that could plausibly distinguish an industrial cause from an otherwise naturally occurring climate event.

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.