Current assessments of bioburden embedded in spacecraft materials are based on work performed in the Viking era (1970s), and the ability to culture organisms extracted from such materials. To circumvent the limitations of such approaches, DNA-based techniques were evaluated alongside established culturing techniques to determine the recovery and survival of bacterial spores encapsulated in spacecraft-qualified polymer materials. Varying concentrations of Bacillus pumilus SAFR-032 spores were completely embedded in silicone epoxy. An organic dimethylacetamide-based solvent was used to digest the epoxy and spore recovery was evaluated via gyrB-targeted qPCR, direct agar plating, most probably number analysis, and microscopy. Although full-strength solvent was shown to inhibit the germination and/or outgrowth of spores, dilution in excess of 100-fold allowed recovery with no significant decrease in cultivability. Similarly, qPCR (quantitative PCR) detection sensitivities as low as ∼103 CFU ml−1 were achieved upon removal of inhibitory substances associated with the epoxy and/or solvent. These detection and enumeration methods show promise for use in assessing the embedded bioburden of spacecraft hardware.

Staphylococcus aureus is routinely recovered from air and surface samples taken aboard the International Space Station (ISS) and poses a health threat to crew. As bacteria respond to the low shear forces engendered by continuous rotation conditions in a Rotating Wall Vessel (RWV) and the reduced gravitational field of near-Earth flight by altering gene expression, we examined the effect of low-shear RWV growth on protein secretion and gene expression by three S. aureus isolates. When cultured under 1 g, the total amount of protein secreted by these strains varied up to fourfold; under continuous rotation conditions, protein secretion by all three strains was significantly reduced. Concentrations of individual proteins were differentially reduced and no evidence was found for increased lysis. These data suggest that growth under continuous rotation conditions reduces synthesis or secretion of proteins. A limited number of changes in gene expression under continuous rotation conditions were noted: in all isolates vraX, a gene encoding a polypeptide associated with cell wall stress, was down-regulated. A vraX deletion mutant of S. aureus SH1000 was constructed: no differences were found between SH1000 and ΔvraX with respect to colony phenotype, viability, protein export, antibiotic susceptibility, vancomycin kill kinetics, susceptibility to cold or heat and gene modulation. An ab initio protein–ligand docking simulation suggests a major binding site for β-lactam drugs such as imipenem. If such changes to the bacterial phenotype occur during spaceflight, they will compromise the capacity of staphylococci to cause systemic infection and to circumvent antibacterial chemotherapy.

The nature of cometary organic matter is of great interest to investigations involving the formation and distribution of organic matter relevant to the origin of life. We have used pyrolysis–Fourier transform infrared (FTIR) spectroscopy to investigate the chemical effects of the irradiation of naturally occurring bitumens, and to relate their products of pyrolysis to their parent assemblages. The information acquired has then been applied to the complex organic matter present in cometary nuclei and comae. Amalgamating the FTIR data presented here with data from published studies enables the inference of other comprehensive trends within hydrocarbon mixtures as they are progressively irradiated in a cometary environment, namely the polymerization of lower molecular weight compounds; an increased abundance of polycyclic aromatic hydrocarbon structures; enrichment in 13C; reduction in atomic H/C ratio; elevation of atomic O/C ratio and increase in the temperature required for thermal degradation. The dark carbonaceous surface of a cometary nucleus will display extreme levels of these features, relative to the nucleus interior, while material in the coma will reflect the degree of irradiation experienced by its source location in the nucleus. Cometary comae with high methane/water ratios indicate a nucleus enriched in methane, favouring the formation of complex organic matter via radiation-induced polymerization of simple precursors. In contrast, production of complex organic matter is hindered in a nucleus possessing a low methane/water ration, with the complex organic matter that does form possessing more oxygen-containing species, such as alcohol, carbonyl and carboxylic acid functional groups, resulting from reactions with hydroxyl radicals formed by the radiolysis of the more abundant water. These insights into the properties of complex cometary organic matter should be of particular interest to both remote observation and space missions involving in situ analyses and sample return of cometary materials.

The last few million years on planet Earth have witnessed two remarkable phases of hominid development, starting with a phase of biological evolution characterized by rather rapid increase of the size of the brain. This has been followed by a phase of even more rapid technological evolution and concomitant expansion of the size of the population that began when our own particular ‘sapiens’ species emerged, just a few hundred thousand years ago. The present investigation exploits the analogy between the neo-Darwinian genetic evolution mechanism governing the first phase, and the memetic evolution mechanism governing the second phase. From the outset of the latter until very recently – about the year 2000 – the growth of the global population N was roughly governed by an equation of the form dN/Ndt=N/T*, in which T* is a coefficient introduced (in 1960) by von Foerster, who evaluated it empirically as about 200 000 million years. It is shown here how the value of this hitherto mysterious timescale governing the memetic phase is explicable in terms of what happened in the preceding genetic phase. The outcome is that the order of magnitude of the Foerster timescale can be accounted for as the product of the relevant (human) generation timescale, about 20 years, with the number of bits of information in the genome, of the order of 10 000 million. Whereas the origin of our ‘homo’ genus may well have involved an evolutionary hard step, it transpires that the emergence of our particular ‘sapiens’ species was rather an automatic process.

This review reports the Brazilian history in astrobiology, as well as the first delineation of a vision of the future development of the field in the country, exploring its abundant biodiversity, highly capable human resources and state-of-the-art facilities, reflecting the last few years of stable governmental investments in science, technology and education, all conditions providing good perspectives on continued and steadily growing funding for astrobiology-related research. Brazil is growing steadily and fast in terms of its worldwide economic power, an effect being reflected in different areas of the Brazilian society, including industry, technology, education, social care and scientific production. In the field of astrobiology, the country has had some important landmarks, more intensely after the First Brazilian Workshop on Astrobiology in 2006. The history of astrobiology in Brazil, however, is not so recent and had its first occurrence in 1958. Since then, researchers carried out many individual initiatives across the country in astrobiology-related fields, resulting in an ever growing and expressive scientific production. The number of publications, including articles and theses, has particularly increased in the last decade, but still counting with the effort of researchers working individually. That scenario started to change in 2009, when a formal group of Brazilian researchers working with astrobiology was organized, aiming at congregating the scientific community interested in the subject and to promote the necessary interactions to achieve a multidisciplinary work, receiving facilities and funding from the University de Sao Paulo and other funding agencies.

For many years, it has been assumed that Jupiter has prevented the Earth from being subject to a punishing impact regime that would have greatly hindered the development of life. Here, we present the fourth in a series of dynamical studies investigating this hypothesis. In our earlier work, we examined the effect of Jupiter's mass on the impact rate experienced by the Earth. Here, we extend that approach to consider the influence of Jupiter's orbital eccentricity and inclination on the impact rate from asteroidal bodies and short-period comets. We first considered scenarios in which Jupiter's orbital eccentricity was somewhat higher and somewhat lower than that in our Solar System, for a variety of ‘Jupiter’ masses. We find that Jupiter's orbital eccentricity plays a moderate role in determining the impact flux at Earth, with more eccentric orbits resulting in a noticeably higher impact rate of asteroids than is the case for more circular orbits. This is particularly pronounced at high ‘Jupiter’ masses. For the short-period comets, the same effect is clearly apparent, albeit to a much lesser degree. The flux of short-period comets impacting the Earth is slightly higher for more eccentric Jovian orbits. We also considered scenarios in which Jupiter's orbital inclination was greater than that in our Solar System. Increasing Jupiter's orbital inclination greatly increased the flux of asteroidal impactors upon the Earth. However, at the highest tested inclination, the disruption to the Asteroid belt was so great that the belt would be entirely depleted after an astronomically short period of time. In such a system, the impact flux from asteroid bodies would therefore be very low, after an initial period of intense bombardment. By contrast, the influence of Jovian inclination on impacts from short-period comets was very small. A slight reduction in the impact flux was noted for the moderate and high inclination scenarios considered in this work – the results for inclinations of 5° and 25° were essentially identical.

The analysis of sulphur isotopic compositions in three sets of surface sulphate samples from the soil zone in the Haughton impact structure shows that they are distinct. They include surface gypsum crusts remobilized from the pre-impact gypsum bedrock (mean δ34S +31‰), efflorescent copiapite and fibroferrite associated with hydrothermal marcasite (mean δ34S −37‰), and gypsum-iron oxide crusts representing weathering of pyritic crater-fill sediments (mean δ34S +7‰). Their different compositions reflect different histories of sulphur cycling. Two of the three sulphates have isotopically light (low δ34S) compositions compared with the gypsum bedrock (mean δ34S +31‰), reflecting derivation by weathering of sulphides (three sets of pyrite/marcasite samples with mean δ34S of −41, −20 and −8‰), which had in turn been precipitated by microbial sulphate reduction. Thus, even in the absence of the parent sulphides due to surface oxidation, evidence of life would be preserved. This indicates that on Mars, where surface oxidation may rule out sampling of sulphides during robotic exploration, but where sulphates are widespread, sulphur isotope analysis is a valuable tool that could be sensitive to any near-surface microbial activity. Other causes of sulphur isotopic fractionation on the surface of Mars are feasible, but any anomalous fractionation would indicate the desirability of further analysis.

In a previous study published in Astrobiology, we focused on the evolution of habitability of a 10 M⊕ super-Earth planet orbiting a star akin to the Sun. This study was based on a concept of planetary habitability in accordance with the integrated system approach that describes the photosynthetic biomass production taking into account a variety of climatological, biogeochemical and geodynamical processes. In the present study, we pursue a significant augmentation of our previous work by considering stars with zero-age main-sequence masses between 0.5 and 2.0 M⊙ with special emphasis on models of 0.8, 0.9, 1.2 and 1.5 M⊙. Our models of habitability consider geodynamical processes during the main-sequence stage of these stars as well as during their red giant branch evolution. Pertaining to the different types of stars, we identify the so-called photosynthesis-sustaining habitable zone (pHZ) determined by the limits of biological productivity on the planetary surface. We obtain various sets of solutions consistent with the principal possibility of life. Considering that stars of relatively high masses depart from the main-sequence much earlier than low-mass stars, it is found that the biospheric lifespan of super-Earth planets of stars with masses above approximately 1.5 M⊙ is always limited by the increase in stellar luminosity. However, for stars with masses below 0.9 M⊙, the lifespan of super-Earths is solely determined by the geodynamic timescale. For central star masses between 0.9 and 1.5 M⊙, the possibility of life in the framework of our models depends on the relative continental area of the super-Earth planet.

The concept of a Galactic Habitable Zone (GHZ) was introduced for the Milky Way galaxy a decade ago as an extension of the earlier concept of the Circumstellar Habitable Zone. In this work, we consider the extension of the concept of a GHZ to other types of galaxies by considering two elliptical galaxies as examples, M87 and M32. We argue that the defining feature of the GHZ is the probability of planet formation which has been assumed to depend on the metallicity. We have compared the metallicity distribution of nearby stars with the metallicity of stars with planets to document the correlation between metallicity and planet formation and to provide a comparison to other galaxies. Metallicity distribution, based on the [Fe/H] ratio to solar, of nearby stars peaks at [Fe/H]≈−0.2 dex, whereas the metallicity distribution of extrasolar planet host stars peaks at [Fe/H]≈+0.4 dex. We compare the metallicity distribution of extrasolar planet host stars with the metallicity distribution of the outer star clusters of M87 and M32. The metallicity distribution of stars in the outer regions of M87 peaks at [Fe/H]≈−0.2 dex and extends to [Fe/H]≈+0.4 dex, which seems favourable for planet formation. The metallicity distribution of stars in the outer regions of M32 peaks at [Fe/H]≈−0.2 dex and extends to a much lower [Fe/H]. Both elliptical galaxies met the criteria of a GHZ. In general, many galaxies should support habitable zones.

Astrobiology must be seen in the context of cosmic evolution, the 13.7 billion-year master narrative of the universe. The idea of an evolving universe dates back only to the 19th century, and became a guiding principle for astronomical research only in the second half of the 20th century. The modern synthesis in evolutionary biology hastened the acceptance of the idea in its cosmic setting, as did the confirmation of the Big Bang theory for the origin of the universe. NASA programmes such as Origins incorporated it as a guiding principle. Cosmic evolution encompasses physical, biological and cultural evolution, and may result in a physical, biological or postbiological universe, each with its own implications for long-term human destiny, and each imbuing the meaning of life with different values. It has the status of an increasingly accepted worldview that is beginning to have a profound effect not only in science but also in religion and philosophy.

The source of Martian atmospheric methane is unknown. On Earth, hydrothermal mineral deposits contain ancient methane together with a host of chemical and geological lines of evidence for the mechanism of gas production. Such deposits are therefore potentially attractive sampling sites on Mars. In order to evaluate this potential, hydrothermal calcite veins were sampled across the Caithness region of Scotland and analysed for methane by an incremental-crushing mass spectrometry technique that may be adaptable to Mars rovers. Methane was detected in all samples. Variations in the quantity of methane released were found to relate directly to the geological history of the localities. Calcite particle size was found to affect measurements in a systematic and informative way. Oxidative weathering had no discernable effect on methane recoverability. These results suggest that the technique is sensitive and informative enough to deserve consideration for missions to Mars.

This study reports the environmental conditions of temperature, moisture and radiation for four years (May 2004 to July 2008) in the area known as Pampas de La Joya in southern Peru, which recently has been considered as a new Mars analogue. The period of evaluation includes the El Niño Southern Oscillation (ENSO) during the months of September 2006 to March 2007, which, despite not having catastrophic effects like its predecessor on 1997–1998, showed an interesting increase in humidity. Our data describe the extreme conditions present in the region and their relationship with the presence of potential habitats that could allow for the survival of micro-organisms. The average environmental temperature was 18.9°C, with a maximum of 35.9°C and a minimum of −4.5°C. The annual average incident solar radiation was 508 W m−2, with high near 1060 W m−2 at noon during the driest period between September and March. The average relative humidity (RH) was 29.5, 20.1 and 20.4% for air, soil and rock, respectively. The RH had higher values at night due to fog during the months of June and August, and during the early morning between December and March. During the months of ENSO event there were four episodes of precipitation (1.1, 1.5, 2.0 and 0.9 mm), of which three increased soil and rock moisture on an average more than 45% and persisted for over 15 days after precipitation, while the atmospheric environment had no significant variations. Finally, quartz rocks and evaporite minerals colonized with micro-organisms were found as the only micro-habitats, in this region, capable of supporting life in this extreme environment.

The study of life remote in space has strong parallels with the study of life remote in time. Both are dependent on decoding those historic phenomena called ‘fossils’, here taken to include biogenic traces of activity and waste products. There is the shared problem of data restoration from incomplete data sets; the importance of contextual analysis of potentially viable habitats; the centrality of cell theory; the need to reject the null hypothesis of an abiogenic origin for candidate cells via morphospace analysis; the need to demonstrate biology-like behaviour (e.g., association with biofilm-like structures; tendency to form clusters and ‘mats’; and a preference for certain substrates), and of metabolism-like behaviour (e.g., within the candidate cell wall; within surrounding ‘waste products’; evidence for syntrophy and metabolic cycles; and evidence for metabolic tiers). We combine these ideas into a robust protocol for demonstrating ancient or extra-terrestrial life, drawing examples from Earth's early geological record, in particular from the earliest known freshwater communities of the 1.0 Ga Torridonian of Scotland, from the 1.9 Ga Gunflint Chert of Canada, from the 3.4 Ga Strelley Pool sandstone of Australia, and from the 3.46 Ga Apex Chert also of Australia.

The number N of detectable (i.e. communicating) extraterrestrial civilizations in the Milky Way galaxy is usually calculated by using the Drake equation. This equation was established in 1961 by Frank Drake and was the first step to quantifying the Search for ExtraTerrestrial Intelligence (SETI) field. Practically, this equation is rather a simple algebraic expression and its simplistic nature leaves it open to frequent re-expression. An additional problem of the Drake equation is the time-independence of its terms, which for example excludes the effects of the physico-chemical history of the galaxy. Recently, it has been demonstrated that the main shortcoming of the Drake equation is its lack of temporal structure, i.e., it fails to take into account various evolutionary processes. In particular, the Drake equation does not provides any error estimation about the measured quantity. Here, we propose a first treatment of these evolutionary aspects by constructing a simple stochastic process that will be able to provide both a temporal structure to the Drake equation (i.e. introduce time in the Drake formula in order to obtain something like N(t)) and a first standard error measure.

This research deals with the fall of the Sikhote-Alin iron meteorite on the morning of 12 February 1947, at about 00:38 h Utrecht, in a remote area in the territory of Primorsky Krai in Eastern Siberia (46°09′36″N, 134°39′22″E). The area engulfed by the meteoritic fall was around 48 km2, with an elliptic form and thousands of craters. Around the large craters the trees were torn out by the roots and laid radially to the craters at a distance of 10–20 m; the more distant trees had broken tops. This research investigated through dendrocronology n.6 Scots pine trees (Pinus Sibirica) close to one of the main impact craters. The analysis of growth anomalies has shown a sudden decrease since 1947 for 4–8 years after the meteoritic impact. Tree growth stress, detected in 1947, was analysed in detail through wood microsection that confirmed the winter season (rest vegetative period) of the event. The growth stress is mainly due to the lost crown (needle lost) and it did not seem to be caused due to direct damages on trunk and branches (missing of resin ducts).

Mars' total atmospheric nitrogen content is 0.2 mbar. One-dimensional (1D) photochemical simulations of Mars' atmosphere show that nitric acid (HNO3(g)), the most soluble nitrogen oxide, is the principal reservoir species for nitrogen in its lower atmosphere, which amounts to a steady-state value of 6×10−2 kg or 4 moles, conditions of severe nitrogen deficiency. Mars could, however, support ∼1015 kg of biomass (∼1 kg N m−2) from its current atmospheric nitrogen inventory. The terrestrial mass ratio of nitrogen in biomass to that in the atmosphere is ∼10−5; applying this ratio to Mars yields ∼1010 kg of total biomass – also, conditions of severe nitrogen deficiency. These amounts, however, are lower limits as the maximum surface-sink of atmospheric nitrogen is 2.8 mbar (9×1015 kg of N), which indicates, in contradistinction to the Klingler et al. (1989), that biological metabolism would not be inhibited in the subsurface of Mars. Within this context, we explore HNO3 deposition on Mars' surface (i.e. soil and ice-covered regions) on pure water metastable thin liquid films. We show for the first time that the negative change in Gibbs free energy increases with decreasing HNO3(g) (NO3−(aq)) in metastable thin liquid films that may exist on Mars' surface. We also show that additional reaction pathways are exergonic and may proceed spontaneously, thus providing an ample source of energy for nitrogen fixation on Mars. Lastly, we explore the dissociation of HNO3(g) to form NO3−(aq) in metastable thin liquid films on the Martian surface via condensed phase simulations. These simulations show that photochemically produced fixed nitrogen species are not only released from the Martian surface to the gas-phase, but more importantly, transported to lower depths from the Martian surface in transient thin liquid films. A putative biotic layer at 10 m depth would produce HNO3 and N2 sinks of −54 and −5×1012 molecules cm−2 s−1, respectively, which is an ample supply of available nitrogen that can be efficiently transported to the subsurface. The downward transport as well as the release to the atmosphere of photochemically produced fixed nitrogen species (e.g. NO2−, NO and NO2) suggests the existence of a transient but active nitrogen cycle on Mars.

At present, bulk liquid water on the surface and near-subsurface of Mars does not exist due to the scarcity of condensed- and gas-phase water, pressure and temperature constraints. Given that the nuclei of soil and ice, that is, the soil solid and ice lattice, respectively, are coated with adsorbed and/or thin liquid films of water well below 273 K and the availability of water limits biological activity, we quantify lower and upper limits for the thickness of such adsorbed/water films on the surface of the Martian regolith and for subsurface ice. These limits were calculated based on experimental and theoretical data for pure water ice and water ice containing impurities, where water ice containing impurities exhibit thin liquid film enhancements, ranging from 3 to 90. Close to the cold limit of water stability (i.e. 273 K), thin liquid film thicknesses at the surface of the Martian regolith is 0.06 nm (pure water ice) and ranges from 0.2 to 5 nm (water ice with impurities). An adsorbed water layer of 0.06 nm implies a dessicated surface as the thickness of one monolayer of water is 0.3 nm but represents 0.001–0.02% of the Martian atmospheric water vapour inventory. Taking into account the specific surface area (SSA) of surface-soil (i.e. top 1 mm of regolith and 0.06 nm adsorbed water layer), shows Martian surface-soil may contain interfacial water that represents 6–66% of the upper- and lower-limit atmospheric water vapour inventory and almost four times and 33%, the lower- and upper-limit Martian atmospheric water vapour inventory. Similarly, taking the SSA of Martian soil, the top 1 mm or regolith at 5 nm thin liquid water thickness, yields 1.10×1013 and 6.50×1013 litres of waters, respectively, 55–325 times larger than Mars’ atmospheric water vapour inventory. Film thicknesses of 0.2 and 5 nm represent 2.3×104–1.5×106 litres of water, which is 6.0×10−7–4.0×10−4%, respectively, of a 10 pr μm water vapour column, and 3.0×10−6–4.0×10−4% and 6.0×10−6–8.0×10−4%, respectively, of the Martian atmospheric water vapour inventory. Thin liquid film thicknesses on/in subsurface ice were investigated via two scenarios: (i) under the idealistic case where it is assumed that the diurnal thermal wave is equal to the temperature of ice tens of centimetres below the surface, allowing for such ice to experience temperatures close to 273 K and (ii) under the, likely, realistic scenario where the diurnal thermal wave allows for the maximum subsurface ice temperature of 235 K at 1 m depth between 30°N and 30°S. Scenario 1 yields thin liquid film thicknesses ranging from 11 to 90 nm; these amounts represent 4×106–3.0×107 litres of water. For pure water ice, Scenario 2 reveals that the thickness of thin liquid films contained on/within Martian subsurface is less than 1.2 nm, several molecular layers thick. Conversely, via the effect of impurities at 235 K allows for a thin liquid film thickness on/within subsurface ice of 0.5 nm, corresponding to 6.0×104 litres of water. The existence of thin films on Mars is supported by data from the Mars Exploration Rovers (MERs) Spirit and Opportunity's Alpha Proton X-ray Spectrometer instrumentation, which have detected increased levels of bromine beneath the immediate surface, suggestive of the mobilization of soluble salts by thin films of liquid water towards local cold traps. These findings show that biological activity on the Martian surface and subsurface is not limited by nanometre dimensions of available water.

Amino acids and nucleic acid bases are very important for the living organisms. Thus, their protection from decomposition, selection, pre-concentration and formation of biopolymers are important issues for understanding the origin of life on the Earth. Minerals could have played all of these roles. This paper discusses several aspects involving the adsorption of amino acids and nucleic acid bases onto minerals under conditions that could have been found on the prebiotic Earth; in particular, we recommend the use of minerals, amino acids, nucleic acid bases and seawater ions in prebiotic chemistry experiments. Several experiments involving amino acids, nucleic acid bases, minerals and seawater ions are also suggested, including: (a) using well-characterized minerals and the standardization of the mineral synthesis methods; (b) using primary chondrite minerals (olivine, pyroxene, etc.) and clays modified with metals (Cu, Fe, Ni, Mo, Zn, etc.); (c) determination of the possible products of decomposition due to interactions of amino acids and nucleic acid bases with minerals; (d) using minerals with more organophilic characteristics; (e) using seawaters with different concentrations of ions (i.e. Na+, Ca2+, Mg2+, SO42− and Cl−); (f) using non-protein amino acids (AIB, α-ABA, β-ABA, γ-ABA and β-Ala and g) using nucleic acid bases other than adenine, thymine, uracil and cytosine. These experiments could be useful to clarify the role played by minerals in the origin of life on the Earth.