Making predictions about aliens is not an easy task. Most previous work has focused on extrapolating from empirical observations and mechanistic understanding of physics, chemistry and biology. Another approach is to utilize theory to make predictions that are not tied to details of Earth. Here we show how evolutionary theory can be used to make predictions about aliens. We argue that aliens will undergo natural selection – something that should not be taken for granted but that rests on firm theoretical grounds. Given aliens undergo natural selection we can say something about their evolution. In particular, we can say something about how complexity will arise in space. Complexity has increased on the Earth as a result of a handful of events, known as the major transitions in individuality. Major transitions occur when groups of individuals come together to form a new higher level of the individual, such as when single-celled organisms evolved into multicellular organisms. Both theory and empirical data suggest that extreme conditions are required for major transitions to occur. We suggest that major transitions are likely to be the route to complexity on other planets, and that we should expect them to have been favoured by similarly restrictive conditions. Thus, we can make specific predictions about the biological makeup of complex aliens.

Extreme environments on Earth often provide similar terrain conditions to landing/operation sites on Moon and Mars. Several field campaigns (EuroGeoMars2009 and DOMMEX/ILEWG EuroMoonMars from November 2009 to March 2010) were conducted at the Mars Desert Research Station (MDRS) in Utah. Some of the key astrobiology results are presented in this special issue on ‘Astrobiology field research in Moon/Mars analogue environments’ relevant to investigate the link between geology, minerals, organics and biota. Preliminary results from a multidisciplinary field campaign at Rio Tinto in Spain are presented.

Cyanobacteria are capable of surviving the adverse conditions of low Earth orbit (LEO). We have previously demonstrated that Gloeocapsa strain OU_20, Chroococcidiopsis and akinetes of Anabaena cylindrica were able to survive 548 days of exposure to LEO. Motivated by an interest to understand how cyanobacteria can survive in LEO, we studied the strategies that Gloeocapsa strain OU_20 employs to survive in its natural environment, the upper region of the intertidal zone. Here, cyanobacteria are exposed to fluctuations in temperature, UV radiation, desiccation and salinity. We demonstrated that an increase in salinity from 6.5‰ (BG-11 medium) to 35.7‰ (similar to that of seawater), resulted in increased resistance to UV radiation (254 nm), vacuum (0.7×10−3±0.01 kPa) and cold temperatures (–20 °C). Concomitantly, biochemical analyses demonstrated that the amount of fatty acids and mycosporine-like amino acids (a UV absorbing pigment) were higher in the stressed cells. Morphological analysis demonstrated that the electron density and thickness of the mucilaginous sheath were also greater than in the control cells. Yet, the control and stressed cells both formed aggregates. As a result of studying the physiological adaptation of Gloeocapsa strain OU_20 in response to salinity, we postulate that survival in the high-intertidal zone and LEO involves a dense extracellular mucilaginous sheath and the formation of aggregates. We conclude that studying the physiological adaptation of cyanobacteria in the intertidal zone provides insight into understanding survival in LEO.

Panspermia (‘seeds everywhere’) postulates that life naturally migrates through space. Laboratory studies of Panspermia often examine the survival of Earth's species under the conditions thought to occur during transfer through space. Much of this research has centred on bacteria, but here we consider seeds themselves. We simulated the extreme accelerations necessary for their hypothetical ejection from a planetary surface and the impacts associated with their arrival on another planet. Seeds of tobacco, alfalfa and cress were fired into water at speeds in the range 1–3 km s−1, corresponding to impact shock pressures of circa 0.24–2.4 GPa. No seeds remained intact and able to germinate, even at the lowest speeds. Although fragmentation occurred, even at 3 km s−1 the size of some of the fragments was about 25% that of the seeds. Thus, whilst the seeds themselves did not survive extreme shocks, a substantial fraction of their mass did and might successfully deliver complex organic materials after impact. These results are discussed with respect to ancient Panspermia and the potential of contemporary impacts to eject living organisms into space.

Life inhabits the subsurface of the Earth down to depths where temperature precludes it. Similar conditions are likely to exist within the traditional habitable zone for objects between 0.1 Earth mass (Mars) and 10 Earth masses (superearth). Long-term cooling and internal radioactivity maintain surface heat flow on the Earth. These heat sources are comparable and likely to be comparable in general within old rocky planets. Surface heat flow scales with mass divided by surface area and hence with surface gravity. The average absolute habitable subsurface thickness scales inversely with heat flow and gravity. Surface gravity varies by only 0.4 g for Mars to 3.15 g for a superearth. This range is less than the regional variation of heat flow on the Earth. Still ocean-boiling asteroid impacts (if they occur) are more likely to sterilize the thin habitable subsurface of large objects than thick habitable subsurface of small ones. Tectonics self-organizes to maintain subsurface permeability and habitability within both stable and active regions on the Earth. Small earthquakes within stable regions allow sudden mixing of water masses. Large earthquakes at plate boundaries allow surface water to descend to great habitable depths. Seismic shaking near major faults cracks shallow rock forming permeable regolith. Strong tidal strains form a similar porous regolith on small bodies such as Enceladus with weak stellar heating. This regolith may be water-saturated within rocky bodies and thus habitable.

Phyllosilicate minerals and hydrated sulphate minerals have been positively identified on the surface of Mars. Studies conducted on Earth indicate that micro-organisms influence various geochemical and mineralogical transitions for the sulphate and phyllosilicate minerals. These minerals in turn provide key nutrients to micro-organisms and influence microbial ecology. Therefore, the presence of these minerals in astrobiology studies of Earth–Mars analogue environments could help scientists better understand the types and potential abundance of micro-organisms and/or biosignatures that may be encountered on Mars. Bulk X-ray diffraction of samples collected during the EuroGeoMars 2009 campaign from the Mancos Shale, the Morrison and the Dakota formations near the Mars Desert Research Station in Utah show variable but common sedimentary mineralogy with all samples containing quantities of hydrated sulphate minerals and/or phyllosilicates. Analysis of the clay fractions indicate that the phyllosilicates are interstratified illite–smectites with all samples showing marked changes in the diffraction pattern after ethylene glycol treatment and the characteristic appearance of a solvated peak at ∼17 Å. The smectite phases were identified as montmorillonite and nontronite using a combination of the X-ray diffraction data and Fourier–Transform Infrared Spectroscopy. The most common sulphate mineral in the samples is hydrated calcium sulphate (gypsum), although one sample contained detectable amounts of strontium sulphate (celestine). Carbonates detected in the samples are variable in composition and include pure calcium carbonate (calcite), magnesium-bearing calcium carbonate (dolomite), magnesium, iron and manganese-bearing calcium carbonate (ankerite) and iron carbonate (siderite). The results of these analyses when combined with organic extractions and biological analysis should help astrobiologists and planetary geologists better understand the potential relationships between mineralogy and microbiology for planetary missions.

The vital ultraviolet- (UV-) protective and photosynthetic pigments of cyanobacteria and lichens (microbial symbioses) that dominate primary production in Antarctic desert ecosystems auto-fluoresce at short wavelengths. We therefore use a long-wavelength (1064 nm) infrared laser for non-intrusive in situ Raman spectrometry of their ecologically significant compounds (especially pigments). To confirm that the power loss at this longer wavelength is justified to avoid swamping by background fluorescence, we compared Raman spectra obtained with excitation at 1064, 852, 830, 785, 633 and 515 nm. These are typical of lasers used for Raman spectroscopy. We analysed communities of the cyanobacterium Nostoc commune and the highly pigmented lichens Acarospora chlorophana and Caloplaca saxicola. These require screening compounds (e.g. pigments such as scytonemin in cyanobacteria and rhizocarpic acid in the fungal symbiont of lichens). They are augmented by quenching pigments (e.g. carotenoids) to dissipate the energy of free radicals generated by penetrating UV. We also analysed organisms having avoidance strategies (e.g. endolithic communities within translucent rocks, including the common cyanobacterium Chroococcidiopsis). These require accessory pigments for photosynthesis at very low light intensities. Although some organisms gave useable Raman spectra with short-wavelength lasers, 1064 nm was the only excitation that was consistently excellent for all organisms. We conclude that a 1064 nm Raman spectrometer, miniaturized using an InGaAs detector, is the optimal instrument for in situ studies of pigmented microbial communities at the limits of life on Earth. This has practical potential for the quest for biomolecules residual from any former surface life on Mars.

First contact with another civilization, or simply another intelligence of some kind, will likely be quite different depending on whether that intelligence is more or less advanced than ourselves. If we assume that the lifetime distribution of intelligences follows an approximately exponential distribution, one might naively assume that the pile-up of short-lived entities dominates any detection or contact scenario. However, it is argued here that the probability of contact is proportional to the age of said intelligence (or possibly stronger), which introduces a selection effect. We demonstrate that detected intelligences will have a mean age twice that of the underlying (detected + undetected) population, using the exponential model. We find that our first contact will most likely be with an older intelligence, provided that the maximum allowed mean lifetime of the intelligence population, τmax, is ≥ e times larger than our own. Older intelligences may be rare but they disproportionately contribute to first contacts, introducing what we call a ‘contact inequality’, analogous to wealth inequality. This reasoning formalizes intuitional arguments and highlights that first contact would likely be one-sided, with ramifications for how we approach SETI.

In the frame of the EXPOSE-R mission outside the Russian Zvezda Module of the International Space Station (ISS) passive thermoluminescence dosimeters were applied to measure the radiation exposure of biological samples. The detectors were located beneath the sample carriers to determine the dose levels for maximum shielding. The dose measured beneath the sample carriers varied between 317 ± 10 and 230 ± 2 mGy, which amount to an average dose rate of 381 ± 12 and 276 ± 2 μGy d−1. These values are close to those assessed for the interior of the ISS and reflect the high shielding of the biological experiments within the EXPOSE-R facility. As a consequence of the high shielding (several g cm−2), the biological samples were predominantly exposed to galactic cosmic heavy ions and trapped protons in the Earth's radiation belts, whereas the trapped electrons did not reach the samples.

Lichen-dominated cryptoendolithic communities from the Dry Valleys of Antarctica have been the subject of much research over recent years owing to their potential as analogues of Martian life forms. Their ability to mobilize iron compounds and organize themselves into distinct coloured biotic zones suggests that they may alter the chemistry of their host rock. By conducting a major, minor and trace element study utilizing inductively coupled plasma atomic emission spectroscopy (ICP-AES) and mass spectrometry (ICP-MS) techniques, we have been investigating the relationship between the microbes and the chemistry of the sandstones. Different layers within a suite of sandstones collected from six localities in the Dry Valleys have been analysed to establish if or how the microbes influence or directly affect the chemical composition of the rocks. Background petrographic studies have shown significant differences in mineralogical maturity between rocks colonized by the communities and those that are not, and the chemistry results have shown significant elemental disparity between colonized and uncolonized rocks. By obtaining accurate percentages of the minerals present in each sample the differences in elemental concentrations could be construed to be caused by the differences in mineralogy between samples. The nature and extent of the concentration differences has led to the conclusion that either the cryptoendolith communities are able to alter their host rock by the solubilization and mobilization of elements that are then subsequently removed or that the organisms are simple opportunists that can only successfully colonize rocks that provide the ideal substrate, being mineralogically mature with ample pore space and less concentrated in the elements tested for.

Homochirality is an essential feature of biology, but how it developed in early life remains unclear. Our aim in this paper is to add to the discussion by taking a somewhat arbitrary but definite sequence of events and examining carefully the chirality at each stage. Our scenario for the development of life starts with the prebiotic, continues through a pre-RNA stage to the RNA world. This leads to the development of proteins and then to the incorporation of DNA in RNA–DNA–protein biochemistry.

We argue that homochirality probably did not develop prebiotically. We see the likely chiral bifurcation point to be during the development of RNA from an achiral pre-RNA. Surprisingly, we find the driving force for this to be enantiomeric cross-inhibition in which the addition of a ‘wrong-handed’ enantiomer to a growing polymer brings the polymerization to a halt. This, it is often argued, is a serious impediment to the development of chiral purity. We suggest that the sign of handedness at this stage was probably determined by chance. We then point out that homochiral RNA was unlikely by itself to lead to homochiral proteins. We identify the additional nonlinear feature required for bifurcation to be the rapid increase in enzymic power available when the amino acids in proteins approach single handedness and structural features such as α-helices and β-sheets become viable. If this is correct, then the handedness of the protein sector is indeed linked to that of RNA. However, the relative sign of the two handednesses will have depended on the precise stereo-sensitive interaction between the RNA and protein systems. We suggest that the most plausible scenario is via the recently discovered RNA binding sites for amino acids, which are both stereo-selective and have contact with the developing genetic code. The detailed steps that determine the handedness are not yet clear and may be specific to the precise development path.

It follows that if biochemistry similar to that on Earth developed extraterrestrially, we would surely have homochirality but at this stage we cannot be sure about the handedness of either the nucleic acid or the protein components.

Gamma-ray bursts (GRBs) are likely to have made a number of significant impacts on the Earth during the last billion years. The gamma radiation from a burst within a few kiloparsecs would quickly deplete much of the Earth's protective ozone layer, allowing an increase in solar ultraviolet radiation reaching the surface. This radiation is harmful to life, damaging DNA and causing sunburn. In addition, NO2 produced in the atmosphere would cause a decrease in visible sunlight reaching the surface and could cause global cooling. Nitric acid rain could stress portions of the biosphere, but the increased nitrate deposition could be helpful to land plants. We have used a two-dimensional atmospheric model to investigate the effects on the Earth's atmosphere of GRBs delivering a range of fluences, at various latitudes, at the equinoxes and solstices, and at different times of day. We have estimated DNA damage levels caused by increased solar UVB radiation, reduction in solar visible light due to NO2 opacity, and deposition of nitrates through rainout of HNO3. In this paper we give a concise review of this work and discuss current and future work on extending and improving our estimates of the terrestrial impact of a GRB.

We discuss whether it is possible to test the universality of biology, a quest that is of paramount relevance for one of its most recent branches, namely astrobiology. We review this topic in terms of the relative roles played on the Earth biota by contingency and evolutionary convergence. Following the seminal contribution of Darwin, it is reasonable to assume that all forms of life known to us so far are not only terrestrial, but are descendants of a common ancestor that evolved on this planet at the end of a process of chemical evolution. We also raise the related question of whether the molecular events that were precursors to the origin of life on Earth are bound to occur elsewhere in the Universe, wherever the environmental conditions are similar to the terrestrial ones. We refer to ‘cosmic convergence’ as the possible occurrence elsewhere in the Universe of Earth-like environmental conditions. We argue that cosmic convergence is already suggested by observational data. The set of hypotheses for addressing the question of the universality of biology can be tested by future experiments that are feasible with current technology. We focus on landing on Europa and the broader implications of selecting the specific example of the right landing location. We have previously discussed the corresponding miniaturized equipment that is already in existence. The significance of these crucial points needs to be put into a wider scientific perspective, which is one of the main objectives of this review.

A hypothesis is proposed about potassium ponds being the cradles of life enriches the gamut of ideas about the possible conditions of pre-biological evolution on the primeval Earth, but does not bring us closer to solving the real problem of the origin of life. The gist of the matter lies in the mechanism of making a delimitation between two environments – the intracellular environment and the habitat of protocells. Since the sodium–potassium pump (Na+/K+-ATPase) was discovered, no molecular model has been proposed for a predecessor of the modern sodium pump. This has brought into life the idea of the potassium pond, wherein protocells would not need a sodium pump. However, current notions of the operation of living cells come into conflict with even physical laws when trying to use them to explain the origin and functioning of protocells. Thus, habitual explanations of the physical properties of living cells have become inapplicable to explain the corresponding properties of Sidney Fox's microspheres. Likewise, existing approaches to solving the problem of the origin of life do not see the need for the comparative study of living cells and cell models, assemblies of biological and artificial small molecules and macromolecules under physical conditions conducive to the origin of life. The time has come to conduct comprehensive research into the fundamental physical properties of protocells and create a new discipline – protocell physiology or protophysiology – which should bring us much closer to solving the problem of the origin of life.

Binaries could provide the best niches for life in the Galaxy. Although counterintuitive, this assertion follows directly from stellar tidal interaction theory and the evolution of lower mass stars. There is strong evidence that chromospheric activity of rapidly rotating young stars may be high enough to cause mass loss from atmospheres of potentially habitable planets. The removal of atmospheric water is most critical. Tidal breaking in binaries could help reduce magnetic dynamo action and thereby chromospheric activity in favour of life. We call this the Binary Habitability Mechanism (BHM) that we suggest allows for water retention at levels comparable to or better than the Earth. We discuss novel advantages that life may exploit, in these cases, and suggest that life may even thrive on some circumbinary planets. We find that while many binaries do not benefit from BHM, high-quality niches do exist for various combinations of stars between 0.55 and 1.0 solar masses. For a given pair of stellar masses, BHM operates only for certain combinations of period and eccentricity. Binaries having a solar-type primary seem to be quite well-suited niches having wide and distant habitable zones with plentiful water and sufficient light for photosynthetic life. We speculate that, as a direct result of BHM, conditions may be suitable for life on several planets and possibly even moons of giant planets orbiting some binaries. Lower mass combinations, while more restrictive in parameter space, provide niches lasting many billions of years and are rich suppliers of photosynthetic photons. We provide a publicly available web-site (http://bit.ly/BHM-calculator or http://bit.ly/BHM-calculator-mirror), which calculates the BHM effects presented in this paper.

The data recently accumulated by the Kepler mission have demonstrated that small planets are quite common and that a significant fraction of all stars may have an Earth-like planet within their habitable zone. These results are combined with a Drake-equation formalism to derive the space density of biotic planets as a function of the relatively modest uncertainty in the astronomical data and of the (yet unknown) probability for the evolution of biotic life, Fb. I suggest that Fb may be estimated by future spectral observations of exoplanet biomarkers. If Fb is in the range 0.001–1, then a biotic planet may be expected within 10–100 light years from Earth. Extending the biotic results to advanced life I derive expressions for the distance to putative civilizations in terms of two additional Drake parameters – the probability for evolution of a civilization, Fc, and its average longevity. For instance, assuming optimistic probability values (Fb~Fc~1) and a broadcasting longevity of a few thousand years, the likely distance to the nearest civilizations detectable by searching for intelligent electromagnetic signals is of the order of a few thousand light years. The probability of detecting intelligent signals with present and future radio telescopes is calculated as a function of the Drake parameters. Finally, I describe how the detection of intelligent signals would constrain the Drake parameters.

We consider the suggestion that, as a matter of caution, the deliberate broadcast of signals to the cosmos should be proscribed. We explore the likely capabilities of extraterrestrial societies that might conceivably pose a threat to our species and show that this suggestion is without merit because even if followed, it would fail to keep our existence secret. In addition, trying to limit signalling activities would be a burden on our descendants, crippling their own activities for the indefinite future. A corollary to these considerations affects the search for extraterrestrial intelligence (SETI): namely, it seems inarguable that technologically advanced beings will assume that other societies are capable of detecting their leakage. Consequently, the premise that SETI should expect to find deliberate beacons from other worlds may be mistaken.

Recent findings on the presence of water on Mars (Baker, V.R. (2006). Geomorphological evidence for water on Mars. Elements2(3), 139–143; DeJong, E. (2006). Geological evidence of the presence of water on Mars. Abstracts from the 40th Western Regional Meeting of the American Chemical Society, Anaheim, CA, January, 2006, pp. 22–25. American Chemical Society, Washington, DC; McSween, H.Y. Jr. (2006). Water on Mars. Elements2(3), 135–137; Mitrofanov, I.G. (2005). Water explorations on Mars. Priroda9, 34–43) strongly suggest that there existed a period of chemical evolution eventually leading to life processes on primitive Mars (Kanavarioti, A. & Maneinelli, R.L. (1990). Could organic matter have been preserved on Mars for 3.5 billion years. Icarus84, 196–202). Owing to the adverse conditions, it is quite likely that the process of chemical evolution would have been suppressed and any living organisms that formed would have become extinct over time on Mars. The presence of water as a necessity for the survival of living organisms and the presence of grey haematite, originated under aqueous conditions, have led us to investigate the possible role of haematite in the chemical evolution on Mars. Our observations suggest that iron oxide hydroxide (FeOOH), a precursor of haematite, has a much higher binding affinity towards ribose nucleotides (the building blocks of RNA) than the haematite itself. This would mean that during the process of haematite formation, especially through the probable process of Fe3+ hydrolysis by aqueous ammonia, the precursors of haematite might have played a significant role in the processes leading to chemical evolution and the possible origin of life on Mars.

We use the critical step model to study the major transitions in evolution on Earth. We find that a total of five steps represents the most plausible estimate, in agreement with previous studies, and use the fossil record to identify the potential candidates. We apply the model to Earth-analogs around stars of different masses by incorporating the constraints on habitability set by stellar physics including the habitable zone lifetime, availability of ultraviolet radiation for prebiotic chemistry, and atmospheric escape. The critical step model suggests that the habitability of Earth-analogs around M-dwarfs is significantly suppressed. The total number of stars with planets containing detectable biosignatures of microbial life is expected to be highest for K-dwarfs. In contrast, we find that the corresponding value for intelligent life (technosignatures) should be highest for solar-mass stars. Thus, our work may assist in the identification of suitable targets in the search for biosignatures and technosignatures.

From a biological point of view, all environments in the Universe can be categorized into one of three types: uninhabitable, uninhabited habitat or inhabited habitat. This paper describes and defines different habitat types in the Universe with a special focus on environments not usually encountered on the Earth, but which might be common on other planetary bodies. They include uninhabited habitats, subtypes of which are sterile habitats and organic-free habitats. Examples of the different types of environments are provided with reference to the Eyjafjallajökull, Iceland. These habitat types are used to identify testable hypotheses on the abundance of different habitats and the distribution of life in the Universe.