Many reasons for why extraterrestrial intelligences might avoid communications with our civilization have been proposed. One possible scenario is that all civilizations follow the lead of some particularly distinguished civilization. This paper will examine the impact the first successful civilization could have on all other subsequent civilizations within its sphere of influence and the ramifications of this as it relates to the Fermi Paradox. Monte Carlo simulation is used to map the inter-arrival times of early civilizations and to highlight the immense epochs of time that the earliest civilizations could have had the Galaxy to themselves.

Gamma-ray bursts (GRBs) are a class of highly energetic explosions emitting radiation in a very short timescale of a few seconds and with a very narrow opening angle. Although, all GRBs observed so far are extragalactic in origin, there is a high probability of a GRB of galactic origin beaming towards the Earth in the past ∼0.5 Gyr. We define the level of catastrophic damage to the biosphere as approximation 100 kJ m−2, based on Thomas et al. (2005a, b). Using results in Melott & Thomas (2011), we estimate the probability of the Earth receiving this fluence from a GRB of any type, as 87% during the last 500 Myr. Such an intense burst of gamma rays would ionize the atmosphere and deplete the ozone (O3) layer. With depleted O3, there will be an increased flux of Solar UVB on the Earth's surface with potentially harmful biological effects. In addition to the atmospheric damage, secondary particles produced by gamma ray-induced showers will reach the surface. Among all secondary particles, muons dominate the ground-level secondary particle flux (99% of the total number of particles) and are potentially of biological significance. Using the Monte Carlo simulation code CORSIKA, we modelled the air showers produced by gamma-ray primaries up to 100 GeV. We found that the number of muons produced by the electromagnetic component of hypothetical galactic GRBs significantly increases the total muon flux. However, since the muon production efficiency is extremely low for photon energies below 100 GeV, and because GRBs radiate strongly for only a very short time, we find that the biological radiation dose from secondary muons is negligible. The main mechanism of biological damage from GRBs is through Solar UVB irradiation from the loss of O3 in the upper atmosphere.

To ensure long-term survival of humans and Earth life generally, strategies need to be in place to recolonize Earth after global catastrophes and to colonize exoplanets. In one strategy of space colonization, the physical barriers erected by time and space are circumvented by sending cryopreserved human and animal embryos to exoplanets rather than adult crews. There the embryos would be developed to neonates in artificial uterus (AU) systems. A similar strategy could also be used to repopulate Earth after human extinction events. In this paper, we review the status and future prospects of these embryonic survival strategies. A critical requirement in each scenario is an AU system for complete ectogenesis, i.e. complete development of embryos to neonates outside the natural womb. While such systems do not yet exist, they may soon be developed to afford clinical assistance to infertile women and reproductive choices to prospective parents. In human survival schemes, AU systems would likely first be used to extend conventional survival missions (e.g. subterranean bunkers) by replacing some adult crew members with cryopreserved embryos. For major mass extinctions and all far future events, adult crews would be entirely replaced by embryos and androids. The most advanced missions would feature orbiting embryo spacecraft for Earth recolonization and analogous interstellar spacecraft for colonizing exoplanets. We conclude that an advanced civilization using such an integrated, embryonic approach could eventually colonize distant parts of its home galaxy and potentially the wider universe.

The Earth is constantly struck by radiation coming from the interstellar medium. The very low energy end of the spectrum is shielded by the geomagnetic field but charged particles with energies higher than the geomagnetic cutoff will penetrate the atmosphere and are likely to interact, giving rise to secondary particles. Some astrophysical events, such as γ-ray bursts and supernovae, when happening at short distances, may affect the planet's biosphere, due to the temporary enhanced radiation flux. Muons are abundantly produced by high-energy cosmic rays in the Earth's atmosphere. These particles, due to their low cross-section, are able to penetrate deep both underground and underwater, with the possibility of affecting biological niches normally considered shielded from radiation. We investigate the interaction of muons produced by high-energy cosmic rays on the Earth's atmosphere using the Geant4 toolkit. We analyse its penetration power in water and crust and also the interaction effects within bacteria-like material according to the particle type and energy, and noticed the possibility of off-track damage due to secondary particles.

Mars is a primary target of astrobiological interest: its past environmental conditions may have been favourable to the emergence of a prebiotic chemistry and, potentially, biological activity. In situ exploration is currently underway at the Mars surface, and the subsurface (2 m depth) will be explored in the future ESA ExoMars mission. In this context, BIOlogy and Mars EXperiment was performed to evaluate the stability and detectability of organic biomarkers under space and Mars-like conditions. Our data suggested that some target molecules, namely melanin, azelaic acid and nucleic acids, can be detected even after 16 months exposure to Low Earth Orbit conditions by multidisciplinary approaches. We used the same techniques as onboard the ExoMars rover, as Raman and infrared spectroscopies and gas chromatograph-mass spectrometer, and polymerase chain reaction even if this is not planned for the imminent mission to Mars. These results should be taken into account for future Mars exploration.

A simple stochastic model for evolution, based upon the need to pass a sequence of n critical steps is applied to both terrestrial and extraterrestrial origins of life. In the former case, the time at which humans have emerged during the habitable period of Earth suggests a value of n=4. Progressively adding earlier evolutionary transitions gives an optimum fit when n=5, implying either that their initial transitions are not critical or that habitability began around 6 Ga ago. The origin of life on Mars or elsewhere within the Solar System is excluded by the latter case and the simple anthropic argument is that extraterrestrial life is scarce in the Universe because it does not have time to evolve. Alternatively, the timescale can be extended if the migration of basic progenotic material to Earth is possible. If extra transitions are included in the model to allow for Earth migration, then the start of habitability needs to be even earlier than 6 Ga ago. Our present understanding of Galactic habitability and dynamics does not exclude this possibility. We conclude that Galactic punctuated equilibrium, proposed as a way round the anthropic problem, is not the only way of making life more common in the Galaxy.

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.

A new method is proposed to search for extraterrestrial life adapted to cold environments far from the Sun. To keep warm, using the light from a distant sun, any life-form must grow a system of optical concentrators, lenses or mirrors, to focus sunlight on to its vital parts. Any light not absorbed, or any heat radiation emitted from the vital parts, will be focused by the optical concentrators into a narrow beam pointing back towards the sun. To search for such life-forms, we should scan the sky with optical and infrared telescopes pointing directly away from the Sun. Any living vegetation will be seen as a bright patch in strong contrast to its dark surroundings, like the eyes of a nocturnal animal caught in the headlights of a car. This method of search may be used either with space-based or with ground-based telescopes. Examples of places where the method would work well are the surfaces of Europa, Trojan asteroids or Kuiper Belt objects. Any life-form that adapted successfully to a vacuum environment would be likely to spread widely over objects with icy surfaces in the outer regions of the solar system.

Environmental conditions have changed in the past of our planet but were not hostile enough to extinguish life. In the future, an aged Earth and a more luminous Sun may lead to harsh or even uninhabitable conditions for life. In order to estimate the life span of the biosphere we built a minimal model of the co-evolution of the geosphere, atmosphere and biosphere of our planet, taking into account temperature boundaries, CO2 partial pressure lower limits for C3 and C4 plants, and the presence of enough surface water. Our results indicate that the end of the biosphere will happen long before the Sun becomes a red giant, as the biosphere faces increasingly more difficult conditions in the future until its collapse due to high temperatures. The lower limit for CO2 partial pressure for C3 plants will be reached in 170(+ 320, − 110) Myr, followed by the C4 plants limit in 840(+ 270, − 100) Myr. The mean surface temperature will reach 373 K in 1.63(+ 0.14, − 0.05) Gyr, a point that would mark the extinction of the biosphere. Water loss due to internal geophysical processes will not be dramatic, implying almost no variation in the surface ocean mass and ocean depth for the next 1.5 billion years. Our predictions show qualitative convergence and some quantitative agreement with results found in the literature, but there is considerable scattering in the scale of hundreds of millions of years for all the criteria devised. Even considering these uncertainties, the end of the biosphere will hardly happen sooner than 1.5 Gyr.

The number of people able to end Earth's technical civilization has heretofore been small. Emerging dual-use technologies, such as biotechnology, may give similar power to thousands or millions of individuals. To quantitatively investigate the ramifications of such a marked shift on the survival of both terrestrial and extraterrestrial technical civilizations, this paper presents a two-parameter model for civilizational lifespans, i.e. the quantity L in Drake's equation for the number of communicating extraterrestrial civilizations. One parameter characterizes the population lethality of a civilization's biotechnology and the other characterizes the civilization's psychosociology. L is demonstrated to be less than the inverse of the product of these two parameters. Using empiric data from PubMed to inform the biotechnology parameter, the model predicts human civilization's median survival time as decades to centuries, even with optimistic psychosociological parameter values, thereby positioning biotechnology as a proximate threat to human civilization. For an ensemble of civilizations having some median calculated survival time, the model predicts that, after 80 times that duration, only one in 1024 civilizations will survive – a tempo and degree of winnowing compatible with Hanson's ‘Great Filter.’ Thus, assuming that civilizations universally develop advanced biotechnology, before they become vigorous interstellar colonizers, the model provides a resolution to the Fermi paradox.

If advanced civilizations appear in the universe with an ability and desire to expand, the entire universe can become saturated with life on a short timescale, even if such expanders appear rarely. Our presence in an apparently untouched Milky Way thus constrains the appearance rate of galaxy-spanning Kardashev type III (K3) civilizations, if it is assumed that some fraction of K3 civilizations will continue their expansion at intergalactic distances. We use this constraint to estimate the appearance rate of K3 civilizations for 81 cosmological scenarios by specifying the extent to which humanity is a statistical outlier. We find that in nearly all plausible scenarios, the distance to the nearest visible K3 is cosmological. In searches for K3 galaxies where the observable range is limited, we also find that the most likely detections tend to be expanding civilizations who have entered the observable range from farther away. An observation of K3 clusters is thus more likely than isolated K3 galaxies.

Finding life in the Universe entirely different to the one evolved on Earth is probable. This is a significant constraint for life-detecting instruments that were sent and may be sent elsewhere in the solar system, as how could we detect life as ‘we don't know it’? How could we detect something when we have no prior knowledge of its composition or how it looks like? Here we argue that disregarding the type of lifeform that could be envisioned, all must share in common the attribute of being entities that decrease their internal entropy at the expense of free energy obtained from its surroundings. As entropy quantifies the degree of disorder in a system, any envisioned lifeform must have a higher degree of order than its supporting environment. Here, we show that by using fractal mathematics analysis alone, one can readily quantify the degree of entropy difference (and thus, their structural complexity) of living processes (lichen growths and plant growing patterns in this case) as distinct entities separate from its similar abiotic surroundings. This approach may allow possible detection of unknown forms of life based on nothing more than entropy differentials of complementary datasets. Future explorations in the solar system, like Mars or Titan, may incorporate this concept in their mission planning in order to detect potential endemic lifeforms.

How special (or not) is the epoch we are living in? What is the appropriate reference class for embedding the observations made at the present time? How probable – or else – is anything we observe in the fulness of time? Contemporary cosmology and astrobiology bring those seemingly old-fashioned philosophical issues back into focus. There are several examples of contemporary research which use the assumption of typicality in time (or temporal Copernicanism) explicitly or implicitly, while not truly elaborating upon the meaning of this assumption. The present paper brings attention to the underlying and often uncritically accepted assumptions in these cases. It also aims to defend a more radical position that typicality in time is not – and cannot ever be – well-defined, in contrast to the typicality in space, and the typicality in various specific parameter spaces. This, of course, does not mean that we are atypical in time; instead, the notion of typicality in time is necessarily somewhat vague and restricted. In principle, it could be strengthened by further defining the relevant context, e.g. by referring to typicality within the Solar lifetime, or some similar restricting clause.

Mechanisms of interstellar panspermia have recently been identified whereby life, wherever it has originated, will disperse throughout the habitable zone of the Galaxy within a few billion years. This re-opens the question of where life originated. The interiors of comets, during their aqueous phase, seem to provide environments no less favourable for the origin of life than that of the early Earth. Their combined mass throughout the Galaxy overwhelms that of suitable terrestrial environments by about 20 powers of ten, while the lifetimes of friendly prebiotic environments within them exceeds that of localized terrestrial regions by another four or five powers of ten. We propose that the totality of comets around G-dwarf Sun-like stars offers an incomparably more probable setting for the origin of life than any that was available on the early Earth.

Atmospheric pressure glow-discharge (APGD) plasmas have been proposed for sterilizing spacecraft surfaces prior to launch. The advantages of APGD plasmas for the sterilization of spacecraft surfaces include low temperatures at treatment sites, rapid inactivation kinetics of exposed microbial cells, physical degradation and removal of microbial cells, physical removal of organic biosignature molecules, and short exposure times for the materials. However, few studies have tested APGD plasmas on spacecraft materials for their effectiveness in both sterilizing surfaces and removal of microbial cells or spores. A helium (He)+oxygen (O2) APGD plasma was used to expose six spacecraft materials (aluminum 6061, polytetrafluoroethylene (PTFE), polycarbonate, Saf-T-Vu, Rastex, and Herculite 20) doped with spores of the common spacecraft contaminant, Bacillus subtilis, for periods of time up to 6 min. Results indicated that greater than six orders of magnitude reductions in viability were observed for B. subtilis spores in as short of time as 40 s exposure to the APGD plasmas. Spacecraft materials were not affected by exposures to the APGD plasmas. However, Saf-T-Vu was the only material in which spores of B. subtilis adhered more aggressively to plasma-treated coupons when compared to non-plasma treated coupons; all other materials exhibited no significant differences between plasma and non-plasma treated coupons. In addition, spores of B. subtilis were physically degraded by exposures to the plasmas beginning at the terminal ends of spores, which appeared to be ruptured after only 30 s. After 300 s, most bacteria were removed from aluminium coupons, and only subtle residues of bacterial secretions or biofilms remained. Results support the conclusion that APGD plasmas can be used as a prelaunch cleaning and sterilization treatment on spacecraft materials provided that the biocidal and cleaning times are shorter than those required to alter surface properties of materials.

Despite tremendous interest in the topic and decades of research, the origins of the major losses of biodiversity in the history of life on Earth remain elusive. A variety of possible causes for these mass-extinction events have been investigated, including impacts of asteroids or comets, large-scale volcanic eruptions, effects from changes in the distribution of continents caused by plate tectonics, and biological factors, to name but a few. Many of these suggested drivers involve or indeed require changes of Earth's climate, which then affect the biosphere of our planet, causing a global reduction in the diversity of biological species. It can be argued, therefore, that a detailed understanding of these climatic variations and their effects on ecosystems are prerequisites for a solution to the enigma of biological extinctions. Apart from investigations of the paleoclimate data of the time periods of mass extinctions, climate-modelling experiments should be able to shed some light on these dramatic events. Somewhat surprisingly, however, only a few comprehensive modelling studies of the climate changes associated with extinction events have been undertaken. These studies will be reviewed in this paper. Furthermore, the role of modelling in extinction research in general and suggestions for future research are discussed.

Astrobiology is usually defined as the study of the origin, evolution, distribution and future of life in the Universe. As such it is inherently interdisciplinary and cannot help but engender a worldview infused by cosmic and evolutionary perspectives. Both these attributes of the study of astrobiology are, and will increasingly prove to be, beneficial to society regardless of whether extraterrestrial life is discovered or not.

In the previous paper ring (Osmanov 2016) (henceforth Paper-I) we have extended the idea of Freeman Dyson and have shown that a supercivilization has to use ring-like megastructures around pulsars instead of a spherical shell. In this work we reexamine the same problem in the observational context and we show that facilities of modern infrared (IR) telescopes (Very Large Telescope Interferometer and Wide-field Infrared Survey Explorer (WISE)) might efficiently monitor the nearby zone of the solar system and search for the IR Dyson-rings up to distances of the order of 0.2 kpc, corresponding to the current highest achievable angular resolution, 0.001 mas. In this case the total number of pulsars in the observationally reachable area is about 64 ± 21. We show that pulsars from the distance of the order of ~ 1 kpc are still visible for WISE as point-like sources but in order to confirm that the object is the neutron star, one has to use the ultraviolet telescopes, which at this moment cannot provide enough sensitivity.

The beaching and stranding of whales and dolphins around the world has been mystifying scientists for centuries. Although many theories have been proposed, few are substantiated by unequivocal statistical evidence. Advances in the field of animal magnetoreception have established that many organisms, including cetaceans, have an internal ‘compass,’ which they use for orientation when traveling long distances. Astrobiology involves not only the origin and distribution of life in the universe, but also the scientific study of how extraterrestrial conditions affect evolution of life on planet Earth. The focus of this study is how cetacean life is influenced by disturbances in its environment that originate from an astrological phenomenon – in the present study that involves solar flares and cetacean beachings. Solar storms are caused by major coronal eruptions on the Sun. Upon reaching Earth, they cause disturbances in Earth's normally stable magnetosphere. Unable to follow an accurate magnetic bearing under such circumstances, cetaceans lose their compass reading while travelling and, depending on their juxtaposition and nearness to land, eventually beach themselves. (1) This hypothesis was supported by six separate, independent surveys of beachings: (A) in the Mediterranean Sea, (B) the northern Gulf of Mexico, (C) the east and (D) west coasts of the USA and two surveys (E and F) from around the world. When the six surveys were pooled (1614 strandings), a highly significant correlation (R2 = 0.981) of when strandings occurred with when major geomagnetic disturbances in Earth's magnetosphere occurred was consistent with this hypothesis. (2) Whale and dolphin strandings in the northern Gulf of Mexico and the east coast of the USA were correlated (R2 = 0.919, R2 = 0.924) with the number of days before and after a geomagnetic storm. (3) Yearly strandings were correlated with annual geomagnetic storm days. (4) Annual beachings of cetaceans from 1998 to 2012 were linearly correlated (R2 = 0.751) with frequency of annual sunspot numbers. Thus, consistently strong statistical correlation evidence indicates that an astronomical phenomenon – solar flares – can cause cetaceans to change their behaviour and become disoriented, which eventually causes them to swim onto a shore and beach themselves.

Several instruments based on immunoassay techniques have been proposed for life-detection experiments in the framework of planetary exploration but few experiments have been conducted so far to test the resistance of antibodies against cosmic ray particles. We present several irradiation experiments carried out on both grafted and free antibodies for different types of incident particles (protons, neutrons, electrons and 12C) at different energies (between 9 MeV and 50 MeV) and different fluences. No loss of antibodies activity was detected for the whole set of experiments except when considering protons with energy between 20 and 30 MeV (on free and grafted antibodies) and fluences much greater than expected for a typical planetary mission to Mars for instance. Our results on grafted antibodies suggest that biochip-based instruments must be carefully designed according to the expected radiation environment for a given mission. In particular, a surface density of antibodies much larger than the expected proton fluence would prevent significant loss of antibodies activity and thus assuring a successful detection.