Laser-ablation inductively coupled plasma mass spectroscopy analyses have been performed on carbonaceous filamentous structures that have been interpreted as fossilized microorganisms containing ~10–50 wt% Fe and on non-carbonaceous filamentous structures that have been interpreted to have been formed abiotically containing ~80 wt% Fe. The obtained laser-ablation profiles of the two structural types show a distinct difference in the iron isotopic variations. The centers of the carbonaceous filaments are enriched in 57Fe and 58Fe and depleted in 56Fe. The surficial parts of the filaments display an opposite behavior of the iron isotopes and are thus enriched in 56Fe and depleted in 57Fe and 58Fe. 54Fe usually follows 57Fe and 58Fe but in some cases it follows 56Fe instead. The outer, surficial parts enriched in 56Fe have been interpreted as iron oxides precipitated on the surfaces of the microorganisms as they mediate oxidation of the iron to achieve metabolic energy. The laser-ablation profiles of the abiotically formed non-carbonaceous filamentous structures do not show the same characteristics as the carbonaceous filaments but only irregular elevations of 56Fe. The characteristic profile patterns of the isotope variations in the microfossils suggest that microbially formed iron oxides may be enriched in 56Fe. If that is the case the isotopic profiles could be used to distinguish abiotically formed iron oxides from biologically formed oxides.

For the first time the kinetic rate constants of the UV photolysis of polyynes C6H2, C8H2, C10H2, C12H2 and C14H2 under rigorously inert atmosphere have been determined in three different solvents: n-hexane, n-heptane and decalin. First- or pseudofirst-order kinetics appear suitable to describe the photolysis of these molecules and k values in the range between 3.0×10−3 s−1 and 4.6×10−3 s−1 have been determined. The unique exception is represented by C6H2 which photolyses more slowly with k=3.2×10−4 s−1. Two different UV sources have been used in the present study: a low-pressure mercury lamp having a monochromatic emission at 253.7 nm and a medium-to high-pressure lamp with a continuous emission between 222 nm and 580 nm. The results are of interest in the understanding, and also the modelling, of the fate of polyynes released by carbon-rich stars in the interstellar medium or the polyynes released by comets in their active phase.

There have been several attempts to answer the question of whether there is, or has ever been, life on Mars. The boldest attempt was the only ever life detection experiment conducted on another planet: the Viking mission. The mission was a great success, but it failed to provide a clear answer to the question of life on Mars. More than 30 years after the Viking mission our understanding of the history and evolution of Mars has increased vastly to reveal a wetter Martian past and the occurrence of diverse environments that could have supported microbial life similar to that on Earth for extended periods of time. The discovery of Terran extremophilic microorganisms, adapted to environments previously though to be prohibitive for life, has greatly expanded the limits of habitability in our Solar System, and has opened new avenues for the search of life on Mars. Remnants of a possible early biosphere may be found in the Martian meteorite ALH84001. This claim is based on a collection of facts and observations consistent with biogenic origins, but individual links in the collective chain of evidence remain controversial. Recent evidence for contemporary liquid water on Mars and the detection of methane in the Martian atmosphere further enhance the case for life on Mars. We argue that, given the cumulative evidence provided, life has and is likely to exist on Mars, and we have already found evidence of it. However, to obtain a compelling certainty a new mission is needed, one which is devoted to the detection of life on Mars.

Mars has surely been scrutinised since the dawn of humankind. Its appearance every couple of years like a drop of blood in the sky led to warlike attributes in the ancient world. In the 16th century Tycho Brahe made accurate observations of the position of Mars that enabled Johannes Kepler to obtain his first two laws of planetary motion. These in turn were explained by Newton's laws of motion and gravity. In the 17th century the first telescope observations were made, but Mars is small and very little surface detail could be discerned.

Throughout the 18th and 19th centuries telescopes improved, revealing many dark areas on the red tinted surface. During the close opposition of 1877 sufficient detail could be seen that enabled Giovanni Schiaparelli to announce that he could see about 40 canali on Mars. This led to the saga of the canals of Mars, finally laid to rest in 1971 when Mariner 9 made observations from Martian orbit showing that the canali/canals do not exist.

Belief that there was life on Mars was widespread in the 19th century. However, the majority of astronomers never believed in Martian intelligence. Least controversial was the view that the dark areas were some form of plant life. This view persisted until Mariner 4 flew past Mars in 1965 and discovered a far thinner atmosphere than previously thought. This was a low point, with impact craters dominating the images. It was Mariner 9 that revealed much more promising landscapes, including volcanic features, and others indicating that water had flowed across the surface, particularly when Mars was young. Thus, the contemporary era of Mars exploration began.

Our picture of Mars today is not only much more complete than that before Mariner 4, in several ways it is quite different. The belief, however, that there might be life on Mars persists – subsurface life cannot be ruled out and, failing that, there might be ancient fossils on Mars.

Heat produced in the mantle and core of the Earth by the decay of radioactive elements and mineral fusion results in large-scale mantle convection. The outer shell of the Earth that floats on the convective mantle is divided into rigid lithospheric plates. Subduction of dense cold plates into the mantle leads to plate tectonics. At divergent plate margins, heat is dissipated through hydrothermal convection cells. As ocean water is entrained into hydrothermal cells it interacts with fresh magmatic rocks and liberates ferrous iron. This iron reduces the ocean water to such an extent that it decomposes and forms hydrogen. Molecular hydrogen, as the most reduced component in the system, forms a basal component to a deep dark biosphere powered by metastable redox gradients. In this paper we review the driving force behind a hydrogen-driven deep biosphere. We present abundant observations of hydrogen produced at natural hydrothermal settings as well as in laboratory experiments. The key mineral reactions responsible for the bulk of this hydrogen production are then presented. A division of the reaction progression into an oxidized state and a reduced state is suggested. The amount of hydrogen produced is insignificant in the oxidized state whereas it becomes proportional to the amount of ferrous iron oxidized in the reduced state. The bulk of basalt-hosted aquifers are expected to reside in the oxidized state because of the low content of ferrous minerals, whereas abundant olivine in ultramafic-hosted systems is responsible for large-scale hydrogen production. Today the majority of the seafloor is basaltic. The Archean seafloor on the other hand consisted of fewer ultramafic exposures, but was dominated by ultramafic magnesium-rich lavas with a higher potential for hydrogen production than the present seafloor.

Mars simulation studies have in the past mainly investigated the effect of the simulation conditions such as UV radiation, low pressure and temperature on pure cultures and much has been learnt about the survival potential of sporeformers such as Bacillus subtilis. However, this approach has limitations as the studies only investigate the properties of a very limited number of microorganisms. In this paper we propose that Mars simulations should be carried out with complex microbial communities of Martian analogues such as permafrost or the deep biosphere. We also propose that samples from these environments should be studied by a number of complementary methods and claim that these methods in combination can provide a comprehensive picture of how imposed Martian conditions affect the microbial community and in particular the survival of its constituents – microbes as well as biological material in general. As an interesting consequence this approach can lead to the isolation of bacteria, which are more recalcitrant to the imposed Martian conditions than the pure cultures that have previously been studied.

The prediction that (due to the limited amount of hydrogen available as fuel in the Sun) the future duration of our favourable terrestrial environment will be short (compared with the present age of the Earth) has been interpreted as evidence for a hard-step scenario. This means that some of the essential steps (such as the development of eukaryotes) in the evolution process leading to the ultimate emergence of intelligent life would have been hard, in the sense of being against the odds in the available time, so that they are unlikely to have been achieved in most of the earth-like planets that may one day be discovered in nearby extrasolar systems. It was originally estimated that only one or two of the essential evolutionary steps had to have been hard in this sense, but it has become apparent that this figure may need upward revision, because recent studies of climatic instability suggest that the possible future duration of our biologically favourable environment may be shorter than had been supposed, being only about 1 Gyr rather than 5 Gyr. On the basis of the statistical requirement of roughly equal spacing between hard steps, it is argued that the best fit with the fossil record is now obtainable by postulating the number of hard steps to be five, if our evolution was exclusively terrestrial, or six, if, as now seems very plausible, the first step occurred on Mars.

In studying the functional and evolutionary significance of compartmentation in biology, it is instructive to consider its thermodynamic context as a conceptual centrepiece of entropy and phase transitions. Here we focus specifically on compartmentation at the intracellular level of microbial organellar cytology. Via a colloid-statistical argument, supplemented with order of magnitude estimates for the relevant physical quantities, we find that the DNA-containing nucleoid of prokaryotes presents a plausible nucleation site for phase-transitional behaviour, provided the genome exceeds some threshold size of the order of 10 Mbp. Large genome size seems capable in this respect of seeding compartmentation effects such as the nuclear envelope of Planctomycetes bacteria, which is widely regarded as a possible precursor to the nuclear envelope of eukaryotes.