Convergent evolution and the search for biosignatures within the solar system and beyond
Introduction
One of the most debated issues in theoretical biology is the contingency vs. convergence or, in other terms, chance vs. necessity problem. This debate is posing the question about the existence of universal laws governing the emergence of analogous forms of biological complexity across the terrestrial and putative alien biospheres. On the one hand, it is possible that the kind of biology we see on Earth and might encounter on other worlds is determined primarily by contingent events occurring in the respective evolutionary history. In contrast to this notion, a small but growing number of researchers is favoring the possible existence of universal laws shaping similar features of independently originating and evolving life forms in comparable planetary environments [1], [2], [3], [4], [5], [6], [7], [8]. The orthodox solution to the problem, however, proposes a scenario in which evolution is rather a stochastically-driven process in which its outcomes are contingent on planetary history and chance mutations. Convergent adaptations, independently and repeatedly evolved complex features, are mostly explained due to ancestral inheritance, i.e. deep homology [9], [10], [11], [12]. Others are suggesting a compromise between these distinct evolutionary forces [13].
Notably, the contingency or chance perspective is essentially a continuation of the “modern evolutionary synthesis”, which presented the core of evolutionary biology since the 1940s. Continuing work on the origin of life and proto-cellular evolution is suggesting that this relatively old evolutionary paradigm is not adequate anymore to fully capture the processes that were active during the onset of emerging biological complexity [14], [15], [16], [17], [18], [19]. Collective phenomena among cohorts of early cells, progenotes, especially the exchange of genetic material via horizontal gene transfer (HGT), are suggested to have determined the emergence or “crystallization” of the first, fully integrated, cells as we know them. These, in turn, were then able to undergo Darwinian, or vertical, evolution. A perspective in which poorly integrated progenotes were engaged in rampant HGT and then evolved towards a Darwinian bottleneck, that could have entailed distinct events of cellularization, is consistent with the notion of convergent evolution [20]. Assuming that similar, if not identical, processes of far off-equilibrium phenomena involving geochemical gradients in aqueous environments [14], [21], [22], could have led repeatedly to the emergence of life in comparable, ancient planetary habitats, alien organisms should have experienced a phase of extensive HGT and ensuing (multiple) cellularization too. From this point onwards it becomes exceedingly difficult to reasonably predict what kind of adaptations putative life, for example, on the icy moons of Jupiter and Saturn, Europa and Enceladus, or on a far-away exoplanet, would evolve in the course of their history. Nonetheless, exactly this type of predictability is essential to the astrobiological endeavor [23], because future planetary exploration missions or space-telescope based exoplanet surveys need to be guided by a defined, or at least constrained, set of possible biosignatures. Here it will be argued that the notion of convergent evolution is pivotal in lending a certain degree of predictability to astrobiology and the related SETI field.
Section snippets
Minimal convergent traits
In order to better understand how the most basic entity, which we could identify as a living organism, should look like, let us turn to the origin of biological evolution again. Life on Earth has evolved in a manner suggestive of a minimum set of prerequisites which comprises liquid water, biogenic elements (C, H, N, O, P, and S) and biologically usable energy (i.e. transducible into chemical bonds for storage and later usage in metabolic reactions). In regard to the most pressing constraint
The possibility of advanced biological complexity on Europa
Next to the water column and seafloor of the deep sea, its underlying sediment presents the largest potential habitat on Earth [35]. On Europa and Enceladus the interaction between the rocky mantle and the overlying water column could lead to hydrothermal processes which may drive the exchange of energy and biogenic elements. In regard to putative hydrothermal systems on these moons, especially in the case of Europa since it is considerably larger than Enceladus, it is conceivable that
Convergent biosignatures
Generally, a biosignature is defined as: “an object, substance and/or pattern whose origin specifically requires a biological agent. The usefulness of a biosignature is determined, not only by the probability of life creating it, but also by the improbability of nonbiological processes producing it. An example of such a biosignature might be complex organic molecules and/or structures whose formation is virtually unachievable in the absence of life. A potential biosignature is a feature that is
Signatures of (extra)terrestrial intelligence
The early Search for Extraterrestrial Intelligence (SETI) enterprise commencing in the early 1960s presented the only genuinely scientific enterprise so far that was seeking to detect signs of extraterrestrial intelligence throughout the galaxy. Until now, however, no radio or optical signal was discerned by ongoing efforts all around the world. Emerging SETI, historically, was accompanied by studies in what was then called “exobiology”, the precursor of astrobiology as we know it today [71],
Conclusions
Here it was shown how convergent evolution appears to be an important conceptual pillar in astrobiology and SETI. First, the hypothesis of universal convergent evolution allows for constraining the vast theoretical landscape of possible biosignatures. Secondly, recommendations for instrument selection of advanced space missions can be derived from qualitative evolutionary modeling of extraterrestrial life on various potential planetary habitats. Thirdly, convergent evolution is opening up
References (103)
SETI in the light of cosmic convergent evolution
Acta Astronaut.
(2014)- et al.
Turnstiles and bifurcators: the disequilibrium converting engines that put metabolism on the road
Biochim. Biophys. Acta
(2013) - et al.
On the universal core of bioenergetics
Biochim. Biophys. Acta
(2013) - et al.
On the origin of genomes and cells within inorganic compartments
Trends Genet.
(2005) - et al.
Europa׳s crust and ocean: origin, composition, and the prospects for life
Icarus
(2000) - et al.
A lander mission to probe subglacial water on Saturn׳s moon Enceladus for life
Acta Astronautica
(2015) The transcension hypothesis: sufficiently advanced civilizations invariably leave our universe, and implications for METI and SETI
Acta Astronaut.
(2012)Fitness of the Cosmos for Life: Biochemistry and Fine- tuning
(2008)Testing evolutionary convergence on Europa
Int. J. Astrobiol.
(2003)Testing the universality of biology: a review
Int. J. Astrobiol.
(2007)
The navigation of biological hyperspace
Int. J. Astrobiol.
Consider the octopus
EMBO Rep.
Evo Devo universe? A framework for speculations on cosmic culture
Can the evolution of multicellularity be anticipated in the exploration of the solar system?
Wonderful life: the Burgess Shale and the Nature of History
Chance and Necessity; An Essay on the Natural Philosophy of Modern Biology
Deep homology and the origins of evolutionary novelty
Nature
Convergent evolution and the limits of natural selection
Eur. J. Philos. Sci.
Chance and necessity in biochemistry: implications for the search for extraterrestrial biomarkers in earth-like environments
Astrobiology
Life is physics: evolution as a collective phenomenon far from equilibrium
Annu. Rev. Condens. Matter Phys.
Biology׳s next revolution
Nature
A new biology for a new century
Microbiol. Mol. Biol. Rev.
The biological Big Bang model for the major transitions in evolution
Biol. Dir.
The cosmological model of eternal inflation and the transition from chance to biological evolution in the history of life
Biol. Dir.
Evolutionary dynamics and information hierarchies in biological systems
Ann. N. Y. Acad. Sci.
On the origins of cells: a hypothesis for the evolutionary transitions from abiotic geochemistry to chemoautotrophic prokaryotes, and from prokaryotes to nucleated cells
Philos. Trans. R. Soc. Lond. B: Biol. Sci.
The fuel cell model of abiogenesis: a new approach to origin-of-life simulations
Astrobiology
The drive to life on wet and icy worlds
Astrobiology
Evolution: like any other science it is predictable
Philos. Trans. R. Soc. B: Biol. Sci.
Design, fabrication, and test of a hydrothermal reactor for origin-of-life experiments
Astrobiology
Serpentinization as a source of energy at the origin of life
Geobiology
Hydrothermal vents and the origin of life
Nat. Rev. Microbiol.
Modeling free energy availability from Hadean hydrothermal systems to the first metabolism
Orig. Life Evol. Biosph.
Serpentinite and the dawn of life
Philos. Trans. R. Soc. B: Biol. Sci.
Hydrothermal exploration and astrobiology: oases for life in distant oceans?
Int. J. Astrobiol.
Hydrothermal systems on Europa
Geophys. Res. Lett.
Methanogenesis as a potential source of chemical energy for primary biomass production by autotrophic organisms in hydrothermal systems on Europa
J. Geophys. Res.: Planets
Evidence for microbial carbon and sulfur cycling in deeply buried ridge flank basalt
Science
Serpentinization, carbon, and deep life
Rev. Mineral. Geochem.
On the forcing mechanism for the H2-driven deep biosphere
Int. J. Astrobiol.
The potential for low-temperature abiotic hydrogen generation and a hydrogen-driven deep biosphere
Astrobiology
Hydrothermal systems in small ocean planets
Astrobiology
Diverse styles of submarine venting on the ultraslow spreading Mid-Cayman Rise
Proc. Natl. Acad. Sci.
Evolution and biogeography of deep-sea vent and seep invertebrates
Science
Hydrothermal vent fields and chemosynthetic biota on the world׳s deepest seafloor spreading centre
Nat. Commun.
Strategy for modeling putative multilevel ecosystems on Europa
Astrobiology
Energy cycling and hypothetical organisms in Europa׳s ocean
Astrobiology
The multiple origins of complex multicellularity
Ann. Rev. Earth Planet. Sci.
The evolutionary-developmental origins of multicellularity
Am. J. Bot.
Origin of Eukaryotic Cells; Evidence and Research Implications for a Theory of the Origin and Evolution of Microbial, Plant, and Animal Cells on the Precambrian Earth
Cited by (4)
Shallow transient liquid water environments on present-day mars, and their implications for life
2018, Acta AstronauticaCitation Excerpt :To assess the habitability of other planetary environments, a minimum criteria for life has been established based on the requirements of Earth biology. Although it is an Earth-centred approach, this strategy identifies the necessary conditions for known life to persist (and, perhaps, to emerge [23]) on another planet [24]. All life on Earth requires access to a minimum quota of nutrients to build biomass [25] and a gradient in chemical energy to fuel metabolism [26].
Organism-substrate interactions and astrobiology: Potential, models and methods
2017, Earth-Science ReviewsCitation Excerpt :Similarly, the detection of life beyond Earth through chemical or isotopic biosignatures may also be difficult. In fact, despite some contrasting views (Flores Martinez, 2015; Pace, 2001), Earth-type biochemistry could not be the only plausible one (Benner et al., 2004; Hoehler et al., 2007; Schulze-Makuch and Irwin, 2006). For these reasons, a biosignature ideally capable of detecting any type of life (herein named ‘universal biosignature’) should be independent from morphology, size and biochemistry of the life form it documents.
Biofluorescent worlds - II. Biological fluorescence induced by stellar UV flares, a new temporal biosignature
2019, Monthly Notices of the Royal Astronomical Society