Convergence to panspermia


New discoveries in astronomy and biology continue to point to Panspermia as the most likely mode of the origin of life on Earth. This paper builds upon the work done by W.M. Napier, 2004 (1), and re-estimates the time for the seeding of the galaxy given the latest 2013 estimates from the Kepler Mission data. We present this “thought experiment” in the form of an opinion paper. We calculate that, from a single point source of origin, the full colonisation of the entire Milky Way galaxy by primitive microbes will take place in a timescale less than the average age of low-mass stars in the galactic disc, 1010 yr (i.e., 10 billion years ago; bya). Our calculation is independent of the location of the “point-source”. The writers believe the probability of the point-source being Earth is infinitesimal compared with it being elsewhere in the galaxy.


Scope of this paper

Although Panspermia, and the Hoyle-Wickramasinghe Model, as an overall hy­pothesis, could apply to not just our Milky Way Galaxy but to the whole Universe, the scope of the calculation, and thought experiment in this paper, is limited to the Milky Way Galaxy.


The earliest evidence of terrestrial life in the form of an enhanced carbon isotope (13C/12C) ratio associated with sediments at 3.82 to 4 billion years ago (bya) coinciding with an epoch of intense comet and asteroid bombard­ment leads naturally to the hypothesis that the impacts themselves were re­sponsible for the start-up of life on the Earth (2). The presence of amino acids and nucleobases in the Murchison meteorite has given credence to the more restricted hypothesis that these molecules served as the components of an Earth-based primordial soup from which life was able to originate (3). However, all attempts to re­produce these processes in the labora­tory have so far not been encouraging (4). The improbability of accomplishing the minimal molecular arrangements, for ex­ample, in the order of amino acids in en­zymes or nucleotides in DNA, by random shuffling of components has made the once unpopular idea of Panspermia ap­pear increasingly more attractive. An ori­gin of life occurring as a singular cosmic event on a galactic or even cosmological scale transferred via panspermic pro­cesses appears to be consistent with all the available data at the present time (5).

Lord Kelvin first suggested that life on Earth may have been carried to Earth via an impacting meteorite, and this idea has recently been recast into the modern form lithopanspermia. This has been dis­cussed recently by several authors in re­lation to impacts onto a life-laden planet such as the Earth. A comet impact, like that which struck Earth 65 million years ago causing the extinction of the dino­saurs, would also have had the effect of ejecting surface rocks that contain terres­trial microbial ecologies. A fraction of this material can be shown to be able to infect embryonic planetary systems in a nearby molecular cloud (1,6). The exchange of life-bearing ejecta would have been facilitat­ed between planetary systems that are contained within star clusters. Numerical calculations show how this could be achieved, so panspermic opportunities are optimised in such cases (7).

Revisiting The Hypothesis Against which this “Thought Experiment” is Conducted

Our 2013 paper formally documents the Panspermia Hypothesis, and the propo­sitions around which the rapidly evolv­ing evidence should be assessed (8). We restate this for the convenience of the reader.

The HOYLE-WICKRAMASINGHE (H-W) model of the Panspermia Hypothesis (8)

Panspermia is the hypothesis that life ex­ists throughout the Universe, distributed by meteoroids, asteroids, comets and planetoids.


Figure 1 | Seeds of Life

The Hoyle-Wickramasinghe Model of the Panspermia Hypothesis defines the following propositions to guide the investigation:

1. That dormant viruses and desiccated DNA/RNA can survive unprotected in interplanetary space (Radiopanspermia)
2. That the seeds of life can survive protected from cosmic rays in asteroids, comets and meteors (Lithopanspermia)
3. That the seeds of life are promulgated from solar system to solar system by a process of comet and asteroid collision with planets; matter ejection from planet to local planets and Moons; and then onwards and outwards from that solar system to an adjacent solar system

In the above propositions of the Hoyle-Wickramasinghe Model, the “seeds of life” include biological microparticles such as bacteria, viruses, spores and pollen (Figure 1). This specifically includes:

1. Desiccated and/or partially inactivated DNA/RNA
2. Live, dormant or fossilized non-cellular life (viruses)
3. Live, dormant or fossilized cellular life (bacteria, archaea)

In the more general Panspermia Hypothesis these “seeds of life” are not as clearly defined as in the Hoyle-Wickramasinghe Model. Also in the Hoyle-Wickramasinghe Model, Litho-Panspermia includes comets. It proposes that comets are the major promulgation “carrier” of the seeds of life, especially from solar system to solar system, and proposes that the center of comets is mostly water, not ice, an ideal environment for bacteria and viruses.

The Thought Experiment
Calculation of the Average Spacing Between Stars

By March 2014, NASA’s Kepler Missionhad discovered 5,537 exoplanets (3,845 candidates + 1,692 confirmed). A recent revision of the size of the habitable zones of stars, taking account of atmospheric greenhouse effects, has led to new estimates of the number of potentially habitable Earth-sized planets around low mass stars in the Galaxy as about N ≈ 1011 (9).

Distributed over the entire volume of the galactic disc V ≈ 7.5 x 1012 ly3 (assumed to be a cylinder of radius 50,000 light year [ly] and thickness ≈ 1000 ly), this gives a mean spacing in the galaxy of (N/V)1/3 ≈ 4 ly between stars with habitable planets.

The spacing could be even closer within the birth clusters of stars. Transfer of viable microbial life across such short distances under interstellar conditions would appear to be entirely feasible.

Propagation Method #1: Lithopanspermia:Cometary Panspermia
The H-W Model sees comets as the primary carrier of the “seed of life” (defined above).

For this paper, comets are considered of two types:

• Short-period comets, which live in the Kuiper Belt and have elliptical orbits in the plane of the solar system ecliptic;
• Longer-period comets, which can have elliptical orbits reaching out to the Oort Cloud (but it is the parabolic Comets, which the writers believe have been involved in “sling shot” transfers from an adjacent star system).

These parabolic comets (which the writers believe include comets like ISON with an eccentricity = > 1 ) are called exocomets in this paper.

This thought experiment imagines a water-bearing exo-comet heading towards an adjacent Sun-like star. As it gets close to perihelion, with good fortune it not only avoids the large Jupiter-sized inner planets, but again, with luck, finds its perihelion is just far enough away from the star for a large fraction of the comet’s mass to make its turn around the star and be slung shot back in the form of fragments and boulders out in a parabolic or even hyperbolic orbit towards our own solar system.

Eventually, these comet fragments coming into the Oort Cloud surrounding our Star (the Sun) are now in parabolic orbits that can interact with Earth and other
planetary bodies and transfer life.

Propagation Method #2: Radiopanspermia
Microscopic forms of life are propagated in space, driven by the radiation pressure from stars.

NOTE: This thought experiment is now focused on this second propagation method.

We consider particles expulsed when the comet above reached the perihelion of its encounter with a star (10). Microorganisms expelled from comets in one planetary system can, under suitable conditions, reach other neighbouring planetary systems through the action of radiation pressure exerted by the light of the central star. The light from the star incident on a virus or dessicated bacterium or clump of bacteria exerts a radially directed outward force P due to transfer of momentum, a photon of energy hν carrying momentum hν/c. The star’s gravitational attraction G acts in the opposite direction and both forces vary inversely with dis­tance from the star. For a star like the Sun with a known mass to luminosity ratio, the ratio P/G becomes a property of the particular dust grain model – the clump of bacteria in our case – that can be cal­culated from the optical properties of the grain material (11). In situations where the ra­tio P/G exceeds unity, grains are expelled from the star. Calculations of this ratio for bacterial grains in the form of spherical clumps possessing thin outer skins of re­duced carbon (graphite) for particles in the vicinity of the Sun show that we have P/G ratios close to 3.

If such a particle is expelled from a comet at a heliocentric distance of Ro, the parti­cles with P/G > 1 would be expelled from the entire solar system with an asymptotic velocity of:

where α = P/G – 1, k is the Universal Gravitational constant, R0 = 1 and M is the solar mass. For α = 0.5, P/G = 1.5 in a typical case we get:

ν≈ 3 ×106 cm/sec

(i.e. 1/10,000th (10-4) of the speed of light)

for expulsion from a heliocentric distance of 1AU (1AU = the mean distance be­tween the Sun and the Earth).

Microorganisms especially viruses and dessicated bacteria, retaining viability thus reach a next neighbouring plane­tary system from an original point source (e.g., the solar system) in a typical time of 40,000 yr. Since accommodation of such microbes within cometary or other am­plification niches in the new system and their exponential replication proceeds on timescales much shorter than 40,000 yr, we can assume that a “wave of colonisa­tion” progresses at an effective speed of approximately ν ≈ 3 x 106 cm/s.

Crossing a typical galactic dimension of 100,000 ly will then be accomplished in a mere 109 yr. In reality, however, the state of readiness of a recipient planetary sys­tem to amplify and redistribute iterant mi­crobes must also be taken into account, but the time delays introduced by this re­finement are likely to be negligible.

Collision of comets and asteroids onto the surfaces of inhabited planets like the Earth could also result in the ejec­tion and transference of genes belong­ing to evolved life-forms (e.g., viruses and bacteria) to neighbouring planetary sys­tems. This process will be particularly im­portant when massive molecular clouds with newly formed stars and planets act as perturbing objects that deflect comets from Oort-type comet clouds. On such a picture, Darwinian evolution will not be confined to a single planetary biosphere but would extend across a biosphere em­bracing the entire galaxy.

These considerations add further to ear­lier arguments that show astronomical spectroscopic studies of interstellar dust matching the predictions of bacteria and their degradation products, and the puta­tive identification of microfossils in meteorites (5,12).

Finally we turn to arguments from genet­ics. Extensive studies of the human ge­nome (and other genomes) have shown the presence of viruses (mainly retro­viruses) making up a large fraction of inert DNA. This can be interpreted in terms of predictions from the Hoyle-Wickramasinghe theory of evolution from space (13). These viral sequences are the relic of invasions from space that led to their insertion in our ancestral line, and they serve a positive role as carrying dor­mant information for further evolution (14).

Thought Experiment Conclusion

That from a single point source of origin the full colonisation of the entire Milky Way galaxy by primitive microbes will take place in a timescale less than the av­erage age of low-mass stars in the galac­tic disc, 1010 yr (i.e., 10 byr). The universe is generally estimated to be 13.8 byr old.

Note: This paper uses the very latest es­timates of the number of habitable Earth-like exoplanets in the Milky Way – now es­timated (June 2013) at 144 billion.

Evaluation of the Thought Experiment

Origin of Life in Comets
Support for the idea that life originated on Earth in a primordial soup is beginning to wear thin in the light of modern geological and astronomical evidence. It is becoming clear that life arose on Earth almost at the very first moment that it could have survived.

During the so-called Hadean Epoch of the Earth, which involved heavy com­etary bombardment, there is clear evi­dence of an excess of the lighter carbon isotope 12C compared with 13C indicating the action of microorganisms that prefer­entially take up the lighter isotope from the environment (2,15,16).

The Hadean epoch in the Earth’s geo­logical history was undoubtedly marked by an exceptionally high frequency of comet and asteroid impacts. It is gen­erally thought that much of the water in the oceans came from comets. Along with the water, comets also brought life. This is the theory of Cometary Panspermia proposed in 1979 by Hoyle and Wickramasinghe (one of the present writers).

Experiments and Evidence

In the formation of a planetary system such as the solar system (and the proto-planetary galaxy) the first solid objects to form are the comets. These icy objects would con­tain the molecules of the parent interstellar cloud, and for a few million years after they condensed would have liquid water interiors due to the heating effect of radio­active decays (5).

If microbial life was already present in the parent interstellar cloud, the newly formed comets serve to amplify and pro­mulgate it on a very short timescale.

Evidence is accumulating for the exis­tence of microbes (viruses, bacteria and other yet unidentified biological entities) in a large number of meteoroids collect­ed on the surface of the Earth as well as in the stratosphere (8).

During the fall of 2014, there are two experiments observers can monitor where evidence could be acquired which would be inconsistent with the theory that both short and long period comets really do carry the seeds of life.

The first is NASA’s initiative monitoring long period Comet Siding Spring from both space and from ground based telescopes (ALMA).

The second is ESA’s experiments in November 2014 on the surface of short-period comet 67P/C-G. The Rosetta Mission has no life detection experiments aboard. But the Micro-Imaging Dust Analysis System (MIDAS) on the Rosetta orbiter is designed to capture dust particles and image them in three dimensions at nanometer scales with an atomic force microscope. The size range of particles to be detected seems to include objects the size of diatoms, bacteria and even viruses—but not DNA fragments. MIDAS has been operating since the beginning of the Rosetta Mission and is now looking at the atmosphere around 67P including the ever growing cometary tails. Other spectroscopy experiments are expected to deliver interesting complex molecule detection results from both the Philae Lander, looking at the surface of Comet 67P as well as from the Rosetta Orbiter looking at the out- pouring tail(s).

2013 saw NASA move its umbrella mis­sion focus from “Search for Water” to the “Difficult Endeavor of Seeking the Signs of Life” (8).

2014 also saw an early discussion on the implications of extraterrestrial life to the study of disasters and to risk management. (17).

Finally, the important role of viruses is being recognized. The U.S. Geological Survey confirmed the importance of vi­ruses as the primary driver of evolution on Earth (18). They stated “Historically, virus­es have been mostly ignored in the field of astrobiology due to the view that they are not alive in the classical sense and if encountered would not present risk due to their host-specific nature”. They recom­mended, “that in our quest for extraterres­trial life, we should be looking for viruses; and while any encountered may pose no risk, the possibility of an encounter with a virus capable of accessing multiple cell types exists”. H

Authors de­clare no conflicts of interest.


About the authors

Professor Chandra Wickramasinghe is a mathematician, astrophysicist and astrobiologist. He is a former Fellow of Jesus College Cambridge, and a former Professor at Cardiff University. Currently, he is Director of the Buckingham Centre for Astrobiology and an Honorary Professor at the University of Buckingham. He is also a Board Member and Director of Research at the Japan-based Institute for the Study of Panspermia and Astroeconomics ( William E. Smith was a student of Professor Herman Bondi, who is best known for his contributions towards the theory of relativity. Mr. Smith is a Chartered IT Professional and UK Chartered Engineer.


  1. Napier WM. A mechanism for interstellar pansper­mia. Mon Not R Astron Soc. 2004;348:46-51.
  2. Mojzsis SJ, Arrhenius G, McKeegan KD, Harrison TM, Nutman AP, Friend CRL. Evidence for life on Earth before 3,800 million years ago. Nature. 1996;384:55-59.
  3. Schmitt-Kopplin P, Gabelica Z, Gougeon RD, Fekete A, Kanawati B, Harir M, et al. High molecular diver­sity of extraterrestrial organic matter in Murchison meteorite revealed 40 years after its fall. PNAS. 2010;107:2763-2768.
    PMid:20160129 PMCid:PMC2840304
  4. Deamer D. First Life: Discovering the connections between stars, cells, and how life began. Los Angeles, California: University of California Press; 2011.
  5. Wickramasinghe JT, Wickramasinghe NC, Napier WM. Comets and the origin of life. Singapore: World Scientific; 2010.
  6. Wallis MK, Wickramasinghe NC. Interstellar trans­fer of planetary microbiota. Mon Not R Astron Soc. 2004;348, 52-57.
  7. Belbruno E, Moro-Martin A, Malhotra R, Savransky D. Chaotic exchange of solid material between plan­etary systems: Implications for lithopanspermia. Astrobiol. 2012;12:754-74.
    PMid:22897115 PMCid:PMC3440031
  8. Smith WE. 2013 – Life is a cosmic phenomenon: The “Search for Water” evolves into the “Search for Life”. Proc SPIE. 2013;8865:88650Q.
  9. Kopparapu RK, Ramirez R, Kasting JF, Eymet V, Robinson TD, Mahadevan S, et al. Habitable zones around main sequence stars: New estimates 2013. Astrophys J. 2013;765:1-16.
  10. Hoyle F, Wickramasinghe NC. Astronomical ori­gins of life. Dordrech: Kluwer; 2000.
  11. Wickramasinghe NC. The astrobiological case for our cosmic ancestry. Int J Astrobiol. 1973; 9:119-29.
  12. Wickramasinghe NC. Bacterial morphologies sup­porting cometary panspermia: A reappraisal. Int J Astrobiol. 2011;10:25-30.
  13. Hoyle F, Wickramasinghe NC. Evolution from space. London: J.M. Dent; 1980.
  14. Wickramasinghe NC. DNA sequencing and predic­tions of the cosmic theory of life. Astrophys Space Sci. 2012;343:1-5.
  15. Manning CE, Mojzsis SJ, Harrison TM. Geology, age and origin of supracrustal rocks at Akilia, West Greenland. Am J Sci. 2006; 306:303-66.
  16. Mojzsis SJ, Harrison TM, Pidgeon RT. Oxygen-isotope evidence from ancient zircons for liquid water at the Earth’s surface 4,300 Myr ago. Nature. 2001;409:178-81.
  17. Neal, M. Preparing for Extraterrestrial Contact. Risk Management. 2014; 16: 63–87.
  18. Griffin, DW. Astrobiology. 2013: 13(8): 774-783.

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