Open Access. ©2020 R. G. Joseph et al., published by De Gruyter. This work is licensed under the Creative Commons Attribution
Open Astron. 2020; 29: 124–157
Rhawn G. Joseph*, Olivier Planchon, Carl H. Gibson, and Rudolph Schild
Seeding the Solar System with Life: Mars, Venus,
Earth, Moon, Protoplanets
Received Jul 08, 2020; accepted Aug 25, 2020
In the space of the entire universe, the only conclusive evidence of life, is found on Earth. Although the
ultimate source of all life is unknown, many investigators believe Earth, Mars, and Venus may have been seeded with life
when these planets, and the sun, were forming in a galactic cluster of thousands of stars and protoplanets. Yet others
hypothesize that while and after becoming established members of this solar system, these worlds became contaminated
with life during the heavy bombardment phase when struck by millions of life-bearing meteors, asteroids, comets and
oceans of ice. Because bolide impacts may eject tons of life-bearing debris into space, and as powerful solar winds may
blow upper atmospheric organisms into space, these three planets may have repeatedly exchanged living organisms for
billions of years. In support of these hypotheses is evidence suggestive of stromatolites, algae, and lichens on Mars, fungi
on Mars and Venus, and formations resembling fossilized acritarchs and metazoans on Mars, and fossilized impressions
resembling microbial organisms on the lunar surface, and dormant microbes recovered from the interior of a lunar
camera. The evidence reviewed in this report supports the interplanetary transfer hypothesis and that Earth may be
seeding this solar system with life.
Mars; Venus; Earth; Moon; Meteors; ALH 84001; Algae; Cyanobacteria; Fungi; Lichens; Stromatolites; Meta-
zoans; Fossils; Interplanetary transfer of life; lithopanspermia; Planetary nebulae
1Seeding the Solar System with
Life: Protoplanets, Mars, Venus,
How and when life began, is unknown. Sir Fred Hoyle
(1982) Nobel laureates Svante Arrhenius (1908), Francis
Crick (1981), Harold Urey (Arnold et al. 1995; Urey 1962,
1966), and other investigators, have theorized that life is
widespread in this universe and was delivered to Earth
via solar winds, meteors, asteroids, and comets from older
planets in distant solar systems (Hoyle and Wickramas-
inghe 2000; Joseph 2009; Joseph and Schild 2010a; Val-
tonen et al. 2008). Yet others have proposed that proto-
Corresponding Author: Rhawn G. Joseph:
Center, Stanford, California, United States of America;
National Center for Scientic Research, Biogéo-
sciences, University of Bourgogne, France
Carl H. Gibson:
Scripps Center for Astrophysics and Space Sciences;
Dept. Aerospace Engineering, University of California, San Diego,
United States of America
Harvard-Smithsonian Center for Astrophysics (Emer-
itus), Cambridge, MA, United States of America
planets, including Earth, were seeded with life when these
worlds rst formed in a galactic cluster within a nebular
cloud amongst thousands of other new born stars (Adams
and Spergel 2005; Fragkou et al. 2019; Johansen and Lam-
brechts 2017; Jones et al. 2019). Therefore, according to
this scenario, as worlds were formed and destroyed (Boyle
and Redman 2016; Stephan et al. 2020) life within this cos-
mic debris may have spread between these protoplanets
(Adams and Spergel 2005; Gibson et al. 2011; Joseph 2009;
Joseph and Schild 2010b; Valtonen et al. 2008) and what
would become Mars, Venus, Earth and its moon, may have
become infested with life before this solar system was es-
tablished. It has also been hypothesized that life may have
been repeatedly transferred between these worlds during
the heavy bombardment phase of this solar system’s sta-
bilization (Gladman et al. 1996, 2005; Mileikowsky et al.
2000a,b) and intermittently thereafter (Beech et al. 2018;
Joseph 2009; Joseph and Schild 2010a; Schulze-Makuch et
al. 2005) via powerful solar winds and life-infested bolides
ejected into space that later crash upon the surface of these
In support of all these theories and scenarios, is
evidence—but no proof—that between 4.2 to 3.7 bya, dur-
ing the heavy bombardment phase, life may have taken
R. G. Joseph et al., Seeding the Solar System with Life: Mars, Venus, Earth, Moon, Protoplanets |125
root on Mars (Clement et al. 1998; Noke 2015; Thomas-
Keprta et al. 2009) and Earth (Nemchin et al. 2008; Nutman
et al. 2016; O’Neil et al. 2008; Rosing and Frei 2004); and
then, over the ensuing billions of years, the inner planets
were repeatedly intermittently seeded with life (Beech et al.
2018; Joseph 2019). Moreover, Earth may have been seeding
the inner planets when tons of rock and soil—and adher-
ing organisms—were ejected into space via powerful solar
winds (Joseph 2009) and following impacts by comets, as-
teroids and meteors (Beech et al. 2018; Gladman et al. 2005;
Joseph 2000; Mileikowsky et al. 2000a,b).
If life was delivered via debris from outside this solar
system, and/or if impacts on Earth also caused the dispersal
of life, this may explain why specimens similar to terres-
trial fungi have been observed on Mars (Joseph et al. 2019,
2020a) and Venus (Joseph 2019; Ksanfomality 2013). This
would also account for why specimens resembling algae,
lichens, stromatolites, and fossilized algae and metazoans
have been observed on Mars (Joseph and Armstrong 2020;
Joseph et al. 2019, 2020a,b; Kaźmierczak 2016, 2020; Noke
2015; Rabb 2018; Rizzo 2020; Rizzo and Cantasano 2009,
2017; Ru and Farmer 2016). The interplanetary transfer
of life would also explain why fossilized impressions re-
sembling "nanobacteria," terrestrial bacteria and micro-
Ediacarans, have been respectively identied in a lunar me-
teorite (Sears and Kral 1998) and lunar soil samples (Joseph
and Schild 2010a; Zhmur and Gerasimenko 1999); and why
dormant spores were found within a lunar camera that had
been sitting on the moon for three years (Mitchell and Ellis
Nevertheless, it must be stressed that there is no con-
clusive proof of current or past life on any planet other than
Earth. As the denitive evidence of life exists only on Earth,
it is also reasonable to hypothesize that after this solar sys-
tem was formed, Earth may have repeatedly seeded neigh-
boring planets and moons with life; the ultimate source of
which, is unknown.
2Genetics and the Improbable
Origins of Life
Be it in the ancient past or following the classic experi-
ments of Miller and Urey (1959a,b) all attempts to fashion
life from non-life have failed. There are published estimates
that it would have taken 100 billion to trillions of years
to fashion the nucleotides that comprise a single macro-
molecule of DNA (Crick 1981; Dose 1988; Horgan 1991; Hoyle
1982; Joseph and Schild 2010a; Kuppers 1990; Yockey 1977).
Further, once that rst DNA molecule had been created,
and based on complex genetic statistical analyses, it could
have taken from 10 to 13 billion years for that rst gene to
undergo sucient duplicate and recombination events to
fashion a minimal genome capable of maintaining the life
of the simplest organism on Earth (Anisimov 2010; Jose et
al. 2010; Joseph and Wickramasinghe 2011; Sharov 2010).
Carsonella, for example, maintains the smallest genome of
all living organisms: 160,000 base-pairs of DNA, and 182
separate genes (Nakabachi et al. 2006); and thus this can
be considered the minimal number of genes necessary to
sustain life. However, Carsonella is parasitic and depends
on a living host, a psyllid insect, to survive. By contrast, the
genome of Mycoplasma genitalium (Fraser et al. 1995), the
smallest free-living microbe, has over 580,000 base pairs
and over 213 genes, 182 of these coding for proteins; and
beginning with the rst gene, it would have taken up to
13 billion years of recombination and duplicative events
to fashion a minimal life-sustaining genome (Joseph and
Wickramasinghe 2011). Estimates are that Earth is only 4.6
billion years in age (Lugmair and Shukolyukov 2001). There-
fore, the rst minimal gene set sucient to sustain life, was
formed at least 6 billion years before Earth and this so-
lar system were established. The establishment of DNA,
however, is just the one step in fashioning a single living
Single cellular microbes are comprised of more than
2,500 small molecules, nuclei acids and amino acids
consisting of 10 to 50 tightly packed atoms, and macro-
molecules and polymeric molecules which precisely inter-
act as a cohesive whole and function together as a living mo-
saic of tissues (Cowan and Talaro 2008; Joseph and Schild
2010a). The thousands of dierent molecules that comprise
a single cellular creature perform an incredible variety of
chemical reactions in concert with that cell’s protein (en-
zyme) products; whereas the smallest of single celled crea-
tures consists of and requires over 700 proteins (Cowan and
Yockey (1977) calculated that the probability of achiev-
ing the linear structure of one protein 104 amino acids long,
by chance, is 2
. The probability of forming just a
single protein consisting of a chain of 300 amino acids is
, or 1 chance in 2.04
(Hoyle 1982). The prob-
ability of creating 700 proteins—the number necessary to
fashion a living mosaic of tissues–might be in excess of 700
(Joseph and Schild 2010a,b). According to "Borel’s
Law" any odds beyond 1 in 10
have a zero probability of
ever happening: "phenomena with very small probabilities
do not occur" (Borel 1962).
As argued by Dose (1988), it appears nearly impossi-
ble for a single cell to have been fashioned by chance or
on Earth. "The diculties that must be overcome are at
126 |R. G. Joseph et al., Seeding the Solar System with Life: Mars, Venus, Earth, Moon, Protoplanets
present beyond our imagination." The chairman of a Na-
tional Academy of Sciences committee which investigated
the evidence, Dr. Harold Klein, concluded it is impossible
to determine how even the simplest bacterium could have
been created (Horgan 1991). As summed up by Kuppers
(1990): "The expectation probability for the nucleotide se-
quence of a bacterium is thus so slight that not even the
entire space of the universe would be enough to make the
random synthesis of a bacterial genome probable."
The logical conclusion is that life, and the genes nec-
essary to maintain life, must have originated on planets
much older than our own.
3Galactic Clusters, Protoplanets,
Solar Systems, and
Interplanetary Transfer of Life
It is completely improbable that life was fashioned and
originated on this planet or in this solar system (Crick
1981; Dose 1988; Hoyle 1982; Yockey 1977) as there was
not enough time and all the constituent elements for the
manufacture of DNA were missing. It would take over 10
billion years to fashion a complete life-sustaining genome
from a single gene; and this solar system is believed to have
formed at least 4.570 Ga when the necessary materials and
elements in the solar nebula began to condense (Lugmair
and Shukolyukov 2001). However, if we accept, as a hypo-
thetical, that life was created somewhere in this galaxy—
which has been estimated to be 13 billion years in age (Pace
and Pasquini 2004; Pasquini et al. 2004)—and/or that the
conditions of nebular clouds somehow fortuitously pro-
duce DNA-equipped living organisms (Joseph and Schild
2010a,b), then it can be predicted that once life began to
replicate, diversify, and evolve, that living organisms were
dispersed to other planets and solar systems in this galaxy,
and infected protoplanets being fashioned in those nebular
Quantitative studies estimate that about one third
of the debris circulating in space between planets will
be ejected from solar systems with Jupiter-sized worlds
(Melosh 2003). Given that some of that some of this de-
bris is ejected from an impacted surface following meteor
strikes, if that debris contains living matter then, hypotheti-
cally, one solar system might seed another; so long as living
organisms or their spores are safely embedded deep within
the matrix of a large meteor, asteroid or comet that is at
10 kg), thereby providing a thick shielding against
UV and cosmic rays (Belbruno et al. 2012; Horneck 1993;
Nicholson et al. 2000).
However, it’s been argued that there is a very low proba-
bility that life can be transferred between solar systems due
to the distance, time, low interstellar density, and because
solar systems are in motion (Melosh 2003). As estimated
by Melosh (2003) of all the meteorites that are ejected from
terrestrial planets following impacts by bolides, only about
one-third are ejected out of the solar system via the gravi-
tational inuences of Jupiter and Saturn. Even during the
heavy bombardment phase of solar system development,
the ejected rocks originating from the surface of one terres-
trial planet would have only a 10
probability of landing in
a terrestrial planet in another solar system. Melosh (2003)
concluded that lithopanspermia between solar systems is
“overwhelmingly unlikely.” Other investigators believe the
odds are actually much greater (Belbruno et al. 2012) par-
ticularly when involving transfer between stellar systems
forming in galactic clusters as they are much closer together
(Adams and Spergel 2005).
Although various scenarios abound, it’s been proposed
that stars and protoplanets rst form in galactic clusters
within turbulent nebular clouds amongst thousands of
other new born stars (Adams 2010; Fragkou et al. 2019;
Johansen and Lambrechts 2017; Jones et al. 2019) with plan-
ets taking up to 10my to become established (Lissauer 1993).
These protoplanets are presumably fashioned in these stel-
lar nurseries by the accumulation of stellar debris, and with
protoplanets of varying size crashing into one another prior
to and after initially becoming captured by a newly forming
stellar system (Boyle and Redman 2016; Joseph and Schild
2010a,b; Stephan et al. 2020). For example, Adams (2010)
calculated that stars are born in clusters of 1,000–10,000
other stars; and with increased density, the probable suc-
cessful transfer of life-bearing debris increases accordingly.
It has been hypothesized that stars and planets re-
main in those clusters for 10my to 30 My or longer (Adams
and Myers 2001). Therefore, as worlds are formed and de-
stroyed (Adams and Spergel 2005; Boyle and Redman 2016;
Stephan et al. 2020) life may be repeatedly transferred be-
tween these protoplanets, carried by the billion trillion tons
of debris that ricochet between these worlds during this
10 to 30 mya episode of supreme chaos and turbulence
(Gibson et al. 2011; Joseph and Schild 2010b; Valtonen et
al. 2008). Therefore, after becoming contaminated with
life, these stars (and billions of planets) will drift away or
are ejected thereby becoming independent, albeit, initially
relatively chaotic solar systems until they stabilize.
R. G. Joseph et al., Seeding the Solar System with Life: Mars, Venus, Earth, Moon, Protoplanets |127
4Habitability and the Heavy
Bombardment Phase of Solar
The proto-planets that would become Earth, Mars, and
Venus may have become contaminated with life before and
after this solar system was established. The early solar sys-
tem was repeatedly subjected to cataclysmic events and
cosmic collisions, which led to major changes aecting the
habitability of the planets orbiting within the inner solar
Mars, Venus, Earth and the Moon, were repeatedly
and continually bombarded by meteors, asteroids, comets,
oceans of ice, and moon-sized debris until approximately
3.8 billion years ago (Chambers and Lissauer 2002; Levison
et al. 2001, 2002; Zappalà et al. 1998). The Late Heavy Bom-
bardment period is believed to have been triggered by the
capture and rapid inward migration of the planets which
resulted in cosmic collisions and the chaotic displacement
of surrounding and adjacent debris elds, thereby trigger-
ing the delivery of planetesimals, asteroids, meteors, and
oceans of water to the inner solar system (Kring and Cohen
2002; Tagle 2008); debris and water that may have harbored
Because Earth was continually bombarded, surface
rocks already established prior to 4.2 bya were pulverized
and vaporized erasing any evidence of life on the surface.
However, once surface rocks, minerals, and metals began
to cool and solidify, biochemical residue indicative of life
began to fossilize, and thus there is evidence of life within
Earth’s oldest rocks, minerals and metals, dated to over 4.2
bya (Nemchin et al. 2008; O’Neil et al. 2008); and which
suggests, life was present from the very beginning. There-
after, and because Earth orbits within the habitable zone,
life began to proliferate and terraform the biosphere (by re-
leasing oxygen and other gasses), and evolve (Joseph 2000,
Earth, Mars, and Venus, all orbit within the habitable
zone, the inner and outer edges of which are located respec-
tively at distances of 0.836 and 1.656 AU from the Sun (Kane
and Gelino 2012). Therefore, Mars (1.52 AU) is located near
the outer edge, while Venus (0.72 AU) is located just within
the inner edge of the habitable zone (Kasting et al. 1993).
Hence, if each of these planets had become contaminated
with life during the protoplanetary stage of development,
then, at least initially, life may have also begun to prolifer-
ate and evolve once their orbits stabilized.
Many scientists agree that ancient Mars was wet and
habitable (Ehlmann et al. 2011; Grotzinger et al. 2014;
Squyres and Knoll 2005; Thomas-Keprta et al. 2009; Vago
et al. 2017). Paralleling the onset and proliferation of life on
Earth, there is evidence—but no conclusive proof–of life on
Mars between 3.7 to 4.2 bya (Clement et al. 1998; Noke 2015;
Joseph et al. 2019; Thomas-Keprta et al. 2009). Moreover,
Martian life may have proliferated and evolved to the level
of metazoans (Joseph and Armstrong 2020; Joseph et al.
2020a; McKay 1996); after which, due to cosmic collisions
or unknown catastrophic events, the Martian geodynamo
was negatively impacted resulting in the loss of its magnetic
shield (Acuña et al. 1999; Arkani-Hamed and Boutin 2004;
Roberts et al. 2009). For example, it is believed that billions
of years ago a planet or moon slammed into the northern
plains of Mars creating an elliptical depression 6,600 miles
long and 4,000 miles wide (Andrews-Hanna et al. 2007)
and which may explain the extreme elliptical orbit or Mars.
However, when and why it lost its geodynamo is unknown;
but in consequence, Mars was no longer protected from so-
lar winds and UV Rays, and suered atmospheric loss and a
cooling and aridication of its climate (Fairén 2017; Jakosky
et al. 2018). Mars, therefore, became a failed Earth; though
how long before the Martian oceans began to evaporate or
freeze, is unknown.
Venus may have also been habitable billions of years
ago (Abe et al. 2011; Cockell 1999; Joseph 2019), and may
have remained habitable and able to sustain a variety of life
forms until at least 700 million years ago, before it lost its
oceans (Way et al. 2016) and its atmosphere exceeded the
ultimate stage of the “moist greenhouse” eect: Ts
(Wolf et al. 2017). When and what caused this catastrophic
alteration in the habitability of Venus is unknown. In conse-
quence, the environment of Venus became so toxic that only
hyper-extremophiles would be able to survive; i.e. fungi
and organisms beneath the surface (Joseph 2019; Ksan-
fomality 2013), or those dwelling in the clouds (Konesky
2009; Limaye et al. 2018; Sagan and Morowitz 1967; Schulze-
Makuch et al. 2004); and for which there is evidence, but
It is also believed that over 4.4 billion years ago a Mars-
sized planet may have struck Earth with so much force that
the ejected mass formed the moon (Belbruno and Gott III
2005). Therefore, Earth was originally a super Earth, much
larger in size, before this solar system stabilized. If life had
already taken root on Earth during the proplanetary phase
of development, then, according to this hypothesis, what
would become the moon would have also been infested
with life that later became extinct, after this Earth-moon
Considered as a hypothetical, if various protoplanets
had become contaminated with life, there is no guaran-
tee life would survive. Life, at least on the surface of these
128 |R. G. Joseph et al., Seeding the Solar System with Life: Mars, Venus, Earth, Moon, Protoplanets
worlds, may be subject to mass extinctions if these planets
assume orbital trajectories outside the habitable zone and
under conditions where water completely evaporates or
becomes permanently frozen. For example, it’s been esti-
mated that the highest surface temperature threshold for a
planet’s habitability is most likely 82
C. Above this thresh-
old, the loss of water by vaporization is irreversible and the
oceans disappear completely in a few million years (Inger-
soll 1969; Kasting 1998; Kasting et al. 2014; Wolf and Toon
2015). However, this does not preclude the possible exis-
tence of "alien" life forms with an adaptive biochemistry
completely unlike the life of Earth.
Although those events leading to the possible ejection
of what became the moon may have led to the extinction of
any life on the lunar surface, this same catastrophic event
may have enhanced the evolutionary potential for life on
Earth. After ejection and/or after the moon began to orbit
Earth, the Earth-Moon system’s tidally driven processes de-
creased Earth’s rotation period over the ensuing billions
of years according to the following estimates: 4.5 bya = 6.1
h; 3 bya = 10.5 h; 2 byr - 14.2 h (Arbab 2009). The presence
of the moon also altered the stabilization of Earth’s obliq-
uity (Laskar et al. 1993) which is subject to variations of
around a mean value of 23.3
. If there was no moon,
these variations would range from nearly 0
up to about
, causing cataclysmic alterations in the climate and bio-
sphere. As Earth would have also been larger—if the moon
had not been ripped from the surface–so to would be the
eects of gravity. In total, without the moon, there would
have been profound eects on the trajectory and evolution
of life such that humans may have never evolved on this
5Meteors, Ejecta, and the
Interplanetary Transfer of Life
It is believed that Earth, Mars, and Venus were struck mil-
lions of times during the period of heavy bombardment
which ended around 3.8 bya (Melosh 2003; Schoenberg et
al. 2002). Given evidence of life on Earth between 4.2 and
3.7 bya (Nemchin et al. 2008; Nutman et al. 2016; O’Neil
et al. 2008; Rosing and Frei 2004), and evidence of life on
Mars during this same time period (Clement et al. 1998;
Noke 2015; Thomas-Keprta et al. 2009) each of these im-
pacts would have also ejected tons of life-bearing debris
into space (Beech et al. 2018; Belbruno et al. 2012; Worth et
al. 2013). As argued by Belbruno et al. (2012): This period of
massive bombardment, therefore, provided a major “win-
dow of opportunity” for the transfer of life-bearing debris
between planets. According to Worth et al. (2013): "such
transfers were most likely to occur during the Late Heavy
Bombardment." Hence, the parallels in the possible mi-
crobial colonization of Earth and Mars between 3.7 and 4.2
bya. However, the interplanetary transfer of life, within this
solar system likely continued over the ensuing billions of
years following meteor strikes (Beech et al. 2018; Belbruno
et al. 2012; Worth et al. 2013) and due to powerful solar
winds (Joseph 2009; Joseph et al. 2019).
It is well established that an ounce of soil contains bil-
lions of microbes, as well as protozoa, algae, fungi, lichens,
and nematodes (Alexander 1991; Sylvia et al. 2004). If a
ton of compacted soil were ejected into space, an estimated
32,000,000,000,000 adhering organisms might be buried
inside and then subsequently deposited on another planet.
As will be explained, a variety of species, including bacte-
ria, algae, fungi, and lichens can survive a violent ejection
from the surface of a planet, direct exposure to space, and
then the crash landing onto the surface of a planet; though
if they survive would depend on how long they are aloft,
the matrix in which they are buried, and the habitability of
the planet upon which they might be deposited.
According to calculations by Beech et al. (2018), given
an impact velocity greater than 23 km/s, this microbial-
laden ejecta could enter the orbits of and intercept Venus,
Mars and other planets within a few weeks, months or years.
Moreover, studies have demonstrated that bolide ejecta pro-
vides nutrients that can sustain trillions of microorganisms,
including algae and fungi, perhaps for thousands of years
(Mautner 1997, 2002). However, ejecta may remain in orbit
for millions of years, whereas yet others may never strike
another planet and instead fall into the sun (Gladman et al.
1996; Melosh 2003).
There are currently 200 known terrestrial impact
craters that are still visible (Earth Impact Database 2020).
Following the end of the great bombardment period, this
planet may have been struck thousands of times (Melosh
1989), which resulted in the ejection of millions of rocks,
boulders and tons of debris into space over the course of
the last 4 billion years (Beech et al. 2018; Gladman et al.
1996; Melosh 1989, 2003; Van Den Bergh 1989). On Earth,
in the last 550 million years there have been a total of 97
major impacts, leaving craters at least 5 kilometers across
(Earth Impact Database 2020), and it’s been estimated that
kg of potentially life-bearing matter
has been ejected from Earth’s surface into the inner solar
system" (Beech et al. 2018). These impacts may have ejected
not just microorganisms, but metazoans, as well as seeds
and plants resulting in the interplanetary transfer of even
complex organisms between planets and inuencing and
impacting the evolution of life on alien worlds as well as on
R. G. Joseph et al., Seeding the Solar System with Life: Mars, Venus, Earth, Moon, Protoplanets |129
Earth due to the possible survival and proliferation of any
organisms buried in those meteors, asteroids and comets,
that struck this planet (Joseph 2000).
Consider, for example, the Chicxulub crater, formed
approximately 66 Mya, and which has a 150 km diameter
(Alvarez et al. 1980). If that impacting asteroid also con-
tained viruses, bacteria, and other living organisms as part
of its cargo, is unknown; but if so, it is reasonable to ask
if surviving extraterrestrial bacteria and viruses may have
sickened life on this planet (Joseph and Wickramasinghe
2010) perhaps contributing to the demise of the dinosaurs
and/or inuencing the evolutionary trajectory of survivors
via horizontal gene transfer (Joseph 2000). In addition to
the possible extraterrestrial delivery of living organisms to
Earth 66mya and creating conditions that led or contributed
to the demise of the dinosaurs (Alvarez et al. 1980), it’s been
estimated, given a 25 km/s impactor velocity, that up to 5.5
kg of debris may have been ejected into space when
that asteroid struck (Beech et al. 2018). That debris may
have included unknown volumes of water, and perhaps
millions of trillions of organisms buried within this ejecta.
Those that survived and were deposited within a habitable
environment, would have likely gone forth and multiplied.
The Chicxulub crater is just one example of an impact-
ejection event. Earth, Mars and Venus were repeatedly
stuck by asteroids and meteors. Over 635,000 impact craters
at least 1 km (0.6 miles) wide, have been located on Mars
(Robbins and Hynek 2012), approximately 1000 impact
craters have been detected on Venus by the Magellan space-
craft (Schaber et al. 1992) and 200 large terrestrial impact
craters have been located on Earth (Earth Impact Database
2020)—whereas the number of those that did not survive
weathering or were eventually buried, is unknown. Of the
60,556 meteorites so far found on Earth, 227 are believed to
have originated on Mars, and 360 are from the Moon (Mete-
oritical Bulletin Database 2020). Meteors from Venus have
not yet been identied. Clearly these planets have been
repeatedly impacted by meteors which survived descent
through the atmosphere without vaporization. Innumer-
able organisms embedded deep within those impacting
meteors may have also survived.
6Surviving Impact, Ejection,
Exposure to Space and Crash
It is well established that microbes buried within debris,
can survive extreme and violent shocks and impact pres-
sures of 100 GPa, and the subsequent hyper-velocity launch
into space (Burchell et al. 2004, 2001; Hazael et al. 2017; Hor-
neck et al. 2008; Mastrapa et al. 2001). By forming spores,
they can even survive long term direct exposure to the frigid
temperatures and vacuum of space despite the cosmic rays,
gamma rays, UV rays, ionizing radiation they encounter
(De la Torre Noetzel et al. 2017, 2020; De Vera et al. 2014,
2019; Horneck et al. 2002; Olsson-Francis et al. 2009). There
is also a high probability of survival after the crash landing
onto the surface of a planet (Burchell et al. 2001; Horneck
et al. 2002; Szewczyk et al. 2005).
Although innumerable meteors disintegrate, it’s been
estimated that those at least ten kilometers across will
punch a hole in the atmosphere and continue their descent;
and upon striking the surface eject tons of dust, rocks, boul-
ders and other debris into space (Covey et al. 1994; Hara
et al. 2010; Van Den Bergh 1989); with some of that debris
possibly passing through that atmospheric hole before air
can rush back in thereby preventing excessive heating (Van
Den Bergh 1989). Other than initial shock pressures, these
masses of ejecta, and surviving organisms buried within,
would not be subject to extremes in heat.
When a comet, asteroid, or meteor passes through
the atmosphere and strikes the surface, rocks, boulders
and debris that are blown upward and ejected by the im-
pact, may pass back through the atmosphere; and in con-
sequence they may be heated to temperatures in excess
C if they pass through after that "hole" has closed
up (Artemieva and Ivanov 2004; Fritz et al. 2005). These
temperatures are well within the tolerance range of ther-
mophiles (Baross and Deming 1983; Kato and Qureshi 1999;
Stetter 2006). Spores can survive shock temperatures of
C (Burchell et al. 2004; Horneck et al. 2002). There-
fore, if the hole in the atmosphere closes up before that
ejecta can pass through, the friction-generated heat might
only kill those organisms riding on the surface. In addi-
tion, exterior heating may only last a few seconds, whereas
ejecta may be covered by a heat-induced fusion crust of
at least 1 mm, which acts as a protective heat shield for
organisms deep within (Cockell et al. 2007); as the thermal
pulse may only extend a few millimeters below the surface
due to low thermal conductivity. Thus, organisms buried
within will not be aected. In fact, the interior may never
be heated above 100
C as the ejecta-surface is acting as a
heat shield (Burchell et al. 2004; Horneck et al. 2002).
Microbes can also resist the shock of a violent impact
casting them into space (Mastrapa et al. 2001; Burchell et
al. 2004, 2001). Bacteria, yeast spores and microorganisms
can survive impacts with shock pressures of the order of
gigapascals (Burchell et al. 2004; Hazell et al. 2010; Meyer
et al. 2011; Willis et al. 2006). Meyer et al. (2011) has demon-
130 |R. G. Joseph et al., Seeding the Solar System with Life: Mars, Venus, Earth, Moon, Protoplanets
strated that bacteria and lichens can survive powerful shock
waves and pressures up to 45 GPa, whereas cyanobacteria
withstand up to 10 GPa; so long as these organisms are
embedded within low porosity rocks.
Further, a substantial number of organisms could eas-
ily survive not just the ejection from a planet, but the de-
scent to the surface (Burchell et al. 2001; Horneck et al.
2002; McLean and McLean 2010). In one study, granite
samples were permeated with spores of Bacillus subtilis
and attached to the exterior of a rocket and launched into
space, reaching a maximum atmospheric entry velocity of
1.2 km/s and temperatures of 145
C (Fajardo-Cavazos et
al. 2005). Although a massive die o was recorded, up to
4.4% directly exposed to these conditions survived—and
one survivor can easily reproduce billions of microbial o-
spring. By contrast, studies have shown that a signicant
number of organisms buried within a meteor will not be
unduly harmed even when crashing into a planet (Burchell
et al. 2001; Horneck et al. 2002; McLean and McLean 2010).
Moreover, there are high survival rates following high at-
mospheric explosions, i.e. the Columbia space shuttle ex-
plosion (Szewczyk et al. 2005), and despite reentry speeds
of up 9700 km h
(McLean et al. 2006). Thus, innumerable
microbes may remain viable despite violent impact-induced
ejection into space and the rapid descent to the surface of
Earth is an obvious source of living organisms that
may have been ejected, jettisoned, cast into space, only
to crash onto the surface of other worlds in this solar sys-
tem beginning over 3.8 bya, thereby repeatedly seeding
Venus, Mars, and other planets with life (Beech et al. 2018;
Fajardo-Cavazosa et al. 2007; Hara et al. 2010; Melosh 2003;
Mileikowsky et al. 2000a,b; Schulze-Makuch et al. 2005)
and vice-versa. Asteroids and meteors striking Earth may
have repeatedly sheared away masses of earth and rock,
and blasted this material (and presumably any adhering
microbes, fungi, algae, and lichens) into space (Beech et al.
2018; Gladman et al. 1996; Hara et al. 2010; Melosh 2003;
Mileikowsky et al. 2000a,b), where they can survive (Hor-
neck et al. 2002; Onofri et al. 2012; De Vera et al. 2019; De
la Torre Noetzel et al. 2020; Novikova 2009; Novikova et
al. 2016; Olsson-Francis et al. 2009). Some of this microbe-
laden debris may have later crashed on Mars (Hara et al.
2010; Schulze-Makuch et al. 2005) where, as demonstrated
by simulation studies, a variety of organisms can also sur-
vive (Cockell et al. 2005; Mahaney and Dohm 2010; Osman
et al. 2008; Pacelli et al. 2016; Sanchez et al. 2012; Selbman
et al. 2015); and the same may be true of organisms de-
posited in the upper clouds of Venus (Joseph 2019; Konesky
2009; Limaye et al. 2018; Sagan and Morowitz 1967; Schulze-
Makuch et al. 2004). Coupled with solar winds blowing high
altitude atmospheric organisms into space (Arrhenius 1908;
Joseph 2009) the interplanetary transfer of microorganisms
within our Solar System is overwhelmingly likely (Beech et
al. 2018; Joseph et al. 2019; Mileikowsky et al. 2000a,b).
7Spores and Space Travel
In the absence of water, nutrients, or under extreme life-
neutralizing conditions, microbes, lichens, fungi and other
organisms may instantly react by forming highly min-
eralized heat or cold shock proteins that enclose and
wrap around their DNA, thereby eliminating all need for
metabolism and altering the chemical and enzymatic reac-
tivity of its genome making it nearly impermeable to harm
(Marquis and Shin 1994; Setlow and Setlow 1995; Sunde et
al. 2009). A dormant spore survives exposure to extreme
heat, cold, desiccation, the vacuum, UV and ionizing radi-
ation of space with just minimal protection (Horneck 1993;
Horneck et al. 1995; Mitchell and Ellis 1971; Nicholson et al.
2000). Survival rates also increase signicantly, up to 70%,
if coated with dust or salt crystals (Horneck et al. 1994).
Although the full spectrum of UV rays are deadly against
spores, some spores, including B. subtilis can even survive
a direct hit (Horneck et al. 2002). If buried below 30 cm of
surface material the eects of heavy ions and secondary
radiation depreciates signicantly and survival rates dra-
matically increase (Horneck et al. 2002). Because of their
small size, it’s been estimated that even those near the sur-
face of ejecta may survive in space for millions of years
being struck by radiation; and up to 25 million years in
space if shielded by 2 meters of meteorite (Horneck et al.
Many species of microbe form colonies. If traveling
through space, those in the outer layers would therefore
create a protective outer colonial crust that blocks out radia-
tion and protects those in the inner layers from the hazards
of space (Nicholson et al. 2000). Therefore, colonies of liv-
ing microbes provide their own protection and need not
As noted, ejected debris may orbit in space for millions
of years before striking another planet. Microbes, lichens,
and fungi may survive life in space for tens of millions of
years via the formation of spores. Cano and Borucki (1995)
have reported that spores, embedded in amber, may remain
viable for 25- to 40-million-years. Vreeland et al. (2000)
have reanimated 250 million-year-old halotolerant bacteria
from a primary salt crystal, whereas Dombrowski (1963)
reanimated spores "isolated from salt deposits from the
R. G. Joseph et al., Seeding the Solar System with Life: Mars, Venus, Earth, Moon, Protoplanets |131
Middle Devonian, the Silurian, and the Precambrian" that
were over 600 million years in age.
Therefore, even if ejecta circulates in orbit for millions
or tens of millions of years, spores embedded beneath the
surface might survive; and if they land on Mars and in the
clouds of Venus, those which can adapt would likely go
forth and multiply.
8Evidence of Life and
Stromatolites on Mars: Parallels
Although considered controversial, NASA’s 1976 Viking La-
beled Release studies, at two landing sites 4,000 miles apart
on Mars, detected evidence of surface biological activity
that could be attributed to a very wide range of microorgan-
isms including aerobic and anaerobic bacteria, as well as
lichens, fungi, and algae (Levin and Straat 1976, 1977, 2016).
Via the Viking "Gas Exchange" experiments, soil samples
were also humidied at ~10
C and a signicant quantity of
was released (Oyama and Berdahl 1977). On Earth, the
humidication of soil will cause a massive proliferation of
photosynthesizing algae/cyanobacteria and an increase in
oxygen production (Lin et al. 2013; Lin and Wu 2014). Levin
et al. (1978) also observed "green patches" on rocks and
hypothesized these may be algae. Therefore, the responses
produced by the LR instruments and the "Gas Exchange"
experiments, and the observations of Levin et al. (1978)
support the likelihood of life.
In 1996, McKay and colleagues reported the discov-
ery of "nanobacteria" in Martian meteorite ALH 84001;
specimens so small that if they had a genome, it could
only house RNA. These ndings were immediately chal-
lenged. As summed up by Martel et al. (2012), "...structures
resembling terrestrial life forms known as nanobacteria–
can be deemed ambiguous at best." Although also sub-
ject to dispute (see Treiman 2003; Steele et al. 2012), evi-
dence of biological residue, carbonates, and fossilized poly-
(Top row): Lake Thetis stromatolites with collapsed domed (Photo credit: Courtesy Government of Western Australia Department
of Mines and Petroleum). (Bottom row) Left: Sol 529. Right: Sol 308. Photographed in Gale Crater: Martian specimens with evidence of
concentric lamination and fossilized fenestrae. (From Joseph et al. 2020a, reproduced with permission).
132 |R. G. Joseph et al., Seeding the Solar System with Life: Mars, Venus, Earth, Moon, Protoplanets
(Top): Lake Thetis stromatolites with collapsed domed
(Photo credit: Lyn Lindeld And TheTravellingLindelds.com, re-
produced with permission). (Bottom) Left: Sol 122. Sol 308. Pho-
tographed in Gale Crater: Martian specimen with evidence of con-
centric lamination and fossilized fenestrae. (From Joseph et al.
2020a, reproduced with permission).
cyclic aromatic hydrocarbons (PAHs)–a byproduct of cellu-
lar decay–were also discovered in Martian meteorite ALH
84001 (Clement et al. 1998; McKay et al. 1996, 2009) at least
25% of which appears to be biological (Thomas-Keprta et al.
2009). Thomas-Keprta et al. (2009) has argued these nd-
ings are indicative of life on Mars over 4.2 bya. As summed
up by Martel et al. (2012) "the presence of polycyclic aro-
matic hydrocarbons, magnetite crystals, carbonate glob-
ules... are compatible with living processes."
In 2002 DiGregorio reported what he believed to be
biosignatures compatible with cyanobacteria in an ancient
paleolake; a hypothesis based on the detailed analysis
of images photographed at Utopia Planitia and Chryse
Planitia—in the same locations where the Viking LR ex-
periments detected biological activity and algae-like green
patches were observed (Levin and Straat 1977, 2016). Di-
Gregorio (2002), observed what he interpreted to be "rock
varnish" typically produced by a wide variety of microor-
ganisms "including epilithic and edolithic cyanobacteria."
DiGregorio hypothesized that Martian cyanobacteria could
have cemented sediments together, fashioning microbial
mats and stromatolites in these ancient Martian lakes. Sub-
sequently, in 2009, Rizzo and Cantasano (2009, 2017) re-
ported evidence of fossilized microbialites based on a de-
tailed examination of Martian sediments resembling stro-
matolites. Additional evidence of microbialites, microbial
mats, thrombolites and stromatolites were subsequently
provided by numerous investigators (Bianciardi et al. 2014,
2015; Joseph et al. 2019, 2020a,c; Ru and Farmer 2016;
Gale Crater is believed to have been host to several lakes
which were repeatedly replenished, and these ancient bod-
ies of water have been likened to the Lake Thetis of Western
Australia which is also home to living and fossilized dom-
ical stromatolites. In March of 2020, a team of 14 experts
in astrobiology, astrophysics, biophysics, geobiology, mi-
crobiology, lichenology, phycology, botany, and mycology
conducted an extensive search of the NASA Mars Gale Crater
image data base and found six concentric-domical Martian
specimens that closely resemble Lake Thetis stromatolites;
ve of which appeared fossilized (Joseph et al. 2020a). This
team also observed numerous other concentric structures,
that although severely decomposed, still retained patterns
similar to domical-concentric stromatolites.
Therefore, over a dozen surface features quite similar
to stromatolites have been observed on Mars. It’s been esti-
mated that the oldest of these Martian stromatolites may be
3.7 billion years in age (Noke 2015); a time period which
coincides with the fashioning of what may be the rst stro-
matolites on Earth 3.7 bya (Garwood 2012; Nutman et al.
2016)—though not all investigators accept this evidence.
Hence, there is evidence (but no proof) that life may
have appeared on Mars between 3.7 to 4.2 bya (Noke
2015; Thomas-Keprta et al. 2009), and that stromatolite
constructing-organism were proliferating (Joseph et al.
2020a); and this parallels the evidence, based on chem-
ical and physical fossils, that life had also appeared on
Earth during this same time period (Nemchin et al. 2008;
O’Neil et al. 2008; Rosing and Frei 2004), some of which
were also constructing stromatolites (Garwood 2012; Nut-
man et al. 2016), during and upon the close of the heavy
bombardment phase when Earth, Mars, and Venus were
pummeled with meteors, asteroids, comets and oceans of
water that may have harbored life.
9Fossils on Mars? Evolution and
Beginning billions of years ago, life on Earth diversied,
adapted to the changing environment, and evolved. By 800
to 600 mya, oxygen levels had signicantly increased to
about 0.1%–3% O
, of modern atmospheric levels (Ader
R. G. Joseph et al., Seeding the Solar System with Life: Mars, Venus, Earth, Moon, Protoplanets |133
(First row): Sol 809 and Sol 869. (Second row) Sol 905 and Sol 905. Specimens photographed in Gale Crater and that are quan-
titatively and statistically nearly identical to Ediacaran fossils of Namacalathus (two, bottom left) and (with the exception of tail length)
Cambrian fossils of Lophotrochozoa (three bottom right). Photos of Namacalathus reproduced from and courtesy of Kontorovich et al. 2008.
Photos of Lophotrochozoa reproduced from and courtesy of Zhang et al. 2014.
134 |R. G. Joseph et al., Seeding the Solar System with Life: Mars, Venus, Earth, Moon, Protoplanets
(First row) fossilized remains of Ediacaran Kimberella. (Bottom two rows): Specimens photographed in Gale Crater, quantitatively
and statistically nearly identical to Ediacaran fossils of Kimberella. Sol 809, Sol 809, Sol 809; Sol 880, Sol 905, Sol 905. Note proboscis
and "zipper-like" appendages.
R. G. Joseph et al., Seeding the Solar System with Life: Mars, Venus, Earth, Moon, Protoplanets |135
et al. 2014; Lyons et al. 2014) thereby leading to an explo-
sion of oxygen-breathing life (Brocks et al. 2017; Lenton et
al. 2014), that included acritarchs followed by Ediacaran-
metazoans (Erin 2015; Xiao et al. 2014; Zhou et al. 2001).
Moreover, despite repeated catastrophic extinction events,
life on Earth never became completely extinguished. In-
stead, each episode of mass extinction was followed by
repopulation and evolutionary innovation (Eldredge and
Gould 1972; Elewa and Joseph 2009; Joseph 2010a,b). There-
fore, if life had taken root, then beginning after 3.7 bya life
may have also evolved on Mars, up until that point in Mar-
tian history when catastrophic events negatively impacted
its internal dynamo, thereby resulting in the loss of its mag-
netic shield, followed by the evaporation and freezing of its
oceans and continual bleeding of atmosphere into space.
However, although speculation abounds, it is unknown as
to when these catastrophes occurred.
Paralleling events on Earth, Kaźmierczak (2016, 2020)
upon searching the Mars Meridiani Planum data base, dis-
covered specimens that resemble mineralized tri-star and
globular fossils with central vesicle-like ornamental cham-
bers. These mineralized spiny bimorphic structures have
thin walls with a cell-like appearance and were discovered
in hydrated sediments that may have once been an ancient
lake, i.e. Endeavor Crater. According to Kaźmierczak (2016)
analyses, morphologically they are similar to terrestrial
fossils variably described as acritarchs (meaning “of un-
certain origin”). The rst acritarchs may have evolved, on
Earth, over 700 million years ago (Arouri et al. 2000; Zhou
et al. 2001). In addition, Kaźmierczak (2020) has presented
evidence of Martian fossils that are strikingly similar to
daughter colonies characteristic of Terran volvocalean al-
gae as well as cell-like enclosures similar to chloroplasts
and modern unicellular green and yellow green algae.
Martian fossils resembling metazoans have also been
observed; many of which resemble one another and were
found in the same location or on adjacent mudstones in
Gale Crater (Joseph et al. 2020b). Subsequent, ongoing stud-
ies have identied over a dozen fossil-like impressions that
are morphologically and statistically identical to Ediacaran
fossils; i.e. Namacalathus and Kimberella (Joseph and Arm-
strong 2020). These fossils were embedded within and atop
Martian mudstones upon the lower lake surface of Gale
Crater; an area that other investigators believe was con-
ducive to the proliferation and fossilization of marine or-
ganisms (Grotzinger et al. 2014, 2015). These metazoan-like
fossils, most protruding from the surface, included spiral,
spherical, and tubular specimens often atop or immedi-
ately adjacent, and many nearly identical to one another
(Joseph et al. 2020a). As determined by molecular clock
studies, metazoans began populating Earth 750 to 800 mya
(Erin 2015) although the rst fossil evidence of metazoans
(the Doushantuo embryos) do not appear in the geological
record until 600 mya (Xiao et al. 2014).
It must be stressed: There is no conclusive proof these
are Martian metazoan fossils. Nevertheless, it is reasonable
to ask: Is it possible that metazoans evolved on Mars? Or
were they deposited on the Red Planet following meteor
strikes and ejection from Earth?
McKay (1996) has argued that "after the origin of life
the key evolutionary steps could have occurred much more
rapidly on Mars than on Earth" and that within a billion
years after life appeared, Mars may have "experienced the
range of biological evolution that would be duplicated on
the Earth only with the start of the Cambrian."
However, if metazoans independently evolved on Earth
and on Mars, then this would suggest that "evolution" is not
random and does not unfold according to Darwinian prin-
ciples, but is genetically coded and follows precise genetic
principles; such that similar species inevitably "evolve" on
planets that are similarly habitable; a genetically governed
and regulated process that Joseph (2000) has likened to
embryology and "evolutionary metamorphosis."
Joseph (2000) has also speculated that since so many
Ediacaran and Cambrian species were of unknown origin,
that possibly the Cambrian explosion may have been due to
the interplanetary transfer of life: "until around 600 million
years ago, just prior to the Cambrian era, the vast major-
ity of life forms sojourning on Earth consisted of single
celled organisms and simple multi-celled creatures com-
posed of less than 11 dierent types of cells. And then
there was a sudden explosion of complex life, including
rather "bizarre" life forms that appeared simultaneously
and multi-regionally throughout the oceans of the Earth"
including numerous species that have an "unknown ori-
gin." Joseph (2000) goes on to argue: "Many creatures (in-
cluding even complex multicellular plants, insects, frogs
and lizards) can also live in a dormant form and withstand
otherwise life neutralizing conditions. Indeed, the capac-
ity to live in a dormant state even under environmental
extremes, may well account not only for the origin of life
on Earth, but to the sudden emergence of at least some of
the complex species during the Cambrian Explosion. In
other words, even complex animal life may have been de-
posited on Earth from outer space, including, perhaps at
least some of the "bizarre" life forms that emerged during
the Cambrian Explosion."
Caenorhabditis elegans is a metazoan, approximately
1mm in length and has a mouth, intestine, male and female
reproductive organs, and an ancestry that extends back
to the Ediacaran era. C. Elegans is a nematode, and some
species of nematode prefer frigid climates (Mullin et al.
136 |R. G. Joseph et al., Seeding the Solar System with Life: Mars, Venus, Earth, Moon, Protoplanets
2002), where temperatures may fall below
Conversely, those that dwell in arid environments can enter
a state of dormancy for up to 28 years if deprived of water
and then become metabolically active when provided mois-
ture (Fielding et al. 1951). Caenorhabditis elegans, therefore,
might be capable of adapting to life on Mars. They can also
survive exposure to space, an explosive reentry into the
atmosphere, and a subsequent crash landing.
On February 2, 2003, numerous members of this
species, ensconced within canisters, survived an explosion,
at speeds of Mach 19, approximately61 km above Earth’s sur-
face, that destroyed the space shuttle Columbia. And these
C. elegans survived an unprotected 660–1,050km/h velocity
reentry into Earth’s atmosphere and the subsequent crash
upon the surface (Szewczyk et al. 2005). After these C ele-
gans were retrieved from the crash site all but two displayed
normal growth and reproductive egg laying behavior. As
argued by (Szewczyk et al. 2005), what they experienced is
analogous to being embedded on the surface of an asteroid
that breaks into fragments upon striking the atmosphere,
and then surviving after those fragments smash into the
Eight hundred million years ago, the Moon and Earth,
were struck by a urry of asteroids that likely profoundly
aected the biosphere (Terada et al. 2020). As summarized
by Terada et al. (2020): "Based on crater scaling laws and
collision probabilities... meteoroids, approximately 30–60
times more powerful than the Chicxulub impact, must have
plunged into the Earth-Moon system."
Soon thereafter, acritarchs, Ediacarans, and thus, the
rst metazoans, began to proliferate in Earth’s oceans,
many having a bizarre appearance, many eventually dy-
ing out and becoming extinct, and many have a completely
unknown ancestral origin—as if they were deposited here
from another planet.
If the hypothesis of McKay (1996) and Joseph (2000) are
correct, it is reasonable to ask: is it possible that Martian
metazoans were transported to Earth, thereby contribut-
ing to or giving rise to the Cambrian Explosion? Or, might
the (presumed) metazoans on both planets have originated
from another world; possibly buried in those meteors that
struck 800mya? Or, conversely, did ejecta from Earth trans-
port metazoans to Mars? One can only speculate.
10 Fossils on the Moon?
In support of the interplanetary transfer hypothesis is the
discovery of fossilized impressions on the surface of the
moon. Specically, in 1970 lunar soil samples were returned
to Earth by the Luna 16 spacecraft in a hermetically sealed
container (Rode et al. 1979) and one of the specimens was
observed to closely resemble a spiral lamentous micro-
Ediacaran, a species which became extinct over 500,000
years ago (Joseph and Schild 2010a). Zhmur and Gerasi-
menko (1999), also identied what they believed to be lu-
nar microfossils of coccoidal bacteria; i.e. siderococcus and
sulfolobus. It is not probable that Ediacarans and coccoidal
bacteria evolved on the moon. Therefore, if these fossilized
impressions are true fossils, they must have been trans-
ported to the lunar surface, possibly while still alive, and
Moreover, what appears to be microfossils of ovoid and
elongated nanobacteria were also discovered in a lunar me-
teorite (Sears and Kral 1998). These lunar "nanobacteria"
however, were even smaller than the "nanobacteria" discov-
ered in Martian meteorite ALH8401. In general "nanobacte-
ria" are so small it would be impossible for them to host a
DNA-based genome, but only an RNA-based genome, like
a virus. If we employ life on Earth as a standard, it is not
likely that the Martian or Lunar "nanobacteria" are true
cellular organisms (Joseph and Schild 2010b).
11 Lunar Life and Survival of the Fit
After sitting 3 years on the moon, a TV camera from the
lunar Surveyor Space Craft was retrieved by Apollo 12 astro-
nauts, and dormant bacterium (Streptococcus mitis) were
found within. Mitchell and Ellis (1971), the scientists who
made this discovery, ruled out contamination due to a sci-
entist’s sneeze or cough because a single droplet of saliva
contains an average of 750 million organisms and billions of
bacteria and a "representation of the entire microbial pop-
ulation would be expected," rather than a single species
that was dormant and then came back to life. Mitchell and
Ellis (1971) therefore, left open the possibility that the cam-
era was contaminated on the moon by lunar Streptococcus
mitis; and not before the camera was sent and not after it
was returned from the lunar surface.
It is possible, however, that there was contamination
and that billions of diverse moisture-dwelling bacteria were
coughed or sneezed into this equipment prior to sending
the TV camera to the moon. Possibly, a diverse colony of
organisms were subsequently transported to the lunar sur-
face within that camera, and only Streptococcus mitis sur-
vived by forming spores and all other bacteria died leaving
not a trace of their existence. Likewise, it can be argued
that only those organisms which can survive ejection from
Earth, Mars, or some other planet, and that can survive the
R. G. Joseph et al., Seeding the Solar System with Life: Mars, Venus, Earth, Moon, Protoplanets |137
subsequent exposure to the intense UV and gamma radia-
tion of space, may go forth and multiply when deposited
on a habitable, watery moon or planet. By contrast, those
that cannot survive a journey through space and which are
deposited on completely uninhabitable moons or planets,
will die, decompose, or, more rarely, their remains may be
12 Solar Winds vs Microbes in the
Stratosphere and Mesosphere
Fungi, lichens, and algae and over 1,800 dierent types of
bacteria ourish within the troposphere, the rst layer of
Earth’s atmosphere (Brodie et al. 2007). Microbes, algae,
fungi, lichens, spores, insects, larva, pollen, seeds, water,
dust and nematodes are often transported to the strato-
sphere and mesosphere due to tropical storms, monsoons,
thunderstorms, hurricanes, tornados, volcanic eruptions
and seasonal and electrostatic upwellings of columns of
air (Dehel et al. 2008; Holton et al. 1995; Randel et al. 1998;
Rohatschek 1996; Van Eaton et al. 2013). Microorganisms,
fungi, and spores have been recovered at 40 km, 61 km
and 77 km above Earth (Imshenetsky et al. 1978; Soen
1965; Wainwright et al. 2010). And once within the strato-
sphere they may be blown into space by powerful solar
winds (Joseph 2009, 2019) where, as shown experimentally,
they can survive (De la Torre Noetzel et al. 2020; De Vera et
al. 2019; Horneck et al. 2002; Nicholson et al. 2000, 2003,
2005; Novikova et al. 2016; Olsson-Francis et al. 2009).
If the dispersal of upper atmospheric organisms into
space occurs continually or only periodically every few
years, decades or centuries, is unknown. However, on
September 24, 1998, a series of coronal mass ejections cre-
ated a shock wave and powerful solar winds that struck
the magnetosphere with such force that oxygen, hydrogen,
helium, water molecules and surface dust gushed from the
upper atmosphere into space (Moore and Horwitz 1998;
Schroder and Smith 2008). For most of every year, the solar
pressure is around two or three nanopascals. However, on
September 24, the pressure increased to ten nanopascals.
Similar events may have occurred repeatedly and more fre-
quently throughout Earth’s history.
For example, data derived from the observation of so-
lar proxies with dierent ages and reconstructions of the
Sun’s radiation and particle environment from 3.5 bya to the
present "indicates a solar wind density up to 1000 times
higher at the beginning of the Sun’s main sequence life-
time" and that gradually dropped to current levels (Lam-
mer et al. 2003). Thus, beginning billions of years ago air-
borne microbes, fungi, lichens, and algae, as well as water
and dust lofted into the upper atmosphere, may have been
swept into space by solar winds and dispersed through-
out the solar system some of which may have landed on
Mars, the Moon, and in the clouds of Venus (Arrhenius
1908; Joseph 2009, 2019).
13 Life in the Clouds of Venus
The clouds of Earth are saturated with water and life (re-
viewed by Joseph 2019). Venus has three cloud layers that
contain high levels of deuterium and trace amounts of wa-
ter (Barstow et al. 2012; Donahue and Hodges 1992), which
could sustain life (Clarke et al. 2013; Cockell 1999; Grin-
spoon and Bullock 2007; Konesky 2009; Seckbach and
Libby 1970; Schulze-Makuch et al. 2004). According to Li-
maye et al. (2018): "The lower cloud layer of Venus" pro-
vides "favorable conditions for microbial life, including
moderate temperatures and pressures (~60
C and 1 atm)."
Konesky (2009) has suggested that organisms similar to
plankton may dwell in the upper atmosphere. Schulze-
Makuch et al. (2004) hypothesized that Venusian clouds,
48 to 65 km above the surface, could harbor aeroplank-
ton which engage in photosynthesis. Sagan and Morowitz
(1967) hypothesized that complex multi-cellular organisms
swim between the thick layers of Venusian clouds where
they metabolize and generate hydrogen as propellants and
a means of oatation. These scenarios are not unreason-
able as trillions of billions of organisms dwell in the clouds
of Earth and are therefore adapted to living in the upper
If life is being deposited in the clouds of Venus via
bolides and solar winds from Earth, it is therefore possible
that some of these organisms that survive the journey may
adapt to life on Venus. However, the possibility of life in
the clouds of Venus is a hypothesis, and not fact.
14 Life Upon and Beneath the
Surface of Venus
The Russian probe Venera 13 landed in the Beta-Phoebe
region of Venus in an area described as a "stony desert"
(Surkov et al. 1983). On Earth, endolithic microorganisms
ourish in hyper-arid stony deserts and under extreme en-
vironmental conditions by colonizing the interior and un-
dersides of rocks (Weirzchos 2012; Pointing and Belnap
2012) within which water molecules may be trapped. Gen-
138 |R. G. Joseph et al., Seeding the Solar System with Life: Mars, Venus, Earth, Moon, Protoplanets
erally, these hot desert micro-habitats are dominated by
lichens, fungi, algae, cyanobacteria and heterotrophic bac-
teria (Pointing and Belnap 2012).
The surface temperature of Venus, as determined by
Venera 7, is 739 K
C (Avduevsky et al. 1971). There
are no known terrestrial organisms which can survive these
temperatures, except, perhaps, as spores. However, basalt
is common on Venus, and basalt has high thermal insu-
lating properties (Eppelbaum et al. 2014). Temperatures
beneath these rocks, and up to 10 m below the surface,
would be much cooler than the surface (Joseph 2019) as
documented on Earth (Al-Temeemi and Harris 2001; Smer-
don et al. 2004). In high temperature environments heat
transfer reduction from the surface to 10 m down can be
as much as 57% (Al-Temeemi and Harris 2001); i.e. 43% of
surface temperature. As calculated by Joseph (2019), at a
depth of 1 m temperatures on Venus might average 407.4
whereas at 10 m, the subsurface temperature may average
C which is within the limit for the hardiest hyper-
thermophiles on Earth (Kato and Takai 2000). Some hy-
perthermophiles have been discovered thriving adjacent to
C thermal vents (Stetter 2006). However, there are no
known terrestrial species which can survive direct exposure
to temperatures above 300
C (Kato and Qureshi 1999; Kato
and Takai 2000).
Venus orbits in the habitable zone, and in addition to
comets, asteroids, and meteors, large amounts of frozen wa-
ter was likely delivered to the surface early in this planet’s
history. Possibly, Venus had oceans as recently as 700 mil-
lion years ago (Way et al. 2016) and was likely habitable
billions of years ago (Abe et al. 2011; Cockell 1999). If the
catastrophic change in the biosphere of Venus was sudden
or took place over millions of years is unknown. However,
if Venus was habitable and inhabited billions of years ago,
from what we know of the adaptive nature of microbial and
other forms of life, even a drastically changing environment
does not obliterate all life. Some organisms form spores,
others evolve and adapt. Likewise, if there had been life on
Venus, to survive they would have had to adapt and evolve
to these hyper-extreme conditions.
15 Fungal Life on Venus?
Any organisms that evolved in response to the changing
Venusian biosphere would require water which also might
be available in the clouds and below ground. For example,
just as occurs in the deserts of Kuwait, moisture and water
may be drawn up from the subterranean depths (Al-Sanad
and Ismael 1992). If so, Venusian organisms living below
ground may be continually supplied with water as it rises
to the surface and before it completely evaporates.
It is also well established that numerous species are
able to colonize and ourish within even the most toxic and
seemingly-life-neutralizing environments, including pools
of radioactive waste (Armstrong 2017; Dighton et al. 2008;
Durvasula and Rao 2018; Gerday and Glansdor 2007; Zh-
danova et al. 2004). It’s also been demonstrated that some
species can survive in Venusian analog environments (Seck-
bach et al. 1970). It’s been hypothesized that thermophilic
photothrophs (Arrhenius 1908; Cockell 1999), algae (Seck-
bach and Libby 1970) and acidophilic microbes (Schulze-
Makuch et al. 2004) could ourish within the Venusian bio-
sphere. Moreover, as reported by Joseph (2019) it appears
that fungi are hyper-extremophiles capable of colonizing
even the most extreme alien environments; and there is
evidence of fungi on Venus (and Mars).
Ksanfomality (2013), based on his examination of en-
hanced panoramic images from the 1975 and 1982 Soviet
VENERA-10, VENERA-13 and VENERA-14 images of the Venu-
sian surface, observed what he interpreted to be a fungal-
shaped specimen at a distance of 15 to 20 cm from the buer
of the landing module and which he estimated to be ele-
vated 3 cm above the surface and with a diameter of approx-
imately 8 cm. Ksanfomality (2013) concluded: "The object
exhibits explicit similarity to terrestrial mushrooms and is
supplied with folded caps."
Examination of panoramic color images from the
1982 VENERA-13 mission, also reveals several well-dened
mushroom-shaped specimens with stalks that protrude
approximately 3 cm from the surface, and with caps that
are approximately 5 cm in diameter, and which resem-
ble the classic terrestrial mushroom (Joseph 2019). These
mushroom-shapes are bordered by a crescent of similarly
shaped specimens, all of which are similar to terrestrial
mushrooms. Moreover, several of these specimens resem-
ble what may be fungal organisms growing on Mars (Joseph
et al. 2019, 2020b). Does this prove there is life on Venus?
16 Fungi on Mars?
Several investigators have reported observations of forma-
tions on Mars that resemble white fungi growing beneath
rock shelters in the dried lake bed of Gale Crater (Joseph
2014; Joseph et al. 2019; Rabb 2018; Small 2015). In addition,
23 specimens similar to fungal "puballs" have been pho-
tographed by the rover Opportunity in Meridiani Planum,
increasing in size over a three days period, twelve of which
R. G. Joseph et al., Seeding the Solar System with Life: Mars, Venus, Earth, Moon, Protoplanets |139
Venus: Specimens resembling fungal-mushrooms. Photographed near the landing struts of the 1982 Soviet probe VENERA-13.
(Reproduced with permisison from Joseph 2019).
Mars. Photographed in Eagle Crater by the rover Opportunity. Comparing Sol 1145-left vs Sol 1148-right: Growth of twenty-three
Martian specimens over three days, twelve of which emerged from beneath the soil and all of which increased in size. Ground level wind
speeds between 40 to 70 m/h are required to move coarse grained soil on Mars, and no strong winds, dust clouds, dust devils, or other in-
dications of strong winds were observed, photographed, or reported during those three days in this vicinity of Mars. Nor does the Sol 1148
photograph show any evidence that the surface has been disturbed by wind, as there are no parallel lineaments, ripples, waves, crests,
or build-up of soil on one side of the specimens as would be expected of a directional wind. Dierences in photo quality are secondary to
changes in camera-closeup-focus by NASA. (Reproduced with permission from Joseph et al. 2020a).
140 |R. G. Joseph et al., Seeding the Solar System with Life: Mars, Venus, Earth, Moon, Protoplanets
Mars. Sol 182. A majority of experts identied these spec-
imens as basidiomycota: fungal "puballs" (Joseph 2016). Note
what appears to be spores littering the surface. (Reproduced with
permission from Joseph et al. 2019).
emerged from beneath the coarse-grained rocky-sandy sur-
face as based on comparisons of Sol 1145 and Sol 1148
(Joseph et al. 2020b) Although on Earth, 20 km/h winds can
displace ne grained sand (Kidron and Zohar 2014) these
specimens are buried in coarse-grained rocky soil, and no
evidence of wind-blown dust in the air, dust devils, dust
storms, or wind-driven soil displacement or buildup was
observed in that vicinity during those three days (Joseph
et al. 2020b). Although it is unknown if these are in fact
living organisms, these observations favor the possibility
that fungi have colonized Mars.
17 Algae and Lichens on Mars?
Oxygen and Photosynthesis
Observations of what may be algae on the surface of Mars
were rst reported by Levin, Straat and Benton in 1978 and
who observed changing patterns on "greenish rock patches"
which were "green relative to the surrounding area." Levin
et al. (1978) speculated that these greenish areas may rep-
resent "algae" or "lichens" growing on Mars.
Mars. Sol 871. Green sphericals upon Martian sand, soil,
rocks and pinnicle-columnar structures resembling terrestrial
stromatolites and thrombolites and algae growing in shallow water,
but may be frozen. On Earth, the greenish-coloration of sand and
rock is due to green cryptoendolithic cyanobacteria. The darkening
in soil coloration may indicate moisture. Photographed in Gale
Crater. (Reproduced with permission from Joseph et al. 2020a).
Mars. Sol 853. Thick-layered clumps of algae-like sub-
stance and "tubular" specimens on top of and adjacent to speci-
mens resembling fossilized bacterial mats, and adjacent to "dim-
pled" lichen-like organisms. Photographed in Gale Crater. (Repro-
duced with permission from Joseph et al. 2020a).
Subsequently, a number of investigators have pub-
lished photos taken by the Mars rovers Spirit and Curiosity,
depicting what they believed to be green algae (Joseph 2014;
Joseph et al. 2020a; Rabb 2018; Small 2015). For example,
R. G. Joseph et al., Seeding the Solar System with Life: Mars, Venus, Earth, Moon, Protoplanets |141
Mars. Sol 305 and Sol 305. Algae-like substances upon fungal-tubular-like specimens, and forming thin layers upon adjacent
rocks. Photographed in Gale Crater. (Reproduced with permission from Joseph et al. 2020a).
Krupa (2017) presented evidence of specimens resembling
green photosynthetic organisms in the Columbia Hills area
of Gusev Crater, adjacent to water pathways that may in-
termittently ll with water. Krupa (2017) noted that "the
hillside...is covered by a very thin layer of green material"
and "green spherules" which resembles algae in the soil.
In addition, a team of 14 established experts conducted an
extensive investigation of the Gale Crater image depository
(Joseph et al. 2020a) and identied specimens resembling
terrestrial algae and lichens. The algae-like specimens ap-
peared as clumps and spherules, and formed cake-like lay-
ers, thin sheet-like layers and thick layered leafy vegetative
masses of material that partially covered Martian rocks,
sand, and fungi-like surface features.
At some point in the evolutionary history of life on
Earth, algae and fungi formed a symbiotic relationship,
thereby fashioning lichens. Lichens consist of at least one
alga that can be a green algae or cyanobacterium (photo-
biont) and at least one fungus (mycobiont). The fungus is
responsible for the lichens’ mushroom shape, bulbous cap,
thallus, and fruiting bodies, whereas the alga photobiont
engages in photosynthesis (Armstrong 2017; Brodo et al.
Lichen-shaped specimens observed in Gale Crater take
a variety of forms, the most common: mushroom-shaped
and nucleated with a visible "dimple" at the center of each
specimen (Joseph et al. 2020a). If these are in fact living
organisms, is unknown. However, hundreds of these lichen-
142 |R. G. Joseph et al., Seeding the Solar System with Life: Mars, Venus, Earth, Moon, Protoplanets
(Top Left): Earth. Lichens growing on the west coast Ireland clis of Moher (Photographed by Dr Jessica M Winder, https:
//natureinfocus.blog. Reproduced with permission). (Top right and bottom) Gale Crater Sol 298: Specimens resembling dimpled lichens
with what may be hyphae along the surface/subsurface. Note hollow apertures in the upper right corner and lower center of photo, and
which resembles an oxygen-gas vents typically produced by photosynthesizing organisms.
R. G. Joseph et al., Seeding the Solar System with Life: Mars, Venus, Earth, Moon, Protoplanets |143
(Top) Sol 232: Specimens similar to gas-vent apertures for the release of oxygen secondary to photosynthesis within microbial
mats; photographed in Gale Crater. (Bottom) Cone-like tubes for the venting of oxygen produced by photosynthesizing algae (reproduced
with permission from Freeman SE, Freeman LA, Giorli G, Haas AF (2018) Photosynthesis by marine algae produces sound, contributing to
the daytime soundscape on coral reefs. PLoS ONE 13(10): e0201766).
Mars. Sol 88 and Sol 37: Specimens resembling the mushroom-shaped lichen Dibaeis baeomyces Photographed in Eage Crater.
(Reproduced with permission from Joseph et al. 2020b).
144 |R. G. Joseph et al., Seeding the Solar System with Life: Mars, Venus, Earth, Moon, Protoplanets
Mars. Sol 35 and Sol 85: Specimens resembling the mushroom-shaped lichen Dibaeis baeomyces and examples of colonies of
lichen-shaped organisms. Photographed in Eagle Crater. (Reproduced with permission from Joseph et al. 2020b).
Mars. Sol 85: Examples of vast colonies of lichen-shaped organisms attached to rocks, and oriented skyward similar to photosyn-
thesizing lichens. Photographed in Eagle Crater. (Reproduced with permission from Joseph et al. 2020b).
like surface features were observed adjacent to specimens
resembling green algae and bubble-like open-cone aper-
tures (Joseph et al. 2020a). It is well established that pho-
tosynthesizing organisms, such as cyanobacteria, respire
oxygen and release gas bubbles via the surrounding ma-
trix and which may become mineralized and fossilized as
open cone apertures (Bengtson et al. 2009; Sallstedt et al.
2018). Therefore, it’s possible that the open-cone apertures
observed in Gale Crater serve to ventilate oxygen respired
Vast colonies consisting of thousands of lichen-
mushroom-shaped specimens that resemble the lichen,
Dibaeis baeomyces, have also been observed in Eagle Crater,
attached by thin stems to the tops of rocks and oriented sky-
ward as is typical of photosynthesizing organisms (Joseph
et al. 2020b). Terrestrial fungi do not engage in photosynthe-
sis; and thus, if these colonies are living photosynthesizing
organisms, then they are most likely lichens.
If the algae and lichen-like Martian structures are in
fact photosynthesizing organisms, this would account for
the distinct seasonal variations in the oxygen content of the
R. G. Joseph et al., Seeding the Solar System with Life: Mars, Venus, Earth, Moon, Protoplanets |145
atmosphere (England and Hrubes 2004) which increases by
approximately 30% in the Summer, and for which no abio-
genic source has been found (Trainer et al. 2019). Earth’s
atmospheric oxygen levels also vary according to the season
and increase during the Spring and Summer due to the bio-
logical activity of photosynthesizing organisms; and these
parallels support the likelihood that oxygen on Mars is also
produced biologically, even more so since Martian atmo-
spheric oxygen is continually replenished despite leaking
into space (Joseph et al. 2020b).
In the space of the entire universe the only conclusive evi-
dence of life is found on Earth. Although the ultimate source
of all life is unknown, many investigators believe Earth,
Mars, and Venus may have been seeded with life before and
after becoming established members of this solar system.
In support of that hypothesis is evidence, but no proof, that
life appeared, in parallel on Mars and Earth 4.2 by and that
stromatolites were being constructed on both planets 3.7
bya. Moreover, there is evidence, but no proof, that life on
Mars may have evolved as suggested by the fossil-like spec-
imens resembling metazoans. There is also evidence—but
no conclusive proof– that fungi have colonized Mars and
Venus, and algae and lichens are ourishing on Mars. By
contrast, only the moon appears to be completely uninhab-
itable and uninhabited—other than by dormant spores—at
least on the surface.
It must be stressed that it is unknown if the surface
features observed on Mars and Venus are abiotic, fossils,
or represent living organisms. Conrmation requires direct
examination, extraction and microscopic analysis. Never-
theless, although there is no denitive, conclusive proof
of life except on Earth, the evidence reviewed in this re-
port, supports the hypothesis that the planets of the inner
solar system may have repeatedly exchanged living organ-
isms beginning billions of years ago, and that Earth may
be seeding the solar system with life.
No Competing Interests:
The authors have no competing
or nancial or non-nancial interests and no funding to
report and will not benet nancially from this article.
All authors have either contributed
directly to the research reviewed, and/or assisted in the
analysis, writing, editing, and /in searching for and refer-
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