

Contents
Technical Sections
Introduction
Target Environments
The Swarm Strategy
Propulsion and Launch
Astrometry and Targeting
Capture at the Target Zone
Design of Capsule Size
Target Selections/Probability
Dark Cloud
Fragment
Protostellar
Condensation
Accretion
Disks/Planets
Biomass Requirements
Missions to Nearby
Stars
Survival/Growth in
Comets
Biological Considerations
Advanced Missions
Resource Requirements
Using Comets as Vehicles
Conclusions |
Directed
Panspermia
- Technical Considerations -

11. Resource
Requirements

Although aimed
at specific targets, the microbial payloads may carry life further in space and time.
First, much of the microbial swarm will miss or
transit the target. Secondly, of the initial 1E13 comets that capture capsules in the
accreting system, up to 99% will be ejected into interstellar space [11], carrying the
microbial content. These embedded capsules, shielded from radiation and preserved at 3 K,
may survive in the comets for many Gyr, until eventually captured in accreting systems in
other regions of the galaxy. Of the 1E11 comets remaining in the accreting system, most
will remain in the cold <10 K Oort cloud which will be eventually ejected into
interstellar space. Therefore the majority of the launched biomass will eventually carry
the microbial payload further into the galaxy. The spread of microbial life by comets is
similar to the proposals of Hoyle and Wickramasinghe [17], but we postulate here a
directed origin.
Future programs may aim intentionally to seed the
entire galaxy. It is interesting to assess the feasibility of such a program.
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Once launched randomly into the
galactic plane at v = 0.01 c, the microbial packets will traverse the galaxy (r = 7E4 ly
[25]) in 7E6 yr. The packets are gravitationally bound to the galaxy and will eventually
perform random paths. At these speeds, mm size capsules will transit all thin regions and
will be captured only in protostellar condensations or denser accretion zones. The mass
ratios above showed that 1E-13 of the captured biomass in these areas will be delivered to
planets. With 100 capsules of 1E-10 kg, ie., a biomass of 1E-8 kg required to seed a
planet, and with star-formation rate of 1 yr-1 in the galaxy, biomass needs to
be launched at the rate of 1E5 kg/yr for 5E9 yr to seed all new stars during the lifetime
of the solar system. For example, the biomass can be dispersed in pulses of 1E12 kg to
seed the population of star-forming clouds as it is renewed every 1E7 yr. The total
required biomass is 5E14 kg, compared for example with the 1E19 kg organic carbon (1%) in
the 1E21 kg total asteroid mass. This resource allows increasing the launched biomass up
to a factor of 2E6 to account for undoubtedly substantial losses.
As a more conservative estimate, assume a 5 au
capture zone, with a volume of 2E36 m3, with the total capture volume of 2E47 m3
about 1E11 stars. With a capture probability of 1E-5 and for delivering 100 captured
capsules of 1E-10 kg each, 1E-3 kg needs to be placed about each star. This corresponds to
a density of 5E-40 kg biomass m-3 in these circumstellar volumes. Assuming that
this is achieved by establishing a similar biomass density through the 5E61 m3
volume of the galaxy, then the total biomass needed in the galaxy is 2.5E22 kg. Renewing
this density each 1E9 yr for the 5E9 yr lifetime of the solar system, to seed every new
planetary system during the first Gyr after its formation, gives a material requirement of
about 1E23 kg, about 10% of the 1% C content in 1E26 kg of the total cometary mass.
The material requirements can be
reduced by many orders of magnitude if the missions are directed to star-forming regions
rather than distributing biomass through the galaxy at random. Of course, the microbial
population may be subject to substantial losses, but may be enhanced in the target zones
by gravitational attraction. The fate of biological objects traversing the galaxy requires
detailed analysis.
It may be possible to grow the necessary large
amounts of microorganisms directly in carbonaceous asteroids or comets. Carbonaceous C1
meteorites, and presumably asteroids, contain water in about the biological ratio of 5:1 H2O/C,
and N in the biological ratio of 10:1 C/N, as well as biologically usable forms of the
other macronutrients S, P, Ca, Mg, Na and K in at least the biological C/X elemental
ratios [19]. Once the nutrient components are extracted, the residual inorganic components
may be used for shielding materials for the microbial capsules.
As a possible method for
converting comets to biomass, the loose icy, cometary matrix may be fragmented and
enclosed in membranes in 1 kg spheres. Warming and melting such a unit, from 10 to 300 K,
requires 5.1E9 J, which can be provided by the solar energy flux of 325 W m-2
at 2 au, incident on the 3.1 m2 cross-section of a 1 m radius object during a
two-months perihelion transit about 2 au. The microbial experiments show that in 6 - 8
days after inoculation, this organic solution will yield microbial densities of >1E8
CFU/ml which can survive for several months [18, 19]. Subsequently, the microbial solution
can be converted to 1 mm "hailstones". These microbial ice capsules can be
accelerated out of the solar system, for example, by first accelerating the comets sunward
into parabolic orbits, and in this manner dispersing the Oort cloud at the rate of 20
comets yr-1 during 5E9 yr. This rate is comparable to the natural rate of 3 new
comets/yr plus up to 1E9 new comets per/year during cometary showers [16], and the task
may be accomplished at the required rate by processing every new comet that arives
naturally from the Oort cloud.
An interesting experiment in this
direction would be to inoculate the sub-crust zone of an inbound comet, and of enclosed
samples of the cometary material embedded in the comet, the latter to allow melting near
the perihelion without evaporation. Embedded sensors could monitor microbial growth during
the perihelion passage and, for a short-period comets, during further passages, to verify
microbial growth in cometary materials and environments. Laboratory microbiology
experiments with returned cometary materials would be also of interest.
The above considerations suggest that a single
technological civilisation can seed the galaxy. Similarly, one past panbiotic civilisation
could have seeded the galaxy, accounting for the rapid emergence of life on Earth and
possibly on Mars [2, 3, 26]. However, if ours is the first technological civilisation, the
potential to seed the galaxy demonstrates the significance of directed panspermia that we
can accomplish. Furthermore, by extrapolation, the material resources of 1E11 solar
systems in one galaxy may be sufficient to seed all the 1E11 galaxies.
Of course these are speculative long-term prospects.
However, even a few comet-based missions in the nearer future, using a small fraction of
the comets material, is sufficient to target one star-forming cloud for a major
biological expansion.
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