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| More on the origins of life (as viewed from 1910)
The following is my translation of an article
called: 'Der Ursprung des Lebens III' von Wilhelm Bölsche. It appeared in a German popular
science magazine, Kosmos Handweiser für Naturfreunde 1910, Heft 6, Seiten 210-215. I'm not aware
of any previous translation.
Part I Part II.
The origin of life (part 3) by Wilhelm Bölsche
In contrast to this is a hypothesis that rests upon indices that are also hypotheses,
as that carries the danger of attempting to justify the unsupported. A common mistake
for the inexperienced is to believe that such a route already leads to genuinely
scientific hypotheses. For example, I have seen an almost steady flow of attempts to
account for the Ice Age coming from lay circles over the years, often careful and
industrious work, but they always stumble over this same stone. Question: how did it
come to pass, that the Earth of the Diluvian period came to suffer from a general
climatic decline? Answer: I assume this was due to something or other in the
cosmological circumstances, a colder area of space or the presence of a dark object
between the Sun and the Earth, which periodically blocks the Sun, or something similar.
However, from such changes in the temperature, what do we know of such a body beyond
nothing whatsoever? "Well, I assume there was one; and that explains everything!" It
is always necessary to be warned against this dangerous sort of conclusion, especially
when one believes in the high value of firmly built hypotheses, and enjoys the
excitement they offer.
Let us consider Arrhenius' idea from this perspective, that the radiation pressure
could drive living spores of bacteria from planet to planet, star to star. Firstly,
we have a number of indices which are obviously not hypothetical, but rather are based
on secure ground.
We are all aware how small bacteria are. When we think of the clearest air and the
bluest sky, then it is already self-evident to the academics of today that there could
be invisible, tiny bits of bacterial dust there, bacteria in a state of so called
spores, like dried seeds, encapsulated with life drifting in a truly dust-like form
which, in favourable conditions in a suitable place, could be reawakened to life and
reproduction with their stored energy. If we think of the smallest of the small from
this dust population of bacterial spores within range of our possibilities of
magnification, reaching the space beyond our atmosphere between planets, it is clear that
they may fall under the influence of radiation pressure to some degree, and be moved.
This organic dust containing the mysterious cells of life, which are affected by the
lightest breeze, would be forced by light waves into the free ocean of the ether.
Precisely as is known to occur with captured cosmic droplets or meteor dust, with the
density of water and a diameter of an astonishing five- or six-thousandth of a
millimetre, they would be driven from the orbit of the Earth to that of Mars within
three weeks and, after fourteen months, reach the orbit of Neptune.
Imagining that the individual lifespans of such minute single cells could be more than
weeks, or even months, may seem counterintuitive. But there are enough wondrous
single-celled organisms on our Earth which, despite all their microscopic smallness,
in no way share the fate of one-day flies, as we might imagine for such small beings.
Single-cellers of this minute size include, for example, the male sperm of higher
animals, and yet such sperm cells typically survive in the womb of the female bats
from autumn, when they arrive, until March or April, which is when the actual fertilisation
of the female egg takes place, and the queen bee hosts such Lilliputian cells of life
in the form of sperm for three to four years. That dried bacteria including the harmful,
for example the infamous causer of typhoid and anthrax, also similarly survive for
years is long known to medicine from bitter experience.
But light pressure would be driving these enduring flecks with their organic content
through a vacuum beyond all moisture into space! And they would be driven into a terrible
cold of at least -200°C.
But we also know: Life on this Earth is infinitely adaptable under all possible
conditions, and it is the bacteria, especially in their enduring form as spores, which
are best able to survive shortages of moisture and extreme cold. But adaptation in
this case would be in entirely unearthly conditions! For this theory to be
credible, these germs of life must be able to endure for more than a couple of
minutes in a cold of -200°C. Our own experiments, however, have punished our lies
of expected probability. MacFadyen placed anthrax spores into liquid oxygen (at a
temperature of -190°C), and it did not kill them; he subjected them to temperatures
reaching -252°C in liquid hydrogen for ten hours -and they survived. Arrhenius
himself even reports of 20 hours, and even six months and longer, by -200°C. These
terrible temperatures were slept through -but they did not result in death.
As one has now become accustomed to these no longer disputed facts, it does not seem
particularly remarkable that, is a similar state of sleep, bacterial spores, and also
seeds of higher plants and algae, can survive weeks and months of absolute dryness
in drying chambers combined with concentrated sulphuric acid and airlessness in
vacuums. The facts of this are simply enormously monstrous. Even the craftiest and
most unscrupulous of hypothesis-smiths would not have dared to invent such things as
supporting hypotheses. But Arrhenius did not require any more hypothetical material,
rather he built upon recognised science.
Naturally enough: his meteor dust, travelling with radiation pressure, should reach
the system of Alpha centauri, the nearest fixed star, after some 9,000 years. And now
he wants to include bacterial spores. A spore of bacteria should live for 9,000
years! That is the decisive element of this hypothesis; the rest stands with only a
couple of relatively minor complications. Gaston Bonnier summarised some arguments
not all too long ago in this journal, and they spoke against the notion of such
lifespans here on Earth. That some organisms can hibernate through such incredible
lengths of time and dryness is an old assumption, which undoubtedly partially belongs
in the field of biological myths. The toad, entombed in rock, which survived for hundreds
of thousands of years, the revitalized Eocene vegetation and the like, are today as
credible as the famous wheat of the mummies. For that last case, and in contradiction
of Herr Bonnier, I would like to point out that a recent, serious German textbook of
natural history still offering this fairy tale a place does not, as far as I am aware,
exist. The strongest evidence for a relatively vast lifespan can still be provided,
as earlier, by certain ancient trees. Even with those, we find earlier estimates
being revised somewhat downwards. Of baobabs, which reach 5,000, or with the famous
Drachenbaum of Humboldt's from Orataya, reportedly even 6,000 years of age, one
today speaks of less, although 3,000 years does remain plausible for some cypresses
and Eiden. However, a tree can only be spoken of as an individual to a limited
degree; it is really a colony of countless generations of shoots, and provides a
closer analogy with a body of coral. One also has to consider the reproductive
viability of the organisms which, as far as we know, is naturally limitless; all
higher life of today is in all probability descended in succession from organisms of
the oldest prehistoric sea and, in this sense, that is a hundred million years or
more; but that is not what came into consideration for Arrhenius. For him, only a
narrower argumentation can be significant.
What makes the story of undiminished vitality for wheat seeds, after thousands of
years in the graves of Egyptian mummies, so improbable, is the nature of the storage
without any sort of special reserves. When conservation is simply left to chance,
then an old spore of moss, after a century with its dried plant, may well be cleanly
and nicely grown in a herbarium, but things do not go further that that as there are
too many possibilities for physical and chemical changes. Thus far is Herr Bonnier
completely correct. What we do not yet actually know, however, is how a plant seed
or, above all, a bacterial spore would behave if consequently subjected to -200°C
in an experiment over thousands of years, in absolute dryness and under vacuum. There
is an undeniable possibility that, if it could survive in such conditions of coldness
and aridity for years, then an endless chain of years could also see it unchanged,
and that would mean viable. Arrhenius has come forward with a relevant calculation
as some evidence. He assumes a progressive loss of vitality in an organic cell with
a chemical process as the cause, and postulates this occurs more slowly at lower
temperatures than higher ones. An increase in the temperature of 10°C raises the
relationships of life functions from 1 to 2.5. The cold of space in the area of the
orbit of Neptune is thought to be -220°C, and that would reduce life processes to a
thousand millionth of their strength at 10°C and, if so, less energy would be expended
in three million years than during a single day at 10°C. According to this
calculation, a bacterial spore transported by radiation pressure could stroll to
Sirius, Arcturus, and even much further, without finding its death. This is naturally
a purely hypothetical conclusion. However, there is something of interest in the thing
with a certain attractiveness, and it is not entirely built of thin air. With time,
it will be possible to experimentally test this mode of thought, and that could
produce serious indices.
Meanwhile, the main hypothesis has another aspect which appears somewhat loose. This
is namely how bacterial spores would actually escape from our earthly atmosphere
(or that of another suitable planet) and reach into the ethereal space. This would
sometimes have to happen for the light journey to begin in earnest. Tiny spores
certainly reach heights and are taken up even by air movements. But the border for this
appears to be in the lower depths of the air ocean. Arrhenius thinks beyond this due
to the repulsive energy of electricity. This would be in the area where, according
to his opinion, discharges of negative electrically loaded cosmic dust (in this case
originating from the Sun) produce the familiar northern lights. A whirl of spores
could come into this critical region from below, become electrically charged, and the
opposing field could redirect them into empty space.
This element of Arrhenius' otherwise sharply focused line of thought necessarily
rests upon the northern lights hypothesis, a hypothesis indeed, but at least it has
not been invented for this purpose, and it does have many advocates. The intensive
repulsion force in the upper regions of our atmosphere has been experimentally
calculated by other renowned researchers before him. Wilhelm Förster sought to
explain the strange zodical light, a particular ball at dawn which has no solid
explanation, as a weak 'comet's tail' produced by the Earth and consisting of tiny
repulsed articles from the upper atmosphere. However, in such circumstances, most
bacterial spores thrown up with the dust would be evaporated. Pulling this is by
the hair would be no help in this case.
All in all, it cannot be denied: with Arrhenius' idea of bacterial transport and
bacterial exchange in space, we have a shot of thought which is to be taken seriously,
but which does not yet have the power of evidence from facts, but it does follow
otherwise orderly rules to a more than sufficient degree.
What would be the most interesting aspect, however, is not possible departures and
further migrations of earthly spores into space, but rather the opposite, such seeds
arriving here from world bodies other than our Earth. We have the seriously proposed
possibility that the actual place of origin for life may have lain somewhere far off
in space, and that this life could have come to us as a belated import.
There is a grave difficulty here, as experimental evidence showing such alien spores
would be immensely difficult to find. We would have great difficulties in recognising
a signature of a bacterial spore showing it to be of cosmic, and not earthly, origins.
Kurd Laßwitz has recently attempted to show in a highly amusing way with direct
connections to Arrhenius, in a fantasy book worthy of reading (Sternentau, die
Pflanze vom Neptuns Mond -'Star dew, the plant from Neptune's moon'), how one
such higher crypto-cell could perhaps look like, and from which a previously unknown
earthly lifeform could develop (in this fantasy instance, the being has a generational
change between plant and animal). Something like that would certainly wake our
attention, but it is presently only an idea in a novel. Should we today discover
a very curious new animal, no zoologist would so simply leap to the conclusion, that
it must be an import from Venus or Mercury.
On the other hand, something would already have been achieved if we were able to say
with certainty, that organic life exists on other world bodies. Presently, we cannot
do so with absolute certainty, so this is strongly still in the stage of a scientific
hypothesis.
Many general probabilities suggest that other planets do carry life, but a strict
basis in fact is not available; and, in order to have an analogy, we must first have
a precise knowledge of what life is; and, in order to support this through observation,
we must be able to vastly improve our vision. Arrhenius himself recently declared
in this journal that Mars is a "without doubt dead world", and that despite the hopes of
many in this regard. Personally, I would not fully concur with his highly intelligent
explanations in this instance. For example, when he assumes that the canals of Mars
are valleys from earthquakes based on an analogy with glowing systems on the surface
of the Moon, and that these systems are also valleys filled with light coloured dust,
then he is explaining something not understood with something else not understood; as
the glowing lines of the Moon, which look like a glimmering varnish across all uneven
surfaces of the ground by a full moon, are actually completely unexplained in reality.
A few aspects of his image of Mars, with its red deserts and salt swamps, are also
reminiscent of, rather than the future, the past situation on our own Earth in around
the Permian and Triassic to geologists; despite deserts and salt steppes, the Earth
hosted a rich animal life. But it is known that the hypothesis of life on Mars is
now swaying in an unsteady mist; there is no secure basis for it, and the sceptics
are correct.
In contrast, I find something else of importance which Arrhenius has not called upon,
something which is within our earthly control and, in a sense, is of consequence
beyond our Earth.
Why, if they are simply a product of our Earth and are bound with it for eternity,
have our bacteria attained their strange characteristics enabling them to withstand
degrees of cold and extreme aridity and air shortages, conditions which do not occur
here? Does it not look as if they have really adapted to our earthly conditions?
In the sense of Darwin, all organic adaptations eventually serve a purpose, even if
only temporarily. Why have we here got a spectrum of adaptations which practically
go far beyond the demands set by our earthly theatre?
One could take this question further. There are a number of forms among our bacteria
which cannot only remain dormant as spores, but which also appear to show capabilities
which are extremely odd, at least for our Earth, but which must be highly advantageous
for sustaining life in differently constructed worlds. There are known bacteria
that use certain amounts of sulphur dioxide for their normal organic processes, a
substance which is generally poisonous for organisms. There are so called anaerobic
bacteria which cannot tolerate the oxygen in air, and depend upon purely chemical
oxygen from mineral substances. If our Earth were to be treated with a dose of
sulphur dioxide, sufficient to immediately kill all other life forms (as certain
Jeremiahs have predicted for chemical poisoning delivered to the Earth from contact
with the tails of comets), or if the atmosphere were to suddenly thin down until
comparable to that of the Moon, we would all asphyxiate, -only sulphur and anaerobic
bacteria would allow life to continue and perhaps to develop to higher forms over the
eons, possibly again rising to intelligent beings from the original forms of
prehistory, and this life would be consequently adapted for sulphur dioxide rich of
airless conditions. The implicated conclusion is close, that life here shows the
hidden possibility of surviving beyond our Earth in the oxygen poverty of moons, or
on planets with strange atmospheres.
This allows us to think of the greater 'Third Kingdom' among our bacteria, with their
curious opposites shown in connection with composition and further development of
an extreme stability here and an adaptability there. Parts of the single-celled
stock developed long ago, through countless generations, to animals and plants, with
their particular characteristics for earthly existence and exploitation. Another
part has stubbornly remained in largely its original condition till today, as a society
which, while certainly hardy, is also sterile in this regard, and indifferent to the
possibilities of development. While the rest of earthly life forms have adapted
increasingly in accord with each other, and a certain harmony has been established
(we can simply think of our bodies as peaceful associations with division of labour
and assistance), we can also see a group of malignants engaged in a terrible and
constant war of destruction against this earthly friendship, the battle of bacteria,
in which our medicine today has become engaged with great energy, and is working ever
further with gathering excitement as to whether it will achieve victory. Are these
sterile and hostile possibilities of life embodiments of those which, under other
planetary conditions, may well have achieved mastery?
On the other hand, the energy still maintained by the more developed earthly life is
astonishing, a great extravagance that makes our own Earth effectively appear almost
unearthly. One can think of the deep sea, where even highly developed life forms
from our upper world, such as fish and crabs, have been able to adapt to an environment
with the pressure of 1,000 atmospheres, in freezing cold with a pronounced content of
carbon dioxide, and sunk in an eternal night. Who would assume, that if we were to
discover a distant planet with such pressure, such temperature and such darkness,
that this planet could support life? And yet, the adaptive possibilities are there:
they are even present in the small elite of the earthly advanced stages of up to a
fish, indeed (as humans are also now pressing into this milieu of the deep sea) even
to the level of a person. One also thinks of animals which internally generate
heat while polar winter reigns outside, and of glowing moss which concentrates light
through a form of burning lens within the cells, and can collect enough light in a
half dark fissure to power its chlorophyll cuisine, - -and one sense, I think, that
in this "life", whatever that is, is generally found something of astronomical
diversity that could develop far beyond the usual level of this Earth, and all forms
could become exceptional. One senses something universal in a speck of a spore,
and one would not wish to conclude that it alone couldn't simply take advantage of
opportunities offered by its role in the whole wide theatre of this wondrous thing,
that which is called life, and it must have caused great changes since the moment of
its beginning.
Simply, naturally, put concisely: already, in the simplest stage of a bacteria, life
had a magic ring, and this allows it to react and endure.
Should it appear that life is a strong universal movement in the sense of Arrhenius'
hypothesis, present everywhere, then this would suggest an adaptation to cosmic chains
far beyond just this Earth, and it would be probable that the origin of life lay
elsewhere in the cosmos. But where are the intermediaries? Is not the inside of
each planet also a typical representative of the cosmos, from which this flower can
blossom when the hour strikes, although always of which only part of its whole energy
can develop in accordance with the precise conditions? Or does the real nursery lie
in some particularly favourable place with a particular concentration of elemental
cosmic energy, and has since been constantly spreading as seeds from there on waves
of radiation through space, conquering the spaces between the stars where, meanwhile,
other causes have produced balls of material, such as the young Earth, for this eternal
colonisation and, as on Earth, in line with the possibilities towards higher
intelligence?
That the original possibilities for origins could differ in strength cannot be
denied. The visible universes already contains endlessly large, and endlessly small,
potentials for spreading and concentrating material. A glowing speck of mist,
containing perhaps only a billionth of the density of our air, or a star which is
many times larger than our own, and which retains all its inner material via pressure,
a planet whose commonest element has the power of our radium: who would want to think
of such possibilities without accepting, that the wondrous qualities found in the
incomprehensibly small volumes of our tiniest bacterial spores, which may result
from cosmic conditions, could not perhaps make the fantastic history of our Earth
appear a comparatively very mundane and small episode. Who might sometimes not say
this. But who, who will prove it...?
Note: This is part three of a three part article. Go to:
Part 1, Part 3.
An index of more of my translations of old Kosmos articles can be found at:
A number of Mesozoic (and post-Mesozoic) location summaries can be found at
Localities.
http://home.arcor.de/ktdykes/meseucaz.htm |