The ecological habitat
(ecohab) of a species is characterized
by a number of defining parameters
(defipars) branched out into two major
categories: the abiotic (abi) and
the biotic (bio) ones, as described
below,
with
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• The abiotic defipar by
being the food sources, the
water sources, the light
sources, the climate, the
temperature ranges, the
altitude, the type (terrestrial,
aquatic, or aerial), and the
territorial boundaries.
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and with
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•The biotic defipar
by being
represented by the living
predators.
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The
ecohab,
as such, is an ecological fermenting
(ecoferm) arena where the successful
species create their unique ecological
enclaves called ecological niches
(ecolons or econiches). An ecological
packing (ecopack or ecopacking)
is being administered to ecohab
by the successful species.
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To
illustrate the ecopacking
mechanism,
we provide a thought
scenario, as
follows:
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Let the ecohab be a grandiose
tree and let consider that
a type of bird, identified as
the Y-bird, populates
on, and feeds from, the top of
the tree.
Now, assume that
another type of bird, identified
as R-bird, has arrived
to occupy and to feed from the
tree. A fight will emerge
between the two bird species Y
and R, pursuant to Darwin's natsel. Assuming that
the resident Y-birds become
victorious, for the defeated R-birds, two and only
two, scenarios could exist:
either the R-birds perish or they
are able to adapt to
occupy the area below the top of
the tree. With that adaptation
of the R-birds, a peaceful
coexistence takes place.
Finally, let's assume
now that the grandiose
tree
attracts another type of bird,
identified as B-bird. Another
fight will commence, pursuant to
Darwin's
natsel, between the
intruding B-birds and the two
resident birds Y and R. Assuming again
that the resident birds become
victorious, for the defeated B-birds again the only
scenarios that could emerge are
either that they will perish, or
that they could adapt of
living at the bottom of the
tree. All that is being
illustrated below:
Remark: From the
presented ecopacking mechanism,
one attribute stands out:
the adaptability to change (adaptoc).
Only species that possess an
ability to adapt to an
environmental change will
survive and trive, those that do
not, will perish.
That adaptoc attribute and
characteristic of survival was
first recognized in 1859 by Charles
Darwin in his seminal work
"On the Origin of the
Species" as marked below:
The adaptoc inheritance of
a species i.e., of the ability
of a species to adapt to
its environment through learning
and remembering is, as
we have seen from the ecopacking mecchanism,
essential for its survival. As
such, successful species would
incorporate a cognitive
mechanism, called biotelligence,
capable of remembering the
"good" and the "bad" of their
environment and using that
stored information for creating
or shaping their environment for
better survival conditions.
!
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As
such,
because of the
paramount role of biotelligence in
delivering adaptoc,
we
say that species
endowed with most
enhanced biotelligence are
best equiped to
survive.
(More
information on the
subject is to be
found in the Biowareness
page.)
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On
Speciation Ecopacking
(Specpack)
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For Charles Darwin,
the "species problem" was how one would
correctly identify one species from another,
in short, how well-defined species are in
the light of their great varieties. Darwin
in his seminal book "On the Origin of
Species" (1859) offered an explanation
of HOW species evolve and diversify, but not
WHY some species can be so close
morphologically and biologically to each
other.
Well,
closeness of some species are due to the ecopacking
that the successful species "packed" into
their ecohab.
The thought bird example provided above
is an example of such a speciation
ecopacking (specpack).
Defining Terran
Life (Terralife) at
its Ultimate Chemical Level
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As
we have seen, plants and algae convert Carbon
Dioxide to organic
matter through the process of photosynthesis.
Natural Selection
(natsel),
as we have seen, continuously
transforms the landscape of Life's
ecolons
by modifying their numbers
and bondaries. With the recognition that the
evolution of Life (evolife)
cannot be separated from natsel,
NASA erroneously defined Life
(at its ultimate chemical level of
existence),
as being a
self-sustained chemical
system capable of Darwinian evolution.
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Well, that NASA definition of Life
is unacceptable in here for the
reason of being placed too
higher up in the tiered
evolutionary structure (TES) of Life. You see, the origin
of Life does not have its
roots in Darwin's Natural
Selection (natsel) principle, but
its popup roots are in
something totally different as
we have seen in here.
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Now, the POPlife
once formed, was required to have, for its
continuous existence and development, food,
defense (from hostile environmental
activity), and shelter. That trio (food,
defense,
shelter)
and denoted as fodesh, forms the existential
platform (exiPLAT) of Life
that continuously is being chiseled by Natural
selection (natsel).
As
such, we can talk
about Life's objective
of existence (obex) as being that of survival
existence (survex), residing on the exiPLAT.
Using TRUTON's lingo, we say that Life's
obex is natsel modulo
survex.
Towards achieving that obex,
natsel
created stunning defense mechanisms against
predators (through elaborate camouflages
and mimicries) that were
incorporated also into strategies for
grabbing their preys.
Another side of Life's
existential expansion of its exiPLAT
is that, through natsel,
it become adept in plundering more rapidly
its existing habitat accelerating, as such,
inadvertently, the depletion of its own
habitation. That inadvertent deterioration,
created additional survival pressure for the
Life.
Thus, the emerging accelerated
downgrading tendency of Life's
habitation acted in opposition to the steady
evolutionary uplifting of its exiPLAT.
Now, in the ecolon,
a skewed ecological balance (skeb)
was progressively shaping up between the two
opposing emerging tendencies (suppression
by the dominant species and degradation
of the habitat), with the degradation
gaining the upper hand that
began now threatening the very existence of
Life.
The
result of that ecological tilt (ecotilt),
as shocking as it may appear to be, that Life
--at its apex-- becames strangulated
by its own success, setting the seeds,
through its strangulated habitat
(stranghab), for its demise, is being
now recognized in here through
The Finitude Theorem
Of Life (FINITOL) in a Ecolon
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Life of the
dominant and most successful
living of any subjugated ecolon cannot
continue to evolve, develop
and expand in perpetuity.
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Proofs:
#1.
The evolution of Life
is propelled by Darwin's Natural
Selection (Natsel) process which,
by 5th FURON, was already proven to have a
finite evolutionary existence.
Thus, the FINITOL is fully
established. A 2nd proof of FINITOL is provided
below.
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#2. Any
ecolon has in it a
succesful dominant species
(domispec). That evolutionary
success (evocess) allows domispec to increase
exponentially the number of its
offspring with no end in sight.
But that is in contradiction to
the Ultimate
Finitude (ULFI) Theorem that was
derived from point 6 of The Ultimate
Marks of Creation (UMOCs) where it is
stated that:
"No
physical
processes can
exist in Nature
without a finite
end. We call
that finitude
characteristic,
the finite value
mark of creation
(FV-UMOC)."
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Thus, the evocess of domispec evolves to the
critical evolutionary
(critev) point where
the ecolon has been
transformed into becoming the domispec's own ecological
graveyard (ecograve).
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The
Grand Corollary of FINITOL: Mass
Extinctions
(Massexes)
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1. The
Self-Induced Mass Extinction
(SIMEX)
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The
dominating species (say, a herbivore), of an
entire habitat say, the terrestrial
habitat (terrahab), will rapidly be
able to overpopulate the land. Being a
herbivore, it will gradually deplete the
entire vegetation which was not able to be
replenished out the massive onslaught that
it has received. Deprived of the food (i.e.,
of the vegetation) and of the oxygen (that
has been produced by the vegetation), that
dominant species was doomed to
self-extinction. By the way, that was
exactly what happened with the dinosaur's
extinction.
PS>
BTW:
The human species will have an identical
fate to the one of the dinosaur as expanded
further below
and in the next
page. We are now
at the beginning of that self-destructive
phase.
2. The Outer
Induced Mass Extinction (OIMEX)
Asides from
the inner
self-induced mass extinction (simex)
triggered by a land dominant species, the aquatic
habitat (aquahab) itself could trigger
mass extinction caused by sudden
catastrophic events such as volcanic
activity. As such, we can have outer
induced mass extinction (oimex) caused
by sudden underwater volcanic eruptions.
Such events occurred indeed in the past
wiping out almost the entire marine life.
The reason for that
catastrophic event was because of the sudden
rise of temperature and depletion of the
oxygen that were at a level where Life
no longer was able to be suported.
3. Cosmic Induced Mass
Extinction (CIMEX)
Arguably
cosmic induced mass extinction (cimex)
events could also impact the survivability
of Life
on Earth. However the probability of such
cosmic catastrophic event to take place is
practically nonexistent. The massive
speculative cosmic theories that are
floating around are just that: cosmic
academic garbage (cacagar).
The academic literature covering that
fantasy needs indeed to find its proper
place in the massive academic trash that
exponentially has been accumulating.
On
the Re-Emergence of Life After
Mass Extinction
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From the central tenets of
TRUTON articulated in the Ultimate
Marks Of (Material) Creation (UMOCs),
we choose two of them:
one, vested in the permanent
existential mark of creation (PE-UMOC),
which states that
"An existing
non-null state can never ever be
made to disappear and thus be
reduced or transformed into Nothingness
--an entity devoid of everything
but its own existence."
[emphasis supplied.]
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and the other, vested in the multitude
existential mark of creation (ME-UMOC),
which states that
"A material
state of existence that was able
to be created in one place, can
be created in a multitude of
other places of similar
conditions as there is no
rationale from barring that to
happen." [emphasis supplied.]
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Armed with those two (2) tenets, we can now
formulate
First
Foundational Theorem on the
Perpetuity of Life
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No
Mass Extinction will be able
to eradicate all Life.
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Proof:
Pockets of Life will always
remain after a mass extinction
because of the variety of ecological
niches (ecolons) that
populated the affected habitat.
The habitants of those ecolons will have now a
unique oportunity to evolve and
expand considerably their arena
of existence by the void created
by the succumbed ecolons.
A prime example of that unique
opportunity arose with the dinosaur
extinction, when the
mammal evolution exploded
abruptly from the nocturnal to
the diurnal life --a subject of
the next page.
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Second
Foundational Theorem on the
Perpetuity of Life
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The cycle
of Life travels and evolves
on a spiral hierarchical
tiered path.
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Proof:
By the 1st
Foundational Theorem above, a new
cycle of
Life (cycol), commencing
after a mass extinction, will
never starts with a clean
slate, as it always will have
in it the surviving species.
As such, those survivors will
constitute the base of the new
emerging cycol. Thus, we can
talk about the evolutionary
tier (evotier) of cycol.
From the available data, we
--the human species--
apparently have arisen and
evolved out of the 5th
mass
extinction (massex). Now, as a
result of our massive
overpopulation and dominance
that accelerated exponentially
the pilferage of Earth's
natural resources, we (as in
the case of the dinosaur) have now
created the conditions needed
for generating a new mass
extinction, the 6th one, where we
are staging our own
self-induced extinction.
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With this rather norrow
blueprint presented herein on Life's
evolutionary trends, we move on to expand
and cover some other related topics of
Evolutionary Biology.
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