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Science Forum Index » Bio Evolution Forum » Digital Genetics and Evolution Theory
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Message |
| Bioteach |
Posted: Wed Feb 07, 2007 8:54 am |
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Guest
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There is a new book on evolution theory: The Evolution of Aging, ISBN
0978870905, by Theodore Goldsmith that discusses digital information
aspects of inheritance and their implications for evolution theory.
Darwin tells us that selective breeding and the corresponding
evolutionary mechanism of natural selection both depend on the natural
variation of characteristics between different individuals. Variation
creates differences for selection to select.
According to the book, natural variation in more complex species is not
actually "natural" in the sense of being a fundamental characteristic of
all living things. Instead, because of the digital nature of the
genetic code, the "natural" intrinsic situation is that members of a
species should nominally tend toward being genetically identical.
"Natural" variation in complex organisms is actually created and
maintained primarily by the action of a long list of complex evolved
mechanisms that process mutations including sexual reproduction, genetic
recombination, certain behaviors, etc. The degree of variation produced
by these mechanisms is described to be much greater than that produced
by the occasional propagatable mutation.
This brings up the issue of how all these variation-producing traits
evolved. It seems to be a somewhat circular situation: organisms are
evolving the means for evolving.
Further, variation considered as an evolved design feature is itself
incompatible with Darwinian evolution as generally understood. If
organisms are striving to propagate their personal designs, then
variation is adverse because it acts to reduce the ability of an
organism to do that. A Darwinian organism would rather clone itself and
therefore propagate ALL of its design characteristics than dilute its
design via sexual reproduction and other evolved variation-producing
characteristics. Cloning is the "natural", easier, route given digital
genetics.
So how did these characteristics evolve? Wouldn't an organism that had
the variation-producing characteristics be at a disadvantage relative to
one that did not (such as one that reproduced by cloning) and therefore
"select out?" An organism that happened to possess an advantageous
design would certainly seem to be less able to propagate that design.
Its descendents would likely be less able to survive, breed, etc. than
would a clone. Somehow variation-producing characteristics were able to
evolve despite fitness disadvantage, apparently because they convey an
evolutionary advantage, an improvement in the capacity for evolution.
The question: Is this a plausible idea? If not, where is the fatal
logical flaw?
If you accept these arguments, Goldsmith then goes on to suggest that
aging, seen as a design feature that deliberately limits life span, also
enhances the evolution process in several different ways. If variation
can evolve, then aging can evolve even though both are fitness-adverse.
This is counter to traditional theories of aging that say that aging is
an adverse "side effect" linked to some beneficial and therefore
evolvable trait such that there is a net Darwinian benefit.
("Beneficial" means a trait that helps in survival or reproduction as in
"survival of the fittest.")
I realize these concepts might seem, at the least, radical, but they are
nonetheless interesting. |
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| Perplexed in Peoria |
Posted: Wed Feb 07, 2007 8:25 pm |
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Guest
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"Bioteach" <bioteach48@yahoo.com> wrote in message news:eqd78l$10dh$1@darwin.ediacara.org...
Quote: There is a new book on evolution theory: The Evolution of Aging, ISBN
0978870905, by Theodore Goldsmith that discusses digital information
aspects of inheritance and their implications for evolution theory.
Darwin tells us that selective breeding and the corresponding
evolutionary mechanism of natural selection both depend on the natural
variation of characteristics between different individuals. Variation
creates differences for selection to select.
According to the book, natural variation in more complex species is not
actually "natural" in the sense of being a fundamental characteristic of
all living things. Instead, because of the digital nature of the
genetic code, the "natural" intrinsic situation is that members of a
species should nominally tend toward being genetically identical.
"Natural" variation in complex organisms is actually created and
maintained primarily by the action of a long list of complex evolved
mechanisms that process mutations including sexual reproduction, genetic
recombination, certain behaviors, etc. The degree of variation produced
by these mechanisms is described to be much greater than that produced
by the occasional propagatable mutation.
This brings up the issue of how all these variation-producing traits
evolved. It seems to be a somewhat circular situation: organisms are
evolving the means for evolving.
Further, variation considered as an evolved design feature is itself
incompatible with Darwinian evolution as generally understood. If
organisms are striving to propagate their personal designs, then
variation is adverse because it acts to reduce the ability of an
organism to do that. A Darwinian organism would rather clone itself and
therefore propagate ALL of its design characteristics than dilute its
design via sexual reproduction and other evolved variation-producing
characteristics. Cloning is the "natural", easier, route given digital
genetics.
So how did these characteristics evolve? Wouldn't an organism that had
the variation-producing characteristics be at a disadvantage relative to
one that did not (such as one that reproduced by cloning) and therefore
"select out?" An organism that happened to possess an advantageous
design would certainly seem to be less able to propagate that design.
Its descendents would likely be less able to survive, breed, etc. than
would a clone. Somehow variation-producing characteristics were able to
evolve despite fitness disadvantage, apparently because they convey an
evolutionary advantage, an improvement in the capacity for evolution.
The question: Is this a plausible idea? If not, where is the fatal
logical flaw?
Two major flawsw and one minor flaw in the argument so far. First, the claim
that "that members of a species should nominally tend toward being
genetically identical" is true only in the limit of infinite population
sizes, infinite amount of time for selection to work, and slow mutation rates.
But in the real world, mutation is producing variation much faster than
natural selection can weed it out, and the only thing that keeps species
as close to genetically identical as they are is drift of nearly neutral
alleles to fixation in finite populations.
Second, the arguments also seem to assume that all members of the population
live in the same environment and that the environment is unchanging. A
considerable amount of the 'natural' variation in populations can be traced
to 'natural' variations in the environment.
The minor flaw appears in the discussion of how the 'evolution of
evolvability' is forbidden by normal selectionist logic. There is some
truth to this if you only consider evolution at a single (organism or
gene) level. But if you also allow for group-level and species-level
selection, then the existence of mechanisms for increasing the generation
of variation becomes plausible.
Quote: If you accept these arguments, Goldsmith then goes on to suggest that
aging, seen as a design feature that deliberately limits life span, also
enhances the evolution process in several different ways. If variation
can evolve, then aging can evolve even though both are fitness-adverse.
This is counter to traditional theories of aging that say that aging is
an adverse "side effect" linked to some beneficial and therefore
evolvable trait such that there is a net Darwinian benefit.
("Beneficial" means a trait that helps in survival or reproduction as in
"survival of the fittest.")
I realize these concepts might seem, at the least, radical, but they are
nonetheless interesting.
The idea that senescence and death exist in sexual organisms for the
*purpose* of allowing the variant young to compete among themselves (without
the older generation siphoning off all of the resources) is hardly an
original one. I've seen enough modeling to convince me that this may
be part of the story, but it is not the full story. The other part is
the sheer difficulty of keeping large complex organisms from simply
wearing out. Some plants (trees, mostly) are designed so that new
generations of tissue can make productive use of the older, worn-out
generations of tissue. Animals (and especially animal central nervous
systems) just can't work that way. |
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| Gil Lawton |
Posted: Wed Feb 07, 2007 8:25 pm |
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Guest
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"Bioteach" <bioteach48@yahoo.com> wrote in message
news:eqd78l$10dh$1@darwin.ediacara.org...
Quote: There is a new book on evolution theory: The Evolution of Aging, ISBN
0978870905, by Theodore Goldsmith that discusses digital information
aspects of inheritance and their implications for evolution theory.
Darwin tells us that selective breeding and the corresponding
evolutionary mechanism of natural selection both depend on the natural
variation of characteristics between different individuals. Variation
creates differences for selection to select.
According to the book, natural variation in more complex species is not
actually "natural" in the sense of being a fundamental characteristic of
all living things. Instead, because of the digital nature of the
genetic code, the "natural" intrinsic situation is that members of a
species should nominally tend toward being genetically identical.
"Natural" variation in complex organisms is actually created and
maintained primarily by the action of a long list of complex evolved
mechanisms that process mutations including sexual reproduction, genetic
recombination, certain behaviors, etc. The degree of variation produced
by these mechanisms is described to be much greater than that produced
by the occasional propagatable mutation.
This brings up the issue of how all these variation-producing traits
evolved. It seems to be a somewhat circular situation: organisms are
evolving the means for evolving.
Further, variation considered as an evolved design feature is itself
incompatible with Darwinian evolution as generally understood. If
organisms are striving to propagate their personal designs, then
variation is adverse because it acts to reduce the ability of an
organism to do that. A Darwinian organism would rather clone itself and
therefore propagate ALL of its design characteristics than dilute its
design via sexual reproduction and other evolved variation-producing
characteristics. Cloning is the "natural", easier, route given digital
genetics.
So how did these characteristics evolve? Wouldn't an organism that had
the variation-producing characteristics be at a disadvantage relative to
one that did not (such as one that reproduced by cloning) and therefore
"select out?" An organism that happened to possess an advantageous
design would certainly seem to be less able to propagate that design.
Its descendents would likely be less able to survive, breed, etc. than
would a clone. Somehow variation-producing characteristics were able to
evolve despite fitness disadvantage, apparently because they convey an
evolutionary advantage, an improvement in the capacity for evolution.
The question: Is this a plausible idea? If not, where is the fatal
logical flaw?
Disclosure: I am a layman, but learning.
This book does seem to address something that Darwin struggled with and was
unable to come up with any mechanism for explaining. (What he termed
"natural selection" was a descriptive term -- descriptive of the before's
and after's of many examples of what goes on in radiation of characteristics
and, what seems to be quite capable of speciation.)
As I understand it, Mendel's work finally became noticed, years after he
published it, among individuals looking for that mechanism.
It seems to me that, just as you indicate, the contemporary state of
research into genetics has come up with lots of data in support of how
characteristics are CONSERVED by DNA in reproduction, but not a conclusive
amount of evidence (to my knowledge) to support how some characterists may
become, as it were, *ARCHIVED* such that they can be accessed and
"tried-out" (so to speak) at times of great stress.
In trying to make sense of much of what strikes this layman as
*circumstantial evidence* but nonetheless *abundant circumstantial evidence*
I have just today pondered why a species can simply be "eliminated" without
being stressed in such a way that its genes could be triggered to
*experiment* with archived potentials to alter the morphology of offspring.
And just TODAY it suddenly occurred to me that a sharp distinction is in
order to distinguish between "stressful invironment" and "simple
environmental attrition."
The decimation of certain types of rhinoceroses, for example, would not
necessarily "stress" the ones that are not killed by poachers in preserves.
In fact, poaching might even be advantageous (in a Malthusian way) in that
the quick rhinocerouses would have food and range which otherwise would have
been eated by the ones shot and hence dead.
While this might lead to *inbreeding* (which might in some way pressure
genes into expressing some alternative "archived characteristics," the
individual rhinocerouses would not necessarily be stressed in their
environment as they would be by, say, geographical changes which would
reduce the food supply and, hence, present *direct somatic stress* and/or
*direct germline stress* (as, for instance, germ cells being hard put to get
the essential nutrients and/or *dietary TRACE ELEMENTS* they require to *do
their job in preparing for, and executing the work of reproduction).
As you can see, this model would NOT be tantamount to a Lamarckian
transmission of *acquired somatic characteristics* (like the notorius
cutting of of mouse's tails, where the mice are well fed and protected in a
laboratory.
But... assuming that genes can, in effect, as it were, *archive and conserve
for possible future use* some prior advantageous morpohological specfic
architectures (as it were), which can be resorted, or fallen back upon
randomly if some stresses alter some otherwise "settled reproductory
dispositions" this might be something worth experimention by microbiological
researchers to CHECK OUT. And, for all this layman knows, there may be
some (or much) checking out of EXACTLY this thesis at this very moment.
This old layman has long been inclined to believe that there is no such
thing as "junk DNA." Maybe there is, mind you. But if there were any
"archived" risidual "programming" (or "information" as currently is a
popular buzz term for it) , which is LEFT OVER from morphological modes
that worked... even many generations earlier, even if not practical in
recent generations, and fallen into disuse, as it were, wouldn't that be a
nice place for it to be warehoused though?
And, another thing to consider is that there might be epigenetic markers we
DON'T EVEN KNOW TO LOOK FOR, YET, which can be changed by stresses on
germline cells (or even TRIGGERED in response to certain chemical messages
by somatic cells and, in a sense,
READ by the germline cells.
This still would not be Lamarckian in nature. Neither would it seem to this
layman unprecedented. After all, the physiology of the human body (and
other organisms) ABOUNDS with examples of direct cell-to-cell responses to
chemical messages in the normal and usual course of homeostasis, as do
general signalers (such as adrenaline) which are produced by organs
specialized for the purpose.
So, if germline cells could respond by resorting to old "vestigial
informational residues" upon being DIRECTLY stressed, or by "reading"
chemical messages of a cell-to-cell or general "signaling chemical messages"
from highly stressed somatic cells... this old layman does not think the
possibility should be deemed ridiculous. I mean, if it were, then some of
the things cells do in the normal course of things SUCH AS producing what
we humans call "consciousness" would be too bizarre to consider, as well.
But calling this "digital?" What does THAT mean? Does the author mean
"binomial" as in the way computers process information as a series of only
two conditions at each juncture, i.e., "yes" vs "no?" or "zero" vs (1)
scenarios? If the author of the book you refer to wished to call this
"digital," so be it. As Turing observed, any mathematical relationship can
be "translated" into an algorithm (i.e. a a format expressing the same
operations, but in a form which gets there by the use of binomial
recursions).
I'm sorry. Did not mean to inundate you. This old fart's brain works that
way. It comes in a flash, but takes many, many words to reduce to writing.
g
re-reading of otherwise disgarded "programming,"
Quote:
If you accept these arguments, Goldsmith then goes on to suggest that
aging, seen as a design feature that deliberately limits life span, also
enhances the evolution process in several different ways. If variation
can evolve, then aging can evolve even though both are fitness-adverse.
This is counter to traditional theories of aging that say that aging is
an adverse "side effect" linked to some beneficial and therefore
evolvable trait such that there is a net Darwinian benefit.
("Beneficial" means a trait that helps in survival or reproduction as in
"survival of the fittest.")
I realize these concepts might seem, at the least, radical, but they are
nonetheless interesting.
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| Tim Tyler |
Posted: Thu Feb 08, 2007 8:42 am |
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Guest
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Bioteach wrote:
Quote: There is a new book on evolution theory: The Evolution of Aging, ISBN
0978870905, by Theodore Goldsmith that discusses digital information
aspects of inheritance and their implications for evolution theory.
Darwin tells us that selective breeding and the corresponding
evolutionary mechanism of natural selection both depend on the natural
variation of characteristics between different individuals. Variation
creates differences for selection to select.
According to the book, natural variation in more complex species is not
actually "natural" in the sense of being a fundamental characteristic of
all living things. Instead, because of the digital nature of the
genetic code, the "natural" intrinsic situation is that members of a
species should nominally tend toward being genetically identical.
"Natural" variation in complex organisms is actually created and
maintained primarily by the action of a long list of complex evolved
mechanisms that process mutations including sexual reproduction, genetic
recombination, certain behaviors, etc. The degree of variation produced
by these mechanisms is described to be much greater than that produced
by the occasional propagatable mutation.
This brings up the issue of how all these variation-producing traits
evolved. It seems to be a somewhat circular situation: organisms are
evolving the means for evolving.
Further, variation considered as an evolved design feature is itself
incompatible with Darwinian evolution as generally understood. If
organisms are striving to propagate their personal designs, then
variation is adverse because it acts to reduce the ability of an
organism to do that. A Darwinian organism would rather clone itself and
therefore propagate ALL of its design characteristics than dilute its
design via sexual reproduction and other evolved variation-producing
characteristics. Cloning is the "natural", easier, route given digital
genetics.
So how did these characteristics evolve? Wouldn't an organism that had
the variation-producing characteristics be at a disadvantage relative to
one that did not (such as one that reproduced by cloning) and therefore
"select out?" An organism that happened to possess an advantageous
design would certainly seem to be less able to propagate that design.
Its descendents would likely be less able to survive, breed, etc. than
would a clone. Somehow variation-producing characteristics were able to
evolve despite fitness disadvantage, apparently because they convey an
evolutionary advantage, an improvement in the capacity for evolution.
The question: Is this a plausible idea? If not, where is the fatal
logical flaw?
The idea that variation-producing characteristics were able to
evolve despite fitness disadvantage because they convey an
improvement in the capacity for evolution - is widely regarded
as not the correct explanation.
In fact there are other, more direct short-term fitness advantages
to diversity-producing traits - such as sexual recombination.
That this is the case can be seen by consideration of organisms
that exhibit facultative parthenogenesis. These organisms can
clone themselves - but often choose not to do so.
Similarly, the idea that variation considered as an evolved design
feature is itself incompatible with Darwinian evolution is
equally incorrect :-(
In fact, clones are often regarded unfavourably by natural
selection - primarily since groups of genetically identical
organisms can easily be exploited by pathogens.
There are other defenses against pathogens besides adapatations that
promote diversity: immune systems, being rare, and very rapid dispersal,
with no parental care.
Immune systems allow some of the advantages of cloning without using
diversity as a defense. However the strategy is typically only
effective in the short term.
Diversity is a simple and reasonably effective defense against
pathogens - it is not surprising to find adaptations that promote it.
--
__________
|im |yler http://timtyler.org/ tim@tt1lock.org Remove lock to reply. |
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| Kent Paul Dolan |
Posted: Sat Feb 10, 2007 8:21 am |
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Bioteach <bioteac...@yahoo.com> wrote:
Quote: Further, variation considered as an evolved design
feature is itself incompatible with Darwinian
evolution as generally understood. If organisms
are striving to propagate their personal designs,
then variation is adverse because it acts to
reduce the ability of an organism to do that. A
Darwinian organism would rather clone itself and
therefore propagate ALL of its design
characteristics than dilute its design via sexual
reproduction and other evolved variation-producing
characteristics. Cloning is the "natural",
easier, route given digital genetics.
This erroneous belief that evolution/reproduction
are _purposive_ is teleology, and cripples pretty
much all rational thought about evolution.
Organisms are not "striving to propagate their
personal designs".
Organisms are behaving in ways that promote
reproduction, because organisms that don't behave in
such ways rapidly lose representation in the gene
pool.
Full stop.
Whatever they produce as offspring, be it clones or
unrecognizable oddities, if it survives and
reproduces successfully in turn, is "fit".
Once teleology is discarded, extirpated root and
branch, rational discussion of evolution has at
least _some_ chance to occur.
Until then, not so.
FWIW
xanthian. |
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| Bioteach |
Posted: Sun Feb 11, 2007 7:41 pm |
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Guest
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Bioteach <bioteach48@yahoo.com> wrote in
news:eqd78l$10dh$1@darwin.ediacara.org:
Quote: There is a new book on evolution theory: The Evolution of Aging, ISBN
0978870905, by Theodore Goldsmith that discusses digital information
aspects of inheritance and their implications for evolution theory.
Darwin tells us that selective breeding and the corresponding
evolutionary mechanism of natural selection both depend on the natural
variation of characteristics between different individuals. Variation
creates differences for selection to select.
According to the book, natural variation in more complex species is
not actually "natural" in the sense of being a fundamental
characteristic of all living things. Instead, because of the digital
nature of the genetic code, the "natural" intrinsic situation is that
members of a species should nominally tend toward being genetically
identical. "Natural" variation in complex organisms is actually
created and maintained primarily by the action of a long list of
complex evolved mechanisms that process mutations including sexual
reproduction, genetic recombination, certain behaviors, etc. The
degree of variation produced by these mechanisms is described to be
much greater than that produced by the occasional propagatable
mutation.
This brings up the issue of how all these variation-producing traits
evolved. It seems to be a somewhat circular situation: organisms are
evolving the means for evolving.
Further, variation considered as an evolved design feature is itself
incompatible with Darwinian evolution as generally understood. If
organisms are striving to propagate their personal designs, then
variation is adverse because it acts to reduce the ability of an
organism to do that. A Darwinian organism would rather clone itself
and therefore propagate ALL of its design characteristics than dilute
its design via sexual reproduction and other evolved
variation-producing characteristics. Cloning is the "natural",
easier, route given digital genetics.
So how did these characteristics evolve? Wouldn't an organism that
had the variation-producing characteristics be at a disadvantage
relative to one that did not (such as one that reproduced by cloning)
and therefore "select out?" An organism that happened to possess an
advantageous design would certainly seem to be less able to propagate
that design. Its descendents would likely be less able to survive,
breed, etc. than would a clone. Somehow variation-producing
characteristics were able to evolve despite fitness disadvantage,
apparently because they convey an evolutionary advantage, an
improvement in the capacity for evolution.
The question: Is this a plausible idea? If not, where is the fatal
logical flaw?
If you accept these arguments, Goldsmith then goes on to suggest that
aging, seen as a design feature that deliberately limits life span,
also enhances the evolution process in several different ways. If
variation can evolve, then aging can evolve even though both are
fitness-adverse. This is counter to traditional theories of aging
that say that aging is an adverse "side effect" linked to some
beneficial and therefore evolvable trait such that there is a net
Darwinian benefit. ("Beneficial" means a trait that helps in survival
or reproduction as in "survival of the fittest.")
I realize these concepts might seem, at the least, radical, but they
are nonetheless interesting.
Quote: FROM Peoria:
Two major flawsw and one minor flaw in the argument so far. First,
the claim that "that members of a species should nominally tend toward
being genetically identical" is true only in the limit of infinite
population sizes, infinite amount of time for selection to work, and
slow mutation rates. But in the real world, mutation is producing
variation much faster than natural selection can weed it out, and the
only thing that keeps species as close to genetically identical as
they are is drift of nearly neutral alleles to fixation in finite
populations.
Second, the arguments also seem to assume that all members of the
population
live in the same environment and that the environment is unchanging.
A considerable amount of the 'natural' variation in populations can be
traced to 'natural' variations in the environment.
Quote: The minor flaw appears in the discussion of how the 'evolution of
evolvability' is forbidden by normal selectionist logic. There is
some truth to this if you only consider evolution at a single
(organism or gene) level. But if you also allow for group-level and
species-level selection, then the existence of mechanisms for
increasing the generation of variation becomes plausible.
I am interpreting "Darwinian" to exclude group selection. The issue
here seems to be the relative importance of mutations vs recombination.
In the Darwinian model, beneficial mutations propagate radially. The
book tries to prove that in complex organisms there are essentially no
beneficial mutations but only mildly adverse mutations that can be
recombined to produce a beneficial result. Various arguments are
offered.
The reason that this is important concerns the feasibility of group
selection. Following the Darwinian model it is hard to get group
selection to work except (maybe) in rather constrained circumstances
such as small groups. The problem is that "individual" disadvantage
seems to operate on a more "short term" basis and would override a
longer term group advantage. (See Tyler below.) Many people totally
disbelieve group selection. Dawkins' selfish gene theory was proposed
as an alternative to group selection, etc. etc. The recombination model
is more amenable to group selection because it is more population
oriented as opposed to individual oriented.
Quote: If you accept these arguments, Goldsmith then goes on to suggest that
aging, seen as a design feature that deliberately limits life span,
also enhances the evolution process in several different ways. If
variation can evolve, then aging can evolve even though both are
fitness-adverse. This is counter to traditional theories of aging
that say that aging is an adverse "side effect" linked to some
beneficial and therefore evolvable trait such that there is a net
Darwinian benefit. ("Beneficial" means a trait that helps in survival
or reproduction as in "survival of the fittest.")
I realize these concepts might seem, at the least, radical, but they
are nonetheless interesting.
The idea that senescence and death exist in sexual organisms for the
*purpose* of allowing the variant young to compete among themselves
(without the older generation siphoning off all of the resources) is
hardly an original one. I've seen enough modeling to convince me that
this may be part of the story, but it is not the full story. The
other part is the sheer difficulty of keeping large complex organisms
from simply wearing out. Some plants (trees, mostly) are designed so
that new generations of tissue can make productive use of the older,
worn-out generations of tissue. Animals (and especially animal
central nervous systems) just can't work that way.
Although everybody recognizes that there is wear or other unrepairable
damage that could accumulate in an organism, it seems to be pretty clear
that wear cannot be the main explanation for observed life span
characteristics. This is because very similar organisms with very
similar cell biology have grossly different life spans. (e.g. mouse and
human, crow and parrot, many other examples) There are also organisms
possessing biological suicide mechanisms that clearly are not
accumulative (e.g. bamboo, octopus). Finally, there are organisms that
do not have any measurable aging (e.g. Pacific rockfish) even at 150
years old when similar organisms have much shorter life spans.
The group benefit of a deliberately limited life span that you mention
was first proposed in 1882. Discussions such as this one on the nature
of aging have been going on since 1859. The book suggests about six
other plausible group benefits of an evolved mechanism that limits life
span.
The currently most respected "main line" aging theories ignore group
selection, adhere to Darwinian theory, and propose that aging is an
unavoidable adverse side-effect of some beneficial function. If you
assume the beneficial function is reproduction related, this then fits
better with the observations than wear. However, the book describes
what appear to be several major logical flaws in the main line theories.
Also attempts at experimental confirmation have not been very
successful.
Quote: FROM Lawton:
But calling this "digital?" What does THAT mean? Does the author
mean "binomial" as in the way computers process information as a
series of only two conditions at each juncture, i.e., "yes" vs "no?"
or "zero" vs (1) scenarios? If the author of the book you refer to
wished to call this "digital," so be it. As Turing observed, any
mathematical relationship can be "translated" into an algorithm (i.e.
a a format expressing the same operations, but in a form which gets
there by the use of binomial recursions).
The genetic code actually is "digital" as opposed to "analog". This is
not a matter of humans choosing to express an analog thing like a
photograph in digital terms. The genetic code consists of a sequence of
letters, words (codons), and messages (genes) and shares characteristics
with any other digital data system. It has to have a format, a
language. While an analog thing is continuously variable, a digital
thing or something controlled by a digital message only has so many
discrete values depending on the "format". The digital nature of
inheritance has many potential consequences for evolution.
It is apparent that this digital genetic data "transmission system"
itself has a very complex design that varies between different
organisms. How did the transmission system that carries the data
evolve? If the fitness design of an organism is driven by the content
of the genetic message, not its carrier, then how did the carrier
evolve? This seems to provide support for group selection. The book
has a very extensive discussion of this.
Quote: FROM Tyler:
The idea that variation-producing characteristics were able to
evolve despite fitness disadvantage because they convey an
improvement in the capacity for evolution - is widely regarded
as not the correct explanation.
In fact there are other, more direct short-term fitness advantages
to diversity-producing traits - such as sexual recombination.
That this is the case can be seen by consideration of organisms
that exhibit facultative parthenogenesis. These organisms can
clone themselves - but often choose not to do so.
Similarly, the idea that variation considered as an evolved design
feature is itself incompatible with Darwinian evolution is
equally incorrect :-(
In fact, clones are often regarded unfavourably by natural
selection - primarily since groups of genetically identical
organisms can easily be exploited by pathogens.
There are other defenses against pathogens besides adapatations that
promote diversity: immune systems, being rare, and very rapid
dispersal, with no parental care.
Immune systems allow some of the advantages of cloning without using
diversity as a defense. However the strategy is typically only
effective in the short term.
Diversity is a simple and reasonably effective defense against
pathogens - it is not surprising to find adaptations that promote it.
This is an argument for how one of the discrepancies (variation
producing features) might be resolved without violating orthodox
Darwinism and embracing some form of group selection. It seems somewhat
implausible that sexual reproduction and all the other complexity
evolved just for this one function, but possible. (Wouldn't there have
been an easier way?)
However, in my view, if you look at the totality: variation, suicide
mechanisms, mating rituals, digital issues, etc. it is very difficult to
conjure a way to escape group selection, certainly from an Occam's Razor
viewpoint. |
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| Tim Tyler |
Posted: Mon Feb 12, 2007 9:40 am |
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Guest
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Bioteach wrote:
Quote: Perplexed wrote:
The idea that senescence and death exist in sexual organisms for the
*purpose* of allowing the variant young to compete among themselves
(without the older generation siphoning off all of the resources) is
hardly an original one. I've seen enough modeling to convince me that
this may be part of the story, but it is not the full story. The
other part is the sheer difficulty of keeping large complex organisms
from simply wearing out. Some plants (trees, mostly) are designed so
that new generations of tissue can make productive use of the older,
worn-out generations of tissue. Animals (and especially animal
central nervous systems) just can't work that way.
Although everybody recognizes that there is wear or other unrepairable
damage that could accumulate in an organism, it seems to be pretty clear
that wear cannot be the main explanation for observed life span
characteristics. This is because very similar organisms with very
similar cell biology have grossly different life spans. (e.g. mouse and
human, crow and parrot, many other examples)
The idea is that lifespan characteristics can be explained
primarily by selection on repair and maintenance mechanisms.
Relatively short-lived creatures allocate more resources to
short-term reproduction at the expense of repair and
maintenance mechanisms. Those that live longer allocate more
resources to repair and maintenance - perhaps because growth
is resource limited, because they have a more plastic
developmental process, or because they provide more parental
care.
Quote: There are also organisms possessing biological suicide mechanisms
that clearly are not accumulative (e.g. bamboo, octopus).
Can you be more specific? There are plenty of causes of
death that are not cumulative - but they need not be
suicidal.
Also, suicide is actually /expected/ in some plants - where
the parents live near the offspring, compete for resources
with them, or act as a parasite reservoir that could
infect them.
In such cases, individual death can be adaptively favoured
by kin selection.
Quote: Finally, there are organisms that do not have any measurable aging
(e.g. Pacific rockfish) even at 150 years old when similar organisms
have much shorter life spans.
I am not sure how negligible senescence bears on the issues of
group selection or adaptive death. An organism with negligible
senescence simply has good repair and maintenance mechanisms.
Indeed, one might ask, if senescence is supposedly adaptively
favoured, why these organisms do not exhibit it.
Quote: The currently most respected "main line" aging theories ignore group
selection, adhere to Darwinian theory, and propose that aging is an
unavoidable adverse side-effect of some beneficial function. If you
assume the beneficial function is reproduction related, this then fits
better with the observations than wear. However, the book describes
what appear to be several major logical flaws in the main line theories.
?
Quote: FROM Tyler:
The idea that variation-producing characteristics were able to
evolve despite fitness disadvantage because they convey an
improvement in the capacity for evolution - is widely regarded
as not the correct explanation.
In fact there are other, more direct short-term fitness advantages
to diversity-producing traits - such as sexual recombination.
That this is the case can be seen by consideration of organisms
that exhibit facultative parthenogenesis. These organisms can
clone themselves - but often choose not to do so.
Similarly, the idea that variation considered as an evolved design
feature is itself incompatible with Darwinian evolution is
equally incorrect :-(
In fact, clones are often regarded unfavourably by natural
selection - primarily since groups of genetically identical
organisms can easily be exploited by pathogens.
There are other defenses against pathogens besides adapatations that
promote diversity: immune systems, being rare, and very rapid
dispersal, with no parental care.
Immune systems allow some of the advantages of cloning without using
diversity as a defense. However the strategy is typically only
effective in the short term.
Diversity is a simple and reasonably effective defense against
pathogens - it is not surprising to find adaptations that promote it.
This is an argument for how one of the discrepancies (variation
producing features) might be resolved without violating orthodox
Darwinism and embracing some form of group selection. It seems somewhat
implausible that sexual reproduction and all the other complexity
evolved just for this one function, but possible. (Wouldn't there have
been an easier way?)
It is not the hypothesis that parasites are /solely/
responsible for the origin and maintenance of sexual
recombination. There is at least one other important theory of
the origin and maintenance of sex: the gene repair theory.
Sex weeds out deleterious mutations by concentrating them in
single bodies, and which then die or fail to reproduce.
However, pressure from parasites is an important reason for
the continued existence of sexuality - and explains much of
its ecological variation.
Sex may seem like a bizarre anti-parasite adaptation, but the
answer to the question of whether there was an easier way
appears to be 'no'.
Life /may/ find other ways of coping with parasites in the
future. It may generate diversity by other means than sexual
recombination, and it may combat pathogens directly, with
medical technology, and a global immune system. If these
approaches to eliminating pathogens are successful, a
question mark may appear over the utility of sexual
reproduction in nature.
However, so far human attempts at pathogen control have been
pretty feeble. Viruses and worms cause billions of dollars of
loss in artificial ecosystems created by humans - in computer
networks. Modern computer systems couldn't be more insecure
if the NSA had designed them itself.
If human beings are really /this/ incompetent or indifferent
to pathogens, perhaps there is little hope of progress in
combating them.
Still, I attrubute the current screw-up to copyright law - which
has created a near monopoly one area. The monopolist has
proved themselves either incompetent or failing to have the
best interests of the people at heart - resulting in the current
pathogen problem.
IMO, there are signs that this type of management screw-up will
have a limited lifespan under the current political system -
too many voters want their MP3s decriminalised, and - according
to current political thought - their wishes outweigh those of
the mega corporations, who want to continue to screw them out
of their dollars.
--
__________
|im |yler http://timtyler.org/ tim@tt1lock.org Remove lock to reply. |
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| Back to top |
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| Bioteach |
Posted: Wed Feb 14, 2007 8:49 am |
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Guest
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Tim Tyler <seemysig@cyberspace.org> wrote in
news:eqqfs8$dql$1@darwin.ediacara.org:
Quote: Bioteach wrote:
Perplexed wrote:
The idea that senescence and death exist in sexual organisms for
the *purpose* of allowing the variant young to compete among
themselves (without the older generation siphoning off all of the
resources) is hardly an original one. I've seen enough modeling to
convince me that this may be part of the story, but it is not the
full story. The other part is the sheer difficulty of keeping
large complex organisms from simply wearing out. Some plants
(trees, mostly) are designed so that new generations of tissue can
make productive use of the older, worn-out generations of tissue.
Animals (and especially animal central nervous systems) just can't
work that way.
Although everybody recognizes that there is wear or other
unrepairable damage that could accumulate in an organism, it seems
to be pretty clear that wear cannot be the main explanation for
observed life span characteristics. This is because very similar
organisms with very similar cell biology have grossly different life
spans. (e.g. mouse and human, crow and parrot, many other examples)
The idea is that lifespan characteristics can be explained
primarily by selection on repair and maintenance mechanisms.
Relatively short-lived creatures allocate more resources to
short-term reproduction at the expense of repair and
maintenance mechanisms. Those that live longer allocate more
resources to repair and maintenance - perhaps because growth
is resource limited, because they have a more plastic
developmental process, or because they provide more parental
care.
There are also organisms possessing biological suicide mechanisms
that clearly are not accumulative (e.g. bamboo, octopus).
Can you be more specific? There are plenty of causes of
death that are not cumulative - but they need not be
suicidal.
Bamboo evidently reproduce by essentially cloning, like grass.
Occasionally they flower and seed. When they flower, they die. Death
is programmed to accompany blooming and clearly not a maintenance issue.
Programmed death is apparently to prevent cloning from dominating sexual
reproduction.
Octopi females stop eating after reproduction and die of self
starvation. Some Polish biologist whose name I do not remember
determined that surgically removing the eyes eliminates this behavior.
No obvious way to make this into a maintenance issue.
Salmon die of old age after mating.
Quote:
Also, suicide is actually /expected/ in some plants - where
the parents live near the offspring, compete for resources
with them, or act as a parasite reservoir that could
infect them.
In such cases, individual death can be adaptively favoured
by kin selection.
Finally, there are organisms that do not have any measurable aging
(e.g. Pacific rockfish) even at 150 years old when similar organisms
have much shorter life spans.
I am not sure how negligible senescence bears on the issues of
group selection or adaptive death. An organism with negligible
senescence simply has good repair and maintenance mechanisms.
Indeed, one might ask, if senescence is supposedly adaptively
favoured, why these organisms do not exhibit it.
Yes the very few organisms that do not appear to age could have really
good repair mechanisms (maintenance, Darwinian, aging is not a benefit
view) or could have lost their ability to age (aging is an evolved
beneficial feature, group selection view). The existence of negligible
senescence doesn't prove anything one way or another, except that SOME
organisms have apparently escaped aging and that it is therefore
possible.
I think there are bigger problems with the maintenance theories:
If an organism can build itself from essentially nothing, how come
repair is such a problem? Replacing a cell shouldn't be very much
different from growing it in the first place. Many cells, (skin, blood)
are replaced often.
Why do things like exercise and other forms of stress seem to extend
life span if maintenance is the issue? This seems the opposite of what
one would expect.
Quote:
The currently most respected "main line" aging theories ignore group
selection, adhere to Darwinian theory, and propose that aging is an
unavoidable adverse side-effect of some beneficial function. If you
assume the beneficial function is reproduction related, this then
fits better with the observations than wear. However, the book
describes what appear to be several major logical flaws in the main
line theories.
?
FROM Tyler:
The idea that variation-producing characteristics were able to
evolve despite fitness disadvantage because they convey an
improvement in the capacity for evolution - is widely regarded
as not the correct explanation.
In fact there are other, more direct short-term fitness advantages
to diversity-producing traits - such as sexual recombination.
That this is the case can be seen by consideration of organisms
that exhibit facultative parthenogenesis. These organisms can
clone themselves - but often choose not to do so.
Similarly, the idea that variation considered as an evolved design
feature is itself incompatible with Darwinian evolution is
equally incorrect :-(
In fact, clones are often regarded unfavourably by natural
selection - primarily since groups of genetically identical
organisms can easily be exploited by pathogens.
There are other defenses against pathogens besides adapatations
that promote diversity: immune systems, being rare, and very rapid
dispersal, with no parental care.
Immune systems allow some of the advantages of cloning without
using diversity as a defense. However the strategy is typically
only effective in the short term.
Diversity is a simple and reasonably effective defense against
pathogens - it is not surprising to find adaptations that promote
it.
This is an argument for how one of the discrepancies (variation
producing features) might be resolved without violating orthodox
Darwinism and embracing some form of group selection. It seems
somewhat implausible that sexual reproduction and all the other
complexity evolved just for this one function, but possible.
(Wouldn't there have been an easier way?)
It is not the hypothesis that parasites are /solely/
responsible for the origin and maintenance of sexual
recombination. There is at least one other important theory of
the origin and maintenance of sex: the gene repair theory.
Sex weeds out deleterious mutations by concentrating them in
single bodies, and which then die or fail to reproduce.
However, pressure from parasites is an important reason for
the continued existence of sexuality - and explains much of
its ecological variation.
Sex may seem like a bizarre anti-parasite adaptation, but the
answer to the question of whether there was an easier way
appears to be 'no'.
Life /may/ find other ways of coping with parasites in the
future. It may generate diversity by other means than sexual
recombination, and it may combat pathogens directly, with
medical technology, and a global immune system. If these
approaches to eliminating pathogens are successful, a
question mark may appear over the utility of sexual
reproduction in nature.
However, so far human attempts at pathogen control have been
pretty feeble. Viruses and worms cause billions of dollars of
loss in artificial ecosystems created by humans - in computer
networks. Modern computer systems couldn't be more insecure
if the NSA had designed them itself.
If human beings are really /this/ incompetent or indifferent
to pathogens, perhaps there is little hope of progress in
combating them.
Still, I attrubute the current screw-up to copyright law - which
has created a near monopoly one area. The monopolist has
proved themselves either incompetent or failing to have the
best interests of the people at heart - resulting in the current
pathogen problem.
IMO, there are signs that this type of management screw-up will
have a limited lifespan under the current political system -
too many voters want their MP3s decriminalised, and - according
to current political thought - their wishes outweigh those of
the mega corporations, who want to continue to screw them out
of their dollars.
--
__________
|im |yler http://timtyler.org/ tim@tt1lock.org Remove lock to
|reply.
Those who do not believe in group selection think that the individual
benefits of sexual reproduction (e.g. pathogen resistance) outweigh the
seemingly major individual disadvantages allowing the major complexities
of sexual reproduction to evolve. Those who do believe in group
selection think that the major group benefits (essentially enabling the
evolution process in complex organisms) outweigh the individual
disadvantages. There is no way that either side can prove their case to
the satisfaction of the other.
My limited experience suggests that once formed, beliefs about group
selection are very deeply held. Someone is about as likely to change
their beliefs about group selection as they are likely to change their
religious beliefs. |
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| Tim Tyler |
Posted: Thu Feb 15, 2007 11:11 am |
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Guest
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Bioteach wrote:
Quote: Tim Tyler <seemysig@cyberspace.org> wrote in
Bioteach wrote:
There are also organisms possessing biological suicide mechanisms
that clearly are not accumulative (e.g. bamboo, octopus).
Can you be more specific? There are plenty of causes of
death that are not cumulative - but they need not be
suicidal.
Bamboo evidently reproduce by essentially cloning, like grass.
Occasionally they flower and seed. When they flower, they die. Death
is programmed to accompany blooming and clearly not a maintenance issue.
Programmed death is apparently to prevent cloning from dominating sexual
reproduction.
In many organisms, vegetative reproduction takes place
when the going is good - and sexual reproduction takes
place when it is not - since the stress may show that the
existing phenotype is not working, and it's time to try
something new.
So maybe it's not sex that causes suicide, but stress that
leads to both death and sexual reproduction.
Also, sex may be a great reproductive effort, which
diverts resources away from maintenance programs to
operate, leading to malfunction and death.
Is there any real evidence that bamboos commit suicide?
Quote: Octopi females stop eating after reproduction and die of self
starvation. Some Polish biologist whose name I do not remember
determined that surgically removing the eyes eliminates this behavior.
No obvious way to make this into a maintenance issue.
Octopus females don't eat in order to care for their eggs.
Isn't eating a type of maintenance? The octopi are
trading bodily maintenance in favour of reproduction.
Quote: Salmon die of old age after mating.
Sex may be a great reproductive effort, which
diverts resources away from maintenance programs
to operate, leading to subsequent malfunction and death.
Quote: I think there are bigger problems with the maintenance theories:
If an organism can build itself from essentially nothing, how come
repair is such a problem? Replacing a cell shouldn't be very much
different from growing it in the first place. Many cells, (skin, blood)
are replaced often.
Nature can do regeneration if it tries. The problem is an
economic one, it makes better economic sense to make new
organisms than trying to repair existing ones. In fact,
it's the same with cars, computers, practically any complex
object - after a while it is cheaper to buy a new one than
to try and fix up the old one.
Quote: Why do things like exercise and other forms of stress seem to extend
life span if maintenance is the issue? This seems the opposite of what
one would expect.
In those cases where stress appears to extend lifespan, it
seems to work by diverting resources away from reproduction
and into maintenance and repair programs.
The classic case is calorie restriction:
http://cr.timtyler.org/why/
Exercise is a bit different, but that is the basic answer.
Quote: Those who do not believe in group selection think that the individual
benefits of sexual reproduction (e.g. pathogen resistance) outweigh the
seemingly major individual disadvantages allowing the major complexities
of sexual reproduction to evolve. Those who do believe in group
selection think that the major group benefits (essentially enabling the
evolution process in complex organisms) outweigh the individual
disadvantages. There is no way that either side can prove their case to
the satisfaction of the other.
AFAICT, neither side is wrong. It's an issue of how much
each theory explains. I'm confident biologists will get to
the bottom of the issue.
--
__________
|im |yler http://timtyler.org/ tim@tt1lock.org Remove lock to reply. |
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