Message-Id: <199710090702.CAA00100@dns.night.net>
Subject: Re: Replicators, was Non Homuncular Memetics
Date: Thu, 9 Oct 97 02:00:19 -0600
From: Mark Mills <mmmills@onramp.net>
To: memetics list <memetics@mmu.ac.uk>
>I'm not sure from the above what the differences are between our
>assumptions about systems and testing. But when you consider how strong a
>term "isomorphism" is, I doubt that you will find isomorphism between
>diploid, triploid, etc chromosomal DNA, and memes. Us diploids, for
>instance beget monoploid organisms, which then fuse into diploid organisms.
>I'd say that this differs considerably from the "life cycle" of memes, and
>causes serious differences between population genetics and population
>memetics, particularly as regards recombination.
Aaron,
Very good points.  
Isomorphism is another of these statistical terms.  I'll try to give it 
the same weight as you give it.  If we can generalize the 'ploid system 
to multiple substrates and stay within some meaningful use of the term 
isomorphism, we might be able to share our views more easily.
I sense in your comments a willingness to consider haploid, diploid, etc. 
systems as within some functional definition of isomorphism.  I suspect 
this is made easy by the use of similar code substrates in each system.  
The substrate is clearly isomorphic.
Am I correct in this assumption?
Recombination mechanics seem to be the criteria for dismissing parallels 
between organic-molecular substrate systems (genetics) and neural 
substrate systems (memetics).
Am I correct in this focus?
I'll try to address these issues.  The following is rather long and 
convoluted.  I apologize in advance.  
I'm going to build a case for saying the brain is a functional isomorph 
of a chromosome despite the substrate differences.  To begin, I'll need 
to describe a code system and draw parallels to each substrate system.  
The key features are code, substrate and a controlled environment.  The 
controlled environment provides energy, rhythm and materials for creating 
and encoding 'blank' substrates.
In genetics, we have a substrate of sugar and phosphate chains.  In 
memetics, the substrate is neural tissue.  The key aspect of any 
substrate is invariance with regard to code.  The substrate needs to 
avoid being 'processed.'  This does not rule out 'shape' factors, though. 
 Shape factors influence code manipulation by timely juxtaposition of 
code units.  At the DNA level, this occurs via helix flexture.  At the 
memetic level, this occurs via selective neural growth and axion 
shielding. 
Genetic coding occurs by sequential fixing of the four DNA bases in a 
helical line upon the substrate.  Neural coding is less well defined, but 
it looks like protein weight factors in the synapses perform the same 
role in the brain.
The genetic process exists within the confines of cellular fluids and 
organelles.  These provide the materials, timing and torque to initiate 
and guide the replication of chromosomes.  In the memetics case, the 
replication of new 'blank' brains is provided by biology.  The controlled 
environmental stimulation needed to encode the brain and produce a 
successful replicator is provided by cultural units like families, tribes 
and nations.
Replication mechanics involve the process used for recreating the 
substrate and recoding 'blanks' to create (relatively) isomorphic 
individuals. In the memetics case, the substrate is recreated via 
biological reproduction.  The 'blank' (infant) is provided with small 
amounts of inherited code (instinct) with which it can build essential 
behaviors required to acquire the remaining code.  This is done via an 
initially self-guided exploration of experiential stimuli.  This stimuli 
is far from random, though.  The environment for collecting experiences 
is carefully controlled by 'related' encoded individuals (adults), quite 
willing to help the 'blank' fill in its code. 
I'd like to suggest the splitting of the DNA double helix into two 
encoded strands which attract free DNA bases into fixed molecular bonds 
with the half-helix blank is functionally isomorphic with the above 
process.  In both cases, the new 'blank' encodes itself based on code it 
embodies in its 'blank' or 'unencoded' state.  In the genetic case, the 
code arrives in the form of free DNA bases provided by the cellular 
environment.  In the memetic case, the code arrives via controlled 
stimulation provided by the cultural environment. The 'choice' of free 
bases is determined by shape features in the 'blank' half chromosome.  
The 'choice' of memorized stimuli retained by a 'blank' brain is 
controlled by a small amount of 'inherited code' (instinct) available at 
birth.  In both cases, the blank is preset to acquire particular codes.
With this in mind, the brain tissue is functional isomorph of the 
sugar-phosphate substrate.  Synapse proteins are the functional isomorph 
of DNA bases.  Culturally controlled environment is the functional 
isomorph of cellular fluids and organelles.
Memetic replication is not mitosis or meiosis, but it is useful to 
carefully compare the mechanical steps required by each replicating 
process.  Though they have different 'means,' they have the same goal and 
functional steps.  Both process produce a functionally identical encoded 
substrate.  Since I have 4 kids, I am well aware of the individual 
differences between parent and child.  All the same, from an objective 
and population view, there are many grounds for isomorphic comparisions 
between parent and child at both biological and cultural levels.
As to genealogical issues, I'll just say one needs to consider both the 
possibility of mutation caused by 'blank' creation (spliting the helix or 
creating an infant) on one hand, and  mutation caused by blank encoding 
(population of second helix or education of the infant), on the other 
hand.  Both features of the replication process produce evolutionary 
(genealogical) change, but the rates of mutation will differ in each.  
Additionally, the functional importance of 'blank' mutation and 
'encoding' mutation differ in genetic and memetic systems.  Thus human 
cultural evolution will mutate at a different rate than biological 
evolution, though they will be linked at fundamental levels. 
The point of all this rhetoric is an intention encourage more biological 
research into memetics.  The biological mechanics of memetic processes 
are important.  Memetics is not an ungrounded science, disconnected from 
the biology of genetic replicators.  The biology of memetics will provide 
a reality that logic can never provide.  Additionally, the biology of 
memes is likely to have an impact on research into autism and help 
thousands of people live better lives.  Finally, it will illuminate 
evolutionary theory by pulling in a new code substrate without destroying 
the isomophism of Darwin's general theory.
Mark
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