[ExI] Do digital computers feel?
Brent Allsop
brent.allsop at gmail.com
Fri Feb 17 05:04:47 UTC 2017
Hi Stathis,
You obviously know more than I know about how neuro transmitters work.
Thanks for helping me to better understand this type of stuff.
As I said, if what you say is true, then it merely falsifies the
prediction that glutamate is what performs the redness quality we
experience.
That is why I always resort to talking about the "simplified theoretical
world". In the simplified world, there are only 3 colors: red, green
and white. And in that simplified world, glutamate has the redness
quality, glycene has the greenness quality, aspartate that has the
whiteness quality, and it is one neuron that binds them all together, so
you can be aware of them all at once. And for Ben's sake: in this
simplified world there are "red and green signals in the optic nerve"
that can be easily inverted.
The goal is to make a very hard topic a little more simple. If one can
understand the qualitative theory I'm trying to describe, and how neuro
substitutuion works with no "hard" problems, and how people in such a
simplified world can "eff the ineffable" by properly qualitatively
interpreting abstracted observation knowledge - then they should be able
to apply the same qualitative theory in the more complex real world.
All that is required is to test for, and find, experimentally, in the
real world, what it is that takes the place of glutamate, glycene,
aspartate, and the single neuron binding system. That job is for the
experimentalists to do, once they understand how to test for it by no
longer being qualia blind (by miss interpreting abstracted observation
information as they all do now) and effing the ineffable by interpreting
what they are observing, qualitatively correctly.
Ben, I don't know if it will help, but I describe the "simplified
theoretical world" in more detail, in this talk:
https://www.youtube.com/watch?v=AHuqZKxtOf4 . But it may not help if
you believe there are not elemental qualities out of which our brain
builds or paints composite qualitative experiences with. It sounds like
you and John Clark agree on this? Do you also, like John, believe that
effing the ineffable is impossible, and thereby, qualia will forever not
be approachable via objective or sharable science?
Brent
On 2/15/2017 8:23 PM, Stathis Papaioannou wrote:
>
> On Wed., 15 Feb. 2017 at 4:48 pm, Brent Allsop <brent.allsop at gmail.com
> <mailto:brent.allsop at gmail.com>> wrote:
>
>
> Hi Stathis,
>
>
> Thanks for expressing all this so concisely. I hope I can be as
> concise so we can make progress with this. I think the key point
> in our misunderstanding is captured by you with this:
>
>
> On 2/14/2017 5:02 AM, Stathis Papaioannou wrote:
>> You're missing the point when you talk about "qualitative
>> representation". *Observable behaviour* is the only thing
>> necessary to consider in order to replicate *observable
>> behaviour*. The argument is that if you ignore qualia and just
>> replicate *observable behaviour* then the qualia will also
>> necessarily be replicated. I gave an example of this which I
>> believe is clear (tell me if not) with the glutamate/glycine swap.
>>
>
> Yes, your answer was very clear. I agree with most of what you
> are saying, but we both believe that the other is missing the
> point. You first want to focus on: "If you ignore qualia and just
> replicate *observable behavior* then the qualia will also
> necessarily be replicated." But even if I do agree with this,
> from how I see things, it is still missing or removing some
> important functionality. In the past you never want to move beyond
> this, because or until this has been settled. The problem is, I
> can't point out the required functionality being removed, until
> you first understand and agree with some other things in the
> qualitative theory. So, this time, could you move beyond that, at
> least for a bit and digest this initial description, then given
> that understanding (if you agree), I'll be able to point out the
> reasons I can't yet accept this functionalist way of doing neuro
> substitution.
>
> Let's start on the subjective side of things, again, with our
> simple 3 element system. The system is experiencing both redness
> and greenness as a unified composite qualitative experience. So,
> there are two qualitative representations of knowledge and there
> is a 3rd part of the system that is binding the two different
> representations into one composite experience. The fact that the
> system is aware of both of these qualitative representations at
> the same time, is the critical base functionality on which the
> comparison system is derived - outputting an indicator that could
> lead to one saying they are consciously aware that they are
> qualitatively the same or not.
>
> So, given that we subjectively know that, would you agree with the
> following? There must be something that is performing the
> functionality of the redness experience, and there is something
> that is performing the functionality of the greenness, and there
> is a 3rd element that is performing the function of binding these
> two representations of information together to make a composite
> experience - enabling the 3rd awareness/comparison neuron to
> indicate whether they are the same or not.
>
> You seem loath to want to go there, instead, first, wanting to
> first focus on: "If you ignore qualia and just replicate
> *observable behavior* then the qualia will also necessarily be
> replicated." But this ignoring of qualia is the problem, and you
> end up removing the most important parts of the functionality we
> want to observe as we neuro substitute.
>
> Let's compare this subjective way of observing things to the
> objective way of observing things, and for the time being assume
> it is glutamate that has or performs the redness experience
> functionality, and it is glycene that performs the greenness
> experience functionality. Given that, with subjective
> observation, we would experience a redness detector and with
> objective observation we would see a glutamate detector. So, what
> the 3rd part of the system (we are assuming it is a single neuron
> for simplicity's sake) is basically an objective and subjective
> comparison system - outputting an indicator as to whether the two
> representations of knowledge are functioning the same or not.
> This functionality derived from the way it binds together
> awareness of the two representations of knowledge to make one
> composite qualitative experience.
>
> Now, when you say you replace glutamate with glycene, and you
> replace the glutamate receptor with a glycene receptor, then
> assert that the comparison neuron will behave the same, you are
> removing the important comparison functionality, or simply
> falsifying the theory that it is only glutamate that reliably
> performs the redness function (if so, necessitating that it be
> something else, yet to be discovered, that is reliably performing
> the redness functionality we know so well). Both representations
> of knowledge are now the same qualitative glycene (or the
> greenness functionality), yet you are asserting that the output is
> still indicating that the two are different. This removal of the
> correct functionality as you do the neuro substitution, is why I
> can't accept your line of reasoning, along with it being the
> source of all the "hard" problems.
>
>
> I started answering point by point but I think it is best to just
> respond to this point, because it seems that you are ignoring what
> neurotransmitters actually do. Neurotransmitters are small molecules
> that are released from the presynaptic neuron and bind to the
> appropriate receptor on the postsynaptic neuron. Receptors are
> proteins in the cell membrane which have special sites to which
> neurotransmitters attach non-covalently (without forming a permanent
> chemical bond), sometimes described as being analogous to a lock and
> key mechanism. As a result of this interaction the receptor protein is
> pulled into a different shape, leading to a cascade of events in the
> neuron. With so-called ionotropic receptors the binding of the
> neurotransmitter opens up channels in the receptor allowing ions to
> move into and out of the neuron: sodium, potassium or calcium ions.
> Since ions are charged entities, this changes the voltage across the
> cell membrane, which can then change the shape of transmembrane
> proteins called voltage-gated ion channels, which can then cause a
> spike in voltage to propagates down the axon of the neuron, and
> ultimately to cause neurotransmitter release at the end of the axon,
> triggering the next neuron in the chain.
>
> Now, if we swap glutamate for glycine in this setup it won't work -
> glycine will not bind to the glutamate receptors. If we swap the
> glutamate receptors for glycine receptors it won't work - glutamate
> will not bind to glycine receptors. But if we swap glutamate for
> glycine and glutamate receptors for glycine receptors, and the glycine
> receptors otherwise have similar properties to the glutamate receptors
> (open similar ion channels when glycine binds), then the neuron will
> behave in the same way in regard to when it will fire, and hence all
> the downstream neurons and the muscles will behave in the same way,
> and the subject will behave in the same way. "The subject will behave
> in the same way" means, among other things, that the subject will say
> in a before/after comparison that the strawberries look red to him in
> exactly the same way as they did before. If you don't agree with this,
> then please point out where in the detailed chain of events I have
> described I have missed something and explain how the
> glutamate/glycine swap (leaving everything else in the brain the same)
> can possibly lead to the subject saying that his qualia have changed.
>
> If you assume the qualia experience functionality will arise or
> emerge in some other way or some other abstracted level, then it
> is this other abstracted location of qualia that can't be ignored,
> and must be able to be reliably compared via composite awareness.
> I am talking about doing a neuro substitution at this level, with
> the required qualia comparison functionality, not the level you
> are talking about, where the qualia being compared is being
> removed. If you are going to claim that a comparison
> functionality can be constructed out of this simplistic lower
> level (I don't see how this could be done), then provide at least
> one theoretically possible description of such (as I have done
> with glutamate, glycene, and a binder neuron to make a composite
> experience), and with that, whatever it is, it will be obvious
> what happens, and why, as the neural substitution occurs.
>
> If you do the neural substitutuion on a system that, instead of
> ignoring and removing qualia comparison, you provide any testable
> theoretical method of really doing the function of qualitative
> comparison, it can be obvious what is going on during the neural
> substitution. Let's do this by having two sets of such identical
> 3 element qualitative comparison systems, one that doesn't change
> and is for constant reference comparison purposes, and the other
> one is the one we will perform the neuro substitution on. We will
> bind these two systems with the same provided binding system in a
> meta comparison functioning system which will monitor and compare
> all the qualities, as the neural substitution takes place on one
> of the systems, so you can prove to everyone, both objectively and
> subjectively, exactly what it is going on, and why both of the 3
> element systems are always indicating: "It is red" even though one
> is the qualia invert of the other after one of the neuro
> substitution steps. If you duplicate all this *observable
> behavior*, including the meta awareness of what is going on with
> both systems, there will be no hard problems when it is neuro
> substituted since you are not removing the most important
> *observable behavior*.
>
> Does that help?
>
>
> Brent Allsop
>
>
>
>
>
>
>
>
>
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