Good job. (your long post) Evolution of language is often given as the reason for the Out of Africa, OoA, event, but the suddenness of OoA, is not compatible with the slow physicological changes you describe (required for flexible functional language more than just a few "alarm calls"). Thus your observtions tend to support my alternative explaination for the OoA event.invert_nexus said:Let's try to bring this back to some form intelligent discussion....The evolution of language in man. ...I'm talking about the biological adaptations that had to take place in man in order for our language to emerge....
My post of 8 Oct 5 in the "about determinism" thread give my views and as you are thoughtful I hope you will read all of it and comment, but here is the part that relates to evolution:
....3) The primary task of living organisms is to stay alive, at least long enough to reproduce. Neural computations require time. The world we would experience, if our experiences were the emergent results of many successive stages of neural transformations would be delayed by a significant fraction of a second. During our evolutionary history nothing truly discontinuous ever happened in our visual environment. (The discontinuous changes in movie and TV scenes did not exist.) None the less, it was essential for our ancestors to have a real-time understanding of their surroundings despite nature’s temporal continuity and our neural delays. - Try ducking a rock thrown towards your head if your only visual experience of it is a display projected into the eyes (electronic goggles) that delay the image by 0.1 seconds! A real-time simulation of the environment, can be achieved in a neural simulation by slightly projecting ahead the sensory information to compensate for neural processing delays.
A real-time simulation would have great survival value. Perhaps the Neanderthals still experienced slightly delayed “emerging transforms” of retinal data when our smaller brained and weaker ancestors perfected a real-time simulation of their environment. (Ecological pressure from the larger and stronger Neanderthals would have accelerated the rate of evolution in our ancestors.) Likewise, the “Out of Africa” mystery, (Why one branch of hominoids, expanded and dominated all others approximately 50,000 years ago.), which is often assumed to be related to the acquisition of “autonomous language” (no gestures required - hands free and education facilitated), might better be explained by the development of the real-time simulation of the environment.
Furthermore, I think everything we perceive as being “real” in our environment, including our physical bodies, is a part of this same simulation, not an emerging result of neural transformations of sensorial data from any of our neural transducers. That is, all of the senses only guide the simulation, feature by feature, to keep it highly faithful to the current external reality. When an abrupt external event unexpectedly occurs (hidden firecracker exploding, etc.), it significantly conflicts with the events projected in our simulation for that moment. We are startled and the simulation must be quickly revised to conform to the unanticipated external reality. This revision requires approximately 0.3 seconds. I think it probable that the simulation is paused while the revision is in progress, but we do not notice as we are also “paused” during this brief interval, just as we are not aware of hours passing while we sleep. I think the unusual electrical activity in the brain associated with the re-initiation of the simulation produces the EEG signal commonly called “P300,” or the “startle spike.” P300 is strongest over the parietal region.3
Why the continuous natural environment should be dissected into “features” and separately processed as a means of achieving a unified perception of the world is a great and unexplained mystery for most cognitive scientists, but easily understood if a simulation of the world is constructed by the brain. The physically sensed world is dissected into “features” for the same reason that a pilot uses a checklist before takeoff. Dividing a complex task into its component details and separately checking each, item by item, feature by feature, improves task performance accuracy. Thus, both the real-time simulation and the dissection of the visual field into features have significant survival value and consequently are probable natural developments in the evolution of creatures as complex as man.
In order to compare the features derived from retinal data with those derived from the simulation, they must be brought to the same neural tissue. Clearly it would be advantages to make this comparison as early as possible in the sequential stages of “computational transforms” of the retinal information. If the simulation is constructed in the parietal region of the brain, then one would expect that the number of neural fiber leaving the parietal cortex and returning to the visual cortex would at least equal those coming there, via the LGN, from the eyes. In fact they are somewhat more numerous. They are called “retrograde fibers” and no plausible reason for their existence has been suggested. Some of the comparison may be made even earlier in the LGN, which is usually considered to be mainly a “relay station” between the eyes and visual cortex. (Both areas have large projections into the parietal cortex, so it can easily “know” when, where and what difference has been detected.) The quantity of retrograde fibers from the visual striate cortex to the LGN slightly outnumbers the number of fibers coming there from the eyes. About this second set of retrograde fibers, DeValois4 states: “It is by no means obvious what function is subserved by this feedback.” (from V1 to LGN) About the retrograde set from the parietal to V1, they state: “Even less is understood (if that is possible) about these feedback connections...” They also note that both sets are “strictly retinotopic,” which is the neuro-physiologist’s way to compactly state that each small part of the visual field is mapped in one-to-one correspondence with neural tissue. That is, the retrograde fibers return to the same small area of processing cells that the prograde fibers enter and these cells are concerned with only a small part of the image on the retina. This approximately equal number of retinotopic retrograde fibers entering the visual cortex, is not only explained by the theory I am suggesting; they are required for the simulation to rapidly correct for unpredictable external events!
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