My F/b response to Bill Trowbridge about evidence for existence of dynamic logical strucutes (DLS) in the brain
Bill’s question:
- Mark A Peaty “Do you have a good reference with neurological evidence for these DLS ? I’d prefer something general, maybe summarizing all we know about them (if such a thing exists), rather than a deep dive for a specific case. But whatever … use your discretion.
- Only in cortical columns?
- Connecting nearby columns?
- In other areas of the brain?
- Distributed everywhere?
- Only in certain area?
- Are there specializations from place to place?”
My Answer: Bill, I learned of cortical columns from reading Vernon B Mountcastle’s contribution to the book The Mindful Brain which he and Gerald Edelman wrote. From Gerald Edelman’s contribution I learned of the concept of neuronal group selection (AKA neural Darwinism). G.Edelman used the term repertoires for the informational-causal effectiveness of such coalitions. He also pointed out that neuronal groups as such are by far most likely to be the underlying parts/bearers of mental information because having a large membership gives:
- robustness through redundancy and the capacity for “graceful degredation”,
- allows widespread interconnectivity across different cortical areas (and elsewhere) which allows exactitude and nuances of meanings, and
- allows associations to occur because individual neurons can be members of many different coalitions. There are other useful attributes also but I can’t think of them right now 😉
Jean Pierre Changeaux in his book Neuronal Man called them singularities and explained that their ‘figurative meaning’ is embodied in the locations of their component parts.
Cortical columns are the fundamental sub components of neural cell assemblies and they are spread all across the cortex, a bit like the pixels of a digital screen. Each local area of cortex therefore has a two dimensional array of columns which can each embody different features of two different environmental (or conceptual) variables.
I first read of the fine detail and processing potential of these arrangements in a Scientific American article in the early ’90s. Some researchers had experimented with bats suspended in little swings which set them moving back and forth. Electrodes set into the bats’ cortices showed various two dimensional representations of things like ‘target’ angular direction versus delay time of echo, ‘target’ direction versus fequency of echo, and so forth. Interlinking of these cortical arrays with other arrays receiving signals from primary processing arrays allows for cross referencing of the analyses performed by primary sensory sheets and synthesis of an analogue representation within the bat’s brain of a moving target insect’s location, velocity, size, and probably other significant features. These ‘other features’ would enable the bat to learn to identify target types and how best to catch them.
This U/T video, from 22:2o onwards for a fair while deals specifically with Vernon B Mountcaste’s discovery. The earlier parts of the video discusses the cortex and its layers (which are visible under a microscope), ie similarity of neuron types prominent at specific distances in from the cortical surface.
NB, I am still processing his (Jeff Hawkins’) assertion that each column has a model of the environment embodied/processed within it. I’m thinking this is akin to the idea that each part of a hologram has the whole of the subject image within it.
His statement may be true but I think that in order to make sense of it one needs to consider the effect upon each and every neuron of its participation in each of the (potentially vast number) of such activations it participates in.
As I understand it the hippocampus is coordinating and sustaining several sets of potential global gestltaten, and the pre frontal cortex is ‘deciding’ which is the most important to be fully activated as the most up to date snapshot of self-in-the-world. The basis of this decision rests upon the emotional charge that has been connected to the component memory/sensory data of each representational ensmble. That emotional charge is the ‘feeling’ related to the item and is the cortical representation of the initial emotion reaction to the raw perceptual information.
I read recently that researchers have discovered that the hippocampus outputs its signals in two waves 90° out of phase with each other. I’m guessing that the first output provokes/sustains/updates the currently active global model of self in the world, whereas the second wave sustains all the other items in short term memory and the parts of other items that were part of the model of self in the world earlier in the day. I imagine there is a kind of fading queue of such ‘new’ memories which are sustained until sleepy time by occasional bouts of reactivation due to enhanced spontaneous bursts of signalling by the member neurons. During sleep of course new memories are consolidated, which may well involve the updating of older forms of the representations involved.
I’m hoping you can see why I use the term dynamic logical structures (DLS) for each of the neuronal ensembles which becomes a self sustaining coalition due to the mutual reciprocal “re-entrant’ cortical signalling they engage in. A point I feel is important is that, for the time such DLS are active, they fulfil the basic requirements of a real thing which exists. Each one is a process which acts as a pathway for degrading the energy of their particular environment, which is a characteristic or all self-sustaining processes, and they also have effects upon their immediate environment which result, in either short term or long term, in increasing the probability of their reactivation in the future.