In Scientific American's March 2010's issue (page 47), Marcus E. Raichle writes in
The Brain's Dark Energy that
... the equivalent of 10 billion bits per second arrives on the retina ... six million bits per second can leave the retina ... 10,000 bits per second make it to the visual cortex ... the amount of information constituting that conscious perception is less than 100 bits per second ...This is to be correlated with the following, in
The role of the thalamus in the flow of information to the cortex, by S Murray Sherman and R W Guillery (
Philos Trans R Soc Lond B Biol Sci. 2002 December 29; 357(1428): 1695–1708.doi: 10.1098/rstb.2002.1161.)
The lateral geniculate nucleus is the best understood thalamic relay and serves as a model for all thalamic relays. Only 5-10% of the input to geniculate relay cells derives from the retina, which is the driving input. The rest is modulatory and derives from local inhibitory inputs, descending inputs from layer 6 of the visual cortex, and ascending inputs from the brainstem. These modulatory inputs control many features of retinogeniculate transmission.That latter citation has been used by Song-Chun Zhu and David Mumford in
A Stochastic Grammar of Images (Foundation and Trends in Computer Graphics and Vision, vol 2, no 4, pp 2590362, 1006) [page 2] to motivate a stochastic grammar approach to human vision.
But stochastic grammars were first motivated by linguistic analysis, where they form a compelling improvement to the grammatical descriptions of Noam Chomsky [See for example my own (shameless publicity)
Form and Interpretation of Relative Clauses in English, Bertrand du Castel, Linguistic Inquiry Volume 9 Number 2 (Spring, 1978) 275-289].
Stochastic grammars are not limited to language analysis nor vision, they extend also to the most intricate human activities, as shown by two World Intellectual Property Organization (WIPO) Patent Cooperation Treaty (PCT) patent applications: (WO/2010/010453)
System and Method for Determining Drilling Activity, by Harry Barrow and Bertrand du Castel, and (WO/2010/010455)
System and Method for Automating Exploration of Production of Subterranean Resources, by Bertrand du Castel and Harry Barrow.
This leads us to stochastic consciousness. While stochastic grammars in vision model our neuronal systems in space first (and then in time, although this is not modeled in the publication mentioned above), stochastic grammars in language and human activities exemplified by the patents above model our neuronal systems in time.
Let's take the time example, although the discussion below also applies in space. The essential of a stochastic grammar is a modular description of stochastic phenomena that extends both in width and depth in a recursive manner. That description amounts to a description of
prior Bayesian probabilities that are then matched with
posterior observations. Those observations allow updating the priors and then go to the next step. In layman's terms, we have a preconceived idea of what the world is like that we constantly update with what we observe, creating anew a preconceived idea of what would happen next.
What's very interesting is how it actually works. Most of the time, we would expect the world to behave our preconceived way. If the car is going on the highway, the next milliseconds it should be going as well. While the landscape is changing, it is also changing in preconceived ways, and we go our merry way as well.
But suddenly, a deer jumps on the highway. While this is part of our priors, i.e. our model of the world, the circuitry involved is in low state of expectation, because the probability of a deer jumping on the highway is low. But the posterior event, i.e. the jump of the deer, matches with the current priors and raises them considerably regarding a deer event. So the priors see a major shift in their probabilities with a new set of prior probabilities that will emphasize, for example, the likelihood that the car hits the deer. Such a major shift in circuitry involves, in the brain, an influx of excitatory neurotransmitter actions to the synaptic connections involved, while inhibitory neurotransmitter actions will lower down the previous priors. That looks very much like consciousness to me.
It is worth nothing that this takes very good care of the questions of top-down and bottom-up attention and their relationship to consciousness. A major adjustment of priors is equivalent to top-down attention, as it prepares the brain for a new set of events, and a major adjustment of posteriors is equivalent to bottom-up attention, as it triggers a major adjustment of priors. In both cases, neurotransmitters shift focus, and that's the feeling of consciousness. I need to look in the literature at whether somebody has correlated specific chemical releases to that feeling. Reading David J. Chalmers seminal
The Puzzle of Conscious Experience, in Scientific American , December 1995 pp62-68 (see also the
original version by Chalmers) where he posits the
hard problem of consciousness, I can't help feeling that perhaps it's less a question of chemical releases than of their glial blood activation.
Let's take for example Chalmer's illustration of Mary, a neuroscientist who is the world's leading expert in color vision but who herself is color-blind (actually, Chalmer says that she has been living in a black and white world). He says that the easy problem of consciousness is the first part and the hard one the later. How to explain that she knows everything about color vision but color experience doesn't evoke a conscious feeling for her? Well, with a stochastic grammar, that's exactly what we would expect. In the former case, Mary has a set of priors that describe her preconceived expectations of a color theory, and that will be met with posteriors which are actual triggers of her theory (like, say, a wavelength measurement). In the latter, the priors are related to natural experience, that for her doesn't involve color. The posteriors don't evoke color either, so there is never a glial blood activation related to a change in the priors due to color. Conversely, for a person without color impairment, a particular set of colors may be different enough from prior expectations to reset priors in a significant way and therefore trigger a perceptible change in glial blood activation. At this point, I'd like to relate brain blood activation to a more immediately understandable phenomenon, that of, for example, blood activation such as blushing, or blood activation such as extra blood in the limbs. In those cases, blood is linked very directly with consciousness; it is natural to ask whether brain glial activation is similarly perceived. Well, I need another plunge into the literature to find out whether changes in the brain blood patterns have been measured while correlated with recognition of consciousness. What's for sure is that the reverse is true, as syncope is a loss of consciousness related to blood insufficiency.
Well, this blog is becoming too big. It's time I convert it into a
knol.
Bertrand du Castel