Open in TheBrain

Bruno Google Lecture 2005

<p>Mar 16, 2011 01:01 PM

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a wonderful overview of vision and the challenges. &#160;delivered at Google in 2005.

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Starts with the evolution of the eye &#160;(cites Michael Land and Russell Fernald work)

see node on evol of eye... wonderful stuff.

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Rhodopsin in billions of years old and is used by essen all seeing creatures...

retinal + difft proteins.

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pit eye then pin hole eye then refrac material for &#160;lens (to allow more light&#160;

and yet maintain focus), &#160;mirrors at back, &#160;spherical lenses in fish.

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how about brain itself: &#160;we are in the pre-Newtonian era in terms of understnading this.

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FLY &#160;compound eye &#160;(gary larsen cartton on lady with fly swatter)

each eye segment has only 7 photoreceptors &#160;per facet.... &#160;

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in insects/ arthropods &#160;eyes are attached to exoskeleton... cannot move...

have to move whole body.

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fly's &#160;turn at 3,000 degrees per second while flying... &#160;mate in the air &#160;etc.

eye speeds are super fast.

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jumping spiders... stalk prey like a cat.

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rods are max sensitive btwn blue and green.

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cones &#160;sensitive at &#160;red, blue and green.

(blue is out of focus... &#160;not may of those blue cones)

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slide with mosaic of cones... most are red cones, some patches of green... uncommon blue.

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head is constant wobbling; &#160;eyes wobbling &#160;BUT

eye mvmt partially compensates for head motion.

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BRUNO &#160;says &#160;&#160;120 cones per degree in fovea &#160;&#160;(fewer than my estimate of 200).

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its a complete mystery how we get a stable visual field with all that motion.

(ie despite cone arrray dancing around).

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photoreceptors first go to horizontal cells &#160;(do lateral inhibition to sharpen resolution)

then to bipolar cells &#160;(relay info)

then to amacrine and finally to ret. ganglion cells.

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fovea: &#160;1 to 1 with retin ganglion cells; &#160;&#160;There are &#160;1M to 1.5 M &#160;ret gangl cells per eye (in each optic nerve)

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He loves the book by Robt Rodeick &#160;(see node) &#160;now deceased, Prof at Univ of Wash

The First Steps in Seeing &#160;&#160;(unfort v expensive).

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for the above, see my node on rods and cones

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as you bring your hand in toward your face... you get no added info cuz

the resolution drops off peripherally in your retina.

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the retinal ganglion cells are gathering impulses from many receptors at the periphery....

taking an average.

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there are 9X as many PARVO gangl cells as there are MAGNO cells.

(the parvos &#160;are the one to ones)

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1M to 1.5 M &#160;fibers in each optic nerve.

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LGN is 1 to 1 with ret ganglion cells &#160;(parvos and magnos are handled in separate layers)

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the LGN is surrounded by an inhibitory layer. called the reticular nucleus.

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There are 10X the number of fibers going BACK from cortex to LGN as from retina to LGN.

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he quotes David Mumford's theory &#160;(cortex is sending a skeleton of what it thinks is going on in visual

world to LGN.

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Marty Usney &#160;&#160;can find exact cell that a partic retin gangl cell stimulates in LGN and in V1

to get exact correspondences.

LGN field is either on center or off center (same as gangl cell)

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V1 pattern is a Gabor &#160;with on or off center &#160;(but that is really only just a minority of cells, like 15% of them)

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What are the other 85% of neurons in V1 doing????

V1 is NOT just a big gabor filter.

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Macaques &#160;(pron muh KACKS) &#160;&#160;v1, v2 and v4 are all retinotopic.

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KEY slide: &#160;&#160;<b>1 mm2 of V1 &#160;is say about 2mm thick</b> and&#160;

has about 100,000 neurons per mm3 &#160;but

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it gets only about <b>800 parvo axons from LGN</b>.

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that is <b>400 from EACH EYE </b> ; &#160;divide that by TWO (a pair of one each of ON cell and OFF cell)

so get 200 nodes or pixels per mm2 of V1 = &#160;or about a 14 by 14 pixel array from retina

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So, &#160;<b>200 pixels are being processed by hundreds of thousands of neurons.</b>

Question: &#160;what is that circuitry doing?

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The STANDARD MODEL (the hubel and wiesel model) is that gabor is convolved with the input.

but it is not this simple

most neurons are NOT firing.

he discusses 5 biases in gathering V1 (or other data)

1) the neurosci &#160;only gather data from neurons that are briskly firing... ignore the others

2) &#160;they use only biased stimuli... &#160;just looking for what works really well

30 artif testing conditions... not natural vision. &#160;etc.

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mean firing rate in mammals of neurons is about one hertz... once per second.

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so, standard model is a biased theory... self-fulfilling prophecy.

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again, look at V1.... &#160;<b>only 5% of input is from LGN</b>... &#160;the other 95% is from other cortical neurons.

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