"Wil Hadden" <(E-Mail Removed)> wrote in message news:<(E-Mail Removed)>...
>
> Excellent, I've had a look at a website detailing Harline's work and it states that
> lateral inhibition is only used for edge detection, though I know it's also used for
> motion detection.
>
> Is that all it's used for or are there other applications.
>
> My research since that posting has pointed me at Adaptive Resonance Theory, which looks to
> formalise an implemntation of lateral inhibition in a biologocally plausable manner.
>
> Can someone remind me of the method which is basically the same as ART 1 and ART 2 put
> together? I can't remember it off the top of my head.
>
> Wil
Hi Wil, I just happened upon this thread. Here are some thoughts and
suggestions .....
1 - take a look at Werblin's site. He got his PhD with John Dowling,
and was the first to record intracellularly from all cell types in the
retina. He's spent the intervening years trying to work out the
details of interactions between various cell types. He has some
"retina movies" - [always a showman].
http://mcb.berkeley.edu/faculty/NEU/werblinf.html
http://mcb.berkeley.edu/labs/werblin/RetinaVideos.htm
2 - regards how horizontal interactions within the retina affect
sensitivity, take a look at old papers by Werblin and Larry Thibos -
about 1977-ish [???]. Lateral inhibition from horizontal cells to
bipolars and back to photoreceptors is responsible for both adjusting
gain/sensitivity, and also for forming the center-surround receptive
fields of bipolar cells.
3 - regards why the vertebrate retina is "upside-down", IIRC, it's
possibly because ... of all cells in the retina, the photoreceptors
have the most severe metabolic requirements and are adjacent to tissue
that can help nourish them. But you might check this. Even so, tiny
cells are basically transparent, so their being physically located
between the cornea and photoreceptors is not as important as one might
imagine.
4 - old ideas were that the amacrine cells were highly
motion-sensitive [Werblin again] and factored into the responses of
motion-detection outputs from the retina. IIRC, Barlow and Levick
[1950s or 60s or so] had a model for for how motion-oriented cells in
rabbit retina might work - basically time-dependent feedforward
signals in the amacrine cell layer.
5 - you might also be interested in one of the all-time great
classical papers about retinal and tectal cell responses - "What the
Frog's Eye Tells the Frog's Brain":
http://www.ai.mit.edu/people/phw/6xxx/lettvin.html
- hope this helps a little ....