Lecture � Neurosciences II

@5 on Thursday, 04 May, 2000

 

gratings of decreasing periodicity � fall-off in contrast sensitivity at very high and very low frequency. between = window of visibility. at the very highest frequency, the spaces seem to get bigger again

 

contrast � white board rubber against blackboard � fraction of reflected light (remains the same under different overall luminosities, giving similar contrast under different light conditions)

 

mosaic of receptors in the Macaque monkey

 

focussing

pupil size � decrease in pupil size �/span> contrast sensitivity, because cuts out spherical aberration from the optical system

 

dots with overlaid gratings (sinosoidal function) �/span> interference (moir�pattern

failure of the Nyquist sampling limit

why don�t we see such high frequency usually, and see everything in the moir�attern � because the optics/lens blurs the image so that it�s not high enough frequency to give rise to that pattern. the properties of the optics and the properties of the mosaic are closely matched

 

very narrow peak of cone density function

reflected in the cortex representation of the visual field � a lot of cortex is devoted to 5deg of the visual angle (the area of a fist held at arm�s length). we are foveal creatures, we need to point our eyes at something to see it at high resolution

 

Enroth-Cugell and Robson, 1966

 

X-cells � similar to P-cells

grating switched on, with a bright bar in the centre of the cell � high response, levelling slightly below

null phase � grating on: left half bright, right half dark � no response = linear spatial summation

Barlow + Mollen � wrong, suggests that this is due to the centre-surrounds � don�t need centre-surround antagonism to cancel out

cells little contrast meters

 

random little grey + white bars flashing across a black background

reverse correlation � listen for when an AP occurs, then look back to when a stimulus occurred

green circle surrounded by doughnut of red, then mutates into red circle

after the stimulus, get a response; when you then take the stimulus away, you get an opposite response

bi-phasic response

 

dancing spots + gratings � totally different methods, give convergent responses

 

take a picture, and flash it across in different positions of the receptive field of the same neuron (in the LGN)

this isn�t a representation of what the brain sees � it�s a representation of what the cell does

the linearity of the firing rate of the cells is related to the fact that we can predict (from arbitrary stimuli) of how the cell is going to respond

criterion of linearity = powerful model

 

Henry Fox-Talbot

rustic barn etc. exhibition on the history of photography

 

in the fovea, P-cells = 95% of the ganglion cells

 

visual receptive fields touch, leaving no gaps

 

 

Parvo + Magno divisions of the LGN � only partly true

assert that you can associate particular functions with the magno and parvo layers of the LGN, asociated cortically with �what� and �where� system

magno are much more sensitive to contrast than the parvo

if you lesion an animal�s magno or parvo cellular layer (can do cleanly/selectively with hibertinic acid???)

parvos make up for their weakness in contrast sensitivity in numbers

isn�t really true that black and white high contrast goes through the magno � need to take into account population, not just individual cells� physiology

Merrigan & Maunsell � measured spatial acuity as a function of eccentricity. knocked out the parvo layers of the LGN, and noticeable supression of the acuity there

if knock out the parvo-cellular layers with acrilimide -