Lec 1-5 Flashcards

1
Q

What is neuroanatomy key points
What different things can we do to help us

A

Various staining and labelling used to reveal groups of anatomically similar neurons. Connections made between individual neruson and the aim is to build a wiring diagram.

  • neuroanatomy, neurophysiology, psychophysics, imaging techniques, cognitive neurophysiology, computational approach.
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2
Q

Describe neuroanatomy, neurophysiology and psychophysics

A

Neuroanatomy- various different staining- similar neurons, wiring diagram

Neurophysiology single cell recordings- cell activity recorded by placing tip of microelectrode close to cell. RGCs respond to appropriate stimulation with action potentials and series of them= spike potential. More rapid spiking more vigorous the response. Cell stimulated and then recorded by microelectrodess determine special action of it.
-experimental ablation-destroying animals brain assess it
-stimulating or inhibiting neural activity- electrical and chemical stimulation of brain to investigate parts of brain on certain behaviours. Eg microoelectrodes can be used current to neuron and experimenter uses psychophysics to see what affects this has.

Psychophysics- non invasive uses behavioural responses to assess how visual stimuli being processed. Responses quantifiable.

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3
Q

Imaging techniques, cognitive neurophysiology and computational approach

A

Imaging techniques- neurophysiology, pet, mri, fair, meg, optical aiming used to show which regions of brain activated by different kinds of stimuli. Optical imaging- pictures of eyes optics.

Cognitive neurophysiology- closed head injury- individuals w brain damage case studies can provide important clues to way brain is structured.

Computational- aims to understand vision by building computer models of visual system. Performance of model compared w psychophysical or neurophysiological data. Not confused w machine vision, both artificial vision system but machine vision no intention of mimicking mammalian vision and cold be several designs for the same goal.

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4
Q

Some of the weird questions and answers

A

Computational approach- dont help under and how robots see this is machine vision.

If an investigator wished to find the slowest speed detected by human visual system whats old be appropriate investigative technique.
Visual psychophysics as detection tasks are simple with it.

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5
Q

Explain the pond analogy in regards to
The distal stimulus
Proximal stimulus
Perception
Computational theory

And what happens to light intensities when hits our receptors and what is processed.

A

Detection, the waves arrive, localisation is when something dropped in, recognition dont really know. Pond analogy

-distal stimulus- physical thing out there in the world- the object dropped in water.
-Proximal stimulus- impression that distal stimulus makes on our sense organs so the pattern of the ripples you see in the waves.
-Perception- our conscious visual experience, our brain analyses the proximal stimulus to work out the distal stimulus- work out smth has been dropped.

-Computational theory= generating a formal understanding of the relationship between the distal and proximal stimulus. We need to understand mapping.

light intensities hit our receptors which transmits a signal, visual cognition leads to our perception. Colour, motion is all being processed, the retinal image also requires interpretation.

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6
Q

Explain bottom up and top down. With analogies.
Also talk about ambiguous figures with an analogy

A

Vision is an active process to make sense of the proximal stimulus:
Bottom up- data driven or descriptive, concerned w description of the proximal image so starts with the retinal image and tries to make sense of it so extracts information from the proximal stimulus and uses it.

Top down- knowledge based or concept driven, using our prior knowledge
(jigsaw analogy- if you look at the box to see where its going then this is top down as knowledge based, if you put similar things together and use shapes and colour this is a bottom up strategy where you are using the description of the proximal image so that’s bottom up)

Bottom up processes build representations that provide cues allowing us to generate a hypothesis that accounts for the data. The final percept is the most successful hypothesis. Some pics the bottom up cues can be the same w 2 different intepretions each is valid so the visual system can flip between the two and we can get the data to fit to either so we can flip back and fourth between them very easily= ambiguous figures when more than one equally good hypothesis fits the data eg necker cube.

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7
Q

Describe hidden figures and accidental assumptions and an analogy
And size constancy

Eg of geometric illusion cues leading to wrong illusion

Sensation and perception

A

Sometimes when we see lots of things it’s because the system doesnt know theres anything meaningful to search for= hidden figure which is when the cues are reduced so the hypothesis is hard to generate. Once we see it its easy to process as visual system is equipped with info on how to make sense of it and uses top down knowledge-> hypothesis. Top down processes stay w us for life= power of memory.

Penroses impossible triangle- assumptions can lead to mistakes. Accidental alignment so where we see a triangle that doesn’t exist in the real world, only on the back of our eye.

size constancy- as an object moves further away from an observer its retinal image gets smaller yet the object appears further away rather than smaller this is due to depth cues eg texture gradients, perspective, motion parallax= visual scene is depth not flat. the visual system uses these cues to scale up the image size with supposed distance to produce perceived size.

Geometric illusions where cues lead to the wrong illusion eg ponzo illusion.

Sensation and perception- study of sensation= encoding basic parameters eg brightness contrast and motion. Perception is to do with how the visual world acc appears to the observer.

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8
Q

Weird qs-
Which a. b. c. d. e.
of the following is not an example of bottom-up processing?
The responses of retinal receptors.
Data driven processing.
The perception of a regular face when looking at a hollow face stimulus from behind. The Marr and Hildreth edge detector.
Doing a jig-saw while ignoring the picture on the box lid.

A

Response of retinal receptors is
Data driven processing is

Marr and hildreth edge detector is as it refers to computational model that detects edges in visual input staring from basic visual info and building up to representation of edges. Starts with raw data the image and processes it to detect edges. So bottom up.

Doing jigsaw ignoring= not top down so bottom up using shapes to try and figure it out and use data.

Perception of regular face when looking at hollow face stimulus from behind- hollow or concave face you often see it as a normal convex face as your brain often expects faces to be convex so this uses top down processes. So we see inside out face but it looks like regular face as your brain normally knows faces are regular so it changes what you see to match this explanation. Brains expectations making you see something different. Top down

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9
Q

Top down processing is the motivating force behind the work of David marr?

What is the Dalmatian dog figure and what is the rat man figure and why in the question ‘in research on perception what is an ambiguous figure’ is it not exemplified by these thigns

A

David marrs work involved understanding computational principles which led to visual perception.
Designed 3 layer framework comp approach etc.

Ratman- ambigious figure= rat or man
Dalmation= dog or shapes abstract ones= amb figure
Though both examples of amb figures and exemplified by perception the q asks for a definition of ambigious figures so read the question carefully. These don’t answer the q eventhough they’re right.

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10
Q

In size constancy when do objects appear to be the same size

A

Objects appear to be the same size when they are physically the same size

Its not about retinal image sizes it’s about distance or angle you view them from. Process of elimination see if any mean the same thing and eliminate them.

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11
Q

The perceived size of a retinal afterimage is larger when viewing a distance surface than a near surace bc of

 what is it not affected by	

When does the acc size of retinal afterimage change

A

Perceived size of retinal afterimage larger distance due to size constancy.

Not affected by distance of the surface against which it is viewed.

Acc size of retinal afterimage changes only when the physical size of the adapting stimulus is changed.

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12
Q

Explain shepherds table and the exam question

A

Visual trick that makes 2 identical tables look different in size.
Longer one appears bigger though both tables re same size.

We learn that the visual system is not able to read off the content of the retinal image.

(Two table tops diff sizes on retina but look same= no as not diff sizes on retina)
(Tables perceived to be diff distances from us when not= no appear to look the same)
Length or legs are removed-no tis the drawing and the entire table

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13
Q

Visible light,
What are EM signals and what are they measured in
What does a variation in wavelengths lead to
What is saturation
What is the amplitude of it

Why aren’t we sensitive to a narrow range of the EM spectrum.

What does em consist of, why sensitive to them, why sensitive to visible part

A

visible light is part of the EM.
Em signals are oscillations measured in wavelengths. Variation in wavelengths leads to a variation in hue. Saturation= purity of colour.
Amplitude of it= intensity and brightness of colour.

Em spectrum consists of a range of signals that travel at a wide variety of speeds. Sensitive to them as they reflect back from physical surfaces. And visible part of it is visible as that is where signals have the greatest amplitude.

Why are we sensitive to a narrow range of the EM spectrum- we can’t be sensitive to all light, filtered out so we are left with narrow bandwidth. Light not coloured- subjective experience.

Rating Martians invaded Venus using x ray guns

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14
Q

Wiring of the retina
Describe how receptor cells hyperpolarise
Cones rods

Explain purkinje shift

Degrees of the visual angle 18 what do we have

A

Retina- back to front. Travels through eyes optics before forming an inverted image on retina. And then everted.

Receptor cells in retina react to light and hyperpolarise in response to amount of light they receive.

Cones- colour vision best bright light, 3 types. Predominate the central fovea 0.5mm. No blue cones in fovea and blue cones are only 10 percent of cone population. Cones most sensitive to 550nm yellow

Rods= low light scotopic conditions more abundant in retinal periphery absent in fovea. Rods more sensitive to blue or green 500nm.

Cones= yellow 550. Rods blue green 500nm. Day yellow objects appear lighter and green objects appear lighter at night= purkinje shift with shift in peak of spectral sensitivity with light levels.

18 degrees of visual angle= optic disc= lack of receptors blind spot. Each eyes is on the nasal side of retina so dont overlap no loss in vision.

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15
Q

Neural circuitry in the retina- graded potentials
Where do rgcs receive their inputs from one or lots recept
Transduction

A

as light increases, graded potentials decrease but at bipolar cells voltage output increases and the retinal ganglion cells are the output stage which sends the signals to brain via optic nerve.
They work via action potentials good for long distance. Retinal ganglion cells receive inputs from several receptors via interneurons (horizontal bipolar and a machine cells) this is known as convergence= optic disc can remain fairly small.

Transduction- we start off with light as an em wave which is transferred to a signal which is a graded voltage then we get image formation on the retina and light absorption by photo pigment and then electrical current in receptor and then neural activity in RGCs and then we have to relay neural impulses to the brain. Graded not as good over long distances.

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16
Q

Rods cones-
Sensitivity to light wavelengths
Metamers
Cones per retina and rods per retina

A

as they have diff sensitivity to light so wide range. When light increases above a certain point rods are bleached and are no longer active but cones can work in these conditions. Cones are selective to diff wavelengths= thousands of colours. We can discriminate colour.

Metamers= physically diff but look identical eg pure yellow and a mix of red and green. As cone types increase less metamers as you can distinguish more colours as if they are physically different they wont look identical so less of these.

Colour deficiency. Rods- do not support colour vision.
More rods nasally than temporally. If we had more temporally we would be able to see our nose.
Cones per retina= 8 million. Rods per retina= 120 million.

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17
Q

Convergence in the retina and why
Explain neural adaptation due to fatigue
Excitatory vs inhibitory response
Visual neurons vs collection of cells
RGCs how do they transmit information and what do they consist of

What is the retinal output and how does the image get to that

A

in retina- optic nerve only has around 1 million fibres but 100 times as many receptors. Rods have high sensitivity low spatial resolution. Higher convergence means its more sensitive to light so receives sm but cant really distinguish between them as well so has a lower spatial resolution.

If you stare at a white spot in black background-> blank paper= black spot due to neural adaptation due to fatigue of these same cells being stimulated over and over and then when they’re not stimulated the firing rates of opposite neurons increases. Smaller size as perception scales down image size eventhough retinal image size same

some response are excitatory others.
Visual neurons have single rf and one response at any one time but a whole collection of cells will have rfs in many different positions producing a spatially distributed pattern of responses.

Image goes through transduction and transformation. The retinal output= neural image.

Retinal ganglion cells transmit info as action potentials higher spike higher stimulus or intensity.
Retinal ganglion cells consist of two concentric subregions called on and off regions sometimes called excitatory and inhibitory regions positive and negative.

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18
Q

RGCs steady state response and increase daycares

A

We find receptive fields throughout vision, they are the region on the retina that when stimulated causes a change a cells response and it either increases or decreases.
Retinal ganglion cells in the retina in the absence of stimulation or under uniform stimulation release spontaneous discharge or background firing rate so certain types cause an increase and others a decrease.

A retinal ganglion cell’s steady state response will increase if light is introduced into its excitatory sub region. And it will also increase if darkness is introduced into its inhibitory subregion as the contribution from the inhibitory region is being reduced. When light is introduced into the cells inhibitory subregion the response decreases bc of its inhibitory influence. A cells response will also decrease is darkness is introduced into its excitatory subregion as the excitatory influence is being reduced.

In general a rgcs response is determined by the algebraic summation of excitatory and inhibitory influences within its receptive field. Bc this summation is additive the cells are said to be linear. To a first approximation the weights of the excitatory and inhibitory regions are equal and this means that if they receive an equal stimulation they will cancel each other out and the response of the cell will be equal to spontaneous discharge.

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19
Q

Rf of a RGC what did they do and what did they find

A

stimulated retina w uniform light to see how they change their responses and they found dimmer increased it but no matter how much light shone into eye the response didnt change they still got continuous spontaneous discharge.

Then removed the light so put it in darkness. Came ot realise that each cell has a small circular region that when stimulated will change the response.

This region was split into two areas- on centre cell (if light shone into centre then cells response went up but if shone into surrounding region went down) and off centre. So they mapped out rfs of each cell and found that if light is shone outside them regions it made no change to cells response at all.

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20
Q

More info
Mexican hat

A

Roughly equal number of on and off centre cells
Some rgcs receive inputs from several receptors

If a bright light is shone into centre of on centre cell= sudden increase in the cells firing rate followed by a gentle decline to a stable level which is higher than the initial response level. This stabilised response level is called the steady-state response. Stimulating excitatory region with light= positive contribution. Stimulating inhibitory region with light= negative contribution to cells output. So a retinal ganglion cells steady state response will increase if light is introduced into its excitatory sub region. A cells response will also decrease if darkness is introduced into a cell’s excitatory subregion as the excitatory influence is being reduced.

Rgcs response= summation of excitatory and inhibitory influences within its rf. bc this summation is additive the cells are said to be linear. To first approximation the excitatory and inhibitory regions are equal so if they receive equal stimulation they cancel each other out and the response of the cell is equal to spontaneous discharge.

The shape of the receptive field looks like a Mexican hat-
narrow but tall centre and the rim is broader but more shallow: total volume of surround eventhough spread over larger area matches the value of the centre which is smaller but taller. This is why there is no net response to diffuse illumination as its cancelled by the inhibitory surround so left w spontaneous discharge. Retinal field size increases with retinal eccentricity. Periphery convergence decreases so we have inputs from many more cons and rods so this is why receptive field size increases with eccentricity.

Diagram the spike trains- plots cells responses as spike trains for 3 different stimuli. Small spot is initially strong response and then levels out and diminishes when stimulus is removed going back to spontaneous discharge. Steady state response after big stimuli presented so response still higher than spontaneous discharge.

Cells response:
light spot in excitatory region- increases + +
dark spot in excitatory- decreases. - +
light spot in inhibitory- decreases + -
dark spot in inhibitory- increases - -
response goes up and down relative to the background firing rate

diagrams with the circles
the spatial arrangement of neighbouring positive and negative regions in a cells rf gives it some interesting properties. RGCs will respond differently from its background firing rate only if there is a d change in luminance eg an edge somewhere within its receptive field.

This diagram shows the steady state response or fitting rates of spatial arrays of neighbouring on centre (middle) and off centre (bottom) rgcs to a light dark luminance border (top) sometimes called a step edge. The responses are shown as a function of the position of the centre of each cells rf so as we move from left to right in the middle and bottom panels of the image we are looking at the response of cells whose rfs are positioned increasingly to the right. The horizontal lines show spontaneous discharge so the firing rate in response to uniform luminance sometimes called background firing rate. The lobes above and below the Laine indicates responses tht are higher and lower than spontaneous discharge.
WHY: this pattern of responses come about consider on centre cells

for those that are positioned so that their whole rf is stimulated by the light region (to the far left) both the on and off regions receive similar input so their contributions will cancel each other out and the cells response will be spontaneous discharge.
Again for cells whose rfs are placed entirely in the dark region so those positioned to the right so neither the on or off regions receive no input so neither on or off is stimulated so neither contribute to cells response and again result is spontaneous discharge
Now for a cell whose rf falls halfway across the light or dark border the on and off regions receive the sa,e amount of light so again same
when a cells rf is just to the left of the border means excitatory centre fully stimulated but inhibitory surround receive less stimulation so contribution from centre is no longer cancelled out by the contribution from the surround and the cells response is greater than spontaneous discharge.
Now if cell is to right of luminance border net decreased less than spontaneous discharge as more darkness in excitatory region and more light in inhibitory region.

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21
Q

Why does this make sense and convolution kernels
Step edge

A

This makes sense as edges provide important info about objects in the world so we must only transmit info about the edges rather than info to the side of the edges to reduce amount of data being transmitted- data compression so reduces the amount of work that has to be done.

We say the pattern of response in the figure is what we get when we convolve the input pattern or the stimulus with a receptive field. In image processing and machine vision rfs are sometimes called convolution kernels as they help us to convolve the stimulus.

Step edge is a step in the luminance profile. Entire retina covered in rfs and there is also an overlap of fields.

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22
Q

Convolution again
What does convolution do to the image
What is the convolution kernel
What is the output

A

This process is convolution= transforms the retinal image to neural image.

There is a convolution kernel at each location we are calculating a response of rf. this calculates responses and firing. Mathematical process occurs to take rfs and apply each case along various locations of images. Converts inputs to outputs. Rf= convolution kernel.

And output is the distribution of responses across space as a result of convolution.

Convolve a stimulus with this rf convolution kernel to produce this output. The response is sent from the eye to the brain and convolution transforms retinal image into neural image and the transformation achieves data compression giving us relevant data of where light is present giving us good info about the step edge. Concentrates it around feature of interest rather than lots of info about spontaneous discharge.

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23
Q

Different types of centre surround cells
Monkeys have p and m. Differences.
Cats= x and y

What are m and p cells and what are differences

A

M cells project forward to the LGN connecting to magnocellular cells.
P cells project forward to LGN conn parvocellular

M cells- transitory- large cell bodies, thick axons, fast conductance, large rfs, sensitive to fast flicker motion, insensitive to wavelength so not colour, few in fovea, high contrast sensitivity. 10 percent of total.

P cells- sustained response- small cell bodies, thin axons, slow conductance, small rfs, insensitive to fast flicker so motion, sensitive to wavelengths so colour, many in fovea, low contrast sensitivity. 80 percent of total.

M cells unselective for wavelength providing an achromatic truly colour blind channel. They receive input from all 3 cone classes but colour blind? This means that the response of the cell will be the same for red green or blue spots on a black background so the cell cannot distinguish between their colours so colour blind.

P cells respond to achromatic stimuli as well as white light contains a mixture of red green and blue wavelengths of light.

Magnocellular cells- achromatic
parvocellular cells- respond to colour and achromatic

24
Q

Opponent colour coding

A

So far we have considered achromatic (black and white) properties of rgcs. But in primates P cells are also sensitive to wavelength which means colours. For both on and off there are four different types. Here we only consider on centre cells:
On red centre and off green surround (most responsive to red light in centre of their rf and are inhibited by green light in the surrounding area)
On green centre and off red surround (most responsive to green in centre of rf and inhibited by red light in surrounding area)
On blue centre and off yellow surround (most responsive blue inhibited yello)
On yellow centre and off blue yellow surround (opposite)

Cells form two opponent systems: red/green and blue/yellow. When oen colour is present in centre of rd its opponent colour in the surrounding area inhibits the cell’s response.
Yellow contribution in blue/yellow weird as there are no dedicated yellow cones in the retina, instead perception of yellow is achieved by combining inputs from red and green cones. When both red and green cones are stimulated simultaneously they signal the presence of yellow to the brain.

-For on green centre and off red surround= red cones feed inhibitory surround and centre is fed by green cones. No input from blue cones for red green rgc.
-Blue on centre yellow surround- centre is fed by blue cones and surround is selective for yellow but we have no yellow selective cones in the eye but red and green make yellow so this is an output of the red and green cones in equal or similar numbers which makes up the yellow selectivity in this case for the surround.

If the question is asking about how a cell responds to a stimulus- think about the centre and the surround not about how the cone responds.

We have both on centre and off centre versions of each cell so with red surround or red centre and same for green blue yellow so 4 of these come in on and off so times 2= 8 colour selective cells.
Magnocellular and parvocellular cells= 10 types
red and green more than blue and yellow remember far fewer blue cones than red and green, parvocellular routine carries red and green. K cells carry blue and green.

Response of a cell with rf on the left and stimulus on right- either goes up, down or same so stays at spontaneous discharge= null response

-Green on-centre cell- most responsive to green light in the centre of its rf, when exposed to white stimulus in the center which contains all wavelengths of light including green the green on centre cell is excited by the presence of green light.
-red surround- Red would provide an inhibitor to the cells response but in this case the surround is black meaning there is no light present to activate the red sensitive cells in the surround therefore there is no inhibitory signal coming from the surround. The green on centre cells response is not inhibited by the red surround. The centre is illuminated with green light so the on centres cell’s response is heightened and the cell receives the green light it wants in the excitatory region of its rf and there is no inhibition from the surround. So response= positive. Increase.

both of these, the responses will cancel out. Centre being stimulated the same in the first one which is cancelled by surround. Second one- centre being inhibited and surround being inhibited as well. So null responses for both.
Wavelength selective cells do not like colour contrast, it requires a difference in luminance contrast to increase or decrease levels of response. This here is uniform illumination.

red in excitatory centre and no green in the inhibitory to inhibit the response. So the on centre will be stimulated as it wants red. But the green wont be as the stimulus is red= difference in luminance contrast. And here the response goes up.

Colour opponent cells respond well to achromatic luminance contrast but they have interesting response properties for colour stimuli.

25
Q

Is the visible part of the em spectrum the part which waves are coloured

Why is it visible

(All reasons its not visible)

A

Waves are not coloured, light isnt coloured in em spectrum it is a subjective experience.

It is visible because that is where signals have the greatest amplitude.

Not bc:
Its the part for which waves are coloured
Visible bc passes through atmosphere
Same as radio 3 apart from wavelengths
Oscillates faster than any other part

26
Q

In vision convolution

A

Is carried out by retinal ganglion cells. Rfs
Involves transforming an image
Doesn’t require a silicon based computer
Not a method of comparing retinal image w object in mem
And not carried out by real position cells

Image has been transduced and transformed into neural image

Rgcs= luminance boundaries or step edge not orientation of them. Thats more simple complex etc.

27
Q

Visual neurons sensitivity to dim light improved if
What is a receptive field

A

Rod to cone ratio of inputs were increased, higher convergence more rf signals so more sensitive.
- rods more sensitive increases in dim light

Not if inhibitory region of rf made larger as less sens. Or not if rf made smaller as this would improve sf and fine detail but not necessarily sens to dim light.
If max firing rate of spont discharge increased yes could improve neuron response but not directly dim sens.
If it’s input from cones or rods removed- cant detect light under normal or low lighting doesnt affect more sens.
Or if receptors selective for greater no of wavelengths of light- more colour vision discrim but for more sens we need more rods more scotopic vision.

Rf= the region on the retina that when appropriately stimulated changes a cells response.

28
Q

Primary visual pathway
Lessers pathways are to what. What are these structures involved with.

A

Primary visual pathway= Lesser pathways are to the superior colliculus (mid-brain) and the pulvinar (thalamus). These structures evolved earlier than the visual cortex and involved w more primitive tasks eg attention and control of eye movements so getting visual system to respond to stimuli. pulvinar receives input from the retina.

LGN and several cortical regions with which its connected. Pulvinar involved in distinguishing between retinal motions that arise from object motion in the external environment and eye movements so involved in aspects of processing visual motion.
What is focused on the fovea appears stable and pulvinar is important in deciding which motion we see.

29
Q

Primary visual pathway- arrangement of optic chiasm and optic tract.

Axons from LGN go where?

A

primary visual pathway- arrangement of optic chiasm and optic tract means each visual hemifield projects to the contralateral hemisphere. Half fibres cross over other half dont. About 90 percent of the retinal output contributes to this pathway.

Left side of the brain takes in temporal retinal information from LE and nasal retinal info from the RE. Ie left hemisphere sees right visual field and right hemisphere sees left visual field. Each hemisphere is sensitive to visual info in the contralateral visual hemifield only. Used to be thought that all the axons leaving the LGN were destined for visual cortex in striate cortex but recently indicates a very small projection to V2 prestriate cortex and another cortical area called MT.

30
Q

LGN facts about it
Layers which layers receive input from what
How much input to lgn is from the retina

Do cells rf alternate but where view in vf?

A

6 layers. Top 4= input from parvo. Bottom 2= mango.
Intermediate layers= koniocellular cells
3 layers per eye

10 percent of input to LGN from retina= but still primary driver of the lgn.
60 percent of input to lgn is from cortex.
30 percent other areas.

Alternating arrangement of inputs from two eyes so sequence of reversals crucial for BV and depth perception. Single unified perception.

So cells rfs alternate but each cell views a similar position within the vf.

31
Q

Bit more info ab lgn
K cells

What colour opponents found in parvo/koniocellular cells
Receptive fields- more variable where

Functional properties of lgn
Purpose of lgn

A

Left lgn receives info from right vf. Each layer stack of 42 neural images. 3 layers a,b,c. 2 further layers alpha beta

Koniocellular cells receive input from retinal k cells and similar in number to magnocellular cells found between other layers.

Functional properties of LGN cells very similar to rgcs eg colour opponent found in parvocellular red/green and koniocellular blue/yellow layers.

However rf size is more variable in the LGN than in the retina.

Purpose of the LGN- relay station between retina and cortex.. but doesnt really need a signal boost at halfway stage as the transmission distance is long to require signals carried by action potentials not graded potentials but not that long. Its bc it would be difficult to have this in the retina as this would increase size of optic nerve and blind spot .

32
Q

Retinotopic mapping and more info. Lower visual areas eg v1 vs cortical areas.

Magnocellular and parvo pathway. What is problem

A

Retinotopic mapping in lower visual areas eg V1 neurons are organised in more orderly fashion= topographic or retinotopic mapping
organized in a sense that they form 2d representation of visual image formed on retina in such a way that neighbouring regions of image are represented by neighbouring regions of visual area.
However, retinotopic representation in cortical areas is distorted- foveal area is represented by relatively larger area in V1 than the peripheral areas.

From LGN- geniculostriate pathway projects via optic radiation to layer 4c of primary visual cortex also called striate cortex. Projection to V1 such hat the cortical image remains top-bottom transposed the left visual field projects to right= contralateral projection. A small central region of the vf projects to both hemispheres and the fovea projects to more posterior regions of cortex.

Magnocellular pathway in layer 4c alpha. Parvocellular in 4c beta
only one synapse between output of retina and input to cortex
contralateral projection. And inversion of neural image doesn’t present a problem for visual system. Problem is getting everything to register with each other in the system.

33
Q

In primary visual pathway talk about no of synaptic sites
V1 and lgnfeedback

A

In primary visual pathway, number of synaptic sites between but not including the retina and initial cortical destination is 1.

V1 to lgn there is some feedback. So minor output from v1 is feedback to retina.

34
Q

What does the retina do,

What do microelectrodes do and what is autoradiography

A

Retina= transduces and transforms and a consequence of this is the retina emphasises luminance boundaries. Retina multiplexes luminance contrast and colour.

Microelectrodes are used to record responses of individual neurons to different visual stimuli.

Autoradiography- injecting substance of radioactive material and transmits into cortex and slice is taken which is pressed up against photographic plate so we are taking a photo of the radioactive parts of the brain responding to stimulus. They presented stimulus to pxs with varying stimulus parameters of bears edges gratings.

35
Q

Layers of the primary visual cortex and magno parvo.

Describe V1 (primary visual cortex) first cortical area baso
How is it mapped

A

Primary visual cortex is split into 6 main layers. 1-3= superficial and 5 and 6 are deep. Most of the input to the primary visual cortex arrives in layer 4c. The magnoceullar pathway terminates in layer 4ca and the parvo in 4cb.

V1 is retinotopically mapped, the spatial ordering of the retina is preserved in the projection to the cortex, though the map is grossly distorted bc the central region of the retina-the fovea- projects to a disproportionately large region of the cortex.

V1 (the primary visual cortex) is retinotopically mapped, meaning it maintains a direct, spatial correspondence with the retina. Each point on the retina maps to a specific point in V1, preserving the layout of the visual scene. The left visual field is processed in the right V1, and the right visual field is processed in the left V1. The fovea (center of vision) has a larger representation in V1, and the mapping keeps the inverted and reversed nature of the retinal image.

36
Q

3 cells in v1- describe them

A

simple cells- rfs discreet, excitatory inhibitory regions but unlike those in retina and lgn these regions are elongated. Preferred stimulus is light vertical bar on a dark background. Selective for orientations, size sf, and position within rf so phase.display little or no maintained discharge in the absence of stimulation but respond to appropriately placed stimulus eg elongated vertical bar. Simple cell response= predicted by amount of light that falls into on and off regions. Selective to orientation and within rf.

Complex cells- have rfs that are not on or off regions, non linear. Respond best to flickering or moving stimuli, have preferred orientations and size like simple but not so specific location for stimulus position so shape within the rf. contours of a particular orientation. Drifting bars= complex cels respond in the same way as they are indifferent to location.

End-stopped/ hypercomplex cell- prefer bars or edges that end within their rf. end stopping is found amongst both simple and complex cells. Similar to complex cells but have inhibitory end stoping on them. Property of all cells but its weak sometimes and stronger in some cases. Cares about orientation. Dont respond to contours that extend behind their receptive field as well. They have to fit within their rf and they care about orientation.

37
Q

describe a columnar organisation of cells in v1

Are all the cortical cells in each column perpendicular or parallel to cortical surface and what do they do
What can hypercolumns response be used to do

A

Most cells in v1= orientation selective.

Columnar organisation for stimulus organisation. All the cortical cells have overlapping rfs and preferred orientations. Each complete set of columns- orientation hypercolumns. So recording from different orientation= different columnar orientation. Each columnar orientation records from different orientations but overlapping rf so

its. a group of cells that process different contour orientations in similar positions in the vf.

Columnar orientation- this column of cells is vertical so different columns prefer different oritentations. But when looking at one column all them rfs in neighbouring cells have overlapping rfs so we are looking at the same part in the visual field.

all cortical cells in each column are perpendicular to cortical surface but have overlapping rfs and similar preferred orientation= hypercol
hypercolumn of cells analyses all orientations at a single location in the vf and the population response of this could be used to code orientation.

38
Q

What does v1 ultimately end up in from retina to lgn v1 and beyond v1

A

Retina lgn is spots edges and bars
V1 simple- orientated edges and bars
V1 complex- orientated edges and bars but not location
V1 end stopped- corner detectors. Orientated edges and bars and location within rf.
beyond v1- “Grandmother detectors” are a theoretical concept suggesting that some neurons respond only to specific, complex stimuli, like the face of your grandmother. This idea implies that certain neurons specialize in recognizing very detailed patterns. However, recognition of complex stimuli is more likely to involve networks of neurons rather than single cells.

39
Q

Do single rfs respond the same to all contrasts or differently-
Does this mean cortical cells are feature detectors

How can we check this

A

Single rf responds to medium contrast at preferred orientation to get medium response. Medium contrast diff orientation= weak response. High contrast diff orientation= medium response.

Cortical cells are selective for orientation of contours edges and bars. Cortical cells are not orientation detectors- not feature detectors bc cant distinguish between responses to see what their preferred orientation was the only thing is that they respond to them.

If we inserted microelectrodes in and took readings to determine preferred orientation we would find cues have same preferred orientation. If it gets the same response in each case it cannot be a feature detector

40
Q

Explain the tilt after effect

Describe blob cells vs single opponent

A

adapt to an orientation for a minute or two and gaze at vertical lines they dont look vertical but look tilted away from orientation of adaptor. Adapt to specific stimulus after the line appears to be tilted in the opposite direction to the original stimulus bc of fatigue of them orientations cells.

cells- and in between interblob cells
blobs= double opponent cells colour selective cells. Example double opponent rf= red green centre excited by red and inhib by green or surround green centre red. Blob cells are found in the centre of ocular dominance columns. Colour contrast.

Single opponent cells good for uniform colour
double likes colour contrast

41
Q

Describe the retinotopic mapping of v1 once again

A

V1 is retinotopically mapped
spatial ordering of retina is preserved eventhough map is grossly distorted as fovea protects to large region of cortex.
In each region 125 000 cells w rf at roughly same retinal position and all of these cells analyse one small region of the world.

42
Q

Eye- ocular dominance columns how were they revealed
Autoradiography explain it again
What has single cell recordings revealed

A

ocular dominance columns revealed using autoradiography

One method= injecting radioactive marker into only one eye and this produces a pattern in the cortex describing cortical arrangements of those cells fed predominantly by one eye.
Image with stripes shows ocular dominance columns in monkey v1 reconstructed from tangential slice through primary visual cortex cortical sections.
Dark bands= anatomical arrangement of neighbouring ocular dominance columns with neighbouring hyperfields(diff areas they examine)

single cell recordings have revealed many cells are binocular eventhough one eye dominates. (So input from one eye mainly and rfs within those areas overlap and we find further subdivision into ocular dominance columns confirmed by single cell recordings)
This confirms it.

43
Q

Cortical cells what are they stained by and what does this reveal

Do they need luminance contrast for blobs to work. Difference between blobs and rgcs.

Can you construct double opponent cells by adding two single opponents together

A

cortical cells are stained for the enzyme cytochrome oxidase which reveal blob cells at the centre of these ocular dominance columns.

Single cell recordings= blobs are specialised for colours (double opponent cells blobs) red/green or blue/yellow and low sfs.
Some evidence that orientation selectivity for them isnt rlly present

wavelength selectivity for blobs is different from opponent cells found in retina and lgn. blobs respond to colour contrast without need for luminance contrast. Unlike an opponent cell in the rgc they would respond well to red berries on a background of green foliage. Rgc wouldnt as same as red green on off so spontaneous discharge here cancels out but these dont need luminance contrast to work.

cannot construct double opponent bu adding two single opponents

44
Q

Where are some cortical cells that are direction specific mainly found. And what do they do

A

some cortical cells and direction specific they will respond to bar drifting in one direction but not in opposite directions
Mainly found in layers 4 and 6

45
Q

Explain what several complex cells provide input to and what this means

Can simple cells be feature detectors
Do all complex cells derive input from simple cells
Describe the general input pathway

A

Many complex cells provide input to each hyper complex cell, allowing them to detect more complex features like corners. They begin to combine simple features or edges from complex cells and wires them together.

As cells are wired together in this hierarchical manner, they can become highly specialized, even responding to specific images, like a familiar face. So you would eventually arrive at a cell which would only respond to the image of your grandmother so highly specialised.

Simple cells not specific enough for feature detectors= ambigous response.
Not all complex cells derive input from simple cells as some complex cells can respond earlier

Generally- lgn to v1 simple cells complex cells hyper complex cells beyond v1

46
Q

Contemporary or current theories what do they concentrate upon
What does this allow them to do

A

current theories concentrate upon pattern of responses across populations of cells rather than responses of individual detectors.
pattern of responses across all cells in hypercolumn.

Allows them to encode info about position, polarity, size, orientation and contrast of luminance changes in one small region of image.

Low contrast preferred orientation same but then increasing it at non preferred orientation brings cells response back as same.
Given response may indicate optimally orientated is low contrast stimulus optimally orientated or non optimally orientated high contrast stimulus.

47
Q

Another graph- changing stimulus contrast does what do the response and what is this used by

Instead of thinking of cells as individual feature detectors what would we think of them as

A

Another graph shows that changing stimulus contrast alters some aspects of response but some can remain unchanged and can be used to code orientation. This is favoured by tilt afteraeffect. Tilted away.

Adaptation cells are fatigued and after respond less than normal so pattern of response to vertical stimulus is skewed with peaks according for cells that signal orientation away from vertical.

Group them with a range of properties.

48
Q

Does v1 multiplex luminance contrast in which colour code 3 or 4.
And what is the standard london tube map an example of

Are complex cells found in striate cortex or not, what do they respond best to and where

A

V1 multiplexes luminance contrast and pure colour in a 4 colour code.

Standard london tube map is an example of topographic stretching. Gets bigger and bigger just how wiring of brain becomes more and more complex when we try and map it out.

Yes they are striate is just primary visual cortex woman. Complex respond to simple like edges and contours. Respond best to within their fr eventhough indifferent of location. Indiff of location within their fr

49
Q

Is it true that a simple cell with a single excitatory lobe and a single inhibitory lobe cannot be made to respond to a light bar stimulus.

Are orientation hypercolumns observed psychophyscially

A

They can by changing firing rate based on orientation.

No they are studied with neuroimaging or neurophysiology.

50
Q

Most of the cells encountered in a short oblique penetration of an electrode through the visual cortex would have what rfs:

A

Rfs scattered all over ve- no as from same place if in specific locations.
Most responsive to oblique contours- orientation preference of hypercolumns varies.
Be stimulated bc electrode passes through their rfs- not all cells are stimulated.
Respond strongly to same stimulus if moved into their rf- depends on orientation remember diff hypercolumns diff orientation

Have receptive fields with progressively rotated orientation- yes as diff orientations so one electrode penetration goes through many diff columns and if progressively rotates as diff orientations change.

51
Q

Huber and Wiesel injected a radioactive amino acid into one eye of a lab animal and after v1 slices subjected to autoradiography. What did they observe.

Same q but both eyes of a lab animal

A

One eye= alternating stripes of radioactivity and non radioactivity.
One eye there is ocular dominance columns so alternating stripes seen with high and low activity areas later called oc dominance columns.

Is radioactivity seen in only one hemisphere- no iss on the entire primary visual cortex so both hemispheres. Ocular dominance and orientation columns not thick thin stripes. They did observe radioactivity but radio and non radio.

Both eyes= radioactivity of almost all cells in both hemispheres. Widespread activation of neurons in both hemispheres diffuse pattern of radioactivity and more cells show it. When 1 eye injected alternating stripes but both the pattern is more diffuse, radioactivity not in all cells but almost all cells in both hemisphere.

52
Q

Visual neurons in striate cortex of left hemisphere receives input from where

A

visual neurons in the striate cortex of the left hemisphere receive input from both the left and right visual fields. However, the majority of the input comes from the contralateral visual field, meaning the right visual field. The input from the ipsilateral visual field, meaning the left visual field, is relatively smaller but still contributes to the overall visual processing in the left hemisphere.

53
Q

A visual neurons transient response
What isnt right

A

Is the spiking activity found in the initial part of the response train. Characteristic pattern of firing aps in response to stimulus presentation.

Requires stimuli to be presented briefly- no depends
Found only in cells that respond to luminance contours= no all in ret and v1
Is the cells firing rate observed several seconds after onset of provocative stimulus- no can be time after
Is only observed when small spots used as stimuli- no all

54
Q

True and false thing about modular organisation of the visual cortex-
Achromotopsia. What can the acc destruction of the modules in v1 result in what condition

Width of whole module one hypercolumns and what area can they process and do they consist of ocular dominance columns

What do interblobs do

How many modules are there in primate v1

A

There are enough modules in v1 for each one to process a single patchwork of 50 by 50 patches as can process the entire vf. Each module consists of a pair of ocular dominance columns. And the width of each hypercolumn is about 1mm.

Cells between blob regions are selective for size and orientation. Interblobs process info about orientation and sf but blobs are more to do with colour processing,

Destruction of modules in v1 results in achromotopsia- false as v1 is basic colour processing, achromotopsia is cv defect can see grey and this is due to damage to v4 rather than v1. V1 damage leads to general scotomas as basic visual processing. Damage to colour processing= achromotopsia= v4.

Damage to v1 can lead to blind sight which is when damage to v1 as lack of conscious visual perception in a specific vf but can demonstrate subconscious visual responsiveness to stimuli presented within that field.

About tens of thousands not millions. V1.

55
Q

More info on tilt aftereffect

A

It is observation post adaptation. It is a pyschophysical phenomenon that suggests that contour orientation is encoded by the distribution of activity across a population of cells.
It is a misperception of a test stimulus.

Not measured using single cell recordings normally psychophysical as human perception to stimulus.
Not misconception of adapting stimulus no we adapt to it.
Not a computational theory

It does not provide evidence that individual cells can be used as feature detectors or to encode simple features eg orientation.

56
Q

If a cortical cell responds to a stimulus that is a vertical luminance contour

A

Some aspects of the stimulus is being represented within the visual system

The organism will not see vertical contour or do defo see vertical contour cortical cell must be simple or have rf with centre surround construction these things arent true. Its TRYE that some aspects of the stimulus is resented within the visual system in some way..

The correct answer is:

e. some aspect of the stimulus is being represented within the visual system.

Explanation:
When a cortical cell responds to a stimulus, such as a vertical luminance contour, it indicates that some aspect of that stimulus is being represented within the visual system. The response of the cortical cell signifies that it is sensitive to the vertical luminance contour, suggesting that this feature is being processed and represented by the visual system. This doesn’t necessarily mean that the organism will perceive a vertical contour (option a), nor does it imply that the cortical cell must be a simple cell (option c) or have a receptive field with a center-surround construction (option d). Therefore, option e is the most accurate choice, as it acknowledges that the cortical cell’s response reflects the representation of the stimulus within the visual system.