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Light
electromagnetic radiation that is visible to our eyes
concentrated in small packets of energy, photons, which travel through space in a wave-like manner
Dual theory of light
light is both a wave and a stream of particles
it propagates like a wave and is absorbed like a particle of energy
Properties of light
wavelength, frequency, amplitude
What does light wavelength correlate with?
perception of colour/hue
What colour is longer wavelengths?
red
What colour is shorter wavelength
blue
eg. ultraviolet is shorter than light, and its close to blue
Sclera
white part around outside of eye; protective thick tissue
What are the two main refractive components of the eye?
cornea and lens
cornea performs most of the refraction and lens is adjustable, making up the rest
Cornea
continuation of sclera; transparent, contains sensory endings; REFRACTIVE
Lens
elastic, transparent, REFRACTIVE
Optic nerve
bundle of axons that transmits visual information to the brain
Zonules of zin
pull lens to make it thin and flat
Emmetropic eye
an eye with perfect vision, also known as 20/20 vision, where light entering the eye focuses perfectly on the retina, producing a crisp, clear image
Accomadation
a change in the curvature of the lens in response to changing object distances
Limit of accommodation
~10 cm in young people; lens can only fatten so much
How does lens accommodate for near objects?
contracting ciliary muscle (ring) and relaxing the zonules of Zinn, making lens fatter
Focal distnace
distance from the refractive surface and point where paralel rays converge
cor
Diopter
unit of measurement of the optical power of a lens
Lens power equation (P)
P = 1/f
Refractive power of the cornea
1/0.024 = ~42 diopters
Would a fat lens have more or less refractive power?
A fatter lens bends light more so it has a higher refractive power
Nodal point
imaginary point near back surface of the lens though which all light rays pass
How does the retinal image compare to the visual scene?
flipped horizontally and vertically
a little blurred around the edges
Hyperopia
farsightedness
focal point is behind the retina, as the lens lack sufficient refractive power
etiehr cornea is not curved enough or eyeball is too shrot
treat with convex lens - add refractive lenses
Myopia
nearsightedness
focal point is in front of retina; lens cannot flatten enough
cornea is too curved, or eyeball is too long
treat with concave lens; reduce refraction
Presbyopia
age-related hardening of the lens and reducation in elasticity of the capsule that encircles the lens
Astigmatism
lack of symmetry in the curvature of the cornea, causes blurred retinal image along the affected direction only
treat with lenses that correct refractive deficit along a particular orientation
Retinal pigment epithelium
absorb any light that isn’t absorbed by the photoreceptors - make sure light ins’t reflected/scattered inside eye
Retinal organization (outside to in)
sclera - pigment epithemium - photoreceptors - bipolar cells - retinal canglion cells
Why are photoreceptors the outermost layer of retina?
to be near retinal pigment epithelium, because is helps regenerate photopigment
What are the only neurons whose axons leave the eye?
retinal ganglion cells
Where do neurons leave the eye?
Optic nerve
properties of photoreceptors
outer segment - store photopigment
inner segment - make photopigment
cell body - nucleus
synaptic terminal
Distance between cell body and synaptic terminal of photoreceptors?
very short - no action potential
Rods
Cylindrical outer segment
90 million
Periphery of retina
One photopigment (colour-blind)
Specialized for night vision
Cones
Conical outer segment
4-5 million
Mostly in fovea
Specialized for day vision
Fine visual acuity = more sensitive
Three photopigments (colour vision)
Distibution of rods and cones in the retina
Cone density is higher in the fovea
Rod density is highest in the periphery
RGC axons leave the eye at the optic disk
Consequence of the fact that there are no rods in the fovea?
under dim illumination, we are effectively blind in the centre 1 deg of our visual field
Rule of thumb (vision)
thumb at arm length is ~2 deg of visual field
Scotpic
Rods are more efficient than cones at converting photon absorption to neural signals thus rods and not cones are active at low light levels
Mesopic
Cones and rods activated
Rods are only active at low light levels; above this level, photopigment cannot be activated any more bleaching
~approx. moonlight
Photopic
Only cones
Cones have mechanisms to prevent bleaching at high light intensities
How does the visual system adjust to changes in illumination?
rods and cones have different ranges
photopigment must be regenerated
pupil size is adjustable irt light
ganglion cells respond best to contrast, not diffuse light
Photopigment bleaching/regeneration
When a photopigment is bleaches (used up), the molecule must be regenerated again; thus, not all photons are captured
Dark adaptation curve
initially mediated by cones’ fast recover but rods take over (recover further; lower threshold)
Photopigment
made in inner segment and stored in outer segment
consists of a protein plus a chromophore
Opsin
photopigment protein, strucutre determines which wavelengths of light the pigment molecule absorbs
Retinal (chromoshore)
absorbs light, changes conformation when bleached
What wavelength of light does rhodopsin absorb?
preferentially absorbs light at about 500nm (green-blue)
Spectrophotometry
measures how much of the incoming light is absorbed by a protein
flash light, record how much is not absorbed
What wavelength is most sensitive in dim conditions?
peak sensitivty is at 500nm
Absorption spectrum of cone opsins
short = blue = 440nm
medium = green = 530nm
long = red= 560nm
Spectral sensitivity of photopic vision
Brain combines input from 3 types of cones to create colour vision, peak is about 550nm
Distribution of cone photopigments
5-10% are blue (S-cones)
30% green (M-cones)
60% Red (L-cones)
Red:green cones
2:1 ratio
Photochromatic interval
difference between just seeing light and being able to tell its colour
Photopic vs scotpic sensitivity
Photopic sensitivity is only higher at very long wavelengths
Othewise, scotpic is typically higher
Purkinje shift
difference in perceived brightness of objects due to spectral shift
Objects of a given colour will appear to shift brightness when you switch between scotopic and photopic systems
What happens when you gradually increase the intensity of a subthreshold light at 450nm?
Scotopic system detects it first – rods have higher sensitivity
At some brightness, you eventually activate the cone system = now we can tell what colour the light is
Dark current
Rhodopsin is inactive, maintaining sensitivity of rods
In the dark, a molecule called cyclic GMP (cGMP) binds to ion channels permeable to Na+ and Ca2+
Keeps them open
Dark current flow of cations (positive charge) into the outer segment in the dark
K+ leaves the cell though K+ leak channels in the inner segment
The Na+/K+ pump maintains the concentrations of Na+ and K+ inside and outside the cell
Results of the dark current…
membrane potential of a photoreceptor is ~-40mV, whereas most have -70mV resting potential
so neurotransmitter glutamate is constantly being released IN DARK
Phototransduciton in the presensce of light
Absorption of light by retinal
Rhodopsin changes conformation à activated
Activated rhodopsin activates a G-protein called transducing
G-protein activates an enzyme called PDE
PDE breaks down cGMP à GMP
cGMP-gated channels close
What happens to the membrane potential when cGMP-gated ion channels close (phototransduction)?
K+ still leaving but its not being balanced by Na+ coming in, so membrane potential gets more negative (DEPOLARIZED)
How does phototransduction compare to the receptor potential generated in other sensory systems?
In other systems, a signal produces hyperpolarization, in phototransudction, a signal produces depolarization
How does phototransduction affect neurotransmitter release?
less glutamate is released
Photopigment
protein (opsin) + chromophore (retinal)
Bipolar cells (vision)
synapse with either rods of cones and pass signals onto retinal ganglion cells (RGCs)
Retinal ganglion cells
only neurons whose axons leave the eye
the only retinal neurons that generate action potentials
part of parallel visual streams
# of photoreceptors vs RGCs
100 million photoreceptors vs 1.25 million ganglion cells
Signals from multiple photoreceptors must converge onto a single RGC
How does photoreceptor-RGC convergence relate to the size of RGC receptive fields
If a neuron response to visual input in larger part of the retina = larger part of the visual field
Midget bipolar cells
few photoreceptors converge onto a single midget cell
in fovea, ratio is 1:1
Diffuse bipolar cells
converge info from many photoreceptors
Visual acuity
measure of the finest detial taht cna be resolved by the eyes
Compare the sensitivity of foveal RGCs to the sensitivity of peripheral RGC in dim diffuse light
Periphery responds better to stimulus 1, because it receives input from many different photoreceptors, so it all adds up to activate the one ganglion cell
Whereas near fovea, dim light only weakly activates the 3 cones so none of them get activated
Compare the ability of the RGCs on the fovea and periphery to discriminate between 3 separate light spots
Near fovea, we can tell when 1 and 3 are activated but not 3, vs periphery the receptive field is large so we can’t discriminate between points
Why/how does foveal vision allow us to see fine details?
retinal neurons (except cones) are shifted to one side to allow light unimpeded access to cones
cones are tightly packed
cones and bipolar cells are connected to each-other in a 1:1 ratio
2 types of bipolar cells
OFF - hyperpolarized by light just like photoreceptors
ON- depolarized by light
Which RGC receives input from midget bipolar cells?
P-ganglion cells
Which RGC receives input from diffuse bipolar cells?
M-ganglion cells
Which RGC projects to parvocellular LGN?
P-ganglion cells
Which RGC projects to magnocellular LGN?
M-ganglion cells
Which RGC has small size, dendritic field?
P-ganglion
Which RGC has large size, dendritic field?
M-ganglion
Which RGC is most numerous? 70% of all RGCs
P-ganglion
Which RGC is less numerous? 10% of all RGCs
M-ganglion
Which RGC is more in fovea?
P-ganglion
Which RGC is found more in periphery?
M-ganglion = more convergence
4 types of RGC
ON - P
OFF - P
ON - M
OFF - M
How do RGCs behave?
All rgcs have a certain level of spontantneous activity (action potential firing)
Firing rate can either increase or decrease in response to light
Retina doesn’t just detect light, rather it detects differences in light in adjacent parts of the retina (spots of light on screen)
RGC receptive field
2 concentric zones: excitatory + inhibitory = center surround antagonism
Why does diffuse light have no effect on firing rate of RGCs?
Because the same amount of inhibition and excitation, so they’re cancelling eachotehr out completely and not producing any change in the firing rate
How to maximize firing rate of RGC?
light up as much excitation region and as little of inhibitory region as possible
How do RGCs filter stimuli by size?
respond best to stimuli that tare the right size to only stimulate excitatory region without hitting inhibitory region
How are RGCs optimized for detecting contrast?
RGCs are most sensitive to differences in the intensity of light in the centre and its surround
Perceptual consequences of centre-surround effects
lightness contrast
lightness constantcy
mach bands
Centre-surround effect - lightness contrast
appearance of one patch of light is affected by other light patches nearby
Centre-surround effects - lightness constancy
An overall change in the ambient illumination affects both objects and the surround in an equal manner resulting in relative constancy of lightness perception
i.e. you realize that the colour of something diddn’t change just because the lighting changed
Mach bands
False impression of a narrow bark band and a narrow light band immediately to boundary when intensity changes abruptly
causes by responses of RGCs that overlap boundary
e.g. cell fires above baseline because entire excitatory region (center) is lit but only part of inhibitory region (surround) is lit - overlaps with darker band
Effect of bipolar to RGC convergence
how we see spatial detail (resolution / acuity)
how little light we need to see (sensitivity)
Usually a trade-off between resolution and sensitivity