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Sensation
refers to the detection of a physical stimulus (such as light, sound, heat, etc.) by early sensory pathways
how cells of the nervous system transduce (convert) these signals into a change in membrane potential and neurotransmitter release.
Perception
refers to the conscious experience and interpretation of sendory information
Sensory Neurons
specialized cells that detect a specific category of physical events such as:
the presence of specific molecules
smell, taste, nausea, pain
physical pressure
touch, stretch, vibration, acceleration, gravity, balance, hearing thirst, pain
temperature
heat, cold, pain
pH (whether a liquid is acidic or alkaline)
sour taste, suffocation, pain
visible light (electromagnetic radiation)
vision
Photoreceptor Cells
sensory cells responsible for vision
in our eyes
transduce visible light into a change in membrane potential which affects amount of NT released
don’t have action potentials
release NT in a graded fashion, dependent on their membrane potential
detect visible light using 4 kinds of photoreceptor cells
around 30% of the cerebral cortex is dedicated to processing info gathered by these cells
Absorption
electrons move into higher energy orbital
Reflection
electrons oscillate within their orbital states, pushing the light backward
Transmission
electrons oscillate within their orbital states, pushing their light forward
primarily observed with air, glass, and water
Seeing Light
colour of an object (at room temp.) is determined by the visible light it reflects (scatters)
ex. object appears orange when it reflects orange light and absorbs all other visible wavelengths
energy of absorbed visible light is usually converted into heat (molecular rotations) via near-field, non-radiative electromagnetic interactions
Vitamin A
undergo a change in shape after absorbing visible light
stabilizes the excited electron in a high energy orbital
one photon of visible light has enough energy to change 3D configuration of vitamin A
Retinal: modified form of vitamin A; perceive visible light
Sunlight
We can perceive much but not all of the radiation that reaches us from the sun.
Retinal
molecule synthesized from vitamin A
is a photopigment, changes shape upon absorbing the energy of visible light
held by the opsin proteins in the photoreceptor cells in our eyes
what absorbs the electromagnetic energy of visible light that allows us to see
when retinal absorbs energy of visible light it activates the opsin protein
this launches an intracellular g protein cascade that changes the membrane potential of photoreceptor cell, affecting how much NT it releases
Opsin
inhibitory metabotropic receptor
light sensitive proteins
undergo a change in shape when the absorb the energy of visible light
acquire this property by holding a molecule of retinal
embedded in the membrane of photoreceptor cells
many opsin proteins encoded in our genome
different ways these opsins hold onto retinal determines the wavelength of light they can absorb (e.g. red vs green light)
Sensory Transduction
process by which sensory stimuli are transduced (converted) into receptor potentials
sensory neurons come in all shapes and sizes
sensory cells that transduce smell and touch are relatively normal neurons
but many others (vision, hearing, taste) are not normal neurons, in part because they don’t have axons or action potentials
Visible Light
has wavelength between 380-750 nm
use 4 kinds of opsin proteins to detect visual light, each hold retinal slightly differently
Types of Photoreceptors
each expresses a different opsin protein
red cone cells express the red cone opsin
blue cone cells express the blue cone opsin
green cone cells express the green cone opsin
rod cells express the rhodopsin protein
last to evolve, 100x more sensitive to light than cone cells are
Cone Receptors: Trichromatic Coding
Blue cone opsins are sensitive to short wavelengths of light (430 nm).
Green cone opsins are sensitive to medium wavelengths of light (535 nm).
Red cone opsins are sensitive to long wavelengths of light (575 nm).
Trichromatic Coding
When red and green light is so close together that our eyes can’t differentiate them, we perceive the color yellow.
There are 3 kinds of light bulbs here: red, green and blue.
Green light (520nm) activates the green cone opsin more than the red cone opsin. Red light (640nm) activates the red cone opsin more than the green cone opsin. The combination of red and green light causes both red and green cone opsins to be activated similar amounts, which is exactly what pure yellow light does (570nm).
Brightness
intensity (total amount of light)
if brightness is 0, there’s no light; perceived as black
Hue
principal colour (dominant wavelength in the light)
if there’s some saturation, then the hue of the light indicates the perceived colour (from 0-360 degrees)
Saturation
purity of colour (the wavelength mixture)
if there’s light, is it saturated with one colour or even mix of colours
0% saturation means that there is an even mix of all the colours, which means there is no perceived colour (gray scale, the central vertical axis of the colour cone)
Protanopia
absences of red cone opsin (1% of males), which makes it difficult to distinguish colours in the green-yellow-red spectrum
red cone cells can sometimes express the green cone opsin, which allows for normal visual acuity
mutations that make the red cone opsin simply act more like the green cone opsin (in terms of the wavelength of light it can detect) produce less pronounced deficits in colour vision (1% of males)
Deuteranopia
absence of green cone opsin 1% of males), which makes it difficult to distinguish colours in the green-yellow-red spectrum
green cone cells can sometimes express the red cone opsin, which allows for normal visual acuity
mutations that make the green cone opsin simply act more like the red cone opsin produce less pronounced deficits in color vision (5% of males).
Tritanopia
absence of blue cone opsin
blue cone cells don’t compensate for this deficit in any way
but there are relatively few blue cone cells, and they are less sensitive to light that the other cone cells, so visual acuity is often not noticeably affected
Cone monochromacy
there is no colour vision when only one of the three cone opsins are functional
Achromatopsia
there is no colour vision when none of the cone cells work
because of a problem with the intracellular signaling cascades shared by all three of the cone cells)
Rod Cell
express the rhodopsin protein
Rhodopsin is 100x more sensitive to light than other cone opsins
is in diff category, not used for colour vision
Lens
consist of several transparent layers
adjust the shape of this lens to focus near or far
Iris
ring of muscle
contraction and relaxation of this muscle determines the size of the pupil
Pupil
determines how much light enters the eye
-coloured part of the eye
Cornea
outer, front layer of the eye
focuses incoming light a fixed amount
laser eye surgery reshapes the cornea
Conjuctiva
mucous membrane that lines the front of the eye
connects to eyelids, preventing things from getting behind the eye
Retina
lines the back part of the eye
contains several layers of cells
photoreceptor cells are located in the furthest back layer in the retina
periphery of the retina only contains rod cells
Fovea
central region of the retina
primarily contains cone cells
equal number of photoreceptor cells, bipolar cells, and retinal ganglion cells
no compression of info
only part if our retina where our visual acuity is good enough to read text (20/20 vision)
supports high resolution, colour vision, only when there is a sufficient amount of light
Optic Disk
where blood vessels leave/enter the eye
also where the optic nerve exits the eye, carrying visual info to the brain
there are no photoreceptor cells in this spot in our retina; our blind spot
Movements of the Eye
eyes are suspended on bony sockets in the front of the skull
six muscles rotate the eye and hold it in place
our eyes scan a scene by making saccadic eye movements
when we maintain focus on an object that is moving (relative to us) our eyes exhibit pursuit movements
Saccadic Eye Movements
rapid, jerky shifts of gaze from one point to another
Pursuit Movements
only time our eyes appear to calm down and move smoothly, slowly
Orgnization of the Retina
light passes through multiple layers of the retina before reaching the photoreceptor cells
activated photoreceptor cells pass visual info forwards (towards front of retina
Visual info (via NT release) goes from
photoreceptor cells → bipolar cells → retinal ganglion cells → brain
Opsin proteins are in the furthest back of the retina
Periphery of our Retina
massive compression (averaging) of visual info ss there are 100x more photoreceptor cells than retinal ganglion cells
our visual acuity in our peripheral vision is about 20/200, which is quite blurry
we can make out general shapes but not details
what we see in our peripheral vision 20 ft away is as detailed as what we see in our fovea 200 ft away
contains high density of rod cells
allows us to easily detect dim light and movement of light, although without any colour info
Peripheral Vision
people have poor visual acuity and are not great at identifying colours in their peripheral vision
we can still make out general shapes, but images look grey, blurry, and unfocused
high visual acuity needed for reading is only possible in the fovea
Cones
most prevalent in the central retina; found in the fovea
sensitive to moderate-to-high levels of light
provide info about hue
provide excellent acuity
Rods
most prevalent in the peripheral retina; not found in the retina
sensitive to low levels of light
provide only monochromatic info
provide poor acuity
Neurons in the Retina
Photoreceptor Cells: synapse on bipolar cells
Bipolar Cells: relay visual info from photoreceptor cells to retinal ganglion cells
Retinal Ganglion Cells (RGCs)
only cells that send info out of the eye
RGCs have axons and action potentials (unlike photoreceptor cells and bipolar cells)
Their axons form on the optic nerve, which exits the retina through the optic disc (blind spot of retina)
Visual Info Pathway: Thalamus
thalamus, specifically the lateral geniculate nucleus
projects to primary visual cortex (V1) in the occipital lobe where visual info enters consciousness
Retina → thalamus → V1 pathway
creates an internal (mental) representation of your entire visual space: the objects in it, their position, and their attentional value
Visual Info Pathway: Midbrain
specifically the superior colliculi
visual info is used here to control fast visually guided reflexive movements
midbrain doesn’t know what you’re looking at, but it can draw your attention to unexpected visual events
Visual Info Pathway: Hypothalamus
visual info is used here to control circadian rhythms such as sleep-wake cycles
hypothalamus doesn’t know what you are looking at, but it knows how much light is present in your environment
Visual Cortex Wiring Diagram
was understood in the 1970s
oversimplification as there are actually tons more pathways most bidirectional (bottom-up and top-down)
Predictive Coding Theory: idea that each node in the network tries to predict what its ascending inputs will look like in the next movements, based on previous experience
idea is that top-down (descending) activity represents sensory predictions that neutralize (cancel out) any correctly predicted bottom-up (ascending) signals
Thus, what propagates up through the network may only be prediction error signals. which inform the brain of how the current movement differs from what was expected
Prediction error signals that ascend through the network would drive learning to improve future predictions