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What are the different types of visual receptors?
Rods and Cones
What are the theories of colour vision?
Trichromatic theory
the opponent-process theory
Retinex theory
What is the dorsal path?
projects through the parietal cortex
the how or where pathway
important for visually guided movements
What is the ventral path?
projects through the temporal cortex
what pathway
identifying and recognising objects
How do we localise sound?
• Time of arrival
• Sound shadow
What are our chemical senses?
Taste and smell
what is the difference between mechanical and chemical senses?
Chemical senses respond to the presence of chemicals, while mechanical senses respond to mechanical displacement of receptors
Cellular Organisation of the Retina
Bipolar cells receive input from visual receptors at the back of the eye
Bipolar cells then synapse with ganglion cells
axons of the ganglion cells form the optic nerve
Amacrine cells synapse with bipolar and ganglion cells
(indirect pathway from bipolar to ganglion cell)
The Fovea
Central portion of the retina allows acute and detailed vision
packed tight with receptors
each receptor in the fovea attaches to a single bipolar cell and a single ganglion cell
knows exactly where the light fell
high spatial resolution
poor low light vision
The periphery of the retina
everywhere else
a greater number of receptors converge into bipolar and ganglion cells
low spatial resolution
convergence of input allows for greater perception of much fainter light in peripheral vision
better in the dark
Convergence of input
1 con to 1 bipolar cell
Lots of rods to lots of bipolar cells
Photoreceptors
respond to photos of light
protein structure that is holing sodium channel open sending inhibition to a bipolar cell when there is no light, when it receives light it changes structure and closes sodium structure and stops sending inhibition and starts sending excitation
light changes the photopigment
Rods
most abundant in the periphery of the eye and respond to faint light (120 million)
10% of visual experience
Cones
most abundant in and around the fovea (6 million per retina)
more light is hitting the fovea so they make up more
colour and detailed vision
colour vision
The perception of colour is dependent upon the wavelength of the light that the object reflects
Trichromatic theory
Colour perception occurs through the relative rates of response by three kinds of cones
short wavelength (blue)
Medium wavelength (green)
Long wavelength (red)
Each cone responds to a broad range of wavelengths, but some more than others
The ratio of activity across the three types of cones determines the colour
The opponent-process theory
Suggests that we perceive colour in terms of paired
opposites
Red vs. green
Blue vs. yellow
Black vs. white
A possible mechanism for the theory is that bipolar
cells are excited by one set of wavelengths and
inhibited by another
Retinex theory
All of the other 2 theories is happening
Suggests that the cortex compares information from various parts of the retina to determine the brightness and colour for each area
Explains how colour perception is consistent despite changes in ambient lighting
colour constancy
Context for colour perception
Retina to thalamus
Ganglion cell axons form the optic nerve
the optic chiasm is the place where the two optic nerves leaving the eye meet
Humans→ half the axons from each eye cross to the other side of the brain (eyes too close together)
most axons of the optic nerve terminate in the lateral geniculate nucleus in the thalamus
some axons project to the superior colliculus → receives visual information
The Path of Visual Input
Retina → optic chiasm → lateral geniculate (thalamus)→ primary visual cortex
Optic chiasm
split information half left goes to the right, half right goes to the left
blue meets blue, red meets left
organised by visual field
Ganglion cells in the pathway to the thalamus
Midget, parasol, bistratified
Midget ganglion cells
Parvocellular pathway
receive information from midget bipolar cells
1 → 1 →1 (fovea)
carry it to the lateral geniculate nucleus to parvocellular neurons that reside there
detailed vision and colour vision
Parasol ganglion cells
Magnocellular pathway
large receptive fields and coming from the periphery
project the magnocellular cells in the lateral geniculate nucleus
detecting movement
not so much colour vision
Bistratified ganglion cells
Koniocellular pathway
some respond to colour
some have large receptive fields that allow them to see movement
super small koniocellular neurons and scattered across the thalamus
Primary visual cortex (V1)
receives input from the lateral geniculate nucleus
located in the occipital lobe
important for conscious visual perception
Hubel and Weisal distinguished various types of cells in the visual cortex
preference for bars of light 3 different types
Simple
complex
end-stopped/hypercomplex cells
Secondary visual cortex (V2)
receives information area from V1
V1 V2 loop
Also receives input directly from the pulvinar nucleus of the thalamus
PN receives information from the superior colliculus
attention gaze type of shifts
Performs additional processing of the visual input
important for binocular disparity
depth perception
comparisons of the eyes
Simple cells
cells that light up in neuro imaging when a specific orientation of a bar of light is presented
Complex cells
respond more to a bar of light across movement
larger visual fields
detect motion
responds to moving bars of light
End-stopped/hypercomplex cells
clear inhibitory and clear excitatory zones
good for detecting things
Facial recognition
Complex
identification, emotion, social cues, communication
2 systems
Core
Inferior occipital gyri, superior temporal sulcus, lateral fusiform gyrus
that is a face
Extended
Using that in some way, recognition of a person, emotion, social cues
Intraparietal sulcus, auditory cortex, limbic system, anterior temporal lobe
Motor perception
The middle temporal cortex contains cells with directional selectivity
a preference for the movement of an object in a particular direction
Medial superior temporal cortex
optic flow
live streaming
everything moves relative to you
I am moving they are static
Both receive input from the magnocellular pathway
Audition
hearing alerts us to useful information
hearing is the detection of sound waves
sound waves are transduced
Process of transduction
Outer ear
Pinna
Middle ear
tympanic membrane vibrates at the same frequency as the sound
vibrates the malleus, incus, stapes to mechanical displacement
gets smaller and smaller down to the Oval window intensity is going up
window into the inner ear
Inner ear
Cochlea
three fluid filled cavities
displacement of fluid
basilar membrane (has the hair cells) and tectorial membrane press against each other which bends hear cells that have mechanically gated channels and opens sodium channels
Theories of pitch perception
Place theory
frequency theory
Pitch theory
Place theory
each are along the basilar membrane has hair cells sensitive to only one specific frequency of sound wave
is it close to the oval window or far away
the biggest displacement of a high frequency is close the start of the basilar membrane
low frequency the back
frequency theory
the basilar membrane vibrates in synchrony with the sound and causes auditory nerve axons to produce action potentials at the same frequency
Pitch theory
combines modified versions of both
low frequency sounds best explained by the frequency theory
for high frequency sounds best explained by place theory
Auditory cortex
The primary auditory cortex (A1) is the destination for most information from the auditory system
located in the superior temporal cortex
Mostly embedded within the Sylvian fissure
Each hemisphere receives information from both ears
Cochlear nucleus → superior olive → Medial geniculate
function of the auditory cortex
Primary sight for processing auditory information
Tonotopic map
cells are more responsive to preferred tones
sound localisation
Sound localisation does not rely on activity of particular sensory receptors
location must be computed within the CNS
2 cues sound shadow and time of arrival
sound shadow
intensity of the sound
sound from the right will be louder in my right ear than left ear (head sound barrier)
time of arrival
right sound comes to right ear first
vestibular sensation
vestibular organ is composed of several structures which detect the position and movement of the head in the ear
the saccule and utricle contain otoliths and hair cells and detect linear acceleration
three semi-circular canals contain a jellylike substance and hair cells detects rotational acceleration
90* angles from each other
Touch sensation
Mechanoreceptors transduce touch/pressure
touch displaces the receptors and opens sodium channels
Include a range of receptor types
Meissner’s corpuscles
light pressure and fast adapting
Merkel’s disks
light pressure and slow adapting
watch on wrist
Ruffini endings
deep pressure and slow adapting
knee movement
Pacinian corpuscles
deep pressure and fast adapting
respond selectively to vibration on skin
Touch sensation to the CNS
Information from touch receptors in the head enters the CNS through the cranial nerves
information from receptors below the head enters the spinal chord via spinal nerves
Taste
Organisation of taste receptors
papillae are structures on the surface of the tongue that contain the taste buds
each papillae may contain up to ten or more taste buds
each taste bud contains approx. 50 million receptors
5 basic tastes
Sweet
sour
bitter
salty
Unami
Labelled-line principle taste
each receptor responds to a limited range of stimuli and ends a direct line to the brain
taste depends on which receptor is activated
we do have a sweet receptor
problem taste experience is so complex there is not a labelled line for each taste
Across-fibre pattern principle taste
each receptor responds to a wider range of stimuli and contributes to the perception of each of them
pattern of activity dictates taste perception
Taste transduction
The saltiness receptor permits sodium ions to cross the membrance
results in depolarisation
sodium from that salt enters into the receptors
Sour receptors detect the presence of acids
hydrogen ions enter into the cell and act on the depolarisation of those cells
Sweetness, bitterness, and umami receptors activate a second messenger system
dislodges something that then send something to the cell
Taste coding in the brain
three cranial nerves are responsible for carrying taste information from different parts of the tongue
cranial nerves project to a structure in the medulla → the nucleus of tractus solitarius
Projections from the NTS reach the thalamus, which then relays taste information to the primary gustatory cortex (anterior insula)
smell
Perception of the activation of olfactory receptors
Olfactory receptors
Olfactory cells line the olfactory epithelium in the rear of the nasal passage
Vertebrates have hundreds of olfactory receptor types, which are highly responsive to some related chemicals and unresponsive to others
transduction occurs via a second messenger system
doesn’t travel very far
Olfaction in the brain
axons from olfactory receptors carry information to the olfactory bulb
similar chemicals excite neighbouring areas
coding is determined by which part of the olfactory bulb is excited
Olfactory information then projects to a range of other regions
collectively referred to as the olfactory cortex
research continues to profile the regions involved in olfaction