Sensory Processing/Perception Flashcards

1
Q

What allows us to perceive depth?

A

Binocular cues: Retinal Disparity and Convergence

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2
Q

What allows us to perceive form?

A

Monocular cues: Relative size, Interposition, Relative height, Shading and contour

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3
Q

What allows us to perceive motion?

A

Monocular cues: Motion paralax (relative motion)

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4
Q

What allows us to perceive constancy?

A

Size constancy

Shape constancy

Color constancy

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5
Q

Perceptual organization

A

Describes how we see and experience different perceptual phenomena in the world around us

Depth

Form

Motion

Constancy

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6
Q

Describe the process of sensory adaptation regarding hearing

A

Inner ear muscle contracts when there’s a loud noise, which dampens the noise and protects ear drum from being damaged. This takes a few seconds to kick in –> doesn’t work for immediate loud noises, i.e. gunshot

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7
Q

Describe the process of sensory adaptation regarding touch

A

Sensory receptors become saturated and stop firing as much –> desensitization

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8
Q

Describe the process of sensory adaptation regarding smell

A

Sensory receptors in nose become desensitized to particular odors

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9
Q

Describe the process of sensory adaptation with proprioception

A

Mechanism not stated in video, but if someone puts on goggles that distort image of world, ie flips images upside down, over time the brain adapts and flips the image rightside up

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10
Q

Describe the process of sensory adaptation regarding sight. How does this differ from sensory adaptation in other modalities?

A

While most other modalities get some kind of down regulation, with sight you can get up or down regulation.

Lots of light: Pupils constrict, rods/cones become desensitized –> down regulation in ability to sense light

Dark: Pupils dilate, rods/cones synthesize more light sensitive molecules –> upregulation in sensitivity

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11
Q

What is Weber’s Law and what kind of relationship does it predict between the JND (incremental threshold) and the background intensity?

A

dI/I = k

Linear relationship

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12
Q
A
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13
Q

T/F: The absolute threshold of stimulation is a fixed, unchanging number

A

False

Can be influenced by: expectations, experiences, motivation, altertness

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14
Q

What are the different types of somatosensation? What determines the intensity for each modality?

A
  1. Thermoception (temperature)
  2. Mechanoception (pressure)
  3. Nociception (pain)
  4. Propioception (position)

For each modality, intensity correlates to neuronal firing rate (low intensity = low rate of firing, high intensity = high rate of firing)

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15
Q

How do somatosensory neurons encode information about timing?

A

Neuron firing may or may not adapt to the stimulus, which provides information regarding stimulus timing.

Non-adapting: The entire time a stimulus is being applied, there is no change in firing rate; each spike is spaced evenly

Slow-adapting: Neurons start off with high firing rate, then slows down over time; slow to adapt to change in stimulus

Fast-adapting: Neurons fires really quickly as soon as stimulus starts, then it will stop firing, then it will start firing again as soon as the stimulus stops

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16
Q

What structures located in the inner ear are particularly important parts of the vestibular system?

A

Semicircular canals: Anterior, lateral, and posterior

Otolith organs: utricle and saccule

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17
Q

What is the fluid located in the semicircular canals? How does it contribute to our vestibular sense?

A

Endolymph

When we rotate along a certain plane → causes endolymph to shift within that particular canal → allows us to sense what plane our head is rotating along

We are also sensitive to how much of fluid is moving and how quickly → we can also get information about the strength of rotation

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18
Q

How do the otolith organs contribute to our vestibular system?

A

They help us detect linear acceleration and head position

Within these structures are calcium carbonate crystals that are attached to hair cells within a viscous gel substance

If we accelerate in a direction or, for example, move from standing up to lying down, this causes the crystals to move because they are heavier than the surrounding gel environment

When they move, they physically pull on the hair cells they’re attached to → triggers an action potential that carries this information to the brain

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19
Q

Describe the physiological process in the semicircular canals that causes dizziness/vertigo

A

As we spin, the endolymph moves along the direction we’re turning, but this liquid doesn’t always stop spinning when we do (especially true if spinning vigorously or for a long period of time)

Continued movement of endolymph → signals sent to brain indicating you’re still moving even after you have stopped → causes dizziness

When fluid finally stops, dizziness subsides

→ Rotating in the opposite direction of how you were originally spinning encourages the movement of the endolymph in that opposite direction → can help stop the original motion of the endolymph by “canceling it out”

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20
Q
A
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21
Q

Describe the physiological process in the otolith organs that causes dizziness/vertigo

A

If you were in a situation without gravity (ie Astronaut), your otolithic organs probably wouldn’t work very well because gravity won’t pull down on them in the same way → concepts of up/down kind of become meaningless → can be really disorienting

Also a danger of scuba diving, because buoyancy can have the same effect as gravity → sometimes results in divers becoming disoriented in water

Especially true when they don’t have visual cues about which way is up and which way is down

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22
Q

Signal Detection Theory

A

Looks at how we make decisions under conditions of uncertainty.

Tries to figure out, at what point is a signal strong enough that we are able to notice it in the first place; at what point are we able to detect a signal?

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23
Q

Describe the 4 possible outcomes of signal detection theory

A

Signal Present, Response “Yes” = Hit

Signal Present, Response “No” = Miss

Signal Absent, Reponse “Yes” = False Alarm

Signal Absent, Response “No” = Correct Rejection

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24
Q

How does the strength of the signal (d’) affect the relative amount of hits/misses/false alarms/correct rejections?

A

If the signal is really strong, you might always get it right (either hit or correct rejection)

Hit>miss

If signal is weak, might get some false alarms and/or misses

Hit

*Note: d’ represents the difference between the means of the noise distribution and signal distribution

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25
Q

What is the difference between top-down and bottom-up processing?

A

Bottom-up Processing: Stimulus influences our perception; No preconceived cognitive constructs about what it is you’re looking at; Data driven; perception of what you’re looking at directs your cognitive awareness of that object

Top-down Processing: Uses your background knowledge/information/expectation to influence perception; Theory driven; our perception/behavior is influenced by our expectation

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26
Q

If you were looking at a ‘where’s waldo?’ image, what kind of processing (top-down or bottom-up) would you be using?

A

Top-down

This allows us to be goal-driven and we’re able to look through the picture and find Waldo.

In contrast, if we were using bottom-up processing, we would just be seeing a bunch of little people and we wouldn’t really be goal driven/trying to do anything

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27
Q

What are the laws outlined by the Gestalt Principles?

A

Similarity: Items that are similar to one another are grouped together by your brain

Pragnanz: Reality os often organized/reduced to the simplest form possible

Proximity: Objects that are close to one another are grouped together

Continuity: Lines are seen as following the smoothest path

Closure: Objects grouped together are seen as a whole

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28
Q

Label the parts of the eye:

A
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29
Q

Conjunctiva

A

Helps protect/moisturize the eyeball; protection from dust

If inflamed → pink eye

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30
Q

Cornea

A

Transparent, thick, fibrous tissue

Anterior ⅙ of the eyeball

Helps bend light; starts to focus the light

Protects front of eyeball

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31
Q

Anterior Chamber

A

From back of cornea to front of lens

Filled with aqueous humor

Helps provide internal pressure to maintain the shape of the eyeball

Allows nutrients/minerals to flow through this space to supply the cells of the cornea, iris, etc.

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32
Q

Aqueous Humor

A

Fluid that fills the anterior chamber

Helps provide internal pressure to maintain the shape of the eyeball

Allows nutrients/minerals to flow through this space to supply the cells of the cornea, iris, etc.

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33
Q

Pupil

A

An opening in the middle of the iris that modulates the amount of light that will be allowed to enter the eyeball

34
Q

Iris

A

The colored part of the eye

Surrounds pupil

Muscle that constricts/relaxes to change size of pupil

Levels of pigmentation in the iris determine eye color

35
Q

Lens

A

Bends and focuses the light on the retina

Lens adjusts how much it focuses the light by changing its shape

36
Q

Ciliary Body

A

Suspensory ligaments + Ciliary Muscles

When ciliary muscle contracts, it’s attached to the suspensory ligaments, which then changes the shape of the lens → changes how much light is bent

Ciliary body secretes the aqueous humor

37
Q

Posterior Chamber

A

Space behind the iris/ciliary muscle

Filled with aqueous humor

38
Q

Vitreous Chamber

A

Filled with vitreous humor

Jelly-like substance that serves to supply pressure to the inside of the eyeball so that the eyeball maintains its round shape; also provides nutrients to cells inside the eyeball

39
Q

Retina

A

Where the ray of light is converted from a physical waveform into an electromagnetic stimulus that the brain can interpret

Packed with cells called photoreceptors

40
Q

Macula (and fovea)

A

A special part of the retina that is particularly rich in cones

Cones are involved in discerning high levels of detail in whatever you’re looking at

Fovea: a little dip in the macula

Almost completely covered in cones (compared to the rest of the retina, which is mostly covered in rods)

Cornea/lens bend light to focus on fovea so you can discern/appreciate fine details

41
Q

Choroid

A

Layer behind the retina

Pigmented black in humans

→ All the light that hits the choroid is absorbed

Network of blood vessels that helps nourish the retina

42
Q

Sclera

A

White, thick, fibrous tissue coat that covers the posterior ⅚ of the eyeball

Attachment point for muscles

Without the sclera, muscles wouldn’t have anything sturdy to attach to and you wouldn’t be able to move your eyes around

Also provides an extra layer of protection and structure to the eyeball

43
Q

Describe the path light takes from entering the to reaching the brain

A

light through the eye to the cornea -
aqueous humor - through pupil -
lens - vitreous humor - retina -
optic nerve - brain - the occipital lobe

44
Q

What are the major differences between rods and cones?

A

Rods: ~120 million; Very sensitive to light; Good for night vision; Found all around the periphery of the retina; contains protein rhodopsin; slow recovery time (takes a longer time to fire again than a cone)

Cones: ~6-7 million; Responsible for color vision; 3 types of cones: Red, green, and blue (named for the color they are sensitive to); Centered in the fovea of the retina –> Lets us see really fine details; contains protein photopsin; fast recovery time

45
Q

When light hits a rod, how does it effect the rod? How does this affect other cells involved in visual processing?

A

Light causes rod to turn off through the phototransduction cascade

When rod is turned off, on-bipolar cellis turnedon(off-bipolar cellis turnedoff), which then turnsontheretinal ganglion cell, which goes to theoptic nerveand then to thebrain

46
Q

Describe the main steps in the phototransduction cascade

A
  1. When light reaches the rod, retinal, a small molecule round in the proteinrhodopsin, changes conformation from bent (cis-retinal) to straight (trans-retinal), which in turn causesrhodopsin to undergo a conformation change as well
  2. Transducin (has alpha, beta, and gamma subunits) breaks away from rhodopsin; the alpha subunit binds to cyclic GMP phosphodiesterase (PDE)
  3. PDE converts cyclic GMP (cGMP) into GMP, which decreases [cGMP] and increases [GMP]
  4. cGMP binding to sodium channels allows sodium to flow into the cell, so decreased [cGMP] actually hyperpolarizes the cell and turns it off
47
Q

What are the two types of bipolar cells and how to they respond to hyperpolarization of rods?

A

On-center bipolar cells normally are being turned off when the rod cell is turned on → when the rod turns off, turns on this bipolar cell

Off-center bipolar cells get turned on when there’s no light → when the rod turns off, turns off this bipolar cell

48
Q

Why is there a dip where the fovea is in the retina?

A

These photoreceptors are connected to other neurons that send axons through the optic nerve and to the brain

Benefit of having no axons in the way of the light: When light hits the fovea, you get a higher resolution; more light is able to hit the cones directly rather than get absorbed by these axons

When light hits the periphery of the eye, it has to go through the axons, and as it’s going through, some of the energy is lost → less light hits rods/cones in the periphery

49
Q

Where do the optics nerves from each eye converge?

A

Optic chiasm

50
Q

All light that hits the temporal side of each eye (does/does not) cross the optic chiasm, while all light that hits the nasal side (does/does not) cross the optic chiasm.

This allows information from the _____ visual field to go to the _____ side of the brain, and vice versa.

A

Does not; does

Right; Left (or left; right)

*Note: light that hits the temporal part of the eyeball does not come from the temporal visual field, but rather comes from the nasal visual field

51
Q

Feature Detection

A

When you’re looking at an object, necessary to break it down to its component features in order to make sense of what you’re looking at; there are many components: color, form, motion

52
Q

Trichromatic Theory

A

Our ability to see color arises from the presence of cones within our retina; 3 major types

Red (60% of cones in eye), Green (30%) and Blue (10%)

Named for the color of light they are sensitive to

53
Q

What pathway is responsible for figuring out the shape of an object?

A

Parvo Pathway

54
Q

The Parvo Pathway is responsible for the _____ aspect of feature detection, and has a high level of ______ resolution and a low level of _______ resolution

A

Shape/form

Spatial

Temporal

*Parvo pathway also helps with color detection

55
Q

Which pathway is responsible for detecting the motion of an object?

A

Magno Pathway

56
Q

The Magno Pathway is responsible for the ______ aspect of feature detection, and has a high level of _______ resolution and a low level of _______ resolution

A

Motion

Temporal

Spatial

57
Q

Describe the main steps that involve hearing

A
  1. Sound is collected by the pinna (the visible part of the ear) and directed through the outer ear canal. 2. The sound makes the eardrum vibrate, which in turn causes a series of three tiny bones (the hammer, the anvil, and the stirrup) in the middle ear to vibrate.
  2. The vibration is transferred to oval window, and then to the snail-shaped cochlea in the inner ear; the cochlea is lined with sensitive hairs which trigger the generation of nerve signals that are sent to the brain.
58
Q

Label the parts of the ear

A
59
Q

What separates the fluid flowing in/out of the cochlea?

A

Organ of Corti

60
Q

How does the organ of corti convert fluid motion into sound?

A
  1. Upper and lower membranes of organ of Corti contain hair cells. The fluid flow pushes down on the top membrane and up on the bottom membrane, causing the hair cells to move back and forth
  2. On the top of the hair cell is the hair bundle, which is composed of a bunch of kinocilium connected to each other by a tip link
  3. Tip link is directly connected to potassium channels. Movement of hair cells stretches on the tip link; as the kinocilium gets stretched, it opens up this gate
  4. Potassium flows into the cell, which activate the opening of calcium channels → now also have calcium flowing into the cell
  5. → cell fires an action potential → stimulates another cell, known as a spiral ganglion cell, which then activates another cell that goes to the brain
61
Q

What range of frequencies can humans hear?

A

20 Hz to 20,000 Hz

62
Q

What method is used in the ear to distinguish different frequencies, and how does it work?

A

Basilar Tuning

Tonotypical Mapping: Hair cells at the base of the cochlea are activated by high frequencies; hair cells at the apex (tip) of the cochlea are stimulated by low frequencies

As sounds with varying frequencies hit the ear, they will stimulate different parts of the basilar membrane

Hair cell fires an action potential that eventually reaches the brain through the auditory nerve and it will be mapped to a particular part of the brain, the primary auditory cortex

63
Q

Describe the visual pathway in the brain, starting with the optic nerve

A

Optic Nerve travels to the Lateral Geniculate Nucleus (LGN) of the thalamus, which preserves the visual map created by the ganglion cells and projects this information to the primary visual cortex, which is located in the occipital lobe

64
Q

Describe the auditory pathway in the brain starting from the auditory nerve

A

First, auditory information goes from the auditory nerve to the cochlear nuclei in the medulla. Axons of the cochlear nuclei synapse with neurons in the inferior colliculus (on the way to the inferior colliculus, some crossing occurs such that auditory information from each ear is sent to the opposite hemisphere).

From there, electrical signals are passed on to the medial geniculate nucleus of the thalamus, which sends information to the auditory cortex in the temporal lobe.

65
Q

What condition results from problems with conduction from the hair cells to the brain? Can it be treated? If so, how?

A

Sensorineural Hearing Loss, aka “nerve deafness

Yes, can be surgically treated with a cochlear implant (however, only restores some degree of hearing)

66
Q

What is the difference between proprioception and kinesthesia?

A

Proprioception: Our ability to sense exactly where our body is in space; our sense of position and balance; Can be thought of as a cognitive awareness of your body in space; more under the surface/subconscious, you’re not overtly thinking about it

Kinesthesia: Movement of your body; Does not include sense of balance; More behavioral

67
Q

What specific receptors sense temperature? What else do they also respond to, and where are they located in the body?

A

TrpV1 receptors are sensitive to both temperature and pain

They are located throughout the whole body

68
Q

Pain/Temperature send information up to the brain through various nerves - what are the different types of fibers and what are the characteristics of each?

A

Aβ Fibers: Fast; Large diameter (lowers resistance) and covered in myelin (increased conductance) → fast signal; Sends message that there’s a change in temperature, it’s really hot, or something is really painful

Aδ Fibers: Medium speed; A little bit smaller in diameter, a little bit less myelin → don’t conduct a signal as quickly as the fast fibers

C Fibers: Slow; Small diameter, unmyelinated → sends a very slow signal

69
Q

Olfactory Epithelium

A

Specialized epithelial tissue inside the nasal cavity that’s involved in smell; Lies on roof of nasal cavity; directly responsible for detecting odors

Is part of the olfactory mucosa

70
Q

Olfactory Mucosa

A

Dime-sized region located high inside the nasal cavity and is the site of olfactory transduction

Contains olfactory receptor neurons

Olfactory receptor neurons have cilia

71
Q

Describe the main steps of the olfactory pathway

A
  1. Olfactory transduction occurs when odorant molecules reach the olfactory mucosa and bind to the olfactory receptor proteins on the cilia (GPCR)
  2. Receptor protein changes shape –> triggers the flow of ions across the receptor-cell membrane and an electrical response is triggered in the cilium
  3. Electrical responses in the cilia spread to the rest of the receptor cell, and from there are passed onto the olfactory bulb of the brain in the olfactory nerve
  4. Inputs from similar receptor neurons go to similar glomeruli (collections of cells within the olfactory bulb)
  5. From the olfactory bulb, mitral cells and tufted cells carry olfactory information to the olfactory cortex, and to the orbitofrontal cortex
72
Q

Pheromones

A

Specialized olfactory cues

A chemical signal that is released by one member of a species and is sense by another member of the species, and it triggers an innate response

Very important in animals, particularly insects: have been linked to mating, fighting, and chemical communications

Sensed in the vomeronasal system, which is within the accessory olfactory epithelium

73
Q

What are the 5 main tastes?

A

Bitter, salty, sweet, sour, umami

74
Q

What are the different types of taste buds?

A

Fungiform, foliate, and circumvallate

75
Q

Which taste buds sense which tastes?

A

All taste buds have receptors for all 5 tastes

76
Q

Labeled Lines Model

A

Each cell has an axon projecting from it, and these axons remain separate all the way to the brain and synapse onto different parts of the gustatory cortex in the brain

All cells that are sensitive to a particular taste synapse in the same part of the brain

77
Q

Individual taste cells are sensitive to how many of the tastes?

A

Each individual taste cell is sensitive to 1 particular taste

78
Q

Which types of taste cells have GPCRs?

A

Sweet, umami, bitter

79
Q

Cells that are sensitive to __________ rely on ion channels

A

Sour, salty

80
Q

What types of receptors are sensitive to:

  1. Sweet
  2. Salty
  3. Sour
  4. Bitter
  5. Umami
A
  1. GPCR
  2. Ion channels
  3. Ion channels
  4. GPCR
  5. GPCR