PSY1002 SEMESTER 2 - WEEK 7 Flashcards

1
Q

why is it important to study classical, operant conditioning

A

study fundamental forms of learning, understand learning foundation, understand stimulus-responses, understand drug addictions, use developing AI

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2
Q

where does simple classical conditioning occurs

A

amygdala and cerebellum

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3
Q

what is classical/operant conditioning in terms of research

A

experimental paradigms leading to highly influential frameworks for associative learning
classical= stimulus-response associations
operant= action-outcome associations

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4
Q

describe appetitive stimuli in classical conditioning

A

want to approach eg: food or hot shower

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5
Q

describe aversive stimuli in classical conditioning

A

animal want to avoid eg: loud noises

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6
Q

give common aversive conditioning paradigms and what it can be applied to

A

eye-blink conditioning, tail pinching, shocks
little Albert
understand phobias formation, anxiety disorder, protective mechanisms (flinching)

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7
Q

explain single-trial learning as part of aversive conditioning

A

evolutionary function- preventing illness (food poisoning)

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8
Q

explain classical conditioning in PTSD

A

develop strong association between situ (CS) and trauma (UCR), with thinking about CS producing severe anxiety (CR) and PTSD develop due to emotion experienced during trauma producing neural activity in amygdala, causes strong conditioned learning which has a slow extinction

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9
Q

define extinction

A

reduction in responding that occurs when CS is presented repeatedly without UCS

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10
Q

outline extinction paradigm

A

study how strong association formed during conditioning is via examining occurrence post conditioning when UCS are removed, presenting a CS alone

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11
Q

what is spontaneous recovery (as shown by Rescorla, 2004 study)

A

after 8 days rest, sudden return to response without reintroductions to stimulus-response
suggests extinction is new type of learning, not forgetting/unlearning

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12
Q

what can spontaneous recovery suggest

A

original learning not fully erased and excitatory association reinforces responses, inhibitory association prevents response. when both equally strong, cancel out each other but after pause inhibitory association become weaker, excitatory more persistent causing reintroduction of CR

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13
Q

sum up simply extinction

A

not unlearning, but learning that association is no longer valid

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14
Q

give advantages of not fully unlearning association

A

environmental change (food available) and not fully unlearning allows flexibility for survival, don’t have to restart acquisisions but can pick up quickly again

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15
Q

give disadvantages of not fully unlearning associations

A

negative implications- unlearnt associations which influence survival, if association is wrong then want to get rid of the learning

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16
Q

define generalisation

A

ability to then also respond with CR, to new stimulus which resembles original CS

17
Q

outline why generalisation is important learning mechansim

A

avoid overtraining for specific stimuli- in real life similar stimuli has similar properties but don’t need to do full acquisition process every time, saving time and evolutionary significance (learn to avoid certain stimuli by generalising negative past outcome)

18
Q

give research example into generailsation

A

ppts had brief interaction with female experimenter, had to ask question, and experimenter responded negative/neutral
students went into another room, asked to approach either one of 2 researchers, significantly more likely to avoid one which looked like original experimenter when she was negative

19
Q

define discrimination

A

ability to then not respond with CR to new stimulus, which resembles original CS

20
Q

explain how discrimination is important learning mechanism

A

allow using for detection in important salient differences in environment

21
Q

outline second-order conditioning

A

existing CS can serve as UCS for pairing with new CS. after consistently pairing CS1 and UCS, CS1 can be UCS for CS2, also triggers CR, leading to long chain of associated stimuli

22
Q

define trial (in a research paradigm)

A

single presentation of a CS-UCS sequenced

23
Q

define block (in a research paradigm)

A

consists of several trials, typically has specific parameter (reward probabilities, trial types etc)

24
Q

define session (in a research paradigm)

A

consists of one or more blocks- different session usually are separated by longer time intervals eg: days

25
Q

what is partial reinforcement

A

intersperse trials where CS isn’t followed by UCS done randomly, so CS followed by UCS with certain probabilities = practical issue as predictable, so instead use delay conditioning (which means CS overlap with UCS- not using a delay)

26
Q

explain blocking in studies

A

first pair CS1+UCS, then post-training add CS2 which is presented with CS1 and followed by UCS
presenting only CS2 doesn’t trigger response (learning is blocked)

27
Q
A