Lecture 9: Learning and Memory 1 Flashcards

1
Q

Who was patient H.M., and why did he undergo brain surgery?

A

H.M. (Henry Molaison) was a patient with severe epilepsy who underwent a bilateral medial temporal lobotomy to treat his condition.

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2
Q

What was the purpose of the medial temporal lobotomy in H.M.’s case?

A

The surgery aimed to alleviate his epilepsy, but it was an invasive and imprecise procedure.

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3
Q

What cognitive impairment did H.M. experience after his surgery?

A

He developed anterograde amnesia, meaning he was unable to form new memories after the surgery.

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4
Q

Who was the main researcher studying H.M.s condition?

A

Brenda Milner, a British-Canadian neuropsychologist, was the first to document the cognitive damage from the surgery.

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5
Q

How many other patients underwent similar surgeries to H.M.?

A

Eight other patients also had the surgery

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6
Q

Why is H.M.’s case considered ethically questionable?

A

The surgery was performed with limited knowledge of its risks and benefits, making its ethical acceptability debatable.

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7
Q

What was William Beecher Scoville’s attitude toward the surgery?

A

Scoville, the surgeon, prioritized action over thought and may have been motivated by career advancement rather than just therapeutic outcomes.

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8
Q

How did H.M.’s case impact medical practices regarding epilepsy surgery?

A

It highlighted the severe cognitive consequences of such surgeries, leading to a shift toward less invasive and more precise methods.

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9
Q

What brain structures were affected by H.M.’s surgery?

A

The surgery damaged the hippocampus (the intended target), amygdala, entorhinal cortex, and fully removed the parahippocampal cortex.

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10
Q

Why is it difficult to attribute H.M.’s memory impairments to a single brain region?

A

Multiple brain structures were damaged, making it impossible to determine which specific area was responsible for the memory deficits.

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11
Q

What was the broader impact of H.M.’s case on neuroscience?

A

It was a crucial starting point for human cognitive neuroscience, helping researchers link brain damage to cognitive functions.

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12
Q

What is the mirror tracing task, and why is it difficult?

A

The mirror tracing task requires tracing an image while viewing it in a mirror, making movements reversed and contradicting previous hand-eye coordination learning.

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13
Q

What type of learning does the mirror tracing task measure?

A

It measures motor skill learning but also requires unlearning previous motor habits, making it not “process pure.”

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14
Q

How is learning measured in the mirror tracing task?

A

Learning is measured by counting the number of tracing errors, which decrease over multiple training days.

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15
Q

What does the error rate on day 3 of the mirror tracing task indicate?

A

It reflects the cumulative learning from day 1 and day 2, showing that learning is retained over multiple days.

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16
Q

How did H.M. perform on the mirror tracing task?

A

He showed a normal motor learning curve, meaning he improved with practice despite his brain lesions.

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17
Q

Why was H.M.’s ability to learn the mirror tracing task surprising?

A

His brain lesions suggested that learning should be impaired, but his ability to improve indicated that motor learning occurs outside the damaged regions.

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18
Q

Could H.M. consciously remember doing the mirror tracing task before?

A

No, if asked, he would say he had never done the task before, despite showing improvement.

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19
Q

What type of memory was impaired in H.M.?

A

His declarative memory (which stores names, dates, facts, and events) was impaired.

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20
Q

What is a single dissociation in cognitive neuroscience?

A

It occurs when a person can do one cognitive task but not another, like H.M. who could learn a motor task but not remember doing it.

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21
Q

What is a double dissociation?

A

It occurs when another person with different brain damage shows the opposite pattern—struggling with motor learning but retaining declarative memory.

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22
Q

What conclusion was initially drawn about the hippocampus from H.M.’s case?

A

Researchers claimed that the hippocampus was crucial for declarative memory but not skill learning.

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23
Q

Why was the claim about the hippocampus overstated?

A

H.M.’s lesions were extensive, making it unclear whether declarative memory relies solely on the hippocampus or a broader network of brain regions.

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24
Q

What did later research reveal about learning and brain areas?

A

Learning requires a wide network of brain regions, rather than being confined to the hippocampus alone.

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25
Q

What was Karl Lashley trying to discover in his experiments?

A

He aimed to find the cortical engram—the specific brain location for learning and memory, particularly in maze navigation.

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26
Q

What were Lashley’s key findings about memory storage?

A

Learning was not stored in one specific location; instead, impairments increased as more cortex was removed, supporting the principle of mass action.

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27
Q

What is the principle of equipotentiality?

A

It suggests that if one part of the cortex is damaged, other areas can take over its function.

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28
Q

How did different types of cortical cuts affect learning performance?

A

Perpendicular cuts had little effect, while undercutting slabs of cortex caused significant impairment, suggesting brain circuits run vertically.

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29
Q

How did Lashley’s research change our understanding of memory in the brain?

A

It showed that memory is widely distributed across the cortex rather than being localized to a single brain area.

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30
Q

Why is it problematic to claim that a specific brain system directly causes a psychological process?

A

True causality requires direct manipulation of the brain system and observing reliable changes in the psychological process, which is ethically impossible in humans.

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31
Q

Why do lesion studies in humans provide limited causal evidence?

A

Brain damage from surgery or accidents is often widespread, affecting multiple systems, and psychological changes may result from other factors like trauma or inflammation.

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32
Q

What is a major limitation of brain imaging techniques like MRI and CT scans?

A

They provide only correlational data with low resolution, meaning they show activity levels but cannot determine what function an area performs.

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33
Q

How can animal studies help establish causal links between brain areas and behaviour?

A

Researchers can precisely manipulate brain function in animals, allowing for controlled experiments on behaviour, though generalising findings to humans is limited.

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34
Q

What is triangulation, and how does it strengthen neuropsychological research?

A

Triangulation combines evidence from human scans, lesion studies, and animal experiments to make stronger inferences about brain-behaviour relationships.

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35
Q

How is the hippocampus removed in monkeys compared to rats?

A

In monkeys, suction is applied from below, whereas in rats, access is gained from the top.

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36
Q

What is a major confound in hippocampal lesion studies across species?

A

The method of removal unintentionally damages different cortical areas—rhinal cortex in monkeys and parietal cortex in rats—potentially influencing results.

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37
Q

Why is it important to acknowledge confounds in lesion studies?

A

Unintended cortical damage may alter results, making it harder to isolate the role of the hippocampus in psychological functions.

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38
Q

What are some more precise techniques for studying brain function?

A

Pharmacological agents (often reversible) allow temporary manipulation, and electrophysiology uses electrodes to stimulate or record neuron activity during tasks.

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39
Q

What is the ultimate goal of these experimental techniques?

A

To enable more accurate causal claims about how specific brain systems contribute to psychological processes.

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40
Q

How is the hippocampus removed in monkeys compared to rats?

A

In monkeys, suction is applied from below, whereas in rats, access is gained from the top.

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41
Q

What is a major confound in hippocampal lesion studies across species?

A

The method of removal unintentionally damages different cortical areas—rhinal cortex in monkeys and parietal cortex in rats—potentially influencing results.

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42
Q

Why is it important to acknowledge confounds in lesion studies?

A

Unintended cortical damage may alter results, making it harder to isolate the role of the hippocampus in psychological functions.

43
Q

What are some more precise techniques for studying brain function?

A

Pharmacological agents (often reversible) allow temporary manipulation, and electrophysiology uses electrodes to stimulate or record neuron activity during tasks.

44
Q

What is the ultimate goal of these experimental techniques?

A

To enable more accurate causal claims about how specific brain systems contribute to psychological processes.

45
Q

How is long-term memory (LTM) categorized?

A

LTM is divided into declarative memory (episodic and semantic) and non-declarative memory (skills and emotional conditioning).

46
Q

What did HM’s case reveal about different types of memory?

A

He had intact procedural skill learning (e.g., mirror tracing) but impaired declarative memory, meaning he could not recall past experiences.

47
Q

Why was HM’s case insufficient to isolate the role of the hippocampus?

A

His lesions were too extensive, affecting multiple brain regions, making it unclear whether the hippocampus alone caused his memory impairment.

48
Q

What is the delayed non-matching to sample task, and why is it used?

A

A primate learns that a previously rewarded object (e.g., a key) will not be rewarded next time, encouraging a win-shift strategy. It helps test episodic memory and hippocampal function.

49
Q

What is the key question researchers aim to answer using this task?

A

Whether hippocampal lesions impair episodic learning in a similar way to HM’s memory deficits.

50
Q

How did selective hippocampal lesions affect memory performance in monkeys?

A

Monkeys with only hippocampal lesions had a small reduction in performance, while larger lesions involving additional cortical areas led to greater deficits.

51
Q

What pattern of impairment was observed with increasing lesion size?

A

The more brain regions were damaged (hippocampus → parahippocampus → perirhinal + entorhinal cortex), the worse the memory impairment became.

52
Q

How does this study relate to Lashley’s principle of mass action?

A

Like Lashley’s findings in maze learning, this study showed that memory is not localized to a single site, but rather, larger lesions cause greater deficits.

53
Q

What does this study suggest about brain organization for memory?

A

It discourages the idea that single brain regions control specific psychological functions, supporting the view that memory relies on large, interconnected networks.

54
Q

How do these findings challenge simple brain-behaviour claims?

A

They show that psychological functions are not confined to single brain areas but depend on integrated systems that extend across multiple regions.

55
Q

Which brain region is responsible for procedural skill learning, such as in the mirror tracing task?

A

The basal ganglia and striatal region support procedural skill learning.

56
Q

What brain area is critical for emotional conditioning, such as fear conditioning?

A

The amygdala plays a key role in emotional conditioning.

57
Q

Which neural structures support low-level motor conditioning and simple reflexes?

A

Eyeblink conditioning relies on the cerebellum, while simple reflexes are controlled by the brainstem, which is closely linked to the cerebellum.

58
Q

How does priming relate to Lashley’s maze learning experiments?

A

Priming—where prior exposure to a stimulus improves response—may have helped rats navigate mazes by sequentially activating memory for the next turn. Cortical lesions likely impaired this process.

59
Q

Why is it misleading to say “Brain area X plays a role in psychological function Y”?

A

Most tasks are not process pure—they require multiple forms of memory. It’s more accurate to say “Brain area X is required for performance of task Y” rather than assuming it only supports a single psychological function.

60
Q

What is Aplysia, and why is it used in learning studies?

A

Aplysia is a sea mollusc used to study cellular learning processes due to its simple nervous system and its gill withdrawal reflex, which responds to threats.

61
Q

How does Aplysia’s gill withdrawal reflex help in studying learning?

A

Researchers tap Aplysia’s siphon, mimicking a potential threat, and measure the extent of gill withdrawal to study learning and memory processes.

62
Q

What is habituation, and how is it demonstrated in Aplysia?

A

Habituation occurs when repeated siphon taps lead to less gill withdrawal, as Aplysia learns the tap is non-threatening.

63
Q

What type of learning is habituation?

A

Habituation is non-associative learning—Aplysia learns that the siphon tap predicts nothing harmful rather than associating two stimuli.

64
Q

Why is the Aplysia model useful for studying neural learning mechanisms?

A

Its simple nervous system allows researchers to track cellular changes during learning, providing insight into basic neural mechanisms.

65
Q

How is the duration of habituation memory measured in Aplysia?

A

By tracking the duration of gill withdrawal in response to siphon taps over multiple testing sessions (T1–T4) and recall tests (R1–R3).

66
Q

What do the recall tests (R1, R2, R3) show about memory retention?

A

R1 (1 day later) and R2 (1 week later) show good retention, but R3 (3 weeks later) shows partial memory decay.

67
Q

Why were two experiments conducted on habituation memory?

A

To ensure the results were reproducible and not just due to chance.

68
Q

What does this study suggest about the stability of habituation memory?

A

Habituation memory is long-lasting but gradually decays over weeks.

69
Q

Why is Aplysia an important model for studying learning?

A

It allows researchers to test cellular mechanisms of learning in a simple and controlled system.

70
Q

What is classical conditioning?

A

It is learning an association between two or more things that are statistically related in the environment.

71
Q

Why has classical conditioning evolved?

A

To help organisms encode statistical regularities in their surroundings for adaptive behavior.

72
Q

What types of organisms have been used to study classical conditioning at the cellular level?

A

Aplysia, fruit flies, honeybees, flatworms, pond snails, anemones, and nematode worms.

73
Q

How does classical conditioning differ from habituation?

A

Classical conditioning involves associating stimuli, while habituation involves ignoring a repeated, irrelevant stimulus.

74
Q

What is an example of classical conditioning in animals?

A

A dog learning to salivate at the sound of a bell after repeated pairings with food (Pavlovian conditioning).

75
Q

What was Pavlov originally studying in dogs?

A

How saliva promotes digestion, collecting saliva to analyze its role.

76
Q

What unexpected observation led Pavlov to study conditioning?

A

Dogs began salivating before food appeared, just upon seeing Pavlov enter the room.

77
Q

How did Pavlov systematically test this phenomenon?

A

He paired a metronome sound (conditioned stimulus) with food (unconditioned stimulus) to create a learned salivary response.

78
Q

What did Pavlov’s experiment demonstrate?

A

Animals can learn associations between neutral stimuli (metronome) and biologically relevant stimuli (food).

79
Q

How did the dogs’ response change after repeated pairings of the metronome and food?

A

They salivated at the metronome alone, expecting food—showing classical conditioning.

80
Q

What is temporal contiguity in classical conditioning?

A

The conditioned stimulus (CS) must occur before the unconditioned stimulus (US) to be effective—acting as a predictive warning signal.

81
Q

What is the blocking effect in conditioning?

A

If an existing CS already fully predicts the US, a new CS won’t be learned—learning only occurs if the new CS improves prediction.

82
Q

Why does blocking demonstrate that conditioning is selective?

A

It shows that the brain optimizes learning by only acquiring useful, non-redundant information about the environment.

83
Q

How does classical conditioning shape daily life?

A

It helps us form expectations—whenever we anticipate something based on past experiences, classical conditioning is at work.

84
Q

How does classical conditioning ensure adaptive behavior?

A

It allows organisms to predict important events, preparing them to respond appropriately to their environment.

85
Q

Why is eye blink conditioning more convenient than Pavlov’s model?

A

It only requires observing an eye blink, rather than collecting saliva, making it easier to measure.

86
Q

What is the reflex pathway in eye blink conditioning?

A

An air puff to the eye naturally triggers a blink via the cranial nerves.

87
Q

How does conditioning occur in eye blink experiments?

A

A sound (CS) is paired with an air puff (US) until the sound alone elicits a blink (CR).

88
Q

What does cerebellar damage reveal about learning?

A

It impairs eye blink conditioning, showing that the cerebellum is crucial for learning conditioned reflexes.

89
Q

How does eye blink conditioning help in neuroscience?

A

It allows researchers to deduce neural circuits involved in simple conditioned reflexes.

90
Q

What is the key difference between classical conditioning and operant learning?

A

Classical conditioning involves learning associations between stimuli, while operant learning involves learning the relationship between one’s own actions and their consequences.

91
Q

How did Thorndike study operant learning?

A

He placed cats in a box, where they learned to press a lever to escape.

92
Q

What did Thorndike observe about the learning curve?

A

Learning was gradual, not sudden insight, as cats became incrementally faster rather than showing an immediate breakthrough.

93
Q

What is Thorndike’s Law of Effect?

A

Behaviours followed by positive outcomes (e.g., escape) become stronger, reinforcing the association between the situation and response.

94
Q

How does the Law of Effect explain learning?

A

It suggests that pleasure strengthens stimulus-response associations, leading to habit formation over time.

95
Q

What is spatial learning, and why is it important?

A

Spatial learning involves understanding where things are in space to aid navigation, such as in maze learning or finding a home location.

96
Q

How did Charles Turner study spatial learning in ants?

A

He observed ants using landmarks like leaves to navigate back to their nest. When he moved the landmarks, the ants searched in the wrong place, showing they relied on landmarks.

97
Q

What did Nico Tinbergen discover about digger wasps?

A

Digger wasps used landmarks to locate their nests. When Tinbergen moved the landmarks, the wasps searched in the wrong location, proving they depended on these cues.

98
Q

What is the Morris water maze, and what does it test?

A

The Morris water maze is an experiment where rats swim to a hidden platform using landmarks outside the bath, testing their spatial learning and memory.

99
Q

How is the hippocampus related to spatial learning?

A

The hippocampus plays a key role in processing spatial memory, and its cellular mechanisms have been studied extensively in the Morris water maze.

100
Q

What are the different types of memory storage?

A

Memory is divided into:
- Sensory buffer (temporary storage for stimuli, e.g., between visual saccades).
- Working memory (short-term holding of information, e.g., remembering a number before writing it down).
- Intermediate memory (requires repeated learning before becoming long-term through consolidation).

101
Q

What are the possible outcomes for information in short-term memory (STM)?

A

Information in STM can either:
- Be used and forgotten or
- Be consolidated into long-term memory (LTM) for later retrieval.

102
Q

How does fear conditioning in rats demonstrate memory consolidation?

A

Rats learn to freeze in a context that signals shock. Memory is tested months later to see if they still recall the association.

103
Q

How does hippocampal damage affect fear memory over time?

A

Lesions to the hippocampus impair memory if done 1 day after learning but not 28 days later, suggesting memory transfers away from the hippocampus over time.

104
Q

What brain region stores fear memory after consolidation?

A

The cortex stores fear memory by day 28, as shown by the fact that cortical lesions impair memory at this stage, but not at day 1.