cog neuroscience Flashcards

1
Q

whats useful about a damaged brain

A

helps us understand how a healthy brain works

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2
Q

N400 electrophysiological signal [how locating processes is valuable]

A

the N400 electrophysiological signal is triggered when we hear a completely unexpected word in a sentence; this is useful for language psych in measuring when prediction occurs in speech comprehension/planning

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3
Q

recording study method

A

a study in which behaviour is changed or manipulated, and the effect on the brain is measured
- CORRELATIONAL technique

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4
Q

strength of recording study technique

A

greater design flexibility and control, offers high temporal and spatial resolution of brain activity

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5
Q

inference studies

A

changing the state of the brain and measuring the effect on behaviour [EX: comparing brain damage ppts to control group]
- CAUSAL inference

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6
Q

limitation of inference studies

A

in brain damage, the brain often reorganises itself and has high plasticity, meaning that the function may not be completely impaired, and will be unique for every ppt

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7
Q

two types of stroke

A

ischemic - blockages in blood vessels cut off blood supply to the brain
hemmorrhagic - the wall of a blood vessel bursts, disrupting flow to brain

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8
Q

single dissociation

A

looking at one case of impairment; weak inference for exploring if two processes are different

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9
Q

double dissociation

A

two contrasting cases of impairment; strong inference for concluding that two processes are independent and can also help locating

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10
Q

association

A

cases with similar performance on all tasks (whether this is impairment or normality)

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11
Q

fractionation assumption

A

the assumption that brain damage can selectively affect different cognitive and neural systems

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12
Q

transparency assumption

A

the assumption that brain lesions can affect existing cognitive systems but do not create new ones

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13
Q

universality assumption

A

the assumption that all cognitive systems are basically the same

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14
Q

critique of transparency assumption

A

neural plasticity is common, so new pathways are often formed after brain damage

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15
Q

critique of universality assumption

A

individual differences are too prominent to assume that cognitive systems are the same - ppl have variation in cognitive ability & cognitive strategies

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16
Q

two proposed models of reading irregular words

A

connectionist ‘triangle’ model - to read irregular words, we use their semantics
dual-route cascaded model - to read irregular words, we use their lexical representation, not their semantics

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17
Q

lesion-symptom mapping

A

find ppts with similar impairments, acquire structural brain scans, identify specific areas & create a lesion overlap map

18
Q

lesion overlap map

A

map of the brain where the areas with the most correlation between ppts is darker (works on a gradient)

19
Q

lesion overlap map in reading

A

study looked at specific reading deficits; found that poor irregular word reading was correlated with damage to the anterior temporal lobe

20
Q

how are lesion overlap maps useful in a clinical setting

A

can predict the statistical probability of specific brain injuries causing specific deficits

21
Q

limits of using natural lesions (3)

A
  • can only use between-subjects design, which can be influenced by individual differences
  • brain damage frequently extends to multiple areas
  • neural plasticity = possible reorganisation of function, so ppts may not have completely lost certain functions
22
Q

transcranial magnetic stimulation

A

a rapidly changing magnetic field is applied to the head, and temporarily disrupts brain functions
= temporary virtual lesions

23
Q

what principle does transcranial magnetic stimulation work off of

A

electromagnetic induction
= the electric charge of one coil creates a magnetic field which induces an electric charge in the second coil (second coil = brain)

24
Q

strengths of transcranial magnetic stimulation (3)

A
  • ppts can act as their own control in within-person design, reducing the effect of individual differences
  • we can know and test what their normal brain function is like’
  • no complications from damage or plasticity
25
Q

limits of transcranial magnetic stimulation (3)

A
  • only stimulates 2-3cm below skull = cannot reach deeper structures
  • higher cognitive functions have less noticeable effects, so exps need careful design
  • cannot study long term processes such as learning
26
Q

how do atoms communicate

A

by passing on action potentials

this is called firing or spiking

27
Q

how do EEGs work [electroencephalography]

A

records changing action potentials

measures microvolts, which are the response of many neurons firing at once

28
Q

limitations of using EEG (2)

A

poor spatial resolution (measures when rather than where)

it’s hard to filter out noise from random firing

29
Q

how do ERPs work [event-related potential]

A

records positive and negative changes in voltage;

these events are named based on their polarity and extent

30
Q

how do MEGs work [magnetoencephalography]

A

similar to EEG but maps brain activity using a magnetic field instead

31
Q

strength of MEG

A

better spatial resolution than EEG

32
Q

how does a PET scan work

A

positron emission tomography
a radioactive tracer is injected into the blood stream, this then flows to where brain activity is taking places and the decay emits positrons which are measured

33
Q

limits of PET scans (3)

A

ppts become exposed to radiation
expensive and complex
the task has to last at least 1 minute for decay to be recorded

34
Q

how does a structural MRI work

A

protons within atoms are always spinning
a magnetic field is used to align them
to take a pic, a frequency is sent out to knock them out of place
we then measure where and how quickly they realign

35
Q

how does a functional MRI work

A

active neurons require more oxygenated blood, an fMRI measure the ratio of oxygenated : deoxygenated blood to see where activity is occurring
- this is called BOLD imaging
the brain is split into a grid of voxels to locate the BOLD contrast

36
Q

limit of fMRI

A

poor temporal resolution as it is a slow process

37
Q

blocked design in MRI

A

showing ppts stimuli in blocks (can lead to them expecting the stimuli and changing behaviour)

38
Q

event-related design in MRI

A

changing the stimuli each time it is shown to reduce expectations and provoke a more realistic response

39
Q

subtraction analysis for fMRI

A

the average of the brain’s ‘on’ activity minus the average of the brain’s ‘off’ activity

40
Q

default mode network

A

the brain network activity while resting; it deactivates during specific tasks

41
Q

multi-voxel pattern analysis (fMRI)

A

using algorithms to differentiate between patterns of activation to classify subsets of activity
= can tell us WHAT info is being coded (not just where/when)