Psychophysiological Methods Flashcards

1
Q

METHODS LIST

A
  • structural/functional Magnetic Resonance (MRI/fMRI)
  • Positron Emission Tomography (PET)
  • Transcranial Magnetic Stimulation (TMS)
  • Transcranial Direct Current Stimulation (TDCS)
  • Electroencephalography (EEG) & Event-Related Potentials (ERPs)
  • eye-tracking
  • pupillometry
  • microelectrode recordings
  • Galvanic Skin Response measurements
  • cardiac measurements (ie. heart-rate)
  • Electromyography (EMG)
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2
Q

MOST WIDELY USED METHODS

A
  • structural/functional Magnetic Resonance (MRI/fMRI)
  • Transcranial Magnetic Stimulation (TMS)
  • Electroencephalography (EEG) & Event-Related Potentials (ERPs)
  • eye-tracking
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3
Q

MAGNETIC RESONANCE: BASICS

A
  • magnetic resonance imagining (MRI) = based on measurement of magnetic resonance (MR) signal
  • when magnetic field that changes over time w/rate of radio waves (radio frequency aka. RF) is applied to hydrogen atoms -> respond/resonate w/measurable magnetic signal
  • aka. magnetic resonance (MR) signal
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4
Q

STRUCTURAL MAGNETIC RESONANCE IMAGING

A
  • MR images are obtained via measuring MR signal from hydrogen atoms in brain
  • ie. images depend on hydrogen amount/density aka. ^ hydrogen = brighter brain areas
  • used by psychologists for for comparing brain structure in individual groups (ie. healthy individuals VS people suffering from psychiatric disorders)/examining brain structure changes as function of experience/training/psychological interventions
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5
Q

FUNCTIONAL MAGNETIC RESONANCE IMAGING (FMRI)

A
  • MRI can also examine brain activity
  • O2 = transported to cells via hemoglobin molecule (oxygehemoglobin aka. Oxy-Hb)
  • transfer of O2 to cells transforms oxyhemoglobin -> deoxygenated hemoglobin (deoxyhemoglobin aka. deoxy-Hb)
  • oxyhemoglobin doesn’t significantly alter MR signal; deoxyhemoglobin does aka. reduces signal
  • ^ active brain areas receive ^ oxygenated blood than they use aka. contain less deoxygenated hemoglobin; deoxygenated hemoglobin reduces MRI signal in such areas less aka. there’s more MRI signal coming from such brain areas
  • hence BOLD fMRI = ^ sensitive to blood flow-rated oxygen supply to this area > oxygen consumption in active area
  • AKA. BOLD fMRI = sensitive to difs in blood flow into active area
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6
Q

FMRI: REVERSE INFERENCE

A
  • scientific interpretation most commonly used by psychologists on basis of fMRI data
  • ie. effectiveness of acupuncture compared brain activity w/ VS w/o acupuncture in people w/chronic pain; found reduced brain activity (blood flow) in brain area set in acupuncture presence
  • areas were previously found activated in studies modulating pain perception
  • conclusion: reduced activation in said regions = objective evidence that pps felt less pain during acupuncture
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7
Q

REVERSE INFERENCE LOGIC

A
  • more general reverse inference: if changes in activation in given brain area = specifically associated w/psychological process then changes in activation point to involvement/modulation of hypothesised psychological process
  • how credible/valid it is depends on if given brain activity patter is also associated w/other psychological processes (specificity)
  • if brain area = activated by multiple psychological process types then activation cannot be taken as evidence of involvement in specific psychological process
  • researchers who make reverse inferences need to provide detailed info on both sensitivity/specificity BUT oft don’t
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8
Q

BOLD FMRI: LIMITS

A
  • blood flow changes associated w/neuronal activity = slow aka. BOLD response to brief stimulus to which pp responds in 1s = 16s
  • aka. fMRI temporal resolution = relatively low (cannot distinguish activations in response to stimuli at interval <3s)
  • scanner = v noisy aka. harder to use auditory stimuli/record vocal responses; one needs to pause scanning while auditory stimulus is presented/while pp is making response aka. “sparse imaging”
  • space in scanner = tight aka. not suitable for individuals w/claustrophobia
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9
Q

ELECTROENCEPHALOPGRAPHY (EEG)

A
  • change in voltage (electricity) recorded from sensors on scalp
  • can extract state of brain (ie. sleep) via EEG frequencies
  • EEG segments associated w/particular stimuli can be analysed separately aka. event-related potentials (EPRs)
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10
Q

FREQUENCY

A
  • oscillation number per unit of time (ie. x4 p/second = 4Hz)
  • EEG has complex frequency patterns
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11
Q

EEG: SLEEP

A

AWAKE & STAGES 1-4 SLEEP
- gradual slowing of EEG (lower frequencies) as sleep becomes deeper
REM SLEEP
- fast (awake-like) EEG seen in Rapid Eye Movement sleep during which most vividly recalled dreams are believed to occur

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12
Q

EVENT-RELATED POTENTIALS (ERPs)

A
  • segments of EEG
  • time-locked to particular events stimuli
  • dif types of stimuli are separately averaged then compared
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13
Q

ERP: LEXICAL DECISION TASK

A
  • pps presented w/words (ie. TALL/readable strings (not words)/non-words ie. TOLB)
  • asked to respond w/1 keypress if stimulus = word & with another if it’s not
  • words start to diverge from non-words at 250ms; clearly dif by 400ms
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14
Q

EEG: EVALUATION

A
  • EEG/ERP has very high temporal resolution aka. it can provide detailed temporal info about processing of stimulus
  • relatively cheap/accessible compared to fMRI
  • BUT has limited spatial resolution aka. it can’t localise activity in brain w/precision/confidence due to complexity of the inverse problem
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15
Q

EEG: THE INVERSE PROBLEM

A
  • inferring cortical generators from known scalp potentials
  • solution = highly uncertain
  • mathematically there is an infinity of cortical current distributions that could result in 1 scalp distribution
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16
Q

NEUROIMAGING & ELCTROPHYSIOLOGY CAUSALITY ISSUE

A
  • both techniques suffer from 1 serious drawback
  • difficult to be certain which (if any) fMRI activations/ERP component modulations are necessary for a given task/psychological process
  • just because fMRI activations/ERP component modulations co-occur w/experimental condition doesn’t mean they cause it or are essential for process to take place
17
Q

TRANSCRANIAL MAGNETIC STIMULATION (TMS)

A
  • large current is briefly discharged into wire coil held on subject’s head
    current generates rapidly changing (increasing) magnetic field around wire coil; this field passes into brain
  • magnetic field generates electric (ionic) current through neurons’ membranes in cortex
18
Q

TMS: MACROSCOPIC RESPONSE

A
  • evoked neural activity (EEG)
  • changes in blood flow/metabolism (PET/fMRI/NIRS/SPECT)
  • muscle twitches (EMG)
  • changes in behaviour
19
Q

TMS: EFFECTS

A
  • can increase/reduce excitability (ease with which neuronal activity is produced by action/stimulus) depending on intensity/number of stimulation pulses
  • in context of goal-directed behaviour (ie. cognitive task) this tends to result in disorganisation of neural activity typically resulting in impaired performance
  • aka. effect is similar to that of neurological lesion (only subtle/reversible/safe)
  • TMS is oft referred to as the virtual lesion technique because of this
20
Q

TMS: TASK-SWITCHING PARADIGM

A
  • pps learned 2 simple classification tasks:
    1) colour task: classify stimulus colour as “warm” (ie. red/orange) or “cold” (ie. blue/green)
    2) shape task: classify shapes as made of straight VS curved lines
  • pps asked to “switch” between tasks; auditory cue specified task to be performed in advance of each stimulus
  • key manipulation = preparation interval
  • interval between cue/stimulus (of CSI) could be longer (750ms)/shorter (200ms)
  • preparation tends to reduce switch cost
21
Q

TMS: STRENGTHS

A
  • can answer critical causality question which cannot be answered using brain measurement methods (ie. fMRI/EEG) aka. is a brain area/structure necessary for performance
  • high temporal resolution/relatively high spatial resolution…
22
Q

TMS: LIMITATIONS

A
  • … BUT “depth coverage” is limited; TMS cannot reach beyond cortex (10-20mm into brain)
  • associated w/strong confounds (side effect) which aren’t easy to control
  • to control for them one typically has a control condition of stimulating over brain area that’s assumed not to be involved in hypothesises process; BUT selecting such an area can be difficult
  • effects of stimulation aren’t confined only to region under coil due to connectivity between regions
23
Q

EYE-TRACKING

A
  • most common technology relied on monitoring pupil position by emitting infrared beam & detecting its reflection from cornea
  • reflection is weaker where pupil is
  • sampling rate can be as high as 1000Hz allowing not only measures of fixations (timing location) but also precise measures of saccades (path/velocity)
  • eye-trackers can be head-mounted (allows more head movement)/remote (less tiring for pps; can be combined w/EEG)
24
Q

FOVEA

A
  • part of retina w/smallest receptive fields (hence best acuity) & highest concentration of cone receptors (only cone receptors can distinguish colours; rod receptors cannot)
  • note that layers of other cells are very thin in fovea so that more light can reach receptor cells
24
Q

FOVEA

A
  • part of retina w/smallest receptive fields (hence best acuity) & highest concentration of cone receptors (only cone receptors can distinguish colours; rod receptors cannot)
  • note that layers of other cells are very thin in fovea so that more light can reach receptor cells
25
Q

WHY DO WE NEED TO MOVE THE EYES?

A
  • there is a resolution (acuity) gradient
  • resolution falls off rapidly along retina as 1 departs from fovea
26
Q

PRIMARY MEASURES

A

FIXATION
SACCADE
PUPIL DIAMETER

27
Q

FIXATION

A
  • when gaze stops on some visual attribute
  • attributes include:
    1) spatial location (where?)
    2) onset latency (when did it start?)
    3) duration (how long?)
28
Q

SACCADE

A
  • the eye-movement
  • attributes include:
    1) amplitude (how far?)
    2) onset (when did its execution start?)
    3) velocity (how fast?)
    4) shape (linear/somewhat curved?)
29
Q

PUPIL DIAMETER

A
  • correlated w/arousal/emotional state
  • ie. perception of emotional signals usually increases pupil size
30
Q

EYE-TRACKING: TASK-SWITCHING

A
  • task-switching paradigm used to examine if one can shift “spotlight” of spatial attention in advance of visual stimulus (face w/letter superimposed onto forehead)
  • face task: identify face & press 1/4 keys corresponding to 1/4 faces
  • letter task: identify 1/4 letters (press 1/4 keys)
  • 2 cue-stimulus intervals (CSIs) to examine preparatory shifts of spatial attention (200/800ms)