Introduction to Event-Related Potentials (ERPs)
Event-Related Potentials (ERPs) are a powerful neurophysiological technique used to study the brain's electrical responses to specific sensory, cognitive, and motor events. By measuring electrical activity via electrodes on the scalp, ERPs offer precise temporal information about how the brain processes a given stimulus, from preparation to post-stimulus processing.
Historical Development of ERP Methodology
- 1929: Hans Berger first demonstrated that brain electrical activity could be recorded non-invasively using scalp electrodes, resulting in the electroencephalogram (EEG).
- 1935–36: Pauline Hallowell Davis isolated ERPs from EEG during quiescent states.
- 1962: Galambos and colleagues published early ERP waveforms.
- 1964: The modern era began with Walter et al.'s discovery of the contingent negative variation (CNV), a cognitive ERP component reflecting preparatory brain activity between warning and target stimuli.
- Later discoveries: Sutton and colleagues identified the P3 (or P300) component linked to stimulus unpredictability.
Significance of ERP Components
- Contingent Negative Variation (CNV): Observed as a negative voltage in frontal electrodes during anticipation between a warning and subsequent target stimulus, indicating cognitive preparation.
- P3 Component: A positive peak occurring approximately 300 milliseconds after stimulus presentation, larger when stimuli are unpredictable.
ERP Experimental Paradigms
The Oddball Paradigm
- Subjects respond to frequent standard stimuli (e.g., "X") and rare target stimuli (e.g., "O") presented on a screen.
- EEG is recorded from multiple electrodes according to the 10-20 system.
- Trials are tagged and averaged to isolate ERP waveforms corresponding to each stimulus type.
- Typical ERP waveform components include P1, N1, P2, N2, and P3, each labeled by polarity (positive/negative) and approximate timing.
- Findings consistently show that rare target stimuli evoke a larger P3 response, especially at parietal midline electrodes (Pz).
Face Processing and the N170 Component
- N170 is a negative ERP peak around 170 ms post-stimulus, maximal over ventral occipito-temporal areas.
- It selectively responds to faces versus non-face objects like houses or cars.
- Demonstrates the brain's rapid ability to differentiate faces within 150 ms.
- Research shows N170 amplitude can be modulated by attention and expertise; experts in bird watching, dog identification, or fingerprint analysis show enhanced N170 responses to their relevant stimuli.
Technical Notes on EEG/ERP Data Collection
- Signals are amplified (e.g., 20,000 times) and digitized for analysis.
- Averaging across trials removes unrelated brain activity noise, isolating stimulus-specific neural responses.
- Electrode placements follow standardized naming conventions indicating brain regions and hemisphere positions, enabling reproducible scalp maps.
Conclusion
ERP methodology bridges the gap between raw EEG data and cognitive neuroscience by enabling the isolation of neural processes with high temporal resolution. Paradigms like the oddball task and face perception research illustrate ERP's utility in elucidating brain functions such as stimulus detection, expectancy, and specialized processing.
Further lectures will expand on these concepts, delving deeper into Fundamentals of Experimental Design in Cognitive Psychology and Designing Reaction Time Experiments in Cognitive Psychology to enhance understanding of how ERP studies fit within broader cognitive experimental methodologies.
Hello and welcome to the course basics of experimental design for cognitive psych. ology. I am Dr. Ark Whmer from
the department of cognitive science at IT Kpur. We're starting the week eight of the course where we are continuing to
discuss about different methodologies that utilize experimental research designs. In this week, I will begin with
discussing about event related potentials in today's lecture and a couple of more lectures.
Now, the ERP technique or the event related potentials technique, it provides a powerful method for exploring
the human mind and brain. The technique involves the measurement of electrical activity in the brain contingent to a
presented stimulus or an event and it provides an index of the temporal processing of that stimulus in the
brain. So that is basically why it is considered very important. Whenever you are presenting a stimulus to the brain,
you want to know what is happening post presentation of that stimulus or in some cases how is the brain preparing for
receiving a particular kind of stimulus uh acting on it while the stimulus is still presented and what happens even
after the stimulus is gone. So all the temporal aspects of cognitive processing are best studied using the event related
potentials technique. Now uh before we uh dive further let's have a brief historical review of how
does this technique develop. So the ERP methodology it seems to have been discovered in the early 1930s and has
now progressed over ensuing uh 100 plus years almost. Uh, one of the first interesting events
was in 1929 when Hans Burgger reported a remarkable set of experiments wherein he showed the that the electrical activity
of the human brain could be measured by place placing an electrode on the scalp amplifying that signal and plotting
changes in the voltage over time. So that is basically the first time people discovered that electronic activity in
the brain can actually be measured and this is uh the contribution of Hans Burgger. This electrical activity that
you could record from electrode on the scalp was referred to as an electroenphiloggram.
Electroenphoggram. Over the following years, uh the EEG or the electrophiloggram proved to be very
useful in both scientific and clinical applications. However, if you look at it, the EEG is a very coarse measure of
brain activity and it cannot be used in its raw form to measure the highly specific neural processes and that are
studied in cognitive neuroscience. The kind of questions you want to ask. So there is always electrical activity in
the brain and it's a summation of a bunch of processes that are going on. But if you want to know what is
happening in the brain contingent to a specific stimulus, then you will you cannot work with the raw EEG form. you
will have to devise new methods. You have to devise a more uh you know uh sharper way of analyzing this data which
is basically what we're going to talk about. As I saying uh EEG represents a mixedup
conglomeration of dozens of different neural sources of activity. It is difficult to isolate individual
neurocognitive processes from the electrophiloggram within the EG. For example, there are
neural responses associated with specific sensory, cognitive, and motor events. And it may be possible to
extract these responses from the overall EEG by means of a simple averaging technique. These specific responses that
you can gain or that you can isolate which are contingent to specific uh actions or specific events referred to
as event related potentials. that is these are the electric potentials that are related to specific events or
specific stimuli which the brain might be processing. Now, one of the first early or one of
the earliest ERP recordings from humans was first reported by Pauline Hallowell Davis. Pauline and Halo Davis in the
years 1935 and 36 when the researchers were able to isolate clear ERPs on single trials during periods in which
EEG was relatively stable in a quason state. The first ERP waveforms were published by Galamos and sheets in 1962.
Now it seems there was a bit of a uh stoppage in ERP research during the years of the world war and it took some
time to come up. Uh so the modern era of ERP research actually begins in the year 1964 when Walter and colleagues reported
the first cognitive ERP component and ERP component that was contingent to uh you know neural processing. That
component is referred to as the contingent negative variation or the CNV component. Now, how did they come about
this or how did they discover this? On each trial in their study, subjects were presented with a warning signal just
like let's say a click sound followed by 100 or followed 500 or 1,000 milliseconds later by a target stimulus.
So, there is a warning signal and uh after that the participant is expecting a stimulus and that target stimulus uh
happens around 5, 500 or 1,000 milliseconds later. In the absence of a task, both both the warning signal and
the target elicited uh the sort of sensory ERP response that would be expected for these stimula. However, if
the subjects were required to uh press a button on detecting the target, a large negative voltage was observed at the
frontal electrode sites uh during the period that separated the warning signal and the target. So between the time the
warning signal has come and the target has not yet appeared and the participants are expecting a target
stimulus to appear there is this negative voltage which is being observed in the frontal areas of the brain in the
frontal electrode sides. This negative voltage was referred to as the contingent negative variation and it was
taken to reflect the subject's preparation of the oncoming target. So the subject is preparing to sort of deal
with this oncoming target and process it. So this new finding encouraged many
researchers to begin exploring cognitive components because now it showed a window that the electrical activity in
the brain which we were calling the electrophiloggram or the EEG can actually be uh analyzed well to slice
out specific electrical events in the brain that are tied to specific events that are tied to specific cognitive
operations that the brain does. So another important step in the same direction was the discovery of the P3
component by Sutton and colleagues and uh here the researchers created a situation in which the subject could not
predict whether the next stimulus would be auditory or it would be visual and they found that the stimulus uh elicited
a large positive component that peaked around 300 milliseconds post the presentation of the stimulus. This
positive component 300 that peaks 300 millconds after the presentation of the similars was named as the P3 component
or the P300 component. This component was found to be much reduced when the conditions were such that the subjects
could predict the modality of the stimulus and the difference in brain responses was attributed to the
difference in the predictability or or the unpredictability of the stimulus. So if the stimulus was unpredictable then
the uh P3 component was slightly larger as opposed to when the uh stimulus was predictable that it was going to come in
an auditory modality and the subject is able to predict that. Now these two uh were the first uh you know cognitive
components that could be isolated from the EEG uh recordings and after these and similar findings researchers
basically uh lapped up the ERP research paradigm through the 1970s and in ' 80s and they look took took upon that to
investigate the general exploration of questions that are uh you know required in cognitive neuroscience.
Now let us explore some examples of how the ERP methodology has been used to investigate cognitive processes. Look at
this. First is the classic oddball uh paradigm. I'm sure everybody knows that in a classic oddball paradigm a
particular stimulus is presented again and again and again and uh very rarely another stimulus is presented uh you
know which the participant has to detect and respond to. Okay. So uh in the classic oddball experiment, subjects
viewed sequences containing it of 80% X's and 20% O's and they had to press a particular button for X's and another
button for O. Each letter was presented on the computer monitor for 100 milliseconds followed by a400
milliseconds blank interstimulus interval. So a stimulus will come and then there's a gap of 1400 millconds
another stimulus will come most of the time that is 80% of the time the stimula will be X's and sometimes it will be O's
when the participant detects an X it presents a particular button when a participant detects an O it presents a
it presses a particular button now when the subjects were engaged in performing this task the researchers recorded the
EEG from several electrodes embedded in the electro electrode cap that was placed on their skull
The EG from each site was amplified by a factor of 20,000 and then converted into digital form for storage on the
digitization computer. So you're basically getting the signal and then storing it for further analysis.
Whenever a stimulus was presented, event codes were sent from the stimulation computer to the EEG digitization
computer where they stored it along with the EEG data. So you're basically tagging or marking the EEG data with
respect to what event is going to happen. Now in each recording session, the
researchers viewed the EEG on the digitization computer, but the stimulus elicited ERP responses were typically
too small to discern within the much larger EEG. EEG was recorded at one electro site from one of the subjects
over a period of 9 seconds. The EEG waveform was first recorded from the PZ electrode site which is on the midline
of the parietital loes where the P3 component was supposed found to be the largest. On a closer examination, it was
cleared there was a consistent pattern in the EEG response to each stimulus which became even clearer when the
continuous voltage was converted into a discrete set of samples for storage on uh the computer. So when the signal was
analyzed further it started becoming clear that the there was contingent electrical activity in the brain with
respect to the stimula. Now the EG was being recorded concurrently from about 20 electrodes placed in the 1020 system
according to the uh protocol set by the American NCilographic society and the system names each electrode using one or
two letters to indicate the general brain region. Say for example FNP for frontal pole, F for frontal, C for
central, P for parietal and O for oxipital and T for temporal. So these are basically how the names of these
components are kept or names of these electrodes are kept actually and a number to indicate the hemisphere uh and
a distance from the midline. So for example, a lowerase Z is is used to represent the number zero which uh
basically indicates that the electrode was placed along the midline of the scalp. All right. So thus f_sub_3 lies
over the frontal cortex to the left of the midline whereas fz lies over the frontal cortex on the midline whereas
f_sub_4 lies on the frontal cortex to the right of the midline. So this is again just some convention that we ought
to be aware of. This is basically the setup. You can see that the uh subject uh an electrode cap is placed on the
subject. These are the active electrodes. There is this reference electrodes. There is the stimulation
computer and monitor. All of these feed into the uh go through the filters and amplifier go to the digitization
computer where the analysis is taking place. These are the different electrode sites uh you know the 20 of them from
which the data is being observed. Here you can see we have zoomed in this region of of the particular signal and
this is basically how that uh signal sort of comes across. You can see this is the average of 80 x's and this is the
average of 20 O's. You can see that there is a difference in the peaks that is observed contingent to X's and
contingent to O's. Now at the end of each recording session, the researchers were performing a simple signal
averaging procedure to extract the ERP waveform elicited by the X's and the ERP waveform that was elicited by the O. The
basic idea that uh was that recording uh eg contains the brain responses to the stimulus plus also other activity that
may be unrelated to the stimulus which basically therefore needs to be extracted to yield a consistent response
by averaging all the trials which had x's and all the trials which had O's. To achieve this, the researchers extracted
the segment of the eg around each x and o and lined up these eg segments with respect to the event codes that mark the
onset of each stimulus. starting from when the stimulus was supposed to come till when the stimulus
has passed they carved out those segments and then they analyze those segments. So after this these were
simply averaged together uh uh you know over the single trial EG waveforms creating one average ERP waveform for
the X's and one average ERP waveform for the O's at each electrode site. So this is what you can see at each electro site
you get particular uh you know waveform for X's and another particular waveform for the O's.
So for the at the uh the voltage at 24 millconds in the average X waveform was computed by taking the voltage that was
measured 24 milliseconds after each X stimulus and averaging all of these voltages together. So this is just you
know a bit of a processing uh you know convention on how this data is uh cleaned. Any brain activity that was
consistently elicited by the stimulus at that time will basically still in the average. However any voltages that were
unrelated to the stimulus will be negative on some trials and will be positive on some trials and therefore
they will c cancel out during the averaging. The resulting average waveform basically will be consisting of
a sequence of positive and negative voltage deflections which we can call peaks and waves or components. And you
can see here that these are named separately. So you have uh P1, you have P1, N1, P2, N2 and P3. So these are the
peaks. This is a first positive peak, second positive peak, third positive peak and the first negative peak and the
second negative peak. This is basically by convention how these waveforms are actually labeled. Alternatively, the
number may indicate the latency of the peak in milliseconds. So sometimes you will also come across ERP components
that have the number which tells the latency or the time period of when that peak is observed. So here we see P1, N1,
P2, N2 and so on. But you can also have a component such as the N170 which basically says that this is a negative
peak which peaks at negative component which peaks at around 170 mconds post stimulus. All right.
Now components may also be given uh paradigm or function based name such as sometimes there are components which are
referred to as the error related negativity or the no go into which is basically observed on the no-go trials
in go no-go experiments. The sequence of ERPs uh peaks basically reflects the flow of information through the brain
the temporality basically. So what how does the brain react first and how does it react second. So all of these peaks
P1 P2 P3 first positive response second. So in in uh chronology P1 will come first, P2 comes second and P3 comes
later. So the sequence of ERP peaks basically reflects the flow of information throughout the brain and the
voltage at each time. uh when the VRP ERP waveform reflects the brain activity that was going on at that precise moment
in time. Now in the experiment that we have just seen the infrequent O stimula elicit a much larger uh P3 wave than the
frequent X uh stimulus a finding that has been replicated with thousands of previous oddball experiments. So you can
look here the infrequent O basically leads to a much larger positive peak which goes over 10. The rare O's
actually uh reflect a much larger P3 component than the very frequent X's. So this is some uh the finding this is a
critical finding in the oddball paradigm and this is something that has been replicated and uh repeated across
several experiments. More specifically, the P3 wave was also at the uh was also largest at the PZ
electrode uh but could be seen at all 20 electrode. So it was observed at all 20 electrodes but it was found to be
largest at the PZ electrode. The P1 wave in contrast was the largest at the lateral occipital uh electrode sites and
was not present in the frontal site. So this is again uh you can differentiate between which are the peaks, where are
they appearing and what time courses they are uh peaking or not peaking. Now here you can see that each ERP component
has a distinctive scalp distribution that reflects the location of the patch of cortex in which it was originally
distributed. So each uh uh ERP component basically has a proper distribution that basically tells us the location of the
scalp where it is coming actually from where it is uh originated from. Now this is about the oddball paradigm. Let's
look at another uh very important ERP paradigm. This these are just examples that we are taking to illustrate how the
ERPs are collected and how they are able to tell something about the brain. Now another uh very interesting experiment
is there which yields a specific N170 component that is a face related component typically peing around 170
milliseconds after stimulus onset and is largest over the vententral areas of the behind areas of the visual cortex. Now,
in a typical uh experiment, in a typical N170 paradigm, photographs of faces and other types of non-face objects such as
houses or cars are flashed on a computer monitor while the subjects are passively viewing the stimula. Okay. The X
presents the time relative to the stimulus onset and the Y presents the magnitude of the neural response. You
can see here the x is the time here and the uh you know uh y-axis is presenting the response in in microvolts that is
contingent to a particular response. Okay. In the scalp map is shown the shading indicates the voltage measured
at each electrode side during the time period of the N 170 response. So you can see here uh there there are these
different shading. They basically tell us uh the amount of voltage that is experienced at different sites when this
particular uh thing when this particular component is isolated. You can see this one is the N 170. It is a negative peak
happening at around 170 milliseconds. Peaking at around 170 millconds. You can see here uh and this is uh happening in
response to face stimula but not in response to any other kinds of stimula. So this is notable because it is larger
when elicit when the eliciting stimulus is a face compared to when the stimulus is a non-face object such as a car or a
house or anything. uh the difference between faces and non-face objects begins approximately it starts at around
150 millconds after the onset of the stimulus and peaks at around uh 170 mconds and then sort of recedes back
which basically would allow us to conclude that the human brain is able to distinguish uh distinguish between faces
and other objects within a very short period of 150 milliseconds. The scalp distribution helps us to know that this
is the same component that is observed in other similar studies of uh the N170 and it suggests that the N170 generator
basically lies somewhere in the visual cortex in the back part in the vententral part of the visual cortex.
Now several researchers have used this N170 uh paradigm and they have basically used it to address interesting questions
about how faces are processed in the brain. For example, some studies have asked whether face processing is
automatic uh by testing whether uh face elicited N170 is smaller when the faces are ignored. So uh if the face is there
and you're not consciously processing it, does the N170 appear again? So that is basically what some people wanted to
look at and the results of these experiments actually indicated that phase processing is at least partially
automatic but it can be modulated under circum some circumstances. So when the PE faces are being uh actively attended
then the nature of the peak versus when the faces are partially ignored is slightly different from each other.
Other studies have used the N170 to ask whether faces are processed in a specialized face module or whether the
same neural processing is also used when PE when people process other sorts of complex uh stimula uh for which they
have extensive expertise. For example, so expertise. So some people have linked the N170 to the role of expertise as
well and therefore very interesting experiments have happened uh and it has been shown that bird experts exhibit an
enhanced one N170 in response to birds. Dog experts exhibit an enhanced N170 in response to dogs and fingerprint experts
exhibit uh an enhanced N170 in response to fingerprints. So there must be some role in 170 with regards to our
expertise in processing faces. That is why it basically is elicited by faces. So that is all uh that I wanted to talk
about in this lecture. We have just initiated a bit on uh uh you know uh ERPs. In the next two lectures I'll take
this uh uh discussion a little bit further. Thank you.
ERPs are brain responses measured via electrodes on the scalp that reflect electrical activity linked to specific sensory, cognitive, or motor events. They provide high temporal resolution, allowing researchers to precisely track how the brain processes stimuli from preparation to response, making them invaluable for studying cognitive functions like attention and perception.
In the oddball paradigm, participants encounter frequent standard stimuli interspersed with rare target stimuli while EEG is recorded. By averaging the brain's responses, researchers isolate ERP components like the P3, which typically shows a larger amplitude for rare, unexpected targets, revealing mechanisms of stimulus detection and cognitive updating.
The N170 is a negative peak around 170 ms after stimulus onset, maximal over occipito-temporal scalp areas, selectively responding to faces rather than non-face objects. It reflects the brain’s rapid and specialized processing of facial features, and its amplitude can be enhanced by attention or expertise, demonstrating neural tuning to relevant visual categories.
EEG signals are amplified (up to about 20,000 times) and digitized for analysis. Averaging multiple trials filters out unrelated background brain activity, isolating the stimulus-specific ERP components. Standardized electrode placement based on the 10-20 system ensures consistency in recording locations across studies.
ERP methodology evolved from Hans Berger's first non-invasive EEG recordings in 1929, through Pauline Hallowell Davis's isolation of ERPs in the 1930s, to Walter et al.'s discovery of the contingent negative variation (CNV) in 1964, which linked brain potentials to cognitive preparation. Later, the P3 component was identified as related to stimulus unpredictability, establishing foundational cognitive ERP markers.
High temporal resolution allows ERPs to track neural activity on the order of milliseconds, revealing the precise timing of cognitive processes such as attention shifts or decision making. This temporal detail surpasses many brain imaging methods like fMRI, which have slower temporal dynamics, thereby enabling a fine-grained understanding of when the brain processes different stimulus features.
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