User Tutorial:EEG Measurement Setup

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This page describes the physical setup required for EEG measurements. EEG utilizes metal electrodes attached to a human subject's scalp, measuring tiny electrical potentials which reflect the brain's electrical activity. Although setting up amplifier and electrodes appears simple and straightforward, a successful, good quality EEG recording requires attention to not-so obvious details, and some practice.

Electrodes

An EEG amplifier measures voltage differences between points on the scalp. This implies that each channel is connected to two electrodes. Usually, measurement is "unipolar" rather than "bipolar", which means that the second electrode is identical for all channels, and called "reference" (Ref). Also, amplifier inputs must be kept within a small voltage range relative to the amplifier's zero (ground) voltage level. This is achieved by connecting yet another electrode, a "ground" (Gnd) electrode, to the subject's scalp.

EEG electrodes are small metal plates that are attached to the scalp using a conducting electrode gel. They can be made from various materials. Most frequently, tin (Sn) and silver/silver-chloride (Ag/AgCl) electrodes are used but there are gold (Au) and platinum (Pt) electrodes as well.

While Sn electrodes have the advantage of being cheap, they introduce a large amount of low-frequency noise ("drifting") below 1Hz. For low-frequency recordings, such as Slow Cortical Potential measurements, or low-noise ERP recordings, Ag/AgCl electrodes are typically used.

Important but often neglected: Using electrodes made from different materials in the same recording will result in DC voltage offsets between electrodes, due to electrochemical contact potentials. Such contact potentials are generally larger than what a typical amplifier tolerates. The result will be a zero or much diminished signal amplitude, and a bad signal-to-noise ratio. This applies to all amplifier inputs, i.e. channels, reference, and ground electrodes must all be made from the same material.

The 10-20 International System

The 10-20 international system is the standard naming and positioning scheme for EEG applications. It is based on an iterative subdivision of arcs on the scalp starting from craniometric reference points: Nasion (Ns), Inion (In), Left (PAL) and Right (PAR) pre-auricular points. The intersection of the longitudinal (Ns-In) and lateral (PAL-PAR) is named the Vertex.

ElectrodePositions1020.PNG

The original 10-20 system included only 19 electrodes (see panel B of the figure). Later on, extensions were proposed so that now you can place over 70 electrodes in standard positions (see panel C of the figure). This extension also renamed four electrodes (marked in black in the figure); the original names were: T3, T5, T4, and T6 for T7, P7, T8, and P8, respectively.

Sometimes, one of the electrodes mounted in these positions is used as reference channel. More often, ear lobe or mastoid (i.e. bony outgrowth behind the ear) are used.

Identifying Brain Areas

Often, it is important to assess whether a given brain signal topology makes sense with regard to a-priori knowledge about sources of interest. In most cases, there is a direct correspondence between major brain features, and electrode positions in the 10-20 international system.

In the image displaying electrode positions above, two of these features are indicated by thin lines, and may be identified easily when using a properly placed EEG cap:

  • The central sulcus (rolandic fissure) separates the frontal lobe from the parietal lobe. Its course corresponds to the thin lines touching CPz-C2-C4 and CPz-C1-C3, respectively. The two gyri immediately neighboring the central sulcus are the
    • primary motor cortex (in frontal direction), and
    • primary sensory cortex (in occipital direction).
  • The course of the lateral sulcus corresponds to the lines C8-FT8-FT10 resp. C5-FT7-FT9. It separates the temporal lobe from the remaining parts of the brain.

Montage Instructions

Acquiring EEG from more than a single location provides spatial information that is useful in interpreting results, and to identify signals and artifacts by their spatial distribution characteristics. Also, linear combinations of signals from different locations may be used to extract signals originating from certain locations.

Attaching 16+2 (or worse 64+2) individual electrodes to the scalp of a subject is not a simple task. And doing it with high geometrical accuracy is a task for very experienced technicians. The difficulty may be greatly alleviated using EEG caps. They are made of elastic fabric (available in different sizes), and electrodes are already fixed in the proper configuration. One proven technique to perform an accurate montage is the following:

  • Mark the vertex on the subject's scalp using a felt-tip pen or some other similar method. To do so, begin by locating the nasion and inion on the subject as indicated in subfigure (A) above. Using a tape measure, find the distance between these two locations. The point midway between the two points, or 50% of the distance, is the vertex. Make a mark at that point for later reference. Other 10-20 points can be located in a similar manner. Distances between points are reported, as percentages of the total distance, in subfigure (A) above.
  • Mark scalp positions for Fpz and Oz.
  • Identify the Cz electrode on the EEG cap and place the cap to position the Cz electrode on the vertex.
  • Keeping Cz fixed, slip the cap onto the head.
  • While ensuring that Cz does not shift, adjust the cap such that:
    • the Fz, Cz Pz line is on the midline;
    • the Fp1-Fp2 line is horizontal, and at the level of the Fpz mark;
    • the O1-O2 line is horizontal, and at the level of the Oz mark.

You can now fix Ref and Gnd electrodes. Usually, Ref is attached to one of the earlobes, or one of the mastoids, in form of a cup electrode using collodium (an adhesive chemical). Some caps have a Gnd electrode embedded on a scalp position; if this is not the case, Gnd is the same kind of electrode as Ref, and should be attached to the earlobe or mastoid opposing the Ref electrode.

Inspecting EEG Signals

BCI2000 may be used to inspect EEG signals without actually recording them. For the sake of this tutorial, we will start up BCI2000 in a configuration suitable for stimulation experiments. However, any configuration will do, and usually you will inspect signals after starting up BCI2000 in the configuration that fits the desired experiment.

  • Make sure that
    • your amplifier is connected to your computer,
    • the amplifier's drivers are installed as described in the manual that came with your amplifier, and
    • the amplifier is switched on.
  • Start BCI2000 by double-clicking the file batch/StimulusPresentation_<YourAmplifier>.bat where YourAmplifier matches the name of your amplifier.
    If there is no such file in the batch directory, and your amplifier is listed in the contributions section, the how-to page on using a contributed source module will provide you with instructions on how to use it with BCI2000.
  • In the BCI2000 operator window, click "Config" and then "Load Parameters..." to load the file parms/examples/StimulusPresentation_SignalGenerator.prm.
  • Load additional parameters for your amplifier by clicking "Load Parameters" again and choosing the parameter file from parms/fragments/amplifiers that corresponds to your amplifier.
    If you are unable to find a parameter file that corresponds to your amplifier and your amplifier is listed in the contributions section, load the SignalGenerator.prm parameter file (also located in parms/fragments/amplifiers) and modify parameters as necessary. In this case, please consult your ADC module's reference page, which is accessible through Contributions:ADCs, for available parameters and their meanings.
  • Switch to the Source tab; for the ChannelNames parameter enter electrode locations corresponding to amplifier channels as a white-space separated list (e.g., Fz CPz Cz CP3 ...).
  • Click "Save", and save your adapted configuration as a system-specific parameter file for later use at parms/fragments/<YourSystem>.prm, or whereever you find appropriate.
  • Close the parameter dialog by clicking the close box its top right corner.
  • Click "Set Config".
  • A window will appear that displays the signal acquired from the amplifier. Initially, the window will be rather small and located in the top left corner of your screen. Adapt it to your liking by moving and resizing it -- its position and size will be remembered across BCI2000 sessions. Right-clicking will bring up a context menu with various options.
  • Reasonable EEG traces should now be visible on the screen as soon as gel is injected.
    Visual inspection can detect the effect of poor contact (excessive mains interference, frequent loss of contact, etc.). You may also want to use an impedance meter to make sure that electrodes have good contact (i.e. that their impedance is below 5-10 k\Omega).
  • When you are done, quit BCI2000 before going to the next step.

EEG Artifacts

Mains Interference

Electrical power lines use sinusoidal voltages with a frequency of 50 or 60 Hz, depending on your country. Generally, 50Hz are used in Europe, Asia, Africa, and parts of South America; 60Hz are used in North America, and parts of South America.

Mains voltage is typically 110 or 230 Volts, and thus exceeds the EEG's 50 to 100 Microvolts by a factor of 2*10^6, or 126 dB. Therefore, mains interference is ubiquitous in EEG recordings, especially if taken outside specially equipped, shielded rooms, and EEG amplifiers usually provide a so-called notch filter that suppresses signals in a narrow band around the mains frequency in question.

Amplifier notch filters are designed to suppress a certain amount of mains interference. When there is mains interference still visible in the signal after activating the amplifier's notch filter, this is often due to high electrode impedance.

MainsInterference.PNG

Eye Blink Artifacts

Eye blink artifacts are generated by fast movement of the eyelid along the cornea, as it happens during an eye blink. By friction between lid and cornea, this movement results in charge separation, with a dominantly dipolar charge distribution, and the dipole moment pointing in up-down-direction.

In the EEG, this is recorded as a positive peak lasting a few tenths of a second, mainly visible in the frontopolar region, but propagating to all the electrodes of the montage, becoming weaker with distance from the front.

Blink artifacts' frequency content is negligible in the alpha band, so they produce no apparent effect on SMR data analysis (if their number is reasonable). At the same time, their amplitude is quite large so that time domain analyses (such as averaged P300 wave forms) can be strongly influenced by their presence.

BlinkArtifacts.PNG

Eye Movement (EOG) Artifacts

EOG artifacts are produced by eye movements, and generated by a frictive mechanism similar to the one underlying blink artifacts but involving retina and cornea rather than cornea alone.

The effect on frontopolar and frontotemporal electrodes can be symmetric or antisymmetric, depending whether the movement is vertical or horizontal, respectively.

The effect of eye movement artifacts on frequency- or time-domain analysis is quite similar to that of blink artifacts, except that their frequency content is even lower, and amplitudes tend to be larger.

EOGArtifacts.PNG

Muscular (EMG) Artifacts

EMG activity must be carefully checked at the beginning of each recording, and verified throughout the recording. Its effect can completely obscure any frequency analysis. Most common sources of EMG are the muscles that lift the eye brows, and those which close the jaw. Both groups are inadvertently contracted as a consequence of a psychological effort. Keeping the mouth slightly open (or the tip of the toungue between the foreteeth) is a good strategy to avoid jaw-generated EMG.

EMGArtifacts.PNG

Next Step

See also

User Tutorial:Mu Rhythm BCI Tutorial, User Tutorial:P300 BCI Tutorial