Identical experimental procedures and EEG acquisition systems were used at all neurophysiology collection sites with high inter-laboratory consistency in recordings (Alexander et al., 1994; Cohen et al., 1994; Kuperman et al., 1995; Rohrbaugh et al., 1997). Subjects were seated comfortably 1 meter from a monitor in a dimly lit sound-attenuated RF-shielded booth (Industrial Acoustics, Inc., Bronx, NY, USA), and wore a 61-channel electrode cap (Electro-Cap International, Inc., Eaton, OH, USA) based on the Extended 10–20 System (Jasper, 1958; Chatrian et al., 1985; Chatrian et al., 1988; Oostenveld and Praamstra, 2001) (Fig. 2), with a reference electrode at the tip of the nose and with a ground electrode at the forehead. The electrooculogram (EOG) was recorded by a supraorbital vertical electrode and by a horizontal electrode on the external canthus of the left eye. Electrode impedances were maintained below 5 kΩ. Electrical activity was amplified 10,000 times using SynAmps2 amplifiers (Compumedics USA, Charlotte, NC) and was recorded continuously over a bandwidth between near-DC (0 Hz) and 100.0 Hz on a Neuroscan system (Versions 4.3–4.5; Compumedics USA, Charlotte, NC) at a sampling
