No abstract

Route learning is a common navigation task affected by cognitive aging. Here we present a novel experimental paradigm to investigate whether age-related declines in executive control of attention contributes to route learning deficits. A young and an older participant group was repeatedly presented with a route through a virtual maze comprised of 12 decision points (DP) and non-decision points (non-DP). To investigate attentional engagement with the route learning task, participants had to respond to auditory probes at both DP and non-DP. Route knowledge was assessed by showing participants screenshots or landmarks from DPs and non-DPs and asking them to indicate the movement direction required to continue the route. Results demonstrate better performance for DPs than for non-DPs and slower responses to auditory probes at DPs compared to non-DPs. As expected we found slower route learning and slower responses to the auditory probes in the older participant group. Interestingly, differences in response times to the auditory probes between DPs and non-DPs can predict the success of route learning in both age groups and may explain slower knowledge acquisition in the older participant group.

The aim of the present study was to determine whether motion history affects motion-onset auditory-evoked potentials (motion-onset AEPs). AEPs were recorded from 33 EEG channels in 16 subjects to the motion onset of a sound (white noise) virtually moving in the horizontal plane at a speed of 60 deg/s from straight ahead to the left (-30 degrees ). AEPs for baseline and adaptation were compared. A stimulus trial comprised three consecutive phases: 2,000 ms adaptation phase, 1,000 ms stationary phase, and 500 ms test phase. During the adaptation phase of the adaptation condition, a sound source moved twice from +30 degrees to -30 degrees to top up preceding adaptation. In the baseline condition, neither top-up nor pre-adaptation were exerted. For both conditions, a stationary sound was presented centrally in the stationary phase, moving leftwards in the test phase. Typical motion-onset AEPs were obtained for the baseline condition, namely a fronto-central response complex dominated by a negative and a positive component, the so-called change-N1 and change-P2 after around 180 and 250 ms, respectively. For the adaptation condition, this complex was shifted significantly into the positive range, indicating that adaptation abolished a negativity within a time window of approximately 160 to 270 ms. A respective shift into the negative range was evident at occipito-parietal sites. In conclusion, while adaptation has to be taken into account as a potential confound in the design of motion-AEP studies, it might also be of benefit in order to isolate AEP correlates of motion processing.

Auditory evoked potentials (AEPs) to motion onset in humans are dominated by a fronto-central complex, with a change-negative deflection 1 (cN1) and a change-positive deflection 2 (cP2) component. Here the contribution of veridical motion detectors to motion-onset AEPs was investigated with the hypothesis that direction-specific adaptation effects would indicate the contribution of such motion detectors. AEPs were recorded from 33 electroencephalographic channels to the test stimulus, i.e. motion onset of horizontal virtual auditory motion (60° per s) from straight ahead to the left. AEPs were compared in two experiments for three conditions, which differed in their history prior to the motion-onset test stimulus: (i) without motion history (Baseline), (ii) with motion history in the same direction as the test stimulus (Adaptation Same), and (iii) a reference condition with auditory history. For Experiment 1, condition (iii) comprised motion in the opposite direction (Adaptation Opposite). For Experiment 2, a noise in the absence of coherent motion (Matched Noise) was used as the reference condition. In Experiment 1, the amplitude difference cP2 - cN1 obtained for Adaptation Same was significantly smaller than for Baseline and Adaptation Opposite. In Experiment 2, it was significantly smaller than for Matched Noise. Adaptation effects were absent for cN1 and cP2 latencies. These findings demonstrate direction-specific adaptation of the motion-onset AEP. This suggests that veridical auditory motion detectors contribute to the motion-onset AEP.