We investigated how landmarks influence the brain’s computation of head direction and found that in a bi-directionally symmetrical environment, some neurons in dysgranular retrosplenial cortex showed bi-directional firing patterns. This indicates dominance of neural activity by local environmental cues even when these conflict with the global head direction signal. It suggests a mechanism for associating landmarks to or dissociating them from the head direction signal, according to their directional stability/utility.
Among the different brain imaging techniques, electroencephalography (EEG) is classically considered as having an excellent temporal resolution, but a poor spatial one. Here, we argue that the actual temporal resolution of conventional (scalp potentials) EEG is overestimated, and that volume conduction, the main cause of the poor spatial resolution of EEG, also distorts the recovered time course of the underlying sources at scalp level, and hence degrades the actual temporal resolution of EEG. While Current Source Density (CSD) estimates, through the Surface Laplacian (SL) computation, are well known to dramatically reduce volume conduction effects and hence improve EEG spatial resolution, its positive impact on EEG temporal resolution is much less recognized. In two simulation studies, we first show how volume conduction and reference electrodes distort the scalp potential time course, and how SL transform provides a much better spatio-temporal description. We then exemplify similar effects on two empirical datasets. We show how the time courses of the scalp potentials mis-estimate the latencies of the relevant brain events and that CSD provides a much richer, and much more accurate, view of the spatio-temporal dynamics of brain activity.
In conflict tasks, the irrelevant stimulus attribute needs to be suppressed for the correct response to be produced. In the Simon task, earlier researchers have proposed that this suppression is the reason that, after an initial increase, the interference effect decreases for longer RTs, as reflected by late, negative-going delta plots. This view has been challenged by observations of positive-going delta plots, even for long RTs, in other conflict tasks, despite a similar necessity for suppression. For late negative-going delta plots to be interpreted as reflecting suppression, a necessary, although maybe not sufficient, condition is that similar patterns should be observed for other conflict tasks. We reasoned that a similar suppression could be present, but hidden, in the Eriksen flanker task. By recording and analyzing electromyograms of the muscles involved in response execution, we could compute delta plots separately for trials that elicited a subthreshold incorrect response activation (partial error). Late negative-going delta plots were observable on partial-error trials, although they were weaker than for the Simon task, reducing the impact of this inversion on the overall distribution. We further showed that this pattern is modulated by time pressure. Those results indicate that mechanisms leading to negative-going delta plots, similar to those observed in the Simon task, are also at play in the Eriksen task. The link between negative-going delta plots and executive online control is discussed.
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