Christina Derichs’s research while affiliated with Heinrich Heine University Düsseldorf and other places

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Publications (2)


Figure 4. Results of the interval duration judgment experiment, with the mask in the temporal center (Experiment 4). Error bars represent SEM. The black dotted line marks averaged duration estimations for the baseline condition and the shaded area represents the standard error. A mask was presented simultaneously with the interval end marker or in the interval center.  
Figure 5. Results of the control condition. A mask is shown either at interval start or at interval end. In separate blocks the mask was shown either simultaneously with an interval marking stimulus or without any simultaneously presented stimulus. Depending on condition subjects either had to judge the interval duration between both interval markers or between mask and the remaining interval marker. Error bars represent SEM.  
Figure 7. (A) Graphical sketch of the neural distributions responding to the first (shown in green), the second (shown in red) and the third (shown in blue) interval marker. The second interval marker is shown on top of a whole-field mask. Since the mask weakens the onset signal of the second interval marker, the corresponding neural response distribution is broader. (B) Summing the distributions corresponding to the first and the second interval marker results in a mixed distribution (shown in black) whose peak is shifted temporally in direction of the peak corresponding to the interval start marker. Reading off the interval duration from the peak of the first interval marker and the mixed distribution yields interval compression. (C) Since the mixed distribution is shifted into direction of the first interval marker, reading off the interval duration from the peak of the third interval marker and the mixed distribution yields interval expansion.  
Temporal binding of interval markers
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December 2016

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88 Reads

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4 Citations

Christina Derichs

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How we estimate the passage of time is an unsolved mystery in neuroscience. Illusions of subjective time provide an experimental access to this question. Here we show that time compression and expansion of visually marked intervals result from a binding of temporal interval markers. Interval markers whose onset signals were artificially weakened by briefly flashing a whole-field mask were bound in time towards markers with a strong onset signal. We explain temporal compression as the consequence of summing response distributions of weak and strong onset signals. Crucially, temporal binding occurred irrespective of the temporal order of weak and strong onset markers, thus ruling out processing latencies as an explanation for changes in interval duration judgments. If both interval markers were presented together with a mask or the mask was shown in the temporal interval center, no compression occurred. In a sequence of two intervals, masking the middle marker led to time compression for the first and time expansion for the second interval. All these results are consistent with a model view of temporal binding that serves a functional role by reducing uncertainty in the final estimate of interval duration.

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Figure 1. (A) Experimental set-up. The monitor was mounted upside down on a plexiglas construction. The image was reflected in a mirror below where it could be seen by the subject. The subject´s hand was placed on a further plane below the mirror. Here the tactile stimulation was applied. This construction enabled us to present visual stimuli at the monitor (reflected in the mirror) and tactile stimuli to the hand at similar perceived positions. Copyright 2016 Martin Hebestreit. (B,C) Possible positions of visual and tactile stimuli in the temporal compression experiment for tactile stimuli presented at the left and the right hand. The visual stimulus (green dot) was always presented at the screen center whereas the position of the tactile stimulus varied (indicated by the positions of the hand). It was presented either at the same position as the visual stimulus or displaced by 12° or by 24°. Fixation (black square) could be at the right or at the left side of the screen. Copyright 2016 Martin Hebestreit. (D) Timecourse of events for the temporal compression experiment. Each trial started with a fixation period of 1000 ms. We next presented the probe interval (shown by gray shaded area). The probe interval lasted 500 ms and started with a tactile stimulus applied for 50 ms. The probe interval ended with a visual stimulus flashed for 16 ms. This visual stimulus was covered by a mask of 50 ms duration. After a break of 1000 ms, the comparison interval (shown by gray shaded area) was presented. The comparison interval had a random duration of 200–800 ms. This interval was also started by a tactile stimulus presented for 50 ms and ended by a visual stimulus flashed for 16 ms.  
Figure 2. (A) Results of the visual-tactile time compression experiment. The perceived duration of the first interval is plotted for the three distances between tactile anchors and visual probes. The dotted line marks the physical duration of the first interval of 500 ms. Error Bars represent SEM. (B) Results of the visual-visual time compression experiment. Error Bars represent SEM.  
Figure 3. (A,B) Arrangement of visual and tactile stimuli in the correspondence matching experiment. In the same condition (A), tactile and visual stimuli are presented at corresponding positions. Copyright 2016 Martin Hebestreit. However, in the different condition (B) tactile and visual stimuli are presented in an opposite orientation. (C) Results of the correspondence matching experiment. The perceived duration of the first interval is plotted on the ordinate. The two arrangements of visual and tactile stimuli (same and different) are shown on the abscissa. The dotted line indicates the physical duration of the first interval of 500 ms. Error bars are SEM.  
Figure 4. (A) Illustration of the first interval in the attention experiment. Two bars were presented to mark the interval start. After 500 ms the interval end marking stimulus was shown. This stimulus was presented in 20% of all trials in the left part of the screen and in 80% in the right part of the screen. (B) In half of the trials the stimulus marking the interval's end was presented on top of a whole field mask. (C) Results from the attention experiment. Data are shown for the " 80% " and the " 20% " condition. Data from trials where the marker of the interval's end was not masked are shown in black and data from masking trials in gray. Error bars represent SEM.  
Figure 5. (A) Graphical illustration of the neural distributions responding to the occurrences of the interval start (shown in green) and the interval end (shown in red) marker. The panel shows distributions for strong onsets of both markers when no mask is presented. (B) Masking the interval end marker weakens its onset signal and the corresponding neural distribution becomes more variable. If the neural distributions responding to the strong onset signal of the interval start marker and the weak signal of the interval end marker are summed, the peak corresponding to the interval end marker shifts in direction of the interval start marker (shown in grey).  
The functional role of time compression

May 2016

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126 Reads

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4 Citations

Multisensory integration provides continuous and stable perception from separate sensory inputs. Here, we investigated the functional role of temporal binding between the visual and the tactile senses. To this end we used the paradigm of compression that induces shifts in time when probe stimuli are degraded, e.g., by a visual mask (Zimmermann et al. 2014). Subjects had to estimate the duration of temporal intervals of 500 ms defined by a tactile and a visual, masked stimulus. We observed a strong (~100 ms) underestimation of the temporal interval when the stimuli from both senses appeared to occur at the same position in space. In contrast, when the positions of the visual and tactile stimuli were spatially separate, interval perception was almost veridical. Temporal compression furthermore depended on the correspondence of probe features and was absent when the orientation of the tactile and visual probes was incongruent. An additional experiment revealed that temporal compression also occurs when objects were presented outside the attentional focus. In conclusion, these data support a role for spatiotemporal binding in temporal compression, which is at least in part selective for object features.

Citations (2)


... For example, a non-target preceding flicker and flutter dilate the perceived duration of a target interval (Droit-Volet and Wearden 2002;Ortega et al. 2012;Wearden et al. 1998), whereas a non-target trailing flicker and flutter compress it Kitazawa 2010, 2011). An interval defined by two flashes is perceived as shorter when a full-field mask is presented temporally close to either of the flashes compared to the no-masking condition (Derichs and Zimmermann 2016;Zimmermann et al. 2014). Moreover, recent studies have examined changes in perceived duration when non-target stimuli are presented before and after the target stimulus (the effect of sandwiching stimulus; Asaoka 2020; Asaoka and Gyoba 2016;Derichs and Zimmermann 2016;Zhou et al. 2015). ...

Reference:

Stimulus (dis)similarity can modify the effect of a task-irrelevant sandwiching stimulus on the perceived duration of brief visual stimuli
Temporal binding of interval markers

... And these two complementary phenomena may also have independently helpful effects for cognition (see also Chunharas et al., 2022). For example, time dilation can improve processing of information within a duration (e.g., Wutz et al., 2015), while time contraction can aid in binding across different stimulus modalities (e.g., Zimmermann et al., 2016). ...

The functional role of time compression