Jasper H. Fabius

Spatiotopic updating facilitates perception immediately after saccades

As the neural representation of visual information is initially coded in retinotopic coordinates, eye movements (saccades) pose a major problem for visual stability. If no visual information were maintained across saccades, retinotopic representations would have to be rebuilt after each saccade. It is currently strongly debated what kind of information (if any at all) is accumulated across saccades and when this information becomes available after a saccade. Here, we use a motion illusion to examine the accumulation of visual information across saccades. In this illusion, an annulus with a random texture slowly rotates and is then replaced with a second texture (motion transient). With increasing rotation durations, observers consistently perceive the transient as large rotational jumps in the direction opposite to rotation direction (backward jumps). We first show that accumulated motion information is updated spatiotopically across saccades. Then, we show that this accumulated information is readily available after a saccade, immediately biasing postsaccadic perception. The current findings suggest that presaccadic information is used to facilitate postsaccadic perception and are in support of a forward model of transsaccadic perception, aiming at anticipating the consequences of eye movements and operating within the narrow perisaccadic time window.

Safe and sensible preprocessing and baseline correction of pupil-size data

Measurement of pupil size (pupillometry) has recently gained renewed interest from psychologists, but there is little agreement on how pupil-size data is best analyzed. Here we focus on one aspect of pupillometric analyses: baseline correction, i.e., analyzing changes in pupil size relative to a baseline period. Baseline correction is useful in experiments that investigate the effect of some experimental manipulation on pupil size. In such experiments, baseline correction improves statistical power by taking into account random fluctuations in pupil size over time. However, we show that baseline correction can also distort data if unrealistically small pupil sizes are recorded during the baseline period, which can easily occur due to eye blinks, data loss, or other distortions. Divisive baseline correction (corrected pupil size = pupil size/baseline) is affected more strongly by such distortions than subtractive baseline correction (corrected pupil size = pupil size − baseline). We discuss the role of baseline correction as a part of preprocessing of pupillometric data, and make five recommendations: (1) before baseline correction, perform data preprocessing to mark missing and invalid data, but assume that some distortions will remain in the data; (2) use subtractive baseline correction; (3) visually compare your corrected and uncorrected data; (4) be wary of pupil-size effects that emerge faster than the latency of the pupillary response allows (within ±220 ms after the manipulation that induces the effect); and (5) remove trials on which baseline pupil size is unrealistically small (indicative of blinks and other distortions).

Object files across eye movements: Previous fixations affect the latencies of corrective saccades

One of the factors contributing to a seamless visual experience is object correspondence—that is, the integration of pre- and postsaccadic visual object information into one representation. Previous research had suggested that before the execution of a saccade, a target object is loaded into visual working memory and subsequently is used to locate the target object after the saccade. Until now, studies on object correspondence have not taken previous fixations into account. In the present study, we investigated the influence of previously fixated information on object correspondence. To this end, we adapted a gaze correction paradigm in which a saccade was executed toward either a previously fixated or a novel target. During the saccade, the stimuli were displaced such that the participant’s gaze landed between the target stimulus and a distractor. Participants then executed a corrective saccade to the target. The results indicated that these corrective saccades had lower latencies toward previously fixated than toward nonfixated targets, indicating object-specific facilitation. In two follow-up experiments, we showed that presaccadic spatial and object (surface feature) information can contribute separately to the execution of a corrective saccade, as well as in conjunction. Whereas the execution of a corrective saccade to a previously fixated target object at a previously fixated location is slowed down (i.e., inhibition of return), corrective saccades toward either a previously fixated target object or a previously fixated location are facilitated. We concluded that corrective saccades are executed on the basis of object files rather than of unintegrated feature information.

Focus of spatial attention during spatial working memory maintenance: Evidence from pupillary light response

ABSTRACT In this experiment, we demonstrate modulation of the pupillary light response by spatial working memory (SWM). The pupillary light response has previously been shown to reflect the focus of covert attention, as demonstrated by smaller pupil sizes when a subject covertly attends a location on a bright background compared to a dark background. We took advantage of this modulation of the pupillary light response to measure the focus of attention during a SWM delay. Subjects performed two tasks in which a stimulus was presented in the periphery on either the bright or the dark half of a black and white display. Importantly, subjects had to remember the exact location of the stimulus in only one of the two tasks. We observed a modulation of pupil size by background luminance in the delay period, but only when subjects had to remember the exact location. We interpret this as evidence for a tight coupling between spatial attention and maintaining information in SWM. Interestingly, we observed particularly strong modulation of background luminance at the beginning and end of the delay, but not in between. This is suggestive of strategic guidance of spatial attention by the content of spatial working memory when it is task relevant.

Investigating the parameters of transsaccadic memory: inhibition of return impedes information acquisition near a saccade target

ABSTRACT A limited amount of visual information is retained between saccades, which is subsequently stored into a memory system, such as transsaccadic memory. Since the capacity of transsaccadic memory is limited, selection of information is crucial. Selection of relevant information is modulated by attentional processes such as the presaccadic shift of attention. This involuntary shift of attention occurs prior to execution of the saccade and leads to information acquisition at an intended saccade target. The aim of the present study was to investigate the influence that another attentional effect, inhibition of return (IOR), has on the information that gets stored into transsaccadic memory. IOR is the phenomenon where participants are slower to respond to a cue at a previously attended location. To this end, we used a transsaccadic memory paradigm in which stimuli, oriented on a horizontal axis relative to saccade direction, are only visible to the participant before executing a saccade. Previous research showed that items in close proximity to a saccade target are likely to be reported more accurately. In our current study, participants were cued to fixate one of the stimulus locations and subsequently refixated the centre fixation point before executing the transsaccadic memory task. Results indicate that information at a location near a saccade landing point is less likely to be acquired into transsaccadic memory when this location was previously associated with IOR. Furthermore, we found evidence which implicates a reduction of the overall amount of elements retained in transsaccadic memory when a location near a saccade target is associated with IOR. These results suggest that the presaccadic shift of attention may be modulated by IOR and thereby reduces information acquisition by transsaccadic memory.

Spatial inhibition of return as a function of fixation history, task and spatial references

In oculomotor selection, each saccade is thought to be automatically biased toward uninspected locations, inhibiting the inefficient behavior of repeatedly refixating the same objects. This automatic bias is related to inhibition of return (IOR). Although IOR seems an appealing property that increases efficiency in visual search, such a mechanism would not be efficient in other tasks. Indeed, evidence for additional, more flexible control over refixations has been provided. Here, we investigated whether task demands implicitly affect the rate of refixations. We measured the probability of refixations after series of six binary saccadic decisions under two conditions: visual search and free viewing. The rate of refixations seems influenced by two effects. One effect is related to the rate of intervening fixations, specifically, more refixations were observed with more intervening fixations. In addition, we observed an effect of task set, with fewer refixations in visual search than in free viewing. Importantly, the history-related effect was more pronounced when sufficient spatial references were provided, suggesting that this effect is dependent on spatiotopic encoding of previously fixated locations. This known history-related bias in gaze direction is not the primary influence on the refixation rate. Instead, multiple factors, such as task set and spatial references, assert strong influences as well.

Feature integration is unaffected by saccade landing point, even when saccades land outside of the range of regular oculomotor variance

The experience of our visual surroundings appears continuous, contradicting the erratic nature of visual processing due to saccades. A possible way the visual system can construct a continuous experience is by integrating presaccadic and postsaccadic visual input. However, saccades rarely land exactly at the intended location. Feature integration would therefore need to be robust against variations in saccade execution to facilitate visual continuity. In the current study, observers reported a feature (color) of the saccade target, which occasionally changed slightly during the saccade. In transsaccadic change-trials, observers reported a mixture of the pre- and postsaccadic color, indicating transsaccadic feature integration. Saccade landing distance was not a significant predictor of the reported color. Next, to investigate the influence of more extreme deviations of saccade landing point on color reports, we used a global effect paradigm in a second experiment. In global effect trials, a distractor appeared together with the saccade target, causing most saccades to land in between the saccade target and the distractor. Strikingly, even when saccades land further away (up to 4°) from the saccade target than one would expect under single target conditions, there was no effect of saccade landing point on the reported color. We reason that saccade landing point does not affect feature integration, due to dissociation between the intended saccade target and the actual saccade landing point. Transsaccadic feature integration seems to be a mechanism that is dependent on visual spatial attention, and, as a result, is robust against variance in saccade landing point.