To establish how many future movements participants planned, we first asked whether participants were faster when extra future targets were visible. To quantify speed, we measured the inter-reach interval (IRI), defined as the time required to move the hand from the boundary of one target to the boundary of the next target (Figure 2). IRI was significantly reduced from Horizon 1 to Horizon 2 for all dwell times. The average reduction of IRI was 206 ms (t₍₁₀₎ = 22.76, p=3.02e-10), 232 ms (t₍₁₀₎ = 27.41, p=4.83e-11), and 246 ms (t₍₁₀₎ = 24.84, p=1.27e-10) for the 75, 200, and 400 ms dwell times, respectively. We also observed a further small 16 ms improvement from H2 to H3 in the 75 ms dwell time condition (t₍₁₀₎ = 3.137, p=5.30e-3). These results suggest that, at least for a dwell time of 75 ms, participants plan two targets ahead of the current reach.

Figure 2

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Because the reduction of IRI from H2 to H3 observed above was small, we performed a second experiment to test whether participants planned two movements into the future. That is, we occasionally displaced the target two reaches in the future (i.e. the +2 target) when the current (i.e. +0) target was captured. If information about the +2 target was not being used, we would expect to see no interruption in the sequence: both the movement toward the unperturbed +1 target, as well as to the jumped +2 target should not differ from unperturbed conditions (Figure 3B, solid line). We tested this prediction in the H3 condition with 75 ms dwell time.

Figure 3

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Our results indicate that participants used the information about the +2 target. We observed a normal reach toward the unperturbed +1 target. The reach time to the +1 target was not reliably different between the jump and no-jump conditions (t₍₉₎ = 0.63, p=0.54; Figure 3C, Execution +1). This was also true for dwell time inside the +1 target (t₍₉₎ = 1.98, p=0.08; Figure 3C, Dwell +1). However, movement time from the +1 to the +2 target was significantly longer in the jump condition (t₍₉₎=5.90, p=2.00e-4; Figure 3C, Execution +2).

One reason for this delay could be that visual displacement of the target was simply a distracting stimulus. However, this explanation is not consistent with our kinematic analysis which revealed participants reached toward the pre-jump +2 target, and then corrected their reach toward the new position of +2 target (Figure 3B, dotted line). We quantified this commitment to the pre-jump +2 target position by measuring the minimum distance between the reach trajectory and the center of the pre-jump +2 target (see Methods). The minimum distance was significantly lower in the jump condition (t₍₉₎=5.78, p=3.00e-4).

Together with the speedup of the overall movement (Figure 2), these results show that the reach to the +2 target was at least partially planned before the target jump, simultaneous with the reach to the +0 target and planning of the reach to the +1 target (Figure 3A).

Our previously described results indicate that multiple future movements are planned at the same time. Consequently, we next asked whether these preparatory processes are independent of each other or if they interact.

We tested whether two future movement plans interact by jumping the position of the +1 target when the +0 target was captured. This was done under the 75 ms dwell time. We compared the speed of the correction in the H2 and H3 conditions (see Figure 4A and Methods). Although the two conditions had similar kinematics, participants could only plan the +1 target in the H2 condition, whereas they could plan both the +1 and +2 targets in the H3 condition (Figure 4A). If the +1 and +2 targets are planned independently, the movement correction to a displacement of the +1 target should be the same in the H2 and H3 conditions. Alternatively, if the movements interact – if they are planned together or share limited resources – the correction should be slower in the H3 condition because some of the resources would be assigned to planning the +2 target.

Figure 4

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Consistent with an interaction between future plans, we found that the corrections for a +1 target jump were longer and slower in the H3 condition than in the H2 condition (Figure 4B). In both conditions, participants failed to correct the movement before arriving at the pre-jump position of the +1 target (Figure 4B). In the H3 condition, both the movement time (t₍₉₎ = 4.85, p=1.80e-3) and the trajectory length (t₍₉₎ = 6.19, p=3.00e-4) of the corrective movement were longer than that of the H2 condition. The longer correction trajectory was due to participants moving onward to the +2 target without having corrected for the displaced +1 target. We again used the minimum distance between the corrective reach trajectory and the +2 target to quantify this effect (Figure 4C). The corrective reaches were closer to the center of the +2 target in H3 condition (t₍₉₎ = 4.28, p=4.00e-3).

In summary, it took more time to update the +1 movement plan when participants could simultaneously plan both the +1 and +2 target as compared to when they could only plan the +1 target. This effect indicates that planning a reach to the +2 target occupied some part of a shared computational resource such that less of the resource was available for updating the reach to the +1 target. These results indicate a clear interaction between the planning processes for future movements.

So far, we have established that people plan reaches to multiple future targets and that these planning processes interact with each other (Figure 5A). An extreme version of such an interaction is that the two future reaches are planned as a single unit, as a ‘motor chunk’ (Figure 5B; Ramkumar et al., 2016). Our data, however, are not consistent with the idea that future reaches are planned as a motor chunk.

Figure 5

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First, an important indicator of chunking is that, after a chunk is executed, there is a short delay until the next chunk is planned. For instance, in the H2 condition, since two targets are shown on the screen at any given time, the participants could execute two fast reaches, followed by a long pause in which they prepared the next chunk of two reaches. However, except for H1 condition, where the participants had to pause and wait for the next target to appear, the speed profiles of other horizon conditions showed no evidence of such pauses (Figure 1—figure supplement 1).

Second, chunked planning predicts that a disturbance in any segment of the chunk would affect the whole chunked segment. We tested this prediction in two types of jump experiments. In the H3 condition, where participants could potentially plan +1 and +2 reaches as one chunk, we occasionally either jumped the position of the +2 target (Figure 5C) or the +1 targets (Figure 5D) when the +0 target was captured. Chunked planning predicts that both jumps should cause a disturbance in the first reach of the chunk, but this did not occur. When we jumped the +2 target, the participants performed the reach to the +1 target in a manner identical to the no-jump condition (t₍₉₎ = 0.60, p=0.56). Additionally, when we jumped the +1 target they still went through the pre-jump +1 target but their movement was significantly shortened by deviating toward the new position of the +1 target (t₍₉₎ = 14.36, p=1.64e-7) (Figure 5E).

In summary, participants were able to correct the second segment of their movement without causing any disturbance in the first segment. This observation provides clear evidence against chucked planning of the future reaches.

The experiments above indicate that reach planning to the +1 and +2 targets interact with each other. Such interactions could allow the motor system to optimize the set of movements leading to systematic co-articulation of movement segments. In other words, when the visual information of the future target is available, each movement in the sequence could be planned in a way that accounts for the movement that comes after it.

Indeed, we observed systematic co-articulation of movements in the H3 condition (Figure 6A). When the +2 target demanded an upcoming rightward turn, the +1 reach curved left, and vice versa (Figure 6B). Although this deviation led to a longer overall trajectory, it reduced the required turning angle at the +1 target. To summarize the effect of future target on curvature, we fit a linear model that predicted the signed curvature value of the current reach based on two independent variables: the turning angle toward the +2 target, and the incoming angle of the previous reach (see Figure 6C and Methods). Note that this model has the advantage over simple averaging because it accounts for the trivial curvature changes caused by the previous movement. The model was fit for each dwell time and horizon separately. Figure 6C shows the average curvature for all possible +1 target angles, corrected for the influence of the last target. To summarize the co-articulation effect across all the angles, we fit a line between five values of angles and the curvature (Figure 6B, black line). The slope of the line summarizes the strength of the curvature effect (Figure 6D) for each dwell time and horizon condition.

Figure 6

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In the H1 and H2 conditions, the slope was not reliably different from zero, indicating no systematic co-articulation. This observation is expected for H1 since the +2 target was not on the screen during the planning or execution of the investigated reach. Notably, we did not observe the curvature effect in the H2 condition in which the +2 target was on the screen only during the execution of the +1 reach. This suggests that co-articulation of segments cannot happen if planning of the next segment happens during the execution of the previous one. In the H3 condition, the slope was reliably smaller than zero for all the dwell time conditions, indicating systematic co-articulation once parallel planning was feasible. In the case of the 75 ms dwell time, the co-articulation kept growing from H3 to H4 (t₍₁₀₎ = 5.54, p=2.60e-03). We observed no reliable increase in co-articulation for Horizon>3 for the 200 ms (t₍₁₀₎ = 0.19, p>0.98) or 400 ms dwell times (t₍₁₀₎ = 0.38, p>0.99).

Overall, we observed less co-articulation for longer dwell times. Dwell time can have a dual role here. On the one hand, longer dwell times mean the participants have more time to benefit from future targets because they see the targets longer, potentially leading to more co-articulation. On the other hand, longer dwell times mean the participants had to stay stationary in the target for longer, making the movements less mechanically integrated, and therefore decreasing the benefit of co-articulation. To distinguish between these potential contributions of dwell time, we plotted the curvature effect versus the time that participants could see both the +1 and +2 targets before starting the +1 movement (Figure 6E). Both horizon and dwell time led to more overlap in planning times. For all dwell time conditions, the curvature effect increased between H2 and H3 conditions, and then saturated after the H4 condition. However, with longer dwell times, the overall rise and saturation of the curvature effect was smaller (F_(2,20) = 16.71, p=6.00e-04), suggesting less interaction between planning processes when the movements are biomechanically separated.

Together, these results show that the biomechanically advantageous co-articulation between segments of the sequence occur when the segments are planned together.

Given that participants used visual information from two targets ahead, we were curious whether the availability of future targets influences participants’ eye-movement strategy, or whether they acquired this information parafoveally.

We collected data from a separate group of 19 participants in the same task, only focusing on Dwell time 75 ms, and H1, H2, and H3 conditions. We found that in ~95% of all reaches in all trials, participants made only one saccade per reach, indicating they primarily focused on the immediate next target with information about subsequent targets likely being processed through parafoveal vision. We assessed the timing of the saccades by measuring the saccade time relative to hand position (Figure 7A and B). The saccade to the next target occurred after the current target disappeared, and right before the hand exited the disappeared target. The relative timing between the saccade and the hand exiting the target was consistent across different horizons (F_(2,36) = 1.92, p=0.16).

Figure 7

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Next, we characterized the fixation location. If the visual information of the next target is received through the parafoveal vision, then it would be beneficial to shift the fixation location toward the future target. As shown in one representative participant (Figure 7C), we found that saccade angle is shifted toward the position of the future target in the H2 and H3 conditions. At the group level, the saccade angle was significantly different for different horizons (F_(8,128) = 12.60, p=3.12e-13). In Horizon 1, as expected, the average saccade angle for different targets was identical since the future target was not shown. For both Horizon 2 and Horizon 3, the angle of the saccade was systematically shifted toward the position of the upcoming target.

Together, these results suggest that information about future targets is received parafoveally, and the fixation location is systematically shifted to facilitate this process.

In a previous finger sequence study, using a similar horizon manipulation to the one used here, we found that participants executed sequences faster when they had information about multiple future finger presses (Ariani et al., 2021). This benefit increased up to horizon of three future finger presses (H3) and then plateaued. Consistent with these findings, we observed a large reduction in movement time when participants were provided with one future reach target (Figure 2, H1 to H2). However, except for the shortest (75 ms) dwell time, the availability of a second future target (H2 to H3) did not further reduce movement time (Figure 2). In these longer (200 and 400 ms) dwell times, we did not observe faster performance for more knowledge of future target positions, likely because the participants had sufficient time to complete planning during the dwell period. Another possible reason for the more pronounced effect of horizon on movement speed in finger presses may be attributed to the nature of the effectors. Specifically, in reaching movements, the arm cannot initiate the next reach before completing the previous one. In contrast, with finger movements, future finger flexions can commence in advance, potentially resulting in faster execution of the sequence (Popp et al., 2022). It is also possible that this difference arises because the transformation of the visual cue to motor plans is faster for the direct spatial mapping used here than for the more abstract number-to-finger mapping used in our previous study (Diedrichsen et al., 2001; Goodman and Kelso, 1980). Even though the planning of multiple future movements, as measured by IRI, could only be seen in shortest dwell times, our experiments with target displacements provide clear evidence that participants had planned two movements ahead (Figure 3). Overall, these observations suggest that the availability of the second reach target can be more significant when faster execution of the task demands faster transformation of visual cue to muscle commands, or when the cue-to-action mapping is more demanding.

If participants plan multiple future movements at the same time, the next question is whether these preparatory processes run independently or if they interact with each other. We investigated these possibilities by jumping the target that participants were about to reach toward. The participants corrected the reach only after initially reaching toward the pre-jump position of the target (Figure 4B). This behavior is similar to that shown in the work by Ames et al., 2019, where target displacement during execution led to an initial commitment to the pre-jump position of the target followed by a smooth corrective reach toward the new target position. Neurally, the authors showed that resource distribution in M1 and PMd is accomplished by re-planning the corrective reach in a subspace orthogonal to the one controlling the ongoing movement (Ames et al., 2019). Here, we asked whether the re-planning process depended on any other planned future movement (Figure 4). Interestingly, the corrections were slower when more future targets were known to the participants (Figure 4B), indicating some interaction between the two future planned reaches. This interaction could come in multiple forms. One possibility is that the neural resources dedicated to re-planning have to be split between preparation of future targets, slowing the re-planning of the next movement (Kornysheva et al., 2019). Alternatively, the two future movements may be prepared as a chunk (Ramkumar et al., 2016), and changing the entire chunk may take longer time than changing a single movement. The latter possibility seems unlikely since the results from jumping the +1 or +2 target within the same horizon of future target can be corrected separately (Figure 5). Either way, by probing the planned state with target perturbations we clearly demonstrate an obligatory interaction between multiple future movement plans.

We also provide evidence that the interactions between future movement plans can optimize kinematics of single reaches for the next reach in the sequence. When the planning processes of two future reaches overlapped sufficiently, we found changes in the curvature of the current reach that anticipated the direction of the next reach target. The curvature was opposite to the direction of the next target, making this co-articulation advantageous from a biomechanical point of view (Figure 6D). The observed curvature interaction can again be either due to fully chunked planning of two elements, or alternatively, due to separate, yet interactive, planning of the two reaches. The former possibility seems less likely since the interaction was observed even when movement segments were fully separated by a long dwell time (Figure 6D, Dwell 400).

What implications do our results have for the neural processes underlying the online planning of multiple future actions? Previous neurophysiological investigations showed that individual neurons can be involved in both the planning and execution of phases of a movement (Churchland and Shenoy, 2007; Crammond and Kalaska, 2000; Elsayed et al., 2016; Kaufman et al., 2014; Pruszynski et al., 2014). Nonetheless, when two movements are concatenated, the planning of the second movement can be proceeded in parallel with the control of the first movement. This lack of interference can be explained by the fact that planning and execution proceed in orthogonal neural subspaces (Zimnik and Churchland, 2021).

The phenomena demonstrated in this study raise the question of how the planning processes for multiple future movements are realized in the brain. One hypothesis is that the two future movements are also planned in orthogonal neural subspaces without any interactions during the planning phase. Under this hypothesis, the co-articulation we report would arise from an interaction between the execution dynamics associated with the current movement and the planning dynamics of the second planned movement. An alternative hypothesis is that the preparation processes of the next two movements directly interact with each other, and possibly are even encoded in partly together (Fusi et al., 2016; Rigotti et al., 2013). Our results are suggestive of the latter scheme since we observed no co-articulation when the next target was only available during execution of the current reach (Figure 6D, H2). Nevertheless, careful electrophysiology experiments are necessary to investigate the exact mechanism by which planning processes interact. The current paradigm provides a useful framework to do so.

In our sequence task, participants switched their gaze location only once per reach, suggesting that information about the location of the next target is perceived parafoveally (Figure 7A). This observation aligns with previous studies (Clavagnier et al., 2007; González-Alvarez et al., 2007; Sivak and MacKenzie, 1990) that found participants keep their visual attention on the current sequence item and can perceive the location of spatial targets even when foveal vision is occluded. However, when comparing gaze locations for conditions Horizon>1, we observed that participants systematically biased their gaze location based on the sequence context. The gaze position shifted toward the next target, potentially allowing for more accurate location estimation (Figure 7C and D). Notably, changes in gaze location were observed even in Horizon 2, despite no changes in the curvature of hand movements in this horizon (Figure 6B). This suggests that information about the next target may first be available in the circuitry that controls eye movements and later in the cortical areas that control voluntary upper limb movements. Further control studies are required to investigate this hypothesis.

Eleven participants (4 female) with an average age of 23.3 years (4.4 SD years) completed five experimental visits for this study (~10 hr data collection per participant); this data was used for IRI (Figure 2) and curvature analysis (Figure 6). Ten of these participants returned for two experimental visits where they were tested on target jump experiments. They were all right-handed with average handedness of 78 (24 SD), measured by the Edinburgh Handedness Inventory. For eye position analysis, we recruited a different group of 20 right-handed participants (2 female) with average age of 21.2 years (2.0 SD years), one participant was excluded from the analysis due to low quality of data (see Eye-tracker analysis below).

All participants reported no prior history of musculoskeletal, neurological, or psychiatric disorders. All the participants provided informed consent in the first session, and they were remunerated CA$ 15 per hour in the seventh and last session of the study. All the procedures were approved by the Health Sciences Research Ethics Board at the University of Western Ontario (Project ID 115088).

Participants performed all experimental trials in an exoskeleton robot (Kinarm, Kingston, ON, Canada). The participants were seated on a height-adjustable chair while their right arm rested comfortably on the robot arm, which supported the elbow and shoulder weight against gravitational force and allowed them to freely move their hand in the horizontal plane. Arm kinematics were recorded at 1000 Hz. All the reaching targets were presented by a horizontally placed monitor onto a mirror which occluded the vision of the participant’s arm (Figure 1A). Participants’ eye movement was recorded using an SR Research Eyelink 1000 at 1000 Hz. The eye tracker also recorded the participants’ head movement by recording the position a bullseye target attached to the participants’ front. The eye position was subtracted from the bullseye position to correct for small head movements during the task.

In each experimental trial, participants performed sequences of 14 reaches. The sequences were generated from a hexagonal grid of equidistant circular targets (see Figure 1A and B). The radii of the targets were 1 cm, and the center of neighboring targets was 4 cm apart. The participants’ arm was occluded – they only saw a circle with radius of 0.5 cm aligned with the tip of their index finger as their hand feedback. The sequences always started from a fixed home target in the center of the working space. We generated sequences according to two rules. First, the next target in the sequence should be a neighbor of the previous target. This ensured that all the reaches were 4 cm apart. Second that there were no loops smaller than five reaches. This ensured that, when multiple future targets were presented, they did not overlap. The participants were instructed to move their right hand in the home target to start a trial. Once the hand was in the home target, either one, two, three, four, or five future targets of the sequence appeared on the screen (depending on the horizon condition); brightness indicated the order of targets, with the brightest target being the immediate next target. The participants were instructed to stay in the home target for 300 ms, after which they received a go cue by the disappearance of the home target. The participants were instructed to always move their hand to the brightest target and stay in the target until it was ‘captured’. Once one target was captured, the captured target disappeared, the brightness of the targets was updated, making the next target the brightest, and a new target appeared at the end of the horizon. This process was repeated until all 14 targets were captured. If the participant failed to stay in the target for the dwell time or the initial wait time in the home target, the trial was interrupted with an error message and rejected. Interrupted trials were repeated later in the session.

Our experiments manipulated two parameters: how much time participants had to stay in each target to capture it (dwell time), and how many future targets were on the screen (horizon). The dwell times could be 75, 200, or 400 ms. In the horizon conditions (H1 to H5), 1–5 future targets were visible. In the case of H1, the task is reduced to a sequential reaction time task, and with longer horizons, participants could potentially plan multiple future movements ahead of time.

The entire experiment had seven sessions. The first five sessions were designed to get a time and curvature analysis in all dwell and horizon conditions. The last two session added the jump experiment.

The first five sessions measured performance in 15 conditions (3 dwell times × 5 horizons). Each session consisted of three blocks of 120 trials for each dwell time, and the horizon was randomized across trials totaling 360 trials per session. The order of dwell time blocks was randomized across five sessions for each participant. Each session of data collection was 1 hr and 15 min on average. As the first step, for each trial, we broke down the full sequence of reaches to their constituting single reaches by segmenting the full sequence trajectory whenever a target was captured. This led to a set of 14 individual reaches starting from each target and ending in the next. For all the analysis we were interested in simultaneous planning and execution processes, therefore we excluded all targets that were visible in the beginning and could therefore be pre-planned. We also excluded one to five targets at the end of each sequence since there was no need to plan future targets anymore. The number of excluded reaches changed with the horizon. For instance, in the H1 condition, we excluded the first and the last reach in the sequence.

Given our hexagonal grid, for each reach, there could be a maximum of five potential next target positions. However, near the boundaries of the workspace, the number of potential next targets decreases so the participants could potentially predict the overall position of the upcoming target and plan for it ahead of time (Glaser et al., 2018). To ensure that this possibility did not affect our results, we only considered reaches with five potential future choices. This excluded the reaches toward and parallel to the boundaries of the workspace.

For the analysis of movement time, we computed IRI, defined as the time the hand entered a one target until it entered the next one. We subsequently averaged IRI values across all the reaches of a trial, all trials, and all sessions of each participant. The IRI contains both the time that the hand passed through the target and the time that the hand was moving between the two targets.

For the curvature analysis, we assessed the effect of the position of the +2 target on the curvature of the reach toward the +1 target. We started by aligning all the reaches: First, we translated the position of the +0 target (where the hand is sitting), the –1 target, the +1 target, and the reach trajectory so that the position of the +0 target is set to the center of the 2D coordinate system (0,0) cm. This ensures that all the reaches start from the same position. Next, we rotated the targets and trajectory around the +0 target so the position of the +1 target rests at (4,0) cm coordinates. This ensures that all the reaches have the same directions. With these transformations, the angle of the line connecting the +1 target to the +2 target, relative to the horizon line, connecting the +0 target to the +1 target, can be either −120,–60, 0, 60, or 120 degrees. The same is true for the angle of the line connecting the –1 target to the +0 target.

Next, we quantified the curvature of +1 reach. We used all the translated and rotated reaches of all the participants. To make the length of the reaches equal, for each reach, we took 100 equally distant spatial samples along the horizontal line connecting the center of the start target to the center of the end target of the reach. Then, we performed a PCA on the matrix containing the y coordinate values of each reach. The size of this matrix was (# reaches × 100). The first and the second PCs were arc-shaped and S-shaped ‘eigen reaches’ each accounting for 72% and 17% of the total variance. We then projected each reach onto the first eigen reach and used the resultant scalar value as a measure of curvature. The absolute value of this scalar shows the amount of the curvature, and the sign indicates the direction of the curve. We used all the reaches of all the participants to calculate the PCs, and then for each participant and condition, the curvature value was calculated separately. This ensured that the comparison between the conditions and averaging across participants are meaningful.

Finally, we were interested in the effect of the +2 target angle on the curvature of the reach to the +1 target. However, the curvature of a reach in a sequence also depends on the previous reach, therefore, to account for this effect, we fitted a linear model that predicted the signed curvature value of each reach based on the position of the previous target (angle of –1 target), next target (angle of +2 target). The angles were one-hot coded, resulting in one regressor for each angle; therefore, the beta values represent the effect of each input angle onto the curvature effect. This process was performed for each of the dwell time and horizon conditions separately. Finally, as summary statistics for the effect of all the one-hot coded values the outgoing target (+2 target effect), we fitted a line to beta values for each of the five angles. We used the slope of this line as a summary of the overall effect. Zero slopes indicated no curvature effect, the value and sign of the slope show the strength and direction of the effect, with a negative slope showing curvature toward the opposite direction of the next target, and vice versa.

For the last two data collection sessions, we focused on the 75 ms dwell condition and two of the horizons (H2, H3). All other parameters including the grid of targets, length of the sequence, size of the targets, etc. were identical to the first five sessions. In these experiments, only one jump of a target could happen in each trial. The jump happened randomly between the 4th and 10th reach of the sequence. We interleaved many no-jump trials in these sessions to avoid anticipation or adaptations for the jumps. The order of these two last sessions was randomized across participants.

The +1 jump experiment consisted of 400 trials, 200 target jumps in H2 and H3, interleaved with 200 no-jump trials with randomized across horizons. In the case of a jump trial, we displaced the next target (+1 target) exactly when the current target (+0 target) was captured. Before the jump, a pre-jump +1 target was shown on the screen, and then, at the moment of the jump, that is when the 75 ms dwell time was satisfied and the current target (+0 target) was captured, we removed the pre-jump +1 target and a new +1 target appeared on the screen. Both the new and pre-jump +1 target were selected in a way that was compatible with the current position of the +2 or +3 targets on the screen, in other words, the jump was compatible with the rules of generating sequence in the task. This jump happened both in the context of Horizon 2, with two future targets, and in Horizon 3, with three future targets presented on the screen.

The +2 jump experiment was performed only in Horizon 3 (H3) condition. There was a total of 300 trials. Two-third of them were no jump; in the remaining one-third, exactly at the movement that the current target (+0 target) was captured, the second future target (+2 target) jumped to a new position, and the position of the next target (+1 target) remained unchanged. Before the jump, we showed a temporary +2 target (pre-jump +2 target) on the screen, and the jump happened with the disappearance of the pre-jump +2 target and the appearance of a new target as the new +2 target.

For pre-processing of eye-tracker data, we first removed trials if the eye position was not recorded for a consecutive 600 ms. This missing data could be due to blinks or the eye tracker momentarily losing the eye position. We removed one participant due to low number of good trials. Then for the remaining trials we first partitioned each trial to 14 segments based on the time point that participants’ hand entered a new target. Then, within each segment we applied a fixed threshold on the derivative of eye position to detect the time point when the saccade occurred. Next, we used the average eye position before and after saccade for analysis of the saccade position. In 95% of the trial only one saccade happened in each reach. The eye position before and after saccade was centered on a circle with radius of 2 cm around the start and end target, respectively. These pre-processing steps were performed blind to the trial type. To analyze the changes in saccade position based on horizon, like curvature analysis, for each participant we first translated and rotated all the reaches and eye positions so that the start target (+0 target) and end target (+1 target) of the reaches are at (0,0) and (4,0) coordinate, respectively. Then for each horizon, we averaged the post-saccade eye position for each possible +2 target position.

We employed a within-subject design. All the analyses were performed in RStudio 22.07.1. For analysis of IRI and curvature effect, we used two-way repeated measures ANOVA. Factors were dwell time (three levels), horizon (five levels: H1 to H5), and (dwell time × horizon) interaction. For comparison between different levels of each significant factor, we adjusted p-values for multiple comparisons using Holm method. For the jump +1 target experiment, we used a repeated measures two-way ANOVA with jump (two levels) and horizon (two levels) as factors. Correction for multiple comparisons was similar to the IRI analysis. The details of statistical analysis including the degrees of freedom, the test statistic, and the p-value are provided in the text.

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.

This work was supported by a CIHR Project Grant to JD and JAP (PJT-175010). JAP received a salary award from the Canada Research Chairs Program.

All the participants provided informed consent in the first session, and they were remunerated CA$ 15 per hour in the seventh and last session of the study. All the procedures were approved by the Health Sciences Research Ethics Board at the University of Western Ontario (Project ID 115088).

1. Preprint posted: November 13, 2023
2. Sent for peer review: December 11, 2023
3. Reviewed Preprint version 1: February 7, 2024
4. Reviewed Preprint version 2: August 1, 2024
5. Version of Record published: September 2, 2024

You can cite all versions using the DOI https://doi.org/10.7554/eLife.94485. This DOI represents all versions, and will always resolve to the latest one.

© 2024, Kashefi et al.

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